Indan Journal of Medical Research Indan Journal of Medical Research Indan Journal of Medical Research Indan Journal of Medical Research
  Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contacts Login  
  Home Print this page Email this page Small font sizeDefault font sizeIncrease font size Users Online: 124       

   Table of Contents      
ORIGINAL ARTICLE
Year : 2015  |  Volume : 141  |  Issue : 6  |  Page : 799-806

Treatment of vitamin D deficiency is an effective method in the elimination of asymptomatic bacterial vaginosis: A placebo-controlled randomized clinical trial


1 Department of Midwifery, School of Nursing & Midwifery, Tehran University of Medical Sciences, Tehran, Iran
2 Reproductive Health Department, Tehran University of Medical Sciences, Tehran, Iran
3 Department of Epidemiology & Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
4 Department of Medical Parasitology & Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran

Date of Submission25-Feb-2013
Date of Web Publication14-Jul-2015

Correspondence Address:
Maryam Modarres
Department of Midwifery, School of Nursing & Midwifery, Tehran University of Medical Sciences, Nosrat st. Tohid sq, Tehran
Iran
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0971-5916.160707

Rights and Permissions
   Abstract 

Background & objectives: Bacterial vaginosis (BV) is the most prevalent vaginal infection in women of reproductive age group which has been found to be associated with vitamin D deficiency. The purpose of this study was to investigate the effectiveness of the administration of 2000 IU/day edible vitamin D for 15 wk to eliminate asymptomatic BV among reproductive age women with vitamin D deficiency.
Methods: A total of 208 women with asymptomatic BV, who were found to be eligible after interviews and laboratory tests, were randomly assigned to a control group (n=106) or an intervention group (n=105). They used vitamin D drops daily for 105 days. Vaginal and blood samples were taken before and after the second intervention using identical methods (Nugent score for BV diagnosis, serum 25-hydroxyvitamin D for vitamin D determination).
Results: The cure rate of asymptomatic BV was 63.5 per cent in the intervention and 19.2 per cent in the control group (P <0.001). The results showed that being unmarried (P=0.02), being passive smoker
(P<0.001), and being in the luteal phase of a menstrual cycle during sampling (P=0.01) were significantly associated with post-intervention BV positive results. After these elements were controlled, the odds of BV positive results in the control group was 10.8 times more than in the intervention group (P<0.001).
Interpretation & conclusions: Among women in reproductive age group with vitamin D deficiency, the administration of 2000 IU/day edible vitamin D was effective in eliminating asymptomatic BV. This treatment could be useful in preventing the symptoms and side effects of BV.

Keywords: Bacterial vaginosis - reproductive age women - vaginal infection - vitamin D


How to cite this article:
Taheri M, Baheiraei A, Foroushani AR, Nikmanesh B, Modarres M. Treatment of vitamin D deficiency is an effective method in the elimination of asymptomatic bacterial vaginosis: A placebo-controlled randomized clinical trial. Indian J Med Res 2015;141:799-806

How to cite this URL:
Taheri M, Baheiraei A, Foroushani AR, Nikmanesh B, Modarres M. Treatment of vitamin D deficiency is an effective method in the elimination of asymptomatic bacterial vaginosis: A placebo-controlled randomized clinical trial. Indian J Med Res [serial online] 2015 [cited 2020 Nov 30];141:799-806. Available from: https://www.ijmr.org.in/text.asp?2015/141/6/799/160707

Bacterial vaginosis (BV) with its high prevalence among vaginal infections is well-known for its adverse effects in pregnancy [1] and the reproductive period [2] . The most important and undesirable consequence of BV is the increased risk of preterm labour in pregnant women [3],[4] , even in asymptomatic infections [5] . [ ] Treatment of symptomatic BV is necessary, but antibiotic therapy for asymptomatic BV is not currently recommended, except among the high risk population [6] . Asymptomatic women do not have clinical complaints, but the Nugent scores of their vaginal discharge confirm BV. Although the aetiology of BV is not well-known, yet risk factors such as vaginal douching, race, smoking, chronic stress, and local immune deficiency have been considered [7] .

