Screening for gestational diabetes mellitus and its prevalence in Bangladesh

  • Subrina Jesmin
    Correspondence
    Corresponding author at: Health & Disease Research Center for Rural Peoples (HDRCRP), Ena Arista, Flat # B-3, House # 802, Road # 3, Baitul Aman Housing Society, Adabor, Shamoli, Dhaka 1207, Bangladesh. Tel.: +88 01721 512282; fax: +81 29 853 3092.
    Affiliations
    Health & Disease Research Center for Rural Peoples (HDRCRP), Ena Arista, Flat # B-3, House # 802, Road # 3, Baitul Aman Housing Society, Adabor, Shamoli, Dhaka 1207, Bangladesh

    Graduate School of Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan
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  • Shamima Akter
    Affiliations
    Health & Disease Research Center for Rural Peoples (HDRCRP), Ena Arista, Flat # B-3, House # 802, Road # 3, Baitul Aman Housing Society, Adabor, Shamoli, Dhaka 1207, Bangladesh

    National Center for Global Health and Medicine (NCGM), 1-21-1 Toyama, Shinjuku-ku, Tokyo 162-8655, Japan
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  • Hidechika Akashi
    Affiliations
    National Center for Global Health and Medicine (NCGM), 1-21-1 Toyama, Shinjuku-ku, Tokyo 162-8655, Japan
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  • Abdullah Al-Mamun
    Affiliations
    Health & Disease Research Center for Rural Peoples (HDRCRP), Ena Arista, Flat # B-3, House # 802, Road # 3, Baitul Aman Housing Society, Adabor, Shamoli, Dhaka 1207, Bangladesh

    Shahid Ziaur Rahman Medical College, Bogra, Bangladesh
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  • Md. Arifur Rahman
    Affiliations
    Health & Disease Research Center for Rural Peoples (HDRCRP), Ena Arista, Flat # B-3, House # 802, Road # 3, Baitul Aman Housing Society, Adabor, Shamoli, Dhaka 1207, Bangladesh

    Shahid Ziaur Rahman Medical College, Bogra, Bangladesh
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  • Md. Majedul Islam
    Affiliations
    Health & Disease Research Center for Rural Peoples (HDRCRP), Ena Arista, Flat # B-3, House # 802, Road # 3, Baitul Aman Housing Society, Adabor, Shamoli, Dhaka 1207, Bangladesh

    Graduate School of Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan
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  • Farzana Sohael
    Affiliations
    Health & Disease Research Center for Rural Peoples (HDRCRP), Ena Arista, Flat # B-3, House # 802, Road # 3, Baitul Aman Housing Society, Adabor, Shamoli, Dhaka 1207, Bangladesh

    Graduate School of Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan
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  • Osamu Okazaki
    Affiliations
    National Center for Global Health and Medicine (NCGM), 1-21-1 Toyama, Shinjuku-ku, Tokyo 162-8655, Japan
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  • Masao Moroi
    Affiliations
    National Center for Global Health and Medicine (NCGM), 1-21-1 Toyama, Shinjuku-ku, Tokyo 162-8655, Japan
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  • Satoru Kawano
    Affiliations
    Graduate School of Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan
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  • Taro Mizutani
    Affiliations
    Graduate School of Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan
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Published:December 26, 2013DOI:https://doi.org/10.1016/j.diabres.2013.11.024

      Abstract

      Background

      The prevalence of gestational diabetes mellitus (GDM) has important health complications for both mother and child and is increasing all over the world. Although prevalence estimates for GDM are not new in developed and many developing countries, data are lacking for many low-income countries like Bangladesh.

      Objective

      To evaluate the prevalence of GDM in Bangladesh.

      Research design and methods

      This cross-sectional study included 3447 women who consecutively visited the antenatal clinics with an average gestation age of 26 weeks. GDM was defined according to WHO criteria (fasting plasma glucose [FPG] ≥7.0 mmol/L or 2-h ≥7.8 mmol/L) and the new ADA criteria (FPG ≥5.3 mmol/L or 2-h ≥8.6 mmol/L OGTT). We also calculated overt diabetes as FPG ≥7.0 mmol/L.

