|Year : 2011 | Volume
| Issue : 4 | Page : 507-521
Past, present & future scenario of thalassaemic care & control in India
Ishwar C Verma, Renu Saxena, Sudha Kohli
Center of Medical Genetics, Sir Ganga Ram Hospital, New Delhi, India
|Date of Submission||18-Aug-2011|
|Date of Web Publication||15-Nov-2011|
Ishwar C Verma
Director, Center of Medical Genetics, Sir Ganga Ram Hospital, Rajender Nagar, New Delhi 110 060
| Abstract|| |
The first case of thalassaemia, described in a non-Mediterranean person, was from India. Subsequently, cases of thalassaemia were documented in all parts of India. Centres for care of thalassaemics were started in the mid-1970s in Mumbai and Delhi, and then in other cities. The parent's associations, with the help of International Thalassemia Federation, greatly helped in improving the care of thalassaemics. Obtaining blood for transfusion was difficult, but the Indian Red Cross Society and the parent's associations played a crucial role in arranging voluntary donations of blood. Chelation with deferoxamine was used sparingly due to the high cost. The Indian physicians conducted trials with deferiprone, and the drug was first approved and marketed in India. Deferasirox is also now being administered. Studies of physical and pubertal growth documented significant retardation, suggesting that generally patients receive inadequate chelation and transfusions. Bone marrow transplantation is available at a number of centres, and cord blood stem cell storage facilities have been established. Information about mutations in different parts of India is available, and ThalInd, an Indian database has been set up. There is a need to set up preimplantation genetic diagnosis and non-invasive prenatal diagnosis. It is argued that too much emphasis should not be placed on premarital screening. The focus should be on screening pregnant women to yield immediate results in reducing the burden of this disorder. Care of thalassaemia has been included in the 12 th 5-year Plan of the Government of India. Many States now provide blood transfusions and chelation free of cost. Although inadequacies in care of thalassaemia remain, but the outlook is bright, and the stage is set for initiating a control programme in the high risk States.
Keywords: Blood transfusion - bone marrow transplantation - carrier screening - chelation - control - cord blood storage - prenatal diagnosis - prevention - thalassaemia care
|How to cite this article:|
Verma IC, Saxena R, Kohli S. Past, present & future scenario of thalassaemic care & control in India. Indian J Med Res 2011;134:507-21
|How to cite this URL:|
Verma IC, Saxena R, Kohli S. Past, present & future scenario of thalassaemic care & control in India. Indian J Med Res [serial online] 2011 [cited 2014 Apr 17];134:507-21. Available from: http://www.ijmr.org.in/text.asp?2011/134/4/507/89888
| The early years|| |
In 1925 in a meeting of the American Pediatric Society, Cooley and Lee reported children of Mediterranean extraction with anaemia, splenomegaly and peculiar changes in bones  . In 1938 Mukerjee  published "the first recorded case of thalassemia on east side of Suez". The case was observed by Dr M. Bose of the Campbell Medical School & Hospital, Calcutta (now Kolkata) in a Hindu boy aged 30 months. This case established that the disease may be found in children of non-Mediterranean parentage, and thus justified scrapping of the designation "Mediterranean disease". Subsequently, in 1939 three reports appeared in India - by Coelho in two Muslim sisters from Bombay  (now Mumbai), by Napier and Dasgupta from Kolkata  , and by Patel and Bhende from Bombay (now Mumbai) in a Brahmin boy of 5 yr  . Cases were recognized and reported from other parts of India, such as Punjab  , Kolkata  , Delhi  , Mumbai  , Bihar  , Orissa  , Andhra Pradesh  , Chandigarh  , and Rajasthan  .
The first case of β-thalassaemia/Hb E disease in India was reported by Chatterjee et al, and that of β-thalassaemia/sickle cell disease by Naik and colleagues . Subsequently other variants haemoglobins were reported - C, D, F, G, H, J, K, L, M, Q (India), G, etc,,,, . Haemoglobins S, D and E were observed to be quite common: Hb S has been found mostly in tribal communities, Hb D in Gujaratis and Punjabis and Hb E in Bengalis, Assamese and Nepalese.
| Molecular studies|| |
The earliest reports of polymorphisms in the β-globin gene in Asian Indians, that gave rise to the characteristic haplotypes of the different mutations, were reported by Kazazian and his colleagues in March 1984  . This group was also the first to report the common seven mutations and their haplotypes in the Indians - Frameshift/8-9 (+G), Nonsense codon 15 (TGG-TAG), Frameshift/41-4 (-TCTT ), Frameshift 41-4 ( TCTT), Frameshift/16 (- C), IVS-1 nt 5 (G-C), 619-bp deletion 13 and 25 nt deletion, at 3' end of the gene. Deletion of 619 bp was shown to be a common mutation in the Asian Indians  . Thein et al showed a single origin of this deletion mutation in the Asian Indians. In the same year, Old and colleagues  showed the feasibility of prenatal diagnosis in Asian Indians by DNA polymorphism analysis. Subsequently several publications emanated from these experts on mutations among Indian subjects, their regional distribution and some rare mutations ,, . They published their experience on prenatal diagnosis using mutation analysis in 1990. Data on the different mutations both from USA and UK were derived from study of subjects going for evaluation of pregnancies to avoid the risk of having an abnormal child. This trend continues even today, as molecular studies are mostly undertaken when women come for prenatal diagnosis.
| Distribution of mutations in different parts of India|| |
The distribution of mutations in various parts of India has been reported by a number of investigators ,,,,,, . New mutations have been reported by the predominant groups working in this field in different parts of India from Vellore , , Mumbai , , Delhi  , and Chandigarh . Old and colleagues published a multi-centric study on mutations in β-thalassaemia major patients from India, Pakistan, Thailand, Iran and Syria  . This paper gives the primer sequences for amplification refractory mutation system (ARMS) technique of all mutations common in these countries. Sinha et al reported a meta-analysis of regional distribution of 8,505 alleles with 64 β-globin gene mutations. Nationally, IVSI-5(G>C), 619-bp del, IVSI-1(G>T), Codon 41/42(-TCCT) and Codon 8/9(-G) comprised the five most common disease mutations, and accounted for 82.5 per cent of all mutations. Codon 15(G>A), codon 30(G>C), cap site +1(A>C), codon 5(-CT) and codon 16(-C) accounted for an additional 11.0 per cent of all mutant alleles. The Western region (Maharashtra, Gujarat and Rajasthan) has a higher prevalence of the 619-bp deletion (14.2%) and IVSI- 1(G>T) (8.7%), and with codon 15(G>A) as the fourth commonest mutation (7.6%). In the northern region (Uttar Pradesh, Punjab, Haryana, Himachal Pradesh, Uttarakhand and Jammu and Kashmir IVSI-5(G>C) accounted for 44.8 per cent of β-thalassaemia alleles. The five most common mutations closely match the national pattern, with codon 16(-C) and -88(C>T) in the list of ten common mutations along with codon 15(G>A), codon 30(G>C) and cap site +1(A>C). The four southern States (Andhra Pradesh, Karnataka, Tamil Nadu and Kerala) have a predominantly Dravidian population, ethnically and culturally quite distinct from the largely Indo-European populations of the north. IVSI-5(G>C) has a prevalence of 67.9 per cent, the 619-bp deletion is present in only 1.8 per cent of cases, whereas the second commonest allele (8.8%) is codon 15(G>A). Poly A site (T>C) is the third most common allele (4.7%). The east region exhibited the highest prevalence of IVS I-5(G>C) at 71.4 per cent, with codon 30(G>C) and codon 15(G>A) the second and third most common alleles, accounting for 5.8 and 5.4 per cent of the total, respectively.
Codon 15 (G>A) occurs in about 35.3 per cent of all subjects resident in Maharashtra. The high percentage of -88(C>T) alleles in cases from Punjab can be ascribed to the frequency of this mutation in the Jat-Sikh community. Likewise, the high prevalence of Codon 5(-CT) in Gujarat (79.7%) is associated with the Lohana and Prajapti communities in that State. Although the Poly A(T>C) allele has been reported in the populations of nine States, 65.6 per cent of cases originated in the adjacent southern States of Tamil Nadu and Karnataka. Gorakshakar et al showed that the mutation codon 47 (+A) was common among the Nicorbarese in Andaman Islands. Two mutations (IVS I-5 (G->C and CD15 (G->A) account for over 90 per cent of the mutant alleles among the tribal populations. The collation of data by Sinha and colleagues has culminated in the establishment of the database for mutations in the β-globin gene in India . The resource ThalInd (http://ccg.murdoch.edu.au/thalind) incorporates and provides data pertinent to molecular genetics, population genetics, genotype-phenotype correlations, disease burden and infrastructural assessment. Importantly, the resource also has been aligned with the administrative health system and demographic resources of the country.
