|Year : 2019 | Volume
| Issue : 3 | Page : 384-388
Impact of tuberculosis on glycaemic status: A neglected association
Darshan Krishnappa1, Surendra K Sharma1, Achintya Dinesh Singh1, Sanjeev Sinha1, AC Ammini2, Manish Soneja1
1 Department of Medicine, All India Institute of Medical Sciences, New Delhi, India
2 Department of Endocrinology, All India Institute of Medical Sciences, New Delhi, India
|Date of Submission||03-Dec-2017|
|Date of Web Publication||24-Jun-2019|
Dr Surendra K Sharma
Department of Molecular Medicine, Jamia Hamdard Institute of Molecular Medicine, Hamdard University, Hamdard Nagar, New Delhi 110 062
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background & objectives: Diabetes mellitus (DM) is an important risk factor for tuberculosis and has received increasing emphasis. However, the reverse association of tuberculosis impacting blood sugar levels has not been well studied. The present study was conducted to evaluate the prevalence of hyperglycemia in patients with tuberculosis and assess its resolution following successful treatment of tuberculosis.
Methods: In this prospective study, a total of 582 patients with tuberculosis were evaluated for hyperglycaemia [DM or impaired glucose tolerance (IGT)] with random blood sugar (RBS) and all patients with RBS >100 mg/dl were subjected to a 75 g oral glucose tolerance test (OGTT). All patients received thrice weekly intermittent Directly Observed Treatment Short Course (DOTS) for tuberculosis. Patients with hyperglycaemia were re-evaluated at the end of anti-tuberculosis treatment with an OGTT and glycated hemoglobin (HbA1c) levels to assess for glycaemic status.
Results: In the present study, 41 of the 582 patients were found to have DM [7%, 95% confidence interval (CI) (5.2, 9.4)] while 26 patients were found to have IGT [4.5%, 95% CI (3, 6.5)]. Three patients were lost to follow up. Of the 26 patients with IGT, 17 [65.4%, 95% CI (46.1, 80.7)] reverted to euglycaemic status following successful treatment of tuberculosis, while the blood sugar levels improved in all patients with DM following treatment of tuberculosis.
Interpretation & conclusions: Our study results show that tuberculosis adversely impacts glycaemic status with improvement in blood sugar levels at the end of successful treatment of tuberculosis. Longitudinal studies with large sample size are required to confirm these findings.
Keywords: Diabetes mellitus - impaired glucose tolerance - pancreatic dysfunction - stress-induced hyperglycaemia - tuberculosis
|How to cite this article:|
Krishnappa D, Sharma SK, Singh AD, Sinha S, Ammini A C, Soneja M. Impact of tuberculosis on glycaemic status: A neglected association. Indian J Med Res 2019;149:384-8
|How to cite this URL:|
Krishnappa D, Sharma SK, Singh AD, Sinha S, Ammini A C, Soneja M. Impact of tuberculosis on glycaemic status: A neglected association. Indian J Med Res [serial online] 2019 [cited 2019 Nov 22];149:384-8. Available from: http://www.ijmr.org.in/text.asp?2019/149/3/384/261111
Surendra K. Sharma - Present address: Department of Molecular Medicine, Jamia Hamdard Institute of Molecular Medicine, New Delhi 110 062, India
A.C. Ammini - Deceased
The adverse impact of diabetes mellitus (DM) on tuberculosis has been well known. Tuberculosis has been found to occur commonly among patients with DM, with general consensus for a unidirectional association between the two conditions since the majority of studies involved patients diagnosed with DM who went on to develop tuberculosis. A multi-centre study showed a prevalence of 13 per cent of DM in tuberculosis. DM is not only associated with an increased risk for tuberculosis, but it may also impact clinical presentation and treatment outcomes. While some studies have reported a higher sputum positivity, longer time to sputum conversion and higher rates of cavitation,, other studies have reported no difference,. This discrepancy may be related to the status of blood sugar control.