      Results

      Prevalence of GDM was 9.7% according to the WHO criteria and 12.9% according to the ADA criteria in this study population. Prevalence of overt diabetes was 1.8%. Women with GDM were older, higher educated, had higher household income, higher parity, parental history of diabetes, and more hypertensive, compared with non-GDM women.

      Conclusion

      This study demonstrates a high prevalence of GDM in Bangladesh. These estimates for GDM may help to formulate new policies to prevent and manage diabetes.

      Keywords

      1. Introduction

      Gestational diabetes mellitus (GDM) is one of the most common medical complications of pregnancy, defined as glucose intolerance with onset or first recognition during pregnancy [
      American Diabetes Association
      Diagnosis and classification of diabetes mellitus.
      ]. GDM can adversely impact perinatal outcome, increase the risk of obesity in offspring and the subsequent development of diabetes in mothers [
      • Sullivan S.D.
      • Umans J.G.
      • Ratner R.
      Gestational diabetes: implications for cardiovascular health.
      ,
      • Krishnaveni G.V.
      • Veena S.R.
      • Hill J.C.
      • Kehoe S.
      • Karat S.C.
      • Fall C.H.
      Intrauterine exposure to maternal diabetes is associated with higher adiposity and insulin resistance and clustering of cardiovascular risk markers in Indian children.
      ,
      • Xiang A.H.
      • Li B.H.
      • Black M.H.
      • Sacks D.A.
      • Buchanan T.A.
      • Jacobsen S.J.
      • et al.
      Racial and ethnic disparities in diabetes risk after gestational diabetes mellitus.
      ]. Overall, GDM rates have been on the rise in all ethnic groups, but most noticeable in Asian countries, where the prevalence rate is around 17% [
      • Dabelea D.
      • Mayer-Davis E.J.
      • Lamichhane A.P.
      • D’Agostino Jr., R.B.
      • Liese A.D.
      • Vehik K.S.
      • et al.
      Association of intrauterine exposure to maternal diabetes and obesity with type 2 diabetes in youth: the SEARCH Case-Control Study.
      ]. Further, among the Asians, South Asians are more prone to have diabetes at an earlier age [
      • Gujral U.P.
      • Pradeepa R.
      • Weber M.B.
      • Narayan K.M.
      • Mohan V.
      Type 2 diabetes in South Asians: similarities and differences with White Caucasian and other populations.
      ] and thus more vulnerable to GDM.
      Among the developing countries several studies has been conducted to estimate the prevalence of GDM, including India [
      • Zargar A.H.
      • Sheikh M.I.
      • Bashir M.I.
      • Masoodi S.R.
      • Laway B.A.
      • Wani A.I.
      • et al.
      Prevalence of gestational diabetes mellitus in Kashmiri women from the Indian sub continent.
      ,
      • Di Cianni G.
      • Volpe L.
      • Lencioni C.
      • Miccoli R.
      • Cuccuru I.
      • Ghio A.
      • et al.
      Prevalence and risk factors for gestational diabetes assessed by universal screening.
      ,
      • Seshiah V.
      • Balaji V.
      • Balaji M.S.
      • Sanjeevi C.B.
      • Green A.
      Gestational diabetes mellitus in India.
      ], China [
      • Yang H.
      • Wei Y.
      • Gao X.
      • Xu X.
      • Fan L.
      • He J.
      • et al.
      Risk factors for gestational diabetes mellitus in Chinese women: a prospective study of 16,286 pregnant women in China.
      ,
      • Zhang F.
      • Dong L.
      • Zhang C.P.
      • Li B.
      • Wen J.
      • Gao W.
      • et al.
      Increasing prevalence of gestational diabetes mellitus in Chinese women from 1999 to 2008.
      ], Sri Lanka [
      • Dahanayaka N.J.
      • Agampodi S.B.
      • Ranasinghe O.R.
      • Jayaweera P.M.
      • Fernando S.
      Screening for gestational diabetes mellitus in Anuradhapura district.
      ], Iran [
      • Agarwal M.M.
      • Dhatt G.S.
      • Zayed R.
      • Bali N.
      Gestational diabetes: relevance of diagnostic criteria and preventive strategies for Type 2 diabetes mellitus.
      ,
      • Keshavarz M.
      • Cheung N.W.
      • Babaee G.R.
      • Moghadam H.K.
      • Ajami M.E.
      • Shariati M.
      Gestational diabetes in Iran: incidence, risk factors and pregnancy outcomes.
      ], and Malaysia [
      • Tan P.C.
      • Ling L.P.
      • Omar S.Z.
      Screening for gestational diabetes at antenatal booking in a Malaysian university hospital: the role of risk factors and threshold value for the 50-g glucose challenge test.
      ]. However, to date no study has been conducted in Bangladesh. Like many developing countries, Bangladesh is also experiencing a high prevalence of diabetes [
      • Guariguata L.
      • Whiting D.R.
      • Hambleton I.
      • Beagley J.
      • Linnenkamp U.
      • Shaw J.E.
      Global estimates of diabetes prevalence for 2013 and projections for 2035 for the IDF Diabetes Atlas.
      ]. In order to effectively manage this condition in a cost effective manner in a low-income country like Bangladesh, it is imperative to identify mothers with GDM early on in their pregnancy. In this manner, lifestyle interventions and treatment may prevent the development of diabetes and other health complications both for mother and offspring, and to avoid high treatment costs. The aim of this study was to determine the prevalence of GDM for the first time among women in Bangladesh by using the World Health Organization (WHO) and the new American Diabetes Association (ADA) criteria.