| Interaction of β-globin gene with other genes|| |
Interaction of β-globin gene with other genes in India has been examined by many investigators ,,,,. Kulozik et al showed the interaction of α gene abnormalities with sickle cell disease. This opened the path for study of the interaction among the various genes in cases of thalassaemia. Garewal et al showed the interaction of mutations in the β-globin with those in the α-globin gene in causing variations in phenotype in subjects from Punjab and Maharashtra. Verma et al  in a multi-centric study showed the interaction of β, α and γ genes in causing thalassaemia intermedia. This study demonstrated that in cases of thalassaemia intermedia when the β-thalassaemia mutations were of the β+ variety, these were accompanied by mutations in the α-globin gene as the ameliorating factor. In the presence of β0 -thalassaemia mutations or Hb E the ameliorating factor was positivity of Xmnl1 (G) polymorphism at -158 (C>T).
| Management|| |
In 1990, an important study on the care of thalassaemic patients in Mumbai highlighted the significant, unavoidable and increasing demand on the public health services by patients with β-thalassaemia major . The situation was also characterized by evasion of the problem, failure of planning, no provisions for prevention, and inadequate treatment leading to premature death among the affected children. Most couples (90%) of reproductive-age felt that prenatal diagnosis was a necessity. Ignorance and prejudice in the community led to social isolation for many families. Another study group reported that most thalassemics were not satisfied with their body image  . Almost all the study subjects felt that the disease did not affect their family or social relationships. The adolescents were anxious about their future health and education. Majority of the subjects (80%) did not discuss their disease and its related problems with their friends. They mainly depended on their parents for monetary and emotional support. Recently they reported on growing up with families of thalassaemics using an accelerated longitudinal design  .
The history of management of thalassaemia in India has followed the success story of thalassemia care in the West. Excellent articles on management of thalassaemia have been published by Indian authors ,,, . Only selected aspects of the management are covered below.
(i) Blood transfusions:
In the initial years the major problem was to obtain blood for transfusions. Marwah  has estimated that in India 2 million units of packed red cells are required for transfusion to thalassaemic patients. The patient organizations were crucially important in ensuring supplies of blood by arranging donations at camps, factories and workplaces. The Indian Red Cross Society (IRCS) also played a stellar role in collecting donations of blood. The Indian Red Cross Society with its 110 blood banks spread across 14 States contributes to about 10 per cent of the demand of blood in the country  . In Delhi, IRCS, blood bank is operational round the clock, collects nearly 30,000 units a year, and supports nearly 50 per cent of thalassaemic children with free supply of blood in the National Capital Region (NCR) territory. Bhattacharya et al used umbilical cord blood to transfuse patients with thalassaemia major, as a source of red cells as well rich source of foetal haemoglobin.
In the early years most of the blood donations were obtained from the relatives or professional donors. Therefore, ensuring safety was difficult, and some cases of transmission of HIV through blood donations were described. In 1987, the Government of India set up the National AIDS Control Organization (NACO )  . One of its main mandates was ensuring safe blood for transfusion by proper screening of blood and blood products throughout the country. In 2003, a National Blood Policy was enacted to ensure safe blood (http://www.naco.nic.in). In 1992-1999 NACO launched a scheme (NACP I) to modernize blood banks by providing government assistance to States to upgrade and provide minimum facilities to blood banks in the public sector, as well as those run by charitable organizations. The assistance facilitated purchase of equipment, consumables, test kits, blood bags, reagents, etc. Many reports appeared on the transmission of HIV, hepatitis B and C viruses in a high percentage of thalassaemic patients who received multiple transfusions during 1990-2003 ,,, . Now, all the blood banks supply blood that has been tested for malaria, syphilis, hepatitis B, HIV and hepatitis C. Currently, there are about 7000 blood banks in the country  . Of these 36.0 per cent are in the Government sector, 14.4 per cent are voluntary, 28.8 per cent are private, 20.7 per cent are private charitable  . Due to the stringent control of blood banks the transmission of infections through blood is now negligible.
( ii) Chelation:
The second major issue was chelation to remove the excess iron in the body resulting from repeated blood transfusions. In the early years desferal (deferoxamine, DFO) was the only chelator available. It was used for almost four decades, and proved its worth. However, its use has a number of problems - it has to be given intravenously for many hours using a pump, and it is expensive. Therefore, compliance is poor. George J. Kontoghiorghes discovered an oral iron chelator deferiprone (L1), a drug designed and developed by academic initiatives  . Indian scientists ,,, and patients contributed immensely in the clinical trials for L1. It was finally approved for use in India in 1994, and in Europe in 1999. It is being used extensively in India and other developing countries. However, it causes joint pains in some patients and agranulocytosis in an occasional patient. Thousands of patients are now treated with L1 worldwide, not only for transfusional iron overload but also for non-iron loading conditions. L1 is set to assume a role of universal antioxidant pharmaceutical and a therapeutic for more than 100 diseases. Deferasirox, once daily oral iron chelator, was the next big advance in this area. It provided an effective oral alternative to deferoxamine (desferal) in the treatment of transfusional haemosiderosis. Several Indian studies have demonstrated the safety and efficacy of Deferasirox in reducing iron burden in patients with beta-thalassaemia who have received many blood transfusions ,,, . Chandra et al reported gastrointestinal symptoms in about 25 per cent of cases, and skin rashes in 5 per cent cases. They observed greyish-brown pigmentation of the skin in 10 per cent children. None of the side-effects necessitated cessation of the drug therapy. They concluded that therapy with deferasirox is safe in paediatric patients with thalassaemia major. However, patients should be carefully monitored for side-effects. The long-term use of effective dose protocols of L1 and combinations with DFO results in the clearance of excess cardiac iron. Trials on effectiveness of combinations of deferiprone with deferasirox are eagerly awaited, as this would be an ideal combination.
(iii) Care of thalassaemics in India:
The first centres for care of thalassaemia were probably started in Mumbai in early 1970s in JJ Hospital and KEM Hospital, followed by All India Institute of Medical Sciences (AIIMS), New Delhi in 1973-1974, Borruka Center, Kolkata in 1985, Sir Ganga Ran Hospital in 1986, and Wadia Hospital for Children in Mumbai in 1987. The Preeti Tuli Thalassemia Center at Sir Ganga Ram Hospital in Delhi was set up in 1994. It was the first dedicated centre which started a free Day Care Clinic with multiple specialists, and routine use of filters during transfusions. Subsequently similar centres were opened in many cities in India.
Shobha Tuli of Thalassemics India and JS Arora of the Federation of Indian Thalassemics (FIT) have played an important role in improving the care of thalassaemics in India by arranging various educational programmes and workshops, by bringing foreign and Indian experts to examine and treat patients of thalassaemia. There are about 60 parent/patient societies of thalassaemia in India, of which about 40 are members of the FIT. Due to the persistent efforts of the thalassaemia societies and the health professionals working in this field, a most significant step has been taken by the Government of India by including the care and management of thalassaemia into the 12 th Five Year Plan. This will pave the way for improving the quality of care and in introducing control programmes in various parts of the country.
Care of thalassaemics in the prominent centres is of a high order. Most of these are led by physicians who have attended the educational conferences organized in India by the thalassaemic societies. The Thalassemia International Federation played a major role by deputing and supporting experts to come to India, and give lectures and conduct workshops. The booklets outlining the optimal care of thalassaemia have also been very useful in educating the patients and doctors. Increasing reports are appearing of endocrinal and cardiac involvement in thalassaemia, which are commonly observed in the second decade, as it takes some time for iron to accumulate in these organs. Adequate chelation therapy delays the onset of these complications. Indeed subjects with thalassaemia major who receive optimal care in India now survive to adulthood. A number of thalassaemic children have married [about 10 in and near Delhi, two in Chandigarh and two in Gujarat (Tuli S, personal communication), and four in Mumbai (Sethi P, personal communication)].
In Jammu a thalassaemia society was formed in 1996, and registered in 2000. Since then the Jammu and Kashmir (J & K) Government has been providing blood transfusions, chelation and other therapies free of cost to 174 patients and also provides free transport to all patients who have to travel from long distances to receive treatment (S. Sethi, personal communication). This was followed by the Delhi State which set up dedicated thalassaemia units in all the Government hospitals and has been providing free blood transfusions and chelation since 2005. The Municipal Corporation of Delhi has also provided the same free facilities in the three hospitals under its care (Kasturba Hospital, Hindu Rao Hospital, Swami Dayanand Hospital). Since 2008 a programme of regular screening of pregnant women has been initiated. The Punjab Government gives free treatment to all thalassaemic children who attend school. The Governments of Gujarat and Maharashtra also provide free therapies for children with thalassaemia. It is hoped that other States would follow suit. It is now up to the thalassaemia societies in the other States to exert pressure on the Governments to provide similar services.