The role of tuberculosis in the development of DM was first suspected by Munkner and Nichols and has since found more favour among researchers with numerous animal and human studies linking a role for tuberculosis in the development of DM,,,. Human studies assessing the reversibility of impaired glucose tolerance (IGT) with the treatment of tuberculosis are, however, limited. This prospective study was carried out to determine the presence of hyperglycaemia (DM and IGT) in patients with tuberculosis and to assess its resolution following successful treatment of tuberculosis.
| Material & Methods|| |
This study was conducted at the All India Institute of Medical Sciences (AIIMS), New Delhi, India. Patients were recruited between May 2012 and December 2013. All patients were followed up for one year after recruitment. All consecutive patients of either sex, aged between 15 and 65 yr presenting to the Directly Observed Treatment, Short-course (DOTS) centre at AIIMS, New Delhi, with a diagnosis of tuberculosis (TB) were enrolled for the study. Both treatment naïve and treatment experienced patients were included. The patients suffering from human immunodeficiency virus (HIV) infection, multidrug-resistant tuberculosis, receiving corticosteroids, aged <15 yr, pregnant women and those not willing for follow up were excluded from the study.
Institutional Ethics Committee of AIIMS, New Delhi, India, approved the study. Written informed consent was obtained from each participant enrolled in the study.
Study design: In this prospective longitudinal study, eligible patients were enrolled after establishing the diagnosis of TB according to previously described criteria. A diagnosis of tuberculosis was made as per the World Health Organization criteria for smear-positive, smear-negative pulmonary TB or extrapulmonary TB,. In all patients, random blood sugar (RBS) was checked using a glucometer (Accu-Chek® Active, Roche Diagnostics, Switzerland). All patients with an RBS more than 100 mg/dl underwent a 75 g oral glucose tolerance test (OGTT) in the morning after eight hours overnight fasting. Patients were diagnosed to have IGT as per the WHO criteria. Patients with IGT were re-evaluated with a 75 g OGTT and glycosylated haemoglobin (HbA1c) at the end of treatment. Patients with persistent IGT were re-evaluated one year after treatment. Patients received category I or category II intermittent thrice weekly anti-tuberculosis therapy from DOTS centre as per the Revised National Tuberculosis Control Programme guidelines.
Statistical analysis: For all comparisons between patients with IGT and those without, Chi-square test or Fisher's exact test was used for categorical data while Student's t test and Wilcoxon rank-sum test were used for continuous data. The analysis was performed using Stata 11.2 for Windows (Stata Corp, College Station, TX, USA).
| Results|| |
A total of 582 patients were recruited in the study. Of these, 35 (6%) patients had type 2 DM. A RBS test was done in the remaining 547 patients, of whom 250 patients had blood sugars above 100 mg/dl and underwent an OGTT. Of these patients, six were newly diagnosed to have DM while 26 patients were found to have IGT, [Figure 1]. Thus, 41 of the 582 patients were found to have DM [7%, 95% confidence interval (CI) (5.2, 9.4)] while 26 patients were found to have IGT [4.5%, 95% CI (3, 6.5)]. Patients with IGT were older than euglycaemic patients (36.5 vs. 31 yr, P <0.05). There were no significant differences between the two groups of patients with respect to body mass index (BMI) or type of tuberculosis. Characteristics of patients with IGT and those with euglycaemic status are described in the [Table 1].
|Figure 1: Study profile for the presence of hyperglycaemia in tuberculosis patients. TB, tuberculosis; RBS, random blood sugar level; OGTT, oral glucose tolerance test; DM, diabetes mellitus; IGT, impaired glucose tolerance.|
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|Table: Characteristics of patients with impaired glucose tolerance and diabetes mellitus (DM)|
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Patients with DM were older than non-diabetic patients (45.6 vs. 31 yr, P <0.001) and were found to have a higher BMI (22.5 vs. 20.4 kg/m). There was no significant difference between the two groups with respect to type of tuberculosis [Table 1].