      2. Data and methodology

      2.1 Study design

      A base-line survey was done in 12 Upzillas of 6 districts under 3 divisions during 2012–2013 in Bangladesh. Twelve GDM corners were established in antenatal clinics, where antenatal care was offered to all pregnant women. A total of 4890 pregnant women, with an average gestation age of 26 weeks, participated in this study. We used the WHO STEPS approach (modified), which entails a stepwise collection of risk factor data based on standardized questionnaires covering the following parameters: demographic characteristics, somatic illnesses, somatic and mental symptoms, medications, life style, and health-related behavior (step 1), basic physical measures (step 2) and basic biochemical investigations, such as blood glucose and cholesterol (step 3). The study was approved by the Ethical Committee of the Health and Disease Research Center of Rural Peoples (HDRCRP), Dhaka, Bangladesh, and conforms to the principles outlined in the Helsinki Declaration. All subjects gave their written informed consent prior to participation.

      2.2 Study subjects

      Of the 4890 subjects, we excluded 1410 subjects who were not fasting. Among the 3480 subjects, who had an oral glucose challenge test (OGCT), 624 women were found to have an abnormal OGCT (≥7.8 mmol/l). Of the 624 subjects who were advised to have an oral glucose tolerance test (OGTT), 591participated and 33 dropped out. Ultimately a total of 3447subjects were included in the present study.

      2.3 Anthropometric and other variables

      Well-trained examiners conducted anthropometric measurements on individuals wearing light clothing and without shoes. Height was measured to the nearest 0.1 cm using the portable stadiometer. Weight was measured in an upright position, to the nearest 0.1 kg, using a calibrated balance beam scale. Body mass index (BMI) was calculated as the body weight (kg) divided by the square of the body height (m2). Blood pressure was measured twice in the right arm in a sitting position using a standard mercury manometer and cuff, to the nearest 2 mmHg, with the initial reading taken at least 5 minutes after the subject was made comfortable, and again after an interval of 15 min. The average systolic blood pressure (SBP) and diastolic blood pressure (DBP) were then estimated. Hypertension was defined as SBP ≥140 or DBP ≥90 or taking antihypertensive medication. Number of parity, history of still birth or abortion, parental history of diabetes, parental history of hypertension, respondent's education, and household income were self-reported.