(iv) Use of wheat grass as therapy:
Based on anecdotal reports by the parents of benefit of wheat grass juice in raising the haemoglobin, three studies have been carried out ,, . In the study by Marwah et al the patients consumed about 100 ml of wheat grass juice daily. Each patient acted as his own control. Of the 16 cases analyzed, blood transfusion requirement fell by >25 per cent in 8 patients, with a decrease of >40 per cent documented in three of these. Choudhry and colleagues  did not find any significant benefit from its use. However, Singh et al treated 40 patients of thalassaemia major with wheat grass tablets (WGT). The mean haemoglobin in the pre WGT was 8.54 ± 0.33 g/dl whereas in WGT period it was 9.13 ± 0.14 g/dl. The decrease in the blood transfusion requirements was by 25 per cent or more in 60.6 per cent cases. The mean interval between the consecutive blood transfusions in pre WGT period was 18.78 ± 4.48 days whereas in WGT period was 24.16 ± 4.78 days. The authors concluded that wheat grass has the potential to increase the haemoglobin levels, increase the interval between blood transfusions and decrease the amount of total blood transfused in patients with thalassaemia major. A double blind randomized study is required to establish efficacy.
(v) Use of hydroxyurea:
Pharmacological agents such as hydroxyurea (HU) have been known to cause induction of foetal haemoglobin and reduce ineffective erythropoiesis, and thus may alleviate the symptoms in thalassaemia intermedia patients. Choudhry et al observed a definite trend of rise in haemoglobin and haemoglobin F on administration of hydroxyurea but the change was statistically insignificant. One study found that response to hydroxyurea correlated with Xmnl1 polymorphism as well as deletions of alpha globin gene  , while another  observed a good response which correlated with Xmnl1 +/+ in 72.7 per cent and alpha gene deletions in 41 per cent of the cases. Raina et al demonstrated that the good response to hydroxyurea correlated with Xmnl1 +/+ genotype and IVS1-I G>T mutation as well as Hb E.
(vi) Bone-marrow haemopoietic stem cell transplantation (BMT):
The first bone marrow transplant centre was established at Tata Memorial Hospital in 1983 in Mumbai. However, they carry out only a limited number of transplants for thalassaemia. The centre at Christian Medical College & Hospital (CMCH), Vellore was started in 1986  . This centre has carried out the maximum number of bone marrow haemopoietic stem cell transplants for thalassaemia in the country, and is second only to the Pesaro centre. At this centre from October 1986 to December 2006, 626 transplants were performed in 595 patients, with 28 patients having more than one transplant  . Thalassaemia accounted for a third of these transplants. Kumar et al performed allogenic haematopoietic SCT in non-Hepa filter rooms. The average cost of allogenic BMT in India is around $15000 to 20000, which is considerably lower than the cost in the West. India needs to develop more transplant centres with adequately trained personnel.
The other centres where BMT is being carried out are in Delhi (All India Institute of Medical Sciences, BL Kapur Hospital, Sir Ganga Ram Hospital, Army Hospital, R and R); Lucknow (Sanjay Gandhi Postgraduate Institute of Medical Sciences), Chennai (Apollo Hospital), Chandigarh (Postgraduate Institute of Medical Education & Research), Pune (Sahayadri Hospital), Bangalore (Narayana Hrudayalaya Hospital, Manipal Hospital and Kidwai Memorial Hospital), Ahmedabad (Gujarat Cancer Research Institute), Thiruvananthapuram (Regional Cancer Center), and Mumbai (Jaslok Hospital). Some of these centers carry out BMT for thalassaemia in a limited number of patients.
(vii) Bone marrow and cord blood stem cell registries:
A major limitation in haematopoietic stem cell transplantation (HSCT) is the availability of a unrelated HLA matched donor. Kanga et al reported that of the 688 patients requiring HSCT, only 39.3 per cent had an HLA matched sibling. Families with sibship size of ? 4 had a higher probability (68.8%) compared with those with sibship size of ? 3 (29.7%). The difficulties in finding an unrelated suitable donor in India are due to the extensive allele and haplotype diversity, and the presence of unique haplotypes in India (HLA-A * 0211, B * 2707, A * 26-B * 08-DRB1 * 03). These limitations are being overcome by establishing unrelated volunteer marrow donor registries. The first one was set up in AIIMS, New Delhi, as the Asian Indian Donor Marrow Registry in 1994. By 2008, 3830 donors have been enrolled (Mehra NK, personal communication). This has been enlarged to a multi-centric project to enroll donors from different cities in India by initiating new registries (Mumbai, Chandigarh, Lucknow, Vellore, Vadodra). Another registry has been started in Mumbai at the Tata Cancer Hospital - Marrow Donor Registry India (MDRI) in 2008. The total number of samples processed for HLA typing till October 2009 was about 3000  . This registry has received a boost as the Salman Khan Foundation has joined as a partner in order to increase the enrolment. DATRI Blood Stem Cell Donors Registry based in Chennai is another important repository  . It has 12,398 donors on its rolls and is listed in the Bone Marrow Donors Worldwide (BMDW). The Cord Stem Cell Registry India (SCRI) has been started by Dr Latha Jagannathan and Dr Velu Nair. Based at Army Hospital (R & R), Delhi, it networks with Rotary blood banks in Bangalore, Chennai and Delhi, Prathama Blood bank in Ahmedabad and Association of Voluntary Blood Donors in Chennai. There are at least ten cord blood storage centres in India. Reliance Life Sciences cord blood repository Mumbai (Relicord) probably has the largest collection. It supplies enriched cord blood stem cells  . There are also some registries abroad that are a source of finding appropriate donors for Indians, e.g., the Asian American Bone Marrow Foundation (AABMF) in USA. In the International Bone Marrow Donor registries about 20,000 Indians are registered. The Bone Marrow Donors Worldwide has 66 stem cell donor registries from 47 countries, and 47 cord blood banks from 28 countries  . The current number of donors and cord blood units in the BMDW database is 18,195,087 (17,707,159 donors and 487,928 CBUs). There are currently 776 users from 488 organizations authorized to access the online BMDW services. More information is provided at the website of World Marrow Organization  .
(viii) Physical growth, endocrinal and bone density changes in thalassaemia major:
Several investigators have studied growth in thalassaemic children , , and others have reported on pubertal development and endocrinal function , . Abnormalities of beta cell function have also been explored  . Significant effects of the disease on growth as well as pubertal growth have been demonstrated suggesting that in most patients optimal treatment is not being provided. Mamtani et al carried out a meta-analysis of bone recovery after zoledronate therapy in thalassaemia-induced osteoporosis.
| Prevention of thalassaemia|| |
The need for prevention of thalassaemia is obvious due to high frequency of the condition, the great expense and difficulties in providing optimal treatment for patients, and the innumerable fatalities from untreated β-thalassaemia. Prevention would not only be a good public health practice, as envisioned in Alma Ata declaration, but it would also be cost-effective, as the ratio of the cost of treatment to prevention is 4:1, as shown in a study from Israel  . It would help tremendously in reducing the burden of the disease for patients, families and the health services. The strongest argument for prevention is that it would ensure the best possible care for the affected, by curbing the increase in their number.
The chief elements of a control programme were developed in 1970s by a team of experts at the World Health Organization, led by Dr Bernadette Modell  . These are (i) Political and financial support, (ii) Improving curative services; (iii) Prenatal diagnosis in couples who have given birth to an affected child , as well as those identified to be at risk, (iv) Prospective antenatal screening, (v) Community carrier screening, (vi) Counselling and prenatal diagnosis, and (vii) Network of centers, and National/Regional working groups. Control programmes in thalassaemia , have the following important components:
Financial support is required for training and employing the manpower required for execution of the control programme (social workers, technicians, doctors, counsellors); purchase of equipment (electronic cell counters, HPLC machines, DNA diagnostic laboratories, or link with a laboratory); and record keeping and information system in a confidential manner.
Education of the professionals and the public should be done using all components of mass media - newspapers, TV and films. An important component is informing the policy makers. The Parent Organizations have a very important role to play in this. Any educational programme on thalassaemia has three main messages - carrier state has no disadvantage, homozygous state is associated with a very severe disorder, that is eventually fatal with no curative therapy, and foetal diagnosis is available and safe. Experience around the world clearly indicates that carrier testing must be voluntary, and mandatory measures should be discouraged. In an analysis of the reasons for the successful control programmes in Cyprus and Greece it was concluded that one of the important steps was the introduction of formal education on thalassaemia in the school curriculum , .
Preventive programmes carried out based on heterozygous detection and counselling to avoid marriage between carriers, without prenatal diagnosis, have not been very effective around the world. In contrast, preventive programmes based on heterozygote detection, counselling and foetal diagnosis have been very effective in reducing birth of thal major infants in Sardinia, Cyprus, Greece and Italy  . The strategy of identifying carriers and asking carriers not to marry carriers (without providing foetal diagnosis) led to no significant difference in the proportion of marriages between heterozygotes as compared with random mating, and no change in the incidence of thalassaemia major in some studies , .