Of the 26 patients with IGT, three patients were lost to follow up, while a 75 g OGTT was repeated and a HbA1c was done at the end of treatment in the remaining 23 patients. All patients with DM were followed up with HbA1c measurements every three monthly and were treated with lifestyle modification measures and oral hypoglycaemic agents (OHA) and/or insulin as appropriate.
Of the 23 patients with IGT, eight patients (34.8%) were found to have persistent IGT while 15 patients were found to be euglycaemic at the end of treatment. Of the eight patients with persistent IGT at the end of treatment, five were lost to follow up while two patients reverted to euglycaemic status one year after completion of treatment and one patient died likely due to severe dengue infection during the dengue outbreak. Thus, 17 of the 26 patients with IGT reverted to euglycaemic status one year after the completion of treatment [65.4%, 95% CI (46.1, 80.7)] [Figure 2]. Of the 41 diabetic patients, six (14.6%) newly detected diabetic patients continued to remain diabetic one year after the completion of treatment.
|Figure 2: Follow up of patients with impaired glucose tolerance (IGT) at the end of treatment and on one-year post-treatment follow up. Abbreviations are as given in Fig.1.|
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Tuberculosis and DM have a bi-directional relationship with each condition adversely impacting the other. There are several mechanisms by which tuberculosis can cause hyperglycaemia: the stress of disease leads to increased release of hormones such as cortisol which increase blood sugars; also release of various cytokines, chemokines and tubercular proteins may cause pancreatic dysfunction, the so-called 'concomitant pancreatitis'. This dysfunction is likely due to increased deposition of amylin within the pancreas consequent to increased beta cell function due to the transient hyperglycaemia at the onset of disease it may also occur due to direct invasion of the pancreas by the mycobacteria which often goes unrecognized,.
In the present study, seven per cent patients were found to have DM. The prevalence of DM varies from as high as 19.5 per cent in Kerala to 6.1 per cent in the Kashmir valley,, A large multi-centric study found 13 per cent prevalence of DM among tuberculosis across India.
IGT was found in 4.5 per cent patients. This was lower compared to other studies which reported the IGT between 10.3 and 14 per cent,. However, these studies have been done in different parts of India and the prevalence IGT has regional variation. In addition, our study had a higher proportion of patients with extrapulmonary TB while the association with hyperglycaemia was higher with pulmonary TB.
The limitation of the present study was that all patients with IGT received advice regarding lifestyle modification which could have also contributed to the improvement in glycaemic status. IGT is considered a risk factor for future development of DM. Although IGT in patients with TB may be related to the stress of infection and often reverts following successful treatment of TB, these patients remain at risk for future development of DM. Further, the progression to DM increases the risk of recurrence of TB. Therefore, patients diagnosed with IGT should receive lifestyle modification and close follow up of blood sugar status and not be neglected as mere cases of transient stress hyperglycaemia.
In conclusion, our study showed the adverse impact of tuberculosis on glycaemic status. Given the high prevalence of active and latent tuberculosis infection in our country and the increasing prevalence of DM, further analyzing this association may contribute to filling the knowledge gap regarding the pathogenesis of DM and eventually enable a permanent cure for this condition. Long-term studies with large sample size are required after completion of anti-TB treatment to determine the reversible nature of these metabolic changes.
Acknowledgment: The authors thank the State Tuberculosis Officer, Delhi for his valuable guidance in the conduct of this study. The authors would also like to thank all the participating patients and Vineet, Rohini, Vinod, Mikashmi and Jigyasa for facilitating the study.
Financial support & sponsorship: The study was supported by the JC Bose National Fellowship awarded to the second author (SKS) (SB/S2/JCB-04/2013), from the Department of Science & Technology, Ministry of Science and Technology, Government of India, New Delhi.
Conflicts of Interest: None.
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