      2.4 Assessment for GDM

      All pregnant women were first screened for GDM using a 1-h 50 g OGCT, performed in the morning after an overnight fast. As we performed a fasting GCT we also measured fasting plasma glucose (FPG) using a glucometer. Subjects with abnormal 1-h blood glucose level (≥7.8 mmol/l) proceeded to an OGTT within one week of the abnormal screening test. Women with abnormal OGCT had a standard 2-h OGTT with a 75-g glucose load administered after a 12–14-h fast with blood collected fasting and 1-h and 2-h.
      GDM was defined according to the 1999 WHO criteria – FPG ≥7.0 mmol/L or 2-h ≥7.8 mmol/L [
      WHO Consultation: definition, diagnosis and classification of diabetes mellitus and its complications: report of a WHO Consultation. Part 1: diagnosis and classification of diabetes mellitus.
      ]. It was additionally defined according to the new ADA criteria of FPG ≥5.3 mmol/L or 2-h ≥8.6 mmol/L after a 2-h OGTT [
      • Metzger B.E.
      • Gabbe S.G.
      • Persson B.
      • Buchanan T.A.
      • Catalano P.A.
      • et al.
      International Association of Diabetes and Pregnancy Study Groups Consensus Panel
      International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy.
      ]. We also calculated overt diabetes according to the new ADA criteria as, FPG ≥7.0 mmol/L [
      • Metzger B.E.
      • Gabbe S.G.
      • Persson B.
      • Buchanan T.A.
      • Catalano P.A.
      • et al.
      International Association of Diabetes and Pregnancy Study Groups Consensus Panel
      International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy.
      ].

      2.5 Statistical analysis

      Differences in anthropometric and socio-demographic characteristics between subjects with GDM and non-GDM were assessed by t-test and Chi-square test for continuous and categorical variables, respectively. Mean ± S.D. and percentage were presented, where appropriate. Two-sided P values of less than 0.05 were considered statistically significant. All analyses were performed using Stata version 12.0 (StataCorp, College Station, Texas, USA).