Premarital screening has been advocated by many investigators and haematologists in India as a preventive strategy. This is a good, perhaps the only option, in countries that do not allow termination of pregnancy, e.g., in Saudi Arabia, the Middle-east and Sri Lanka. Experience gained in the running the control programme for thalassaemia in Iran is instructive. The program was started in 1995. Their policy is based on couple screening  . In an autosomal recessive disorder this makes good sense  . All couples wanting to marry are required to be checked for carrier status of thalassaemia in order to receive a permit for marriage registration. The male is tested first by determining the red blood cell indices. If he is a carrier as suggested by red cell indices the woman is screened. If the results are abnormal, haemoglobin A2 (HbA2) is performed. Couples in which both partners are confirmed to be carriers receive counselling. In the original report by Samavat and Modell  over a period of 5 years (1997-2001) 2.7 million couples were tested all over Iran, of whom 10,290 were at risk. Of these, 53 per cent decided to get married, 29 per cent separated, and 18 per cent were uncertain. Five years later Karimi et al reported on screening of 1,038,371 couples in Southern Iran from 1995 to 2004. Of these, 5,182 (0.4%) were diagnosed to be carriers; 1932 refused marriage, while 2798 (54%) proceeded to marry in spite of knowing the carrier status. This happened because of the existing cultural practice. It quickly became apparent, however, that those being tested wanted to have prenatal diagnosis available. This pressure led to ethical discussions by Muslim scholars and others, resulting in a fatwah that allowed abortion during the first 16 wk after the last menstrual period, when the foetus was diagnosed with thalassaemia. The latter was offered only since 2002. Results revealed that in 1995, 1999 and 2004, 296, 94 and 56 β-thalassaemia homozygotes, respectively, were born (2.53, 1.07 and 0.82 patients per 1000 births). Even in Saudi Arabia and UAE more and more couples are choosing prenatal diagnosis, and it is only a question of time when this will be introduced.
In countries where prenatal diagnosis is available, most of the people prefer prenatal diagnosis rather than using the information about carrier status for choosing a marriage partner. This is because marriage is a complex social phenomenon, and marriage partners are selected for a strong personal preference, family or traditional reasons. When a planned marriage is called off, it results in social embarrassment, stigma to the young people involved and their families. An earlier study in Arta area of Greece is revealing  . There is a 20 per cent carrier rate in the area. All young people of marriageable age were screened and counselled. Assessment at the end of 2 years showed no measurable effect on choice of partner. In a study in Montreal, Canada, high school children were screened for carrier status of thalassaemia and Tay Sach disease, and six years later were asked the question " Do you think that a couple planning to marry, who found they were carriers, should change their marriage plans? Would you change your own marriage plans". The answer was most revealing - 80 per cent thought that other couples would change their marriage plans, but only 10 per cent thought they would change their own plans  .
The Cyprus programme is often used to justify premarital counselling. Initially the model in Cyprus was based on screening and counselling of subjects, and marriage between carriers was discouraged. This approach proved unacceptable to the general public, and was soon abandoned, because of evasions. Once prenatal diagnosis became available within Cyprus health service, confidential premarital screening was mandated by the Church, but there was no compulsion that carriers should not marry carriers. The objective was that people should know their carrier status and after marriage get the foetus tested in those cases where both the husband and wife were carriers. A study showed that 98 per cent of at risk couples detected prior to marriage proceeded to marry, but opted for prenatal diagnosis during pregnancy. It has been reported that less than 5 per cent of the fall in thalassaemia major births is due to separation of engaged couples, while about 80 per cent is due to prenatal diagnosis and selective abortion , .
Which strategy is likely to succeed in India? If the policy of premarital screening were to be successful, control of thalassaemia in India should have been achieved a long time ago, because this course of action has been available for decades. For the reasons given above the policy of identifying carriers and advising carriers not to marry carriers is not likely to be successful, given the current state of knowledge of the general public about science and genetics. Chattopadhya  observed that blood is deeply valued in the Bengali kinship system, and that this genetic mutation is perceived to be corrupting the blood. Being a thalassaemia carrier (i.e., having thalassaemia minor) renders an individual unfit as a suitable marriage partner because of beliefs related to purity of blood, its association with the continuity of the lineage, and subsequent transmission of desirable traits to future generations. The risk of non-marriage affects women disproportionately, and parents are not inclined to test their daughters because of the possibility of not being able to marry them off to eligible suitors. The stigma associated with having thalassaemia minor (TMI) is a deterrent to the disclosure of thalassaemia status as well as to testing. Tamhankar et al carried out premarital testing for thalassaemia carrier state in three groups: extended family members of diagnosed cases of thalassaemia/haemoglobinopathies, unmarried adult cases of anaemia attending the hospitals' outpatient department and adult college students. As much as 99 per cent of prospective carrier couples married even after knowing their high-risk status and opted for prenatal diagnosis.
This reinforces the view that over-emphasis on premarital screening should be avoided in India. The policy should determine the carrier status of subjects before reproduction, or during early pregnancy, so that prenatal diagnosis can be obtained in the at risk couples. Strategy for screening programmes for β-thalassaemia should be to sensitize the community to the problem, establish haematological technologies for screening, and molecular and obstetric techniques for prenatal diagnosis. However, the programme should not begin until all components are in place.
How should the carriers be identified? The technique to be used should be affordable, applicable, and accurate. Should one use naked eye single tube red cell osmotic fragility test (NESTROFT), or electronic cell count, or HbA 2 estimation using HPLC? No doubt HPLC is the best, but in view of large numbers of subjects requiring screening in India, the better option would be use electronic cell counters for measuring red cell indices. If only one partner has to be screened the husband should be preferred because it avoids the anaemia of pregnancy disturbing the red cell indices. One of the two partners must clearly be shown to be negative for thalassaemia carrier status. In case of any doubtful result HPLC analysis should be done. In rural areas where electronic cell counters are not available, initial analysis may be by NESTROFT. This should work out well because most investigators have pointed out that NESTROFT has a sensitivity of over 90-95 per cent, and a negative result picks out the normal very well ,,, .
The other important observation made in India is that concomitant iron deficiency is present in many β-thalassaemia carriers,, . It was shown that once iron deficiency is established, therapy with iron leads to a significant rise in haemoglobin. The authors demonstrated that in β-thalassaemia carriers HbA2 decreased in the presence of iron deficiency, but the fall was slight, and it never reached the normal range. Another important contribution was recognizing the unique sequence in HbA 2 and developing antibodies against HbA 2 . These antibodies were used to measure HbA 2 by ELISA technique , .
The next issue is who should be screened? There are a number of options - pregnant women, relatives of the affected, high school or college students, or the community at large. There is little doubt that the primary focus of screening in developing countries, including India, should be pregnant women. This yields results immediately, in terms of reducing the burden. Screening of high school or college students is good to create awareness, but by the time they are to marry many tend to forget their carrier status. Colah and colleagues  screened 5682 school children (age 11-18 yr) from 75 schools in Mumbai city between 1984 and 1988. Of these, 153 (2.7%) were found to be β-thalassaemia heterozygotes. After 20 years it was possible to locate only 71 of the 153 children who were carriers of β-thalassaemia. Only 47 of these 71 families could be contacted. Only 12 of the 47 individuals contacted (26%) recollected that they were β-thalassaemia carriers. None of the 41 individuals who were now married had revealed their carrier status or had their partners tested before marriage. However, 11 individuals had their spouses tested for haemoglobinopathies after marriage. This shows that screening of school students is unlikely to make a significant reduction in the burden of thalassaemia.
Cascade or inductive screening identifies many more carriers than general population screening, as was shown in a study in Pakistan . The investigators screened 15 large families with segregating β-thalassaemia genes through a proband, who was a known carrier. They also examined eight families from the same region without a history of β-thalassaemia. Because of consanguinity 31 per cent of those tested in the first category were found to be carriers, while there was none in those without a family history of thalassaemia. Inductive screening is not a new approach - it is used regularly in every genetics clinic. In Sardinia, Cao & Galanello  were able to identify more than 90 per cent of the couples who were at risk for producing a child with β-thalassaemia, by examining only 11 per cent of the population. Gorakshakar and Colah screened 691 relatives of affected subjects and detected 151 to be β-thalassaemia carriers (21.9%). As compared with other approaches, the percentage of β-thalassaemia carriers identified was 5-6 times higher using this cascade screening approach. Tamhankar et al  tested (i) extended family members of diagnosed cases of thalassaemia, (ii) unmarried adult cases of anaemia attending the hospitals' outpatient department, and (iii) adult college students for carrier status of β-thalassaemia. The yield of carriers from the three groups was 78.17, 19.51 and 4.04 per cent, respectively. The number of prospective high-risk couples detected were 154, 48 and 2 from the three groups, respectively.
In 1990, Sangani et al collected information on the attitudes toward screening for thalassaemia among 200 families of index cases residing around Mumbai. Twenty per cent of these families had expressed an unfavourable reaction from their relatives. Hence, these parents were secretive about their child having thalassaemia major to avoid social stigmatization. Yagnik  followed up 70 carriers and 127 non carrier who were identified during screening of high-risk communities 5-7 years after counselling. Of these, 46 per cent of the carriers had got all their siblings tested while 42 per cent had not informed their siblings about their carrier status. Saxena & Phadke  interviewed 100 parents of children with thalassaemia using a pre-designed questionnaire. The results showed that 96 per cent of them were willing to share information on their thalassaemic children with relatives and friends. However, only 14 families got themselves tested, while another 34 families could not do so due to non availability of screening facilities in the nearby town, high cost of the test, and lack of sufficient motivation.