An important factor is the higher incidence of BV among Blacks [8] , who have a higher prevalence of vitamin D deficiency compared to their white counterparts [9] . Due to the role of vitamin D in the regulation of the immune system [10] , this finding led to the hypothesis that vitamin D could be a modulator of genital immunity and its deficiency might lead to BV. Bodnar et al[11] confirmed the relationship between vitamin D deficiency and BV in pregnant women. Though cross-sectional studies have failed to confirm this relationship in non-pregnant women [11],[12] , more research has been done in this area [12] . The impact of vitamin D consumption and compensating for its deficiency on eliminating BV has not been studied. The objective of this study was to examine the effect of 2000 IU/day edible vitamin D in eliminating asymptomatic BV among reproductive age women with vitamin D deficiency.


   Material & Methods Top


This placebo-controlled randomized clinical trial was conducted between June 2011 and March 2012. The study was performed at the gynaecology clinic of Imam Khomeini Hospital, Tehran, Iran, among reproductive age women. Using 95 per cent power and 95 per cent significance level (two-sided) to detect a 20 per cent success in the experimental group, a sample size of 101 per group (total of 202) was estimated. Due to the risk of loss during the screening process, however, more women were enrolled at the beginning (211).

The study was approved by the ethics committee of Tehran University of Medical Sciences and was registered at the Registry of Clinical Trials website with No: IRCT201105096284N2. Written consent was obtained from all participants before enrolment.

Women in the age group of 18-35 yr with asymptomatic BV and vitamin D deficiency, who had maintained a stable medical condition during the previous six months, were eligible for the study. Asymptomatic BV was defined by Nugent score and lack of complaint about vaginal odour and/or abnormal discharge on direct questioning. Screening for vitamin D deficiency [serum 25(OH)D < 75 nmol/l] was done for those with confirmed asymptomatic BV. Exclusion criteria were symptomatic BV (because they required antibiotic therapy), any complaint of vaginal itching, burning, and/or irritation on direct questioning, the detection of a vaginal or cervical infection upon gynaecologic examination, pathological obesity,

tobacco use, history of hypercalcaemia or nephro-lithiasis, current pregnancy, hepatic or renal dysfunction (based on history), malignancy or malabsorption, the current use of medications that suppress immunity or interfere with vitamin D metabolism, and consumption of vitamin D supplements or antibiotics.

A questionnaire was used to collect data on demographic characteristics, reproductive history, and lifestyle of women. During the first visit, women were screened for BV and vitamin D levels. Screening of BV included two phases: vaginal pH determination and Nugent scoring. Amsel's criteria is not applicable in the diagnosis of asymptomatic BV [13] ; therefore, the pH of vaginal discharge was tested using a colour strip (Universalindikator Merck, Germany). Simultaneously, gynaecological examination was performed using a non-lubricated speculum. Women who had a vaginal pH > 4.5 entered the second phase of BV screening, and samples of their vaginal discharge were collected by Dacron swab. These samples taken from the vaginal wall by swabs were spread on a glass slide and were dried at room temperature. These were passed through the flame of a Bunsen burner several times to induce heat fixation. The vaginal slides were evaluated by Nugent scoring. This scoring system has been considered to be a reliable and cost-effective method for the laboratory evaluation of BV [14] . In this study, a Nugent score of 7-10 was considered as evidence of BV.

During this screening visit, blood samples were also collected. Serum samples were stored in aliquots at -20°C until the analysis time. EIA (enzymatic immuno assay) kits (Immuno Diagnostic Systems, UK) were used to measure the serum 25(OH)D at the beginning of the study and after the intervention. The serum samples of women confirmed as BV positive were screened for hypovitaminosis. Given the recommended concentration of vitamin D [15],[16] , women with levels below 75 nmol/l were considered vitamin D deficient.