      3. Results

      The mean age of our study population was 22 ± 4 years (mean ±SD), with a median schooling of 7 years. Among the pregnant women only 7.7% had a basic knowledge about GDM. Only 51.6% women were receiving antenatal care during their pregnancy.
      Table 1 shows the characteristics of the study population who completed the OGCT. The majority (38.4%) were in the 20–24 year age group, education below 5 years (43.8%), and household income more than 15,000 Tk (31.1%). More than half of the pregnant women were zero parity women (51.5%) and had normal BMI (18.5–23.0) (55.3%).
      Table 1Characteristics of study population completing a 1-h OGCT test.
      Subjects screened, n (%)Subjects with abnormal OGCT, n (%)
      Age (years)
       <201029 (29.8)192 (32.5)
       20–241323 (38.4)186 (31.5)
       25–29855 (24.8)159 (26.9)
       ≥30240 (7.0)54 (9.1)
      Education (years of schooling, %)
       ≤51509 (43.8)273 (46.2)
       5–101368 (40.2)192 (32.5)
       ≥10552 (16.0)126 (21.3)
      Monthly household income (Tk)
       <8000945 (27.4)96 (16.2)
       8000–10,000702 (20.4)111 (18.8)
       10,001–15,000729 (21.1)153 (25.9)
       >15,0001071 (31.1)231 (39.1)
      Number of parity
       01776 (51.5)252 (42.6)
       11101 (31.9)208 (34.5)
       2408 (11.8)75 (12.7)
       ≥3162 (4.7)60 (10.2)
      Pregnancy weight status (BMI, kg/m2)
       Under weight (<18.5)498 (14.4)171 (28.9)
       Normal (18.5–23.0)1905 (55.3)297 (50.2)
       Overweight (23.0–25.0)474 (13.8)69 (11.7)
       Obese (≥25.0)570 (16.5)54 (9.1)
      Table 2 shows total and age-specific prevalence of GDM and overt diabetes. The total prevalence of GDM was 9.7% according to WHO criteria and 12.9% according to the ADA criteria. The prevalence of overt diabetes was 1.8% using the ADA criterion. The prevalence of GDM increased significantly with increased age for both ADA and WHO criteria. Fig. 1 shows the overlap of GDM cases diagnosed by the ADA and WHO criteria.
      Table 2Age-specific prevalence of gestational diabetes mellitus (GDM) and overt diabetes.
      Age group (years)Prevalence of GDM ADA criteria, n (%)WHO criteria, n (%)Overt diabetes, n (%)
      <2075 (7.3)102 (9.9)6 (0.58)
      20–24306 (11.6)90 (6.8)18 (1.4)
      25–29159 (18.6)102 (11.9)21 (2.5)
      ≥3060 (25.0)42 (17.5)18 (7.5)
      Total447 (12.9)336 (9.7)63 (1.8)
      Figure thumbnail gr1
      Fig. 1Overlap of cases of GDM as diagnosed by the ADA and WHO criteria for a 2–h 75 g OGTT.
      Table 3 shows age-adjusted prevalence of GDM for WHO criteria according to the characteristics of the study population. GDM was higher among women with higher education, higher monthly household income, and those who had higher parity. Prevalence was also higher among women with hypertension, currently seeking antenatal care, no previous history of still birth/abortion, and parental history of hypertension and diabetes.
      Table 3Age-adjusted prevalence of GDM according to WHO criteria.
      CharacteristicsPrevalence (95% Cl)
      Education (years of schooling)
       ≤510.9 (8.5–14.0)
       5–96.2 (4.3–8.8)
       ≥1013.0 (8.9–18.7)
      Monthly income of household (Tk)
       <80004.5 (2.7–7.3)
       8000–10,0009.7 (6.5–14.2)
       10,001–15,0009.7 (6.6–14.1)
       >15,00013.3 (10.1–17.3)
      Number of parity
       07.4 (5.4–10.1)
       19.8 (7.1–13.4)
       212.9 (7.9–20.3)
       ≥322.7 (12.0–38.6)
      Antenatal care
       Yes12.6 (10.2–15.4)
       No5.1 (3.5–7.4)
      Still birth/abortion
       Yes5.6 (2.7–11.1)
       No9.8 (8.1–11.8)
      Hypertension
       Yes22.9 (13.9–35.1)
       No8.7 (7.1–10.5)
      Parental history of hypertension
       Yes13.7 (7.6–23.3)
       No9.1 (7.5–10.9)
      Parental history of diabetes
       Yes9.9 (8.3–11.9)
       No4.0 (1.7–9.4)
      Table 4 shows differences in anthropometric and socio-demographic characteristics of the study population according to GDM. There were significant differences in age, education, monthly household income, parity, presence of hypertension, parental history of diabetes, and those who were seeking antenatal care during pregnancy (P < 0.05 for all).
      Table 4Differences in anthropometric and socio-demographic characteristics according to gestational diabetes mellitus (GDM) status (WHO criteria).
      GDM (n = 112)Non-GDM (n = 1037)P value
      Based on chi-square test for categorical variables, t-test for continuous variables.
      Age (years)23.7 ± 5.5
      Mean±S.D. (all such values).
      22.2 ± 3.9<0.001
      Education (years of schooling, %)0.004
       ≤552.742.8
       5–1025.941.8
       ≥1021.415.4
      Monthly household income (Tk)0.004
       <800014.328.8
       8000–10,00020.520.4
       10,001–15,00022.321.0
       >15,00042.929.8
      Parental history of hypertension (yes, %)9.86.20.14
      Parental history of diabetes (yes, %)10.54.50.04
      Number of parity
       044.456.9<0.001
       129.629.2
       214.110.4
       ≥311.93.4
      Antenatal care (yes, %)75.055.2<0.001
      Still birth/abortion (yes, %)7.19.20.48
      Hypertension (yes, %)13.44.3<0.001
      a Based on chi-square test for categorical variables, t-test for continuous variables.
      b Mean ± S.D. (all such values).