The largest programme of screening for thalassaemia in the population has been carried out in Gujarat by the Indian Red Cross Society in Ahmedabad and other cities  . From 2004 to 2010, they screened 370,117 subjects for carrier status, among whom there were 173,112 students, 45,000 youths and 8,377 pregnant women. Carrier rate has varied from 4.3 to 5.0 per cent. Testing was done using the HPLC system.
An important project was carried out under the Prime Minister's Jai Vigyan Thalassaemia Control Programme, in six cities in India with a high prevalence of haemoglobinopathies - Mumbai (Maharashtra), Vadodora (Gujarat), Dibrugarh (Assam), Kolkata (West Bengal), Ludhiana (Punjab) and Bangalore (Karnataka) , . Screening was done in 29,898 college students, and 26,916 pregnant women. The prevalence of β-thalassaemia trait varied from 1.5 to 3.4 per cent among college students, and 1.3 to 4.2 per cent among pregnant women. A high frequency of carriers was observed among certain communities - Vellalas, Sindhis Aroras, Lohanas, Mandls, Pillais, Jains, Khatirs and Baidyas. Essential recommendations of this extensive study were as follows: Multimedia awareness programmes should be a continuous process; adequate number of centres should be established so that people do not have to travel long distances for the tests; NESTROFT (osmotic fragility) test, though cheap, cannot be recommended as the only test for preliminary screening, it should be combined with RBC indices measured on a cell counter; the blood count should be done within 48 h after collection; mean corpuscular haemoglobin (MCH) was more stable parameter than mean corpuscular volume (MCV); HbA 2 estimation by HPLC was the most accurate method for diagnosis of β-thalassaemia heterozygotes. Considering the cost involved in using HbA 2 , assay it was recommended that all samples that are Nestroft +ve or have MCV less than 80 fl, or MCH less than 27 pg/cell should be screened further for HbA 2 ; high MCV values were observed in 1.7 per cent of carriers suggesting concomitant vitamin B12 or folic acid deficiency; and need for ensuring screening early in pregnancy.
We carried out a pilot study (unpublished) on prevention of β-thalassaemia in a district hospital in Delhi. Using NESTROFT, 2300 women were screened for carrier status of β-thalassaemia, at the local site. All those with positive or doubtful results had an HbA 2 estimated. Sixty two (2.7%) women were confirmed to be carriers. Only 43 husbands could be examined and eight (18.6%) turned out to be carriers. This was surprising, but not totally unexpected, given that marriages are not completely random, and occur most commonly among the same castes. Of these 8 couples, prenatal diagnosis was carried out in 6, as one refused, and in one the pregnancy was too advanced. Of the six examined, two had affected foetuses, two foetuses were carriers and two foetuses were normal. This averted the birth of two affected children. Calculation of cost of the care of two affected children for a period of ten years covered the entire cost of screening and prenatal diagnosis in the study subjects, highlighting that the preventive screening and prenatal diagnosis are cost effective.
| Prenatal diagnosis|| |
A number of investigators have described their experience with prenatal diagnosis in India ,, . This was provided first in Delhi. Initially samples for prenatal diagnosis were sent to John Old in Oxford. However, with his help the ARMS/RFLP analysis using restriction enzymes (RE) method to detect the mutations was set up locally. By 1996 prenatal diagnosis was performed in 415 cases in All India Institute of Medical Sciences, New Delhi  . In rapid succession it was established in Christian Medical College in Vellore  , and in Mumbai at the National Institute of Immunohaematology and Wadia Hospital for Children  . Currently prenatal diagnosis is available in the following centres in India: Delhi - Sir Ganga Ram Hospital, All India Institute of Medical Sciences, Mumbai - National Institute of Immunohaematology, Wadia Hospital for Children, Vellore - Christian Medical College and Hospital, Lucknow - Sanjay Gandhi Postgraduate Institute of Medical Sciences, Hyderabad - Center for DNA Fingerprinting and Diagnostics, and Center for Cellular and Molecular Biology; Chandigarh - Postgraduate Institute of Medical Education and Research, and a few commercial laboratories.
The important steps for prenatal diagnosis can be listed as: (i) Be certain both parents are carriers. Even in families with an affected child who is on blood transfusions it is better to establish that the parents are carriers by haematological studies. Sometimes one of the parents turns out to be Hb E or sickle cell disease. If there is no affected child, special care should be taken to ensure that parents are carriers. Electronic cell count should invariably be done to support the results of HbA 2 by HPLC. Estimation of HbA 2 by electrophoresis is not always reliable. (ii) When one of the partners is a carrier, take particular care that the other partner is not a carrier. This is because they may carry mild or 'silent' mutations of β-globin gene. In those with borderline values of red cell indices or HbA 2, it is better to sequence their β-globin gene. Garewal and colleagues, showed that Jat Sikhs, a subcaste of Punjabis, have a very high prevalence of the mild beta ++ promoter region mutation -88 (C-T). "Mild" mutations are also reported from South India , - cap site +1 (A>C), poly A (T>C), -28 (A>G), and -88 (C>T). (iii) Know which combination of alleles is significant. For example, the combinations of the following alleles lead to clinical manifestations and require prenatal diagnosis: β-Thal/β-Thal (Thalassaemia major), β-Thal/HbS (Sickle/β-Thalassaemia), β-Thal/HbE (E/β-Thalassaemia), HbS/HbS (sickle cell anaemia), HbS/HbD Pb/Hb C (SCD/Symptomatic). On the other hand, the following combinations do not require prenatal diagnosis because these do not lead to any clinical problem: β-Thal/Hb D Punjab/Iran, β-Thal/Hb C/Hb Q, homozygous Hb E, Hb D Punjab/Hb D Iran.
| The techniques for identification of mutations|| |
There are 64 β-globin mutations reported in Indians so far as recorded in the ThalInd database  . The most popular technique for mutation detection is the ARMS technique. This was developed by Newton and colleagues  , and applied for molecular diagnosis for thalassaemia by John Old and group ,, . It has proved to be a good technique, and easy to learn. However, its disadvantage is that separate primers are required to analyze each mutation and the normal sequence at that site. Restriction enzyme method can be applied for many of the mutations, while reverse dot-blot is used by the groups at Mumbai (NIIH)  and Vellore  . Earlier most investigators tested the mutations in stages - the five commonest mutations along with Hb E and Hb S, then the eight other common mutations, then the rare ones. The unknown mutations were screened by denaturing gradient gel electrophoresis (DGGE), single strand conformation polymorphism (SSCP), or temporal temperature gradient gel electrophoresis (TTGE), and the resulting fragment sequenced. As the facility of sequencing has become more widely available, most investigators proceed to sequence once testing for the common seven mutations is negative. Another useful technique has been to test cord blood by HPLC analysis for prenatal diagnosis in those cases where mutations are not known, or in those women who present late in pregnancy , .
| Future of thalassaemia care in India|| |
The international situation changed in 2006 with the recognition by the Executive Board of the World Health Organization that thalassaemia and sickle cell anaemia were major global health problems which needed to be urgently addressed, a move reinforced by their inclusion in the current Global Burden of Disease Study  . This was accompanied by adoption of the resolution WHA63.17 in May 2010, to redress the limited focus to date on preventing and managing birth defects, especially in low- and middle-income countries  . Weatherall  pointed out that the major problem for the future lies in the unwillingness of governments and international health agencies to accept that thalassaemias present a health burden in developing countries comparable to that of other major diseases. He suggested that more detailed information on frequency and economic data is required to provide evidence for the health burden posed by thalassaemias in the developing world. The Government of India is proposing to provide sufficient funds to the care and control of thalassaemia in India.
Currently in most cities thalassaemia care centres have been established, both in the private sector as well the Government hospitals. Paediatricians and paediatric haematologists looking after these centres have sufficient training and skills to manage these cases. What needs to be done is to supply free or subsidized blood transfusions as well chelating agents in all States in India, as has been done in a number of States like Jammu and Kashmir, Delhi, Maharashtra and Gujarat.
The programme of prevention through carrier screening and prenatal diagnosis should receive the highest priority in the future, in order to reduce drastically the birth of affected children. Talks have been ongoing for initiating control programmes in the cities and States that have a high prevalence of carriers of B-thalassaemia, yet no concrete programmes have been started. The 6-centre study on control  has been extremely useful in providing the basics of organizing and running a control programme in India. Even without a control programme in place we must motivate the obstetricians to screen every woman at first visit for carrier status of thalassaemia, haemoglobin E and sickle cell disease. As far as feasible, husband should be screened at the same time.