The eligible participants were randomized at the second visit by the block randomization method. A computer-generated randomization was used to create the sequence of allocation; 53 blocks with size of four were used to achieve equal sample sizes across both groups. Each participant had an identification number and was assigned to a study group based on randomization list; 105 participants were randomly entered into the intervention group and consumed two drops/day of vitamin D3 edible oily solution (Equivalent to 2000 IU/day of vitamin D3) with the largest meal of the day [17] for 105 days ([Figure 1]). This dosage of vitamin D was recommended by the Food and Nutrition Board [18] . Studies which used this dosage of vitamin D for enhancing immune activity considered a 12-wk intervention [19],[20] . As the participants in this study were vitamin D deficient, so the intervention period was increased to 15 wk.
Figure 1. Flowchart showing the trial profile. After screening process, 211 eligible women used 2 drops/day of randomly chosen solutions for 15 wk. Asymptomatic BV was evaluated by Nugent score; score of 0-3 was defined as BV negative (score of 4-6 was not seen at all). Three women did not continue the study.

Click here to view


The control group used placebo drops (sesame oil), which had the same appearance, colour, taste and smell as the vitamin D 3 drops, for the same duration. The solutions of vitamin D and placebo were labelled as B and A, respectively; blinding was maintained by concealing information about real constituents of these solutions. Phone calls were made to the participants every two weeks to ensure the proper use of the drops. Participants were instructed to return to the clinic in case of abnormal vaginal discharge. Five women complained of vaginal discharge; they were confirmed to have symptomatic BV during the study using Nugent score (Figure). At this point they stopped the solution intake and were referred to a gynaecologist. Due to the importance of this outcome, however, we computed them as a persistent BV positive in data analysis.

After 15 wk, participants were told to stop the intake of solutions and were referred to the clinic. At this follow up visit, vaginal and blood samples were collected again and analyzed. A clinical cure of asymptomatic BV was defined as having a Nugent score of 0-3.

At the end of the study, women were informed of their group, BV status, and level of vitamin D.

Statistical analysis: Data were analyzed using the SPSS 16.0 statistical package (SPSS Inc, Chicago, Illinois, USA). The chi-squared test was used to compare distributions of independent variables between the two groups and by asymptomatic BV status (after intervention). Regression logistic was used to control confounding variables.


   Results Top


Of the 211 women, three (1 from the control group and 2 from the intervention group) were excluded in the first weeks of the study (2 women did not continue use of the drug; 1 woman used antibiotics). The average age of the 208 study participants was 29.4 ± 4.8 yr (range 18-35 yr); the average age of women was 29.6 ± 4.5 yr in the control group and 29.2±5.0 yr in the intervention group. [Table 1] presents characteristics of the study participants in the two groups. No significant difference was found in any of the parameters between the two groups.
Table 1. Characteristics of the participants included in the study


Click here to view


[Table 2] demonstrates the mean values of Nugent score, vaginal pH and serum 25(OH)D; the changes of these values in the two groups are shown with 95% CI (confidence interval).
Table 2. mean values of laboratory test results


Click here to view


The cure rate was 63.5 per cent in the intervention and 19.2 per cent in the control group (P <0.001). Intervention, marital status, menstrual phase at the time of sampling and passive smoking had significant relationships with the dependent variable (bacterial vaginosis) ([Table 3]).
Table 3. Outcomes of logistic regression analysis for controlling confounding factors on elimination of bacterial vaginosis


Click here to view


Being married, sampling in the proliferative phase, and not being a passive smoker increased the chance of BV clearance after the intervention.


   Discussion Top


Our results showed that the use of 2000 IU/day vitamin D for 15 wk was an effective treatment method for asymptomatic BV among vitamin D-deficient, reproductive age women. The findings also indicated that married status, not being a passive smoker, and being in the proliferative phase of the menstrual cycle during sampling, were related to the cure of BV. A high prevalence of vitamin D deficiency among reproductive age group women was seen in (97%, 211/218) the study participants; 36 per cent of our participants (218/605) were confirmed as having asymptomatic BV. Bodnar et al[12] found that the prevalence of BV decreased when vitamin D levels were elevated. Hensel et al[12] used data from NHANES (National Health and Nutrition Examination Survey) and reported that the association between BV and vitamin D deficiency was meaningful only among pregnant women; in non-pregnant women, this relationship was not confirmed. This finding could be due to higher amounts of circulating 25(OH)D in pregnant women [21] . The production of cathelicidins is higher among pregnant women, and it can lead to more immunity against BV. Intervention using a daily and constant dosage of vitamin D might be appropriate for increasing the circulating 25(OH)D in the non-pregnant women as done in the current study.