      4. Discussion

      This is the first study to estimate the prevalence of GDM in Bangladesh. We also compared prevalence according to WHO and ADA criteria. We found that the prevalence of GDM was 9.7% according to WHO criteria and 12.9% according to the ADA criteria and the prevalence of overt diabetes was 1.8% according to ADA criterion.
      The prevalence of GDM observed and reported here (9.6% and/or 12.9%) is comparable with other studies published from South Asian and South East Asian countries, including India, Sri Lanka, and Malaysia [
      • Di Cianni G.
      • Volpe L.
      • Lencioni C.
      • Miccoli R.
      • Cuccuru I.
      • Ghio A.
      • et al.
      Prevalence and risk factors for gestational diabetes assessed by universal screening.
      ,
      • Dahanayaka N.J.
      • Agampodi S.B.
      • Ranasinghe O.R.
      • Jayaweera P.M.
      • Fernando S.
      Screening for gestational diabetes mellitus in Anuradhapura district.
      ,
      • Tan P.C.
      • Ling L.P.
      • Omar S.Z.
      Screening for gestational diabetes at antenatal booking in a Malaysian university hospital: the role of risk factors and threshold value for the 50-g glucose challenge test.
      ]. By contrast, this prevalence is lower than a Middle Eastern study from Qatar (16.3%) [
      • Agarwal M.M.
      • Dhatt G.S.
      • Zayed R.
      • Bali N.
      Gestational diabetes: relevance of diagnostic criteria and preventive strategies for Type 2 diabetes mellitus.
      ] and the United Arab Emirates (20.6%) [
      • Bener A.
      • Saleh N.M.
      • Al-Hamaq A.
      Prevalence of gestational diabetes and associated maternal and neonatal complications in a fast-developing community: global comparisons.
      ], but higher than Iran (4.8%) [
      • Keshavarz M.
      • Cheung N.W.
      • Babaee G.R.
      • Moghadam H.K.
      • Ajami M.E.
      • Shariati M.
      Gestational diabetes in Iran: incidence, risk factors and pregnancy outcomes.
      ] and Turkmenistan (6.3%) [
      • Parhofer K.G.
      • Hasbargen U.
      • Ulugberdiyewa A.
      • Abdullayewa M.
      • Melebayewa B.
      • Annamuhammedov A.
      • et al.
      Gestational diabetes in Turkmenistan: implementation of a screening program and first results.
      ]. Overall prevalence of GDM varies from 4% to 6% in USA [
      • Dabelea D.
      • Snell-Bergeon J.K.
      • Hartsfield C.L.
      • Bischoff K.J.
      • Hamman R.F.
      • McDuffie R.S.
      • et al.
      Increasing prevalence of gestational diabetes mellitus (GDM) over time and by birth cohort: Kaiser Permanente of Colorado GDM Screening Program.
      ,
      • Ferrara A.
      • Kahn H.S.
      • Quesenberry C.P.
      • Riley C.
      • Hedderson M.M.
      An increase in the incidence of gestational diabetes mellitus: Northern California, 1991–2000.
      ] and 2–6% in European countries [
      • Buckley B.S.
      • Harreiter J.
      • Damm P.
      • Corcoy R.
      • Chico A.
      • Simmons D.
      • et al.
      Gestational diabetes mellitus in Europe: prevalence, current screening practice and barriers to screening. A review.
      ]. Thus, prevalence of GDM seems greater in developing countries from Asians. However, it is important to note that the prevalence of GDM varies widely according to the specific cut-off points used in the various studies. The variation may be also due to time lag, specific study subject, environmental diversity, dietary habits, and other national or sub-national socio-behavioral factors. It is also difficult to compare disease prevalence, particularly for diabetes, with results from older literature because of the rapid epidemiologic and demographic transitions occurring in most developing countries.
      In this study, presence of GDM was significantly higher among older, higher educated, higher household income, higher parity and hypertensive women. Consistent with our study, previous studies had been shown higher age was associated with GDM [
      • Zargar A.H.
      • Sheikh M.I.
      • Bashir M.I.
      • Masoodi S.R.
      • Laway B.A.
      • Wani A.I.
      • et al.
      Prevalence of gestational diabetes mellitus in Kashmiri women from the Indian sub continent.
      ,
      • Di Cianni G.
      • Volpe L.
      • Lencioni C.
      • Miccoli R.