There is a need to increase the number of centres in India able to perform prenatal diagnosis, and provide this facility at a subsidized cost, or free for the poor, and introduce quality control programmes. An important challenge is to develop pre-implantation genetic diagnosis as many couples are distressed by having affected children in consecutive pregnancies. Investment in non invasive techniques for prenatal diagnosis would be worthwhile, as this would help to provide prenatal diagnosis in peripheral areas also. The facilities for voluntary cord stem cell storage should be established in the Government sector, as currently most of these exist in the private sector at a huge cost. Centres for bone marrow transplantation need to be expanded and facility subsidized. The need of the hour is to introduce control programmes in the high risk States.
| References|| |
|1.||Cooley TB, Lee P. Series of cases of splenomegaly in children with anemia and peculiar bone changes. Tr Am Pediatr Soc 1925; 37 : 19. |
|2.||Mukherji, M. Cooley's anaemia (erythroblastic or Mediterranean anaemia). Indian J Pediatr 1938; 5 : 1-7. |
|3.||Coelho C. Erythroblastic anemia- Cooley's anemia. Med Bull Bombay 1939; 7 : 291-3. |
|4.||Napier LE, Shorten JA, Das Gupta CR. Cooley's erythrolblastic anaemia. Indian NI Gaz 1939; 74 : 660-4. |
|5.||Patel ND, Bhende YM. Erythroblastic anaemia with kyphosis and cirrhosis of liver. Indian J Pediatr 1939; 6 : 217-22. |
|6.||Malhotra RP, Chhuttani PN. Case of Cooley's anaemia. Indian Med Gaz 1944; 79 : 198-9. |
|7.||Chaudhuri KC. Erythroblastic anaemia of Cooley. Indian J Pediatr 1947; 14 : 76-80. |
|8.||Ghai OP, Varma KP, Taneja PN. Hemoglobinopathies in north India - 1. Hemoglobin D trait and hemoglobin D thalassemia. Indian J Child Health 1961; 10 : 334-41. |
|9.||Sharma RS, Parekh JG, Shah KM. Hemoglobinopathies in Western India. J Assoc Physicians India 1963; 11 : 969-73. |
|10.||Sinha KP, Prasad LS, Saran A. Hemoglobinopathy in Bihar. J Indian Med Assoc 1964; 42 : 219-23. |
|11.||Praharaj KC, Mohanta KD, Kar RS, Swain U, Nanda BK. Haemoglobinopathy in Orissa. Indian Pediatr 1969; 6 : 533-7. |
|12.||Laxman S, Mathur YC, Chandra H, Reddi YR. Haemoglobinopathy in Andhra Pradesh. Indian J Pediatr 1971; 38 : 365-7. |
|13.||Dash S, Dash RJ. Spectrum of haemolytic anaemias in Punjab, North India. Trop Geogr Med 1980; 32 : 312-6. |
|14.||Jain RC. Prevalence of abnormal haemoglobin, thalassaemia & G-6 PD deficiency among the hospital population of Udaipur (Rajasthan). Indian J Med Res 1984; 80 : 332-8. |
|15.||Chatterjee JB, Saha AK, Ray RN, Ghosh SK. Hemoglobin E-thalassemia disease. Indian J Med Sci 1957; 11 : 553-64. |
|16.||Naik SK, Kothari BV, Jhaveri CL, Sukumaran PK, Sanghvi LD. Fatal hemolytic anemia presumably due to the combination of sickle cell and thalassemia gene; case report. Indian J Med Sci 1957; 11 : 244-9. |
|17.||Swarup S, Ghosh SK, Chatterjee JB. Haemoglobins E and K and thalassemia in an Indian family with evidence of interaction between haemoglobin E and thalassaemia. J Indian Med Assoc 1966; 46 : 587-90. |
|18.||Sukumaran PK, Merchant SM, Desai MP, Wiltshire BG, Lehmann H. Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families. J Med Genet 1972; 9 : 436-42. |
|19.||Ajmani M, Sharma A, Talukder G, Bhattacharyya DK. Genetic interaction of beta-thalassaemia (Hb âT-) & haemoglobin E (Hb âE) in populations of Eastern India. Indian J Exp Biol 1977; 15 : 455-7. |
|20.||Kumar S, Rana M, Handoo A, Saxena R, Verma IC, Bhargava M, et al0. Case report of HbC/â -thalassemia from India. Int J Lab Hematol 2007; 29 : 381-5. |
|21.||Chatterjee JB. Haemoglobinopathies, glucose-6-phosphate dehydrogenase deficiency and allied problems in the Indian subcontinent. Bull World Health Organ 1966; 35 : 837-56. |
|22.||Kazazian HH Jr, Orkin SH, Antonarakis SE, Sexton JP, Boehm CD, Goff SC, et al. Molecular characterization of seven beta-thalassemia mutations in Asian Indians. EMBO J 1984; 3 : 593-6. |
|23.||Wood S, Daya M, Allanson JE, Kirby L, Coupland R, Gray GR. Partial deletion of the beta-globin gene: a common beta-thalassaemia allele in Asian Indians. Can J Genet Cytol 1984; 26 : 296-301. |
|24.||Thein SL, Old JM, Wainscoat JS, Petrou M, Modell B, Weatherall DJ. Population and genetic studies suggest a single origin for the Indian deletion beta thalassaemia. Br J Haematol 1984; 57 : 271-8. |
|25.||Old JM, Petrou M, Modell B, Weatherall DJ. Feasibility of antenatal diagnosis of â thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations. Br J Haematol 1984; 57 : 255-63. |
|26.||Thein SL, Hesketh C, Wallace RB, Weatherall DJ. The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: application to prenatal diagnosis. Br J Haematol 1988; 70 : 225-31. |
|27.||Old JM, Varawalla NY, Weatherall DJ. Rapid detection and prenatal diagnosis of â-thalassaemia: studies in Indian and Cypriot populations in the UK. Lancet 1990; 336 : 834-7. |
|28.||Varawalla NY, Old JM, Sarkar R, Venkatesan R, Weatherall DJ. The spectrum of â-thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis. Br J Haematol 1991; 78 : 242-7. |
|29.||Verma IC, Saxena R, Thomas E, Jain PK. Regional distribution of â-thalassemia mutations in India. Hum Genet 1997; 100 : 109-13. |
|30.||Vaz FE, Thakur CB, Banerjee MK, Gangal SG. Distribution of â-thalassemia mutations in the Indian population referred to a diagnostic center. Hemoglobin 2000; 24 : 181-94. |
|31.||Colah R, Gorakshakar A, Nadkarni A, Phanasgaonkar S, Surve R, Sawant P, et al. Regional heterogeneity of â-thalassemia mutations in the multi ethnic Indian population. Blood Cells Mol Dis 2009; 42 : 241-6. |
|32.||Bandyopadhyay A, Bandyopadhyay S, Basak J, Mondal BC, Sarkar AA, Majumdar S, et al. Profile of â-thalassemia in eastern India and its prenatal diagnosis. Prenat Diagn 2004; 24 : 992-6. |
|33.||Venkatesan R, Sarkar R, Old JM. â-Thalassaemia mutations and their linkage to â-haplotypes in Tamil Nadu in southern India. Clin Genet 1992; 42 : 251-6. |
|34.||Agarwal S, Naveed M, Gupta UR, Kishore P, Agarwal SS. Characterization of â-thalassaemia mutations in 57 â-thalassaemia families seen at Lucknow. Indian J Med Res 1994; 100 : 106-10. |
|35.||Garewal G, Fearon CW, Warren TC, Marwaha N, Marwaha RK, Mahadik C, et al. The molecular basis of â thalassaemia in Punjabi and Maharashtran Indians includes a multilocus aetiology involving triplicated alpha-globin loci. Br J Haematol 1994; 86 : 372-6. |
|36.||Shaji RV, Edison ES, Poonkuzhali B, Srivastava A, Chandy M. Rapid detection of â-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis. Clin Chem 2003; 49 : 777-81. |
|37.||Edison ES, Shaji RV, Devi SG, Moses A, Viswabandhya A, Mathews V, et al. Analysis of â globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity. Clin Genet 2008; 73 : 331-7. |
|38.||Nadkarni A, Pawar A, Mudera VC, Mohanty D, Colah R. Clinical heterogeneity of silent-gene â-thalassemia among Indians. Ann Hematol 1995; 70 : 61-4. |
|39.||Old JM, Khan SN, Verma I, Fucharoen S, Kleanthous M, Ioannou P, et al. A multi-center study in order to further define the molecular basis of â-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reaction. Hemoglobin 2001; 25 : 397-407. |
|40.||Sinha S, Black ML, Agarwal S, Colah R, Das R, Ryan K, et al0. Profiling â-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes. Hugo J 2009; 3 : 51-62. |
|41.||Gorakshakar AC, Das MK, Phanasgaokar SP, Nadkarni AH, Colah RB, Mohanty D. Origin of the codon 47 (+A) â-thalassaemia mutation among the Nicobarese of the Andaman and Nicobar islands in India. Br J Haematol 2007; 139 : 345-6. |
|42.||Sinha S, Black ML, Agarwal S, Das R, Bittles AH, Bellgard M. ThalInd, a â-thalassemia and hemoglobinopathies database for India: defining a model country-specific and disease-centric bioinformatics resource. Hum Mutat 2011; 32 : 887-93. |