The effect of vitamin D on BV elimination can be explained by the impact of vitamin D on the immune system, especially in the local immunity of the vagina. Cytokines were considered the main factor linking BV and vitamin D [11],[22] . Yusupov et al[20] evaluated the effectiveness of 2000 IU/day of vitamin D on serum cytokines levels and found it to be ineffective. They proposed that cytokines could not be the mediating factor between vitamin D and asymptomatic BV, although Ryckman et al[23] reported a significant difference between the cytokines and chemokines of BV positive and negative women. It has been suggested that adequate levels of 25(OH)D can protect women from BV by aiding in the production of cathelicidins [24] . Based on these findings, our assumption is that higher serum 25(OH)D levels increase the production of cathelicidins and thereby enhance the immunity of the genital tract. BV clearance in the control group could be due to the improvement in vaginal health. We did not repeat the questionnaire at the end of the intervention, so analysis of these changes was not possible. The failure of some women to respond to treatment could be due to concurrent parameters weakening vaginal immunity.

Almost all of our participants were vitamin D-deficient, while Bodnar et al[25] demonstrated that only 46 per cent of Black women (the high risk population) from the USA were vitamin D-deficient. This considerable difference may be partly explained by cultural and social behaviours of women in this study. Because of high percentage of vitamin D deficiency among Iranian mothers (86%) [26] and similar findings of the current study, prevention and treatment policies should be applied in the general population.

In a trial, the same dosage of vitamin D was used to increase serum cytokines [20] , the percentage of people with normal levels of vitamin D (>75 nmol/l) rose from 23 to 73 per cent in the intervention group, whereas in our intervention group levels of vitamin D before and after intervention were 0 and 46.2 per cent, respectively.

It has been demonstrated that everyone does not have the same response of serum 25(OH)D level to the standard treatment; difference in response of vitamin D levels is not related to the age [27] . But in the current study we found that it could be related with parity and gravidity. Frequent pregnancies could lead to severe reduction of maternal vitamin D reserves for a long time. This deprivation can decrease the response to vitamin D treatment. The dosage of vitamin D used in the current had no adverse effects. The safety of a dose of 4000 IU/day for at least six months for pregnant women was confirmed by Hollis et al[28] .

Risk factors of asymptomatic BV resistance recognized in our study had been identified as the risk factors of BV in another research [29],[30] . Smoking is known to have an adverse effect on the metabolism of vitamin D [31 ] which can lead to vitamin D deficiency [32] and make treatment difficult. Mania-Pramanik et al[33] revealed that BV and infertility were significantly associated, regardless of tubal damage. In our study, a positive history of infertility (in the past years and not currently) was related to BV, but the relationship was not meaningful.

The main strength of this study was the measurement of 25(OH)D in two stages (baseline and after intervention). The lack of laboratory analysis of factors such as parathyroid hormone (PTH), calcium and phosphorous, the inability of the dosage or duration of intervention to increase the level of vitamin D in participants to normal ranges for all cases, and the lack of investigation into the immune factors at both stages of the study were weaknesses of this clinical trial; genital co-infections were not evaluated by standard laboratory tests before or after the intervention, so their rates were disregarded. The limitations of this study were performing vitamin D measurements in two different seasons, and not using DNA-based tests to enhance sensitivity and specificity for BV detection. In the current study, vaginal sampling from women was performed without considering their menstrual cycle phase. It would have been better to consider sampling in the proliferative phase as an inclusion criterion. Adding a follow up period for the evaluation of serum 25(OH)D levels and BV status would be considered in future studies.