|43.||Kulozik AE, Kar BC, Serjeant GR, Serjeant BE, Weatherall DJ. The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene. Blood 1988; 71 : 467-72. |
|44.||Nadkarni AH, Gorakshakar AC, Mohanty D, Colah RB. Alpha genotyping in a heterogeneous Indian population. Am J Hematol 1996; 53 : 149-50. |
|45.||Panigrahi I, Marwaha RK, Kulkarni K. The expanding spectrum of thalassemia intermedia. Hematology 2009; 14 : 311-4. |
|46.||Verma IC, Kleanthous M, Saxena R, Fucharoen S, Winichagoon P, Raizuddin S, et al. Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations. Hemoglobin 2007; 31 : 439-52. |
|47.||Oberoi S, Das R, Panigrahi I, Kaur J, Marwaha RK. Xmn1-(G) ã polymorphism and clinical predictors of severity of disease in â-thalassemia intermedia. Pediatr Blood Cancer 2011; 57 : 1025-8. |
|48.||Sangani B, Sukumaran PK, Mahadik C, Yagnik H, Telang S, Vas F, et al. Thalassemia in Bombay: the role of medical genetics in developing countries. Bull World Health Organ 1990; 68 : 75-81. |
|49.||Khurana A, Katyal S, Marwaha RK. Psychosocial burden in thalassemia. Indian J Pediatr 2006; 73 : 877-80. |
|50.||Khairkar P, Malhotra S, Marwaha RK. Growing up with the families of â-thalassaemia major using an accelerated longitudinal design. Indian J Med Res 2010; 132 : 428-37. |
|51.||Choudhry VP, Desai N, Pati HP, Nanu A. Current management of homozygous beta thalassemia. Indian Pediatr 1991; 28 : 1221-9. |
|52.||Lokeshwar MR. Progress in the management of thalassemia. Indian Pediatr 2006; 43 : 503-6. |
|53.||Dubey AP, Parakh A, Dublish S. Current trends in the management of beta thalassemia. Indian J Pediatr 2008; 75 : 739-43. |
|54.||Agarwal MB. Advances in management of thalassemia. Indian J Pediatr 2009; 76 : 177-84. |
|55.||Marwaha N. Whole blood and component use in resource poor settings. Biologicals 2010; 38 : 68-71. |
|56.|| http://www.indianredcross.org, accessed on August 5, 2011. |
|57.||Bhattacharya N, Mukherijee K, Chettri MK, Banerjee T, Mani U, Bhattacharya S. A study report of 174 units of placental umbilical cord whole blood transfusion in 62 patients as a rich source of fetal hemoglobin supply in different indications of blood transfusion. Clin Exp Obstet Gynecol 2001; 28 : 47-52. |
|58.||Ramani KV, Mavalankar D, Govil D. Management of blood transfusion services in India: An illustrative study of Maharashtra and Gujarat States, W.P. No. 2007-03-09, March 2007. Ahmedabad: Indian Institute of Management; 2007. |
|59.||De M, Banerjee D, Chandra S, Bhattacharya DK. HBV & HIV seropositivity in multi-transfused haemophilics & thalassaemics in eastern India. Indian J Med Res 1990; 91 : 63-6. |
|60.||Choudhry VP, Acharya SK. Hepatitis B, C & D viral markers in multitransfused thalassemic children: long-term complications and present management. Indian J Pediatr 1995; 62 : 655-68. |
|61.||Sur D, Chakraborty AK, Mukhopadhyay SP. Dr. P. C. Sen Memorial Award Paper. A study of HIV infection in thalassaemia patients of rural Bengal. Indian J Public Health 1998; 42 : 81-7. |
|62.||Marwaha RK, Bansal D, Sharma S, Kumar S, Trehan A, Duseja A, et al. Seroprevalence of hepatitis C and B virus in multiply transfused beta-thalassemics: results from a thalassemic day care unit in north India. Vox Sang 2003; 85 : 119-20. |
|63.||Chaudhury N. Need to change present regulatory framework for blood banks in India. Asian J Trans Med 2011; 5 : 1-2. |
|64.||Kontoghiorghes GJ. The proceedings of the 17th International Conference on Chelation: application of effective chelation therapies in iron loading and non iron loading conditions, and the gap in the prevention and treatment policies on thalassemia between developed and developing countries. Hemoglobin 2009; 33 : 283-6. |
|65.||Agarwal MB, Gupte SS, Viswanathan C, Vasandani D, Ramanathan J, Desai N, et al. Long-term assessment of efficacy and safety of L1, an oral iron chelator, in transfusion dependent thalassaemia: Indian trial. Br J Haematol 1992; 82 : 460-6. |
|66.||Agarwal MB. Oral iron chelation: a review with special emphasis on Indian work on deferiprone (L1). Indian J Pediatr 1993; 60 : 509-16. |
|67.||Adhikari D, Roy TB, Biswas A, Chakraborty ML, Bhattacharya B, Maitra TK, et al. Efficacy and safety of oral iron chelating agent deferiprone in beta-thalassemia and hemoglobin E-beta thalassemia. Indian Pediatr 1995; 32 : 855-61. |
|68.||Choudhry VP. Oral deferiprone--controversies on its efficacy and safety. Indian J Pediatr 1998; 65 : 825-8. |
|69.||Gomber S, Saxena R, Madan N. Comparative efficacy of desferrioxamine, deferiprone and in combination on iron chelation in thalassemic children. Indian Pediatr 2004; 41 : 21-7. |
|70.||Goel H, Girisha KM, Phadke SR. Long-term efficacy of oral deferiprone in management of iron overload in beta thalassemia major. Hematology 2008; 13 : 77-82. |
|71.||Dubey AP, Sudha S, Parakh A. Deferasirox: the new oral iron chelator. Indian Pediatr 2007; 44 : 603-7. |
|72.||Agarwal MB. Deferasirox: oral, once daily iron chelator - an expert opinion. Indian J Pediatr 2010; 77 : 185-91. |
|73.||Chandra J, Chaudhary H, Pemde H, Singh V, Dutta AK. Safety and efficacy of deferasirox in multitransfused Indian children with â-thalassaemia major. Ann Trop Paediatr 2011; 31 : 47-51. |
|74.||Marawaha RK, Bansal D, Kaur S, Trehan A. Wheat grass juice reduces transfusion requirement in patients with thalassemia major: a pilot study. Indian Pediatr 2004; 41 : 716-20. |
|75.||Choudhary DR, Naithani R, Panigrahi I, Kumar R, Mahapatra M, Pati HP, et al. Effect of wheat grass therapy on transfusion requirement in beta-thalassemia major. Indian J Pediatr 2009; 76 : 375-6. |
|76.||Singh K, Pannu MS, Singh P, Singh J. Effect of wheat grass tablets on the frequency of blood transfusions in thalassemia major. Indian J Pediatr 2010; 77 : 90-1. |
|77.||Choudhry VP, Lal A, Pati HP, Arya LS. Hematological responses to hydroxyurea therapy in multitransfused thalassemic children. Indian J Pediatr 1997; 64 : 395-8. |
|78.||Panigrahi I, Dixit A, Arora S, Kabra M, Mahapatra M, Choudhry VP, et al. Do alpha deletions influence hydroxyurea response in thalassemia intermedia? Hematology 2005; 10 : 61-3. |
|79.||Italia KY, Jijina FJ, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, et al. Response to hydroxyurea in â-thalassemia major and intermedia: experience in western India. Clin Chim Acta 2009; 407 : 10-5. |
|80.||Raina A, Verma IC, Saxena R, Kaul D, Khanna VK. Relation of Xmn-1 polymorphism and five common Indian mutations of thalassaemia with phenotypic presentation in â-thalassaemia. J K Sci 2006; 8 : 139-43. |
|81.||Chandy M. Stem cell transplantation in India. Bone Marrow Transplant 2008; 42 : S81-4. |
|82.||Kumar R, Naithani R, Mishra P, Mahapatra M, Seth T, Dolai TK, et al. Allogeneic hematopoietic SCT performed in non-HEPA filter rooms: initial experience from a single center in India. Bone Marrow Transplant 2009; 43 : 115-9. |
|83.||Kanga U, Panigrahi A, Kumar S, Mehra NK. Asian Indian donor marrow registry: All India Institute of Medical Sciences experience. Transplant Proc 2007; 39 : 719-20. |
|84.||Suryanarayan D. Marrow donors on the rise, but they are not enough. DNA, Mumbai. May 12, 2010. |
|85.|| http://www.relicord.com, accessed on October 4, 2011. |
|86.|| http://www.bmdw.org/, accessed on August 5, 2011. |
|87.|| http://www.worldmarrow.org/, accessed on August 5, 2011. |
|88.||Gomber S, Dewan P. Physical growth patterns and dental caries in thalassemia. Indian Pediatr 2006; 43 : 1064-9. |
|89.||Merchant RH, Shirodkar A, Ahmed J. Evaluation of growth, puberty and endocrine dysfunctions in relation to iron overload in multi transfused Indian thalassemia patients. Indian J Pediatr 2011; 78 : 679-83. |
|90.||George A, Bhaduri A, Choudhry VP. Development of secondary sex characteristics in multitransfused thalassemic children. Indian J Pediatr 1997; 64 : 855-9. |
|91.||Khairwa A, Chaudhary A, Jat KR. Assessment of glucose tolerance in multi-transfused adolescent and young adult patients with beta thalassemia. Indian J Pediatr 2011; 78 : 1297-8. |
|92.||Mamtani M, Kulkarni H. Bone recovery after zoledronate therapy in thalassemia-induced osteoporosis: a meta-analysis and systematic review. Osteoporos Int 2010; 21 : 183-7. |
|93.||Ginsberg G, Tulchinsky T, Filon D, Goldfarb A, Abramov L, Rachmilevitz EA. Cost benefit analysis of a national thalassemia prevention programme in Israel. J Med Screening 1998; 5 : 120-6. |
|94.||Guidelines for control of hemoglobin disorders. World Health Organization hereditary disease program. WHO/HDP/HB/gl/94.1. Geneva: WHO; 1994. |
|95.||Cao A, Galanello R, Rosatelli MC. Prenatal diagnosis and screening of the haemoglobinopathies. Baillieres Clin Haematol 1998; 11 : 215-38. |
|96.||Verma IC, Choudhry VP, Jain PK. Prevention of thalassemia: a necessity in India. Indian J Pediatr 1992; 59 : 649-54. |
|97.||Angastiniotis MA, Model B. Prevention of thalassemia in Cyprus. Lancet 1981; 1 : 369-70. |
|98.||Angastiniotis MA, Kyriakidou S, Hadjiminas M. How thalassemia was controlled in Cyprus. World Health Forum 1986; 7 : 291-7. |
|99.||Stamatoyannopoulos G. Probelms of screening and counseling in the hemoglobinopathies. In: Motulsky AG, Lenz W, editors. Birth defects. Amsterdam: Excerpta Medica; 1974. p. 268-76. |
|100.||Gamberini MR, Lucci M, Vullo C, Anderson B, Canella R, Barrai I. Reproductive behavior of families segregating for Cooley's anaemia before and after the availability of prenatal diagnosis. J Med Genet 1991; 28 : 523-9. |
|101.||Samavat A, Modell B. Iranian national thalassemia screening programme. BMJ 2004; 329 : 1134-7. |
|102.||Haddow JE. Couple screening to avoid thalassemia: successful in Iran and instructive for us all. J Med Screen 2005; 12 : 55-6. |
|103.||Karimi M, Jamalian N, Yarmohammadi H, Askarnejad A, Afrasiabi A, Hashemi A. Premarital screening for â-thalassaemia in Southern Iran:options for improving the programme J Med Screen 2007; 14 : 62-6. |
|104.||Zeesman S, Clow CL, Cartier L, Scriver CR. A private view of heterozygosity:eight year follow-up study on carriers of Tay - Sachs gene detected by high- school screening in Montreal. Am J Med Genet 1984; 18 : 769-78. |
|105.||Chattopadhyay S. 'Rakter dosh' - corrupting blood: The challenges of preventing thalassemia in Bengal, India. Soc Sci Med 2006; 63 : 2661-73. |
|106.||Tamhankar PM, Agarwal S, Arya V, Kumar R, Gupta UR, Agarwal SS. Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India. Prenat Diagn 2009; 29 : 83-8. |
|107.||Silverstroni E, Bianco I. Screening for microcytemia in Italy: Analysis of data collected in the past 30 years. Am J Hum Genet 1975; 27 : 198-212. |
|108.||Mehta BC, Iyer PD, Gandhi SG, Ramnath SR, Patel JC. Diagnosis of heterozygous beta-thalassemia in a population with high prevalence of iron deficiency. Indian J Med Sci 1973; 27 : 832-5. |
|109.||Gomber S, Madan N. Validity of Nestroft in screening and diagnosis of â-thalassemia trait. J Trop Pediatr 1997; 43 : 363-6. |
|110.||Mamtani M, Das K, Jawahirani A, Rughwani V, Kulkarni H. Is NESTROFT sufficient for mass screening for beta-thalassaemia trait? J Med Screen 2007; 14 : 169-73. |
|111.||Saraya AK, Kumar R, Sehgal AK. Iron status in heterozygous beta-thalassemia: detection of coexisting iron deficiency by transferrin saturation and serum ferritin. Birth Defects Orig Artic Ser 1988; 23 : 9-18. |
|112.||Madan N, Sikka M, Sharma S, Rusia U. Frequency of coincident iron deficiency and beta-thalassaemia trait. J Clin Pathol 1996; 49 : 1021. |
|113.||Madan N, Sikka M, Sharma S, Rusia U. Phenotypic expression of hemoglobin A2 in â-thalassemia trait with iron deficiency. Ann Hematol 1998; 77 : 93-6. |
|114.||Menon SR, Khatkhatay MI, Dandekar SP, Patel ZM. Development and validation of an ELISA for hemoglobin-A2: a novel method for â-thalassemia screening in developing countries. J Immunoassay Immunochem 2004; 25 : 135-46. |
|115.||Ravindran MS, Patel ZM, Khatkhatay MI, Dandekar SP. Beta-thalassaemia carrier detection by ELISA: a simple screening strategy for developing countries. J Clin Lab Anal 2005; 19 : 22-5. |
|116.||Colah R, Thomas M, Mayekar P. Assessing the impact of screening and counselling high school children for â-thalassaemia in India. J Med Screen 2007; 14 : 158. |
|117.||Ahmed S, Saleem M, Modell B, Petrou M. Screening extended families for genetic hemoglobin disorders in Pakistan. N Engl J Med 2002; 347 : 1162-8. |
|118.||Cao A, Galanello R. Effect of consanguinity on screening of thalassemia. N Engl J Med 2002; 347 : 1200-2. |
|119.||Gorakshakar AC, Colah RB. Cascade screening for beta-thalassemia: A practical approach for identifying and counseling carriers in India. Indian J Community Med 2009; 34 : 354-6. |
|120.||Yagnik H. Post counseling follow up of thalassemia in high risk communities. Indian Pediatr 1997; 34 : 1115-8. |
|121.||Saxena A, Phadke SR. Feasibility of thalassaemia control by extended family screening in Indian context. J Health Popul Nutr 2002; 20 : 31-5. |
|122.||Indian Red Cross Society (IRCS), Gujarat State Branch. Annual Report 2009-2010. Ahmedabad: IRCS, Gujarat State Branch; 2010. |
|123.||Colah R, Surve R, Wadia M, Solanki P, Mayekar P, Thomas M, et al. Carrier screening for beta-thalassemia during pregnancy in India: a 7-year evaluation. Genet Test 2008; 12 : 181-5. |
|124.||Mohanty D, Colah R, Gorakshakar. Jai Vigyan S & T Mission Project on community control of thalassemia syndromes - Awareness, screening, genetic counseling and prevention. New Delhi: Indian Council of Medical Research; 2008. |
|125.||Muralitharan S, Srivastava A, Shaji RV, Mathai M, Srivastava VM, Dennison D, et al. Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique. Natl Med J India 1996; 9 : 70-1. |
|126.||Saxena R, Jain PK, Thomas E, Verma IC. Prenatal diagnosis of beta-thalassaemia: experience in a developing country. Prenat Diagn 1998; 18 : 1-7. |
|127.||Thakur (Mahadik) C, Vaz F, Banerjee M, Kapadia C, Natrajan PG, Yagnik H, et al. Prenatal diagnosis of beta-thalassaemia and other haemoglobinopathies in India. Prenat Diagn 2000; 20 :194-201. |
|128.||Garewal G, Das R, Ahluwalia J, Marwaha RK, Varma S. Nucleotide -88 (C-T) promoter mutation is a common beta-thalassemia mutation in the Jat Sikhs of Punjab, India. Am J Hematol 2005; 79 : 252-6. |
|129.||Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians. Eur J Haematol 2007; 79 : 417-21. |
|130.||Newton CR, Graham A, Heptinstall LE, Powell SJ, Summers C, Kalsheker N, et al. Analysis of any point mutation in DNA - the amplification refractory mutation system (ARMS). Nucleic Acids Res 1989; 17 : 2503-16. |
|131.||Wadia MR, Phanasgaokar SP, Nadkarni AH, Surve RR, Gorakshakar AC, Colah RB, et al. Usefulness of automated chromatography for rapid fetal blood analysis for second trimester prenatal diagnosis of beta-thalassemia. Prenat Diagn 2002; 22 : 153-7. |
|132.||Rao S, Saxena R, Deka D, Kabra M. Use of HbA estimation by CE-HPLC for prenatal diagnosis of beta-thalassemia; experience from a tertiary care centre in north India: a brief report. Hematology 2009; 14 : 122-4. |
|133.|| http://www.who.int/healthinfo/global_burden_disease/en/, accessed on October 4, 2011. |
|134.|| http://data.worldbank.org/about/country-classifications, accessed on October 4, 2011. |
|135.||Weatherall DJ. Keynote address: The challenge of thalassemia for the developing countries. Ann N Y Acad Sci 2005; 1054 : 11-7. |