In conclusion, the treatment of vitamin D deficiency using 2000 IU/day edible vitamin D for 15 wk was an effective way to cure the asymptomatic BV. We recommend vitamin D therapy for the prevention or management of BV among deficient women. By treating vitamin D deficiency, preterm labour and other adverse effects of BV may be prevented.


   Acknowledgment Top


This project was funded and supported by Tehran University of Medical Sciences (TUMS); grant no: 90-01-28-13331.

 
   References Top

1.
Ryckman KK, Williams SM, Kalinka J. Correlations of selected vaginal cytokine levels with pregnancy-related traits in women with bacterial vaginosis and mycoplasmas. J Reprod Immunol 2008; 78 : 172-80.  Back to cited text no. 1
    
2.
Verstraelen H, Verhelst R, Vaneechoutte M, Temmerman M. The epidemiology of bacterial vaginosis in relation to sexual behaviour. BMC Infect Dis 2010; 10 : 81.  Back to cited text no. 2
    
3.
Carey JC, Klebanoff MA. Is a change in the vaginal flora associated with an increased risk of preterm birth? Am J Obstet Gynecol 2005; 192 : 1341-6; discussion 1346-7.  Back to cited text no. 3
    
4.
Donders GG, Van Calsteren K, Bellen G, Reybrouck R, Van den Bosch T, Riphagen I, et al. Predictive value for preterm birth of abnormal vaginal flora, bacterial vaginosis and aerobic vaginitis during the first trimester of pregnancy. BJOG 2009; 116 : 1315-24.  Back to cited text no. 4
    
5.
Leitich H, Kiss H. Asymptomatic bacterial vaginosis and intermediate flora as risk factors for adverse pregnancy outcome. Best Pract Res Clin Obstet Gynaecol 2007; 21 : 375-90.  Back to cited text no. 5
    
6.
Workowski KA, Berman SM. Sexually transmitted diseases treatment guidelines, 2006. MMWR Recomm Rep 2006; 55 : 1-94.  Back to cited text no. 6
    
7.
Neggers YH, Nansel TR, Andrews WW, Schwebke JR, Yu KF, Goldenberg RL, et al. Dietary intake of selected nutrients affects bacterial vaginosis in women. J Nutr 2007; 137 : 2128-33.  Back to cited text no. 7
    
8.
Allsworth JE, Peipert JF. Prevalence of bacterial vaginosis: 2001-2004 National Health and Nutrition Examination Survey data. Obstet Gynecol 2007; 109 : 114-20.  Back to cited text no. 8
    
9.
Looker AC, Dawson-Hughes B, Calvo MS, Gunter EW, Sahyoun NR. Serum 25-hydroxyvitamin D status of adolescents and adults in two seasonal subpopulations from NHANES III. Bone 2002; 30 : 771-7.  Back to cited text no. 9
    
10.
Shin JS, Choi MY, Longtine MS, Nelson DM. Vitamin D effects on pregnancy and the placenta. Placenta 2010; 31 : 1027-34.  Back to cited text no. 10
    
11.
Bodnar LM, Krohn MA, Simhan HN. Maternal vitamin D deficiency is associated with bacterial vaginosis in the first trimester of pregnancy. J Nutr 2009; 139 : 1157-61.  Back to cited text no. 11
    
12.
Hensel KJ, Randis TM, Gelber SE, Ratner AJ. Pregnancy-specific association of vitamin D deficiency and bacterial vaginosis. Am J Obstet Gynecol 2011; 204 : 41.e1-9.  Back to cited text no. 12
    
13.
McGregor JA, French JI. Bacterial vaginosis in pregnancy. Obstet Gynecol Surv 2000; 55 (Suppl 1) : 1-19.  Back to cited text no. 13
    
14.
Mohanty S, Sood S, Kapil A, Mittal S. Interobserver variation in the interpretation of Nugent scoring method for diagnosis of bacterial vaginosis. Indian J Med Res 2010; 131 : 88-91.  Back to cited text no. 14
    
15.
Bischoff-Ferrari HA, Giovannucci E, Willett WC, Dietrich T, Dawson-Hughes B. Estimation of optimal serum concentrations of 25-hydroxyvitamin D for multiple health outcomes. Am J Clin Nutr 2006; 84 : 18-28.  Back to cited text no. 15
    
16.
Bischoff-Ferrari HA. Optimal serum 25-hydroxyvitamin D levels for multiple health outcomes. Adv Exp Med Biol 2008; 624 : 55-71.  Back to cited text no. 16
    
17.
Mulligan GB, Licata A. Taking vitamin D with the largest meal improves absorption and results in higher serum levels of 25-hydroxyvitamin D. J Bone Miner Res 2010; 25 : 928-30.  Back to cited text no. 17
    
18.
Institute of Medicine (US). Dietary reference intakes: for calcium, phosphorus, magnesium, vitamin D, and fluoride.Washington DC: National Academies Press; 1997.  Back to cited text no. 18
    
19.
Li-Ng M, Aloia JF, Pollack S, Cunha BA, Mikhail M, Yeh J, et al. A randomized controlled trial of vitamin D3 supplementation for the prevention of symptomatic upper respiratory tract infections. Epidemiol i0 nfect 2009; 137 : 1396-404.  Back to cited text no. 19
    
20.
Yusupov E, Li-Ng M, Pollack S, Yeh JK, Mikhail M, Aloia JF. Vitamin d0 and serum cytokines in a randomized clinical trial. Int J Endocrinol 2010; 2010 : pii:305054.  Back to cited text no. 20
    
21.
Hollis BW, Wagner CL. Vitamin D and pregnancy: skeletal effects, nonskeletal effects, and birth outcomes. Calcif t0 issue i0 nt 2013; 92 : 128-39.  Back to cited text no. 21
    
22.
Yudin MH, Landers DV, Meyn L, Hillier SL. Clinical and cervical cytokine response to treatment with oral or vaginal metronidazole for bacterial vaginosis during pregnancy: a randomized trial. Obstet Gynecol 2003; 102 : 527-34.  Back to cited text no. 22
    
23.
Ryckman KK, Williams SM, Krohn MA, Simhan HN. Racial differences in cervical cytokine concentrations between pregnant women with and without bacterial vaginosis. J Reprod Immunol 2008; 78 : 166-71.  Back to cited text no. 23
    
24.
Grant WB. Adequate vitamin D during pregnancy reduces the risk of premature birth by reducing placental colonization by bacterial vaginosis species. m0 Bio 2011; 2 : e00022-11.  Back to cited text no. 24
    
25.
Bodnar LM, Simhan HN, Powers RW, Frank MP, Cooperstein E, Roberts JM. High prevalence of vitamin D insufficiency in black and white pregnant women residing in the northern United States and their neonates. J Nutr 2007; 137 : 447-52.  Back to cited text no. 25
    
26.
Kazemi A, Sharifi F, Jafari N, Mousavinasab N. High prevalence of vitamin D deficiency among pregnant women and their newborns in an Iranian population. J Womens Health (Larchmt) 2009; 18 : 835-9.  Back to cited text no. 26
    
27.
Ryan P. Vitamin D therapy in clinical practice. One dose does not fit all. Int J c0 lin p0 ract 2007; 61 : 1894-9.  Back to cited text no. 27
    
28.
Hollis BW, Johnson D, Hulsey TC, Ebeling M, Wagner CL. Vitamin D supplementation during pregnancy: double-blind, randomized clinical trial of safety and effectiveness. J Bone Miner Res 2011; 26 : 2341-57.  Back to cited text no. 28
    
29.
Harville EW, Savitz DA, Dole N, Thorp JM Jr, Herring AH. Psychological and biological markers of stress and bacterial vaginosis in pregnant women. BJOG 2007; 114 : 216-23.  Back to cited text no. 29
    
30.
Thorsen P, Vogel I, Molsted K, Jacobsson B, Arpi M, Moller BR, et al. Risk factors for bacterial vaginosis in pregnancy: a population-based study on Danish women. Acta Obstet Gynecol Scand 2006; 85 : 906-11.  Back to cited text no. 30
    
31.
Brot C, Jorgensen NR, Sorensen OH. The influence of smoking on vitamin D status and calcium metabolism. Eur j0 c0 lin n0 utr 1999; 53 : 920-6.  Back to cited text no. 31
    
32.
Zhao G, Ford ES, Tsai J, Li C, Croft JB. Factors associated with vitamin D deficiency and inadequacy among women of childbearing age in the United States. ISRN Obstet Gynecol 2012; 2012 : 691486.  Back to cited text no. 32
    
33.
Mania-Pramanik J, Kerker SC, Salvi VS. Bacterial vaginosis: a cause of infertility? Int J STD AIDS 2009; 20 : 778-81.  Back to cited text no. 33
    


    Figures

  [Figure 1]
 
 
    Tables

  [Table 1], [Table 2], [Table 3]


This article has been cited by
1 Research Progress of Vitamin D Deficiency and Gestational Diabetes Mellitus
?? ?
Medical Diagnosis. 2020; 10(03): 150
[Pubmed] | [DOI]
2 Relationship between vitamin D status and the vaginal microbiome during pregnancy
Kimberly K. Jefferson,Hardik I. Parikh,Erin M. Garcia,David J. Edwards,Myrna G. Serrano,Martin Hewison,Judith R. Shary,Anna M. Powell,Bruce W. Hollis,Jennifer M. Fettweis,Jerome F. Strauss III,Gregory A. Buck,Carol L. Wagner
Journal of Perinatology. 2019;
[Pubmed] | [DOI]
3 Associations between dietary micronutrient intake and molecular-Bacterial Vaginosis
Susan Tuddenham,Khalil G. Ghanem,Laura E. Caulfield,Alisha J. Rovner,Courtney Robinson,Rupak Shivakoti,Ryan Miller,Anne Burke,Catherine Murphy,Jacques Ravel,Rebecca M. Brotman
Reproductive Health. 2019; 16(1)
[Pubmed] | [DOI]
4 Vitamin D in the Middle East and North Africa
Marlene Chakhtoura,Maya Rahme,Nariman Chamoun,Ghada El-Hajj Fuleihan
Bone Reports. 2018;
[Pubmed] | [DOI]
5 Factors of the epidemiological triad that influence the persistence of human papilloma virus infection in women with systemic lupus erythematosus
S Méndez-Martínez,M García-Carrasco,E A Jiménez-Herrera,C Mendoza-Pinto,I Etchegaray-Morales,P W Barahona-Rubio,J L Gálvez-Romero,P Munguía-Realpozo,C O Muñóz-Guarneros,M L Cedillo-Ramírez,S E Silva-Gómez,G Linares-Fleites,A Rojas-Vallaraga
Lupus. 2018; 27(9): 1542
[Pubmed] | [DOI]
6 Vitamin D: effects on pregnancy, maternal, fetal and postnatal outcomes
A K Eremkina,N G Mokrysheva,E A Pigarova,S S Mirnaya
Terapevticheskii arkhiv. 2018; 90(10): 115
[Pubmed] | [DOI]
7 Serum vitamin D status and bacterial vaginosis prevalence and incidence in Zimbabwean women
Abigail N. Turner,Patricia Carr Reese,Pai Lien Chen,Cynthia Kwok,Rebecca D. Jackson,Mark A. Klebanoff,Raina Fichorova,Tsungai Chipato,Charles S. Morrison
American Journal of Obstetrics and Gynecology. 2016;
[Pubmed] | [DOI]
8 Bacterial Vaginosis Biofilms: Challenges to Current Therapies and Emerging Solutions
Daniela Machado,Joana Castro,Ana Palmeira-de-Oliveira,José Martinez-de-Oliveira,Nuno Cerca
Frontiers in Microbiology. 2016; 6
[Pubmed] | [DOI]



 

Top
 
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Acknowledgment
   Material & Methods
   Discussion
   Results
    References
    Article Figures
    Article Tables

 Article Access Statistics
    Viewed2156    
    Printed14    
    Emailed3    
    PDF Downloaded571    
    Comments [Add]    
    Cited by others 8    

Recommend this journal