      • Cuccuru I.
      • Ghio A.
      • et al.
      Prevalence and risk factors for gestational diabetes assessed by universal screening.
      ,
      • Seshiah V.
      • Balaji V.
      • Balaji M.S.
      • Sanjeevi C.B.
      • Green A.
      Gestational diabetes mellitus in India.
      ,
      • Hossein-Nezhad A.
      • Maghbooli Z.
      • Vassigh A.R.
      • Larijani B.
      Prevalence of gestational diabetes mellitus and pregnancy outcomes in Iranian women.
      ] indicating that older age is an independent risk factor for GDM irrespective of race and ethnicity. In a previous study, Bener et al. did not find a significant difference between education, household income, and GDM status of women [
      • Bener A.
      • Saleh N.M.
      • Al-Hamaq A.
      Prevalence of gestational diabetes and associated maternal and neonatal complications in a fast-developing community: global comparisons.
      ]. In our study higher education and higher income groups were more likely to engage in sedentary work that may relate to obesity and GDM. Obesity and associated type 2 diabetes or cardiovascular disease are a growing challenge in developing world [
      • Hossain P.
      • Kawar B.
      • El Nahas M.
      Obesity and diabetes in the developing world – a growing challenge.
      ]. Overweight or obesity is associated with GDM in all racial and ethnic groups [
      • Kim S.Y.
      • Saraiva C.
      • Curtis M.
      • Wilson H.G.
      • Troyan J.
      • Sharma A.J.
      Fraction of gestational diabetes mellitus attributable to overweight and obesity by race/ethnicity, California, 2007–2009.
      ].
      Regarding parity and hypertension, the results of our study were consistent with previous studies [
      • Zargar A.H.
      • Sheikh M.I.
      • Bashir M.I.
      • Masoodi S.R.
      • Laway B.A.
      • Wani A.I.
      • et al.
      Prevalence of gestational diabetes mellitus in Kashmiri women from the Indian sub continent.
      ,
      • Agarwal M.M.
      • Dhatt G.S.
      • Zayed R.
      • Bali N.
      Gestational diabetes: relevance of diagnostic criteria and preventive strategies for Type 2 diabetes mellitus.
      ,
      • Keshavarz M.
      • Cheung N.W.
      • Babaee G.R.
      • Moghadam H.K.
      • Ajami M.E.
      • Shariati M.
      Gestational diabetes in Iran: incidence, risk factors and pregnancy outcomes.
      ], wherein higher parity and gestational hypertension were significantly associated with GDM. Also prevalence of GDM was higher among women with parental history of hypertension and as with other studies, parental history of diabetes was associated with GDM [
      • Di Cianni G.
      • Volpe L.
      • Lencioni C.
      • Miccoli R.
      • Cuccuru I.
      • Ghio A.
      • et al.
      Prevalence and risk factors for gestational diabetes assessed by universal screening.
      ,
      • Yang H.
      • Wei Y.
      • Gao X.
      • Xu X.
      • Fan L.
      • He J.
      • et al.
      Risk factors for gestational diabetes mellitus in Chinese women: a prospective study of 16,286 pregnant women in China.
      ,
      • Yang X.
      • Hsu-Hage B.
      • Zhang H.
      • Yu L.
      • Dong L.
      • Li J.
      • et al.
      Gestational diabetes mellitus in women of single gravidity in Tianjin City, China.
      ]. Thus, women with higher parity, presence of hypertension, and parental history diabetes should be considered a high-risk group and compulsory screening should be considered in these specific groups of pregnant women.
      There are some limitations to our study. We only performed OGTT in women who had abnormal OGCT and there will be some women with a normal OGCT who would have GDM if they had an OGTT. On the other hand, a greater proportion of women with an abnormal OGCT is likely to have an abnormal OGTT which would tend to exaggerate the prevalence of GDM. The combined effect of these on the overall prevalence of GDM is not known. Another limitation relates to cross-sectional design of our study which could have resulted in selection bias during case recruitment because we only examined pregnant women who had an antenatal check-up during a limited time interval and in selected clinics, and thus the results may not be generalizable to all Bangladeshi women.
      In conclusion, this study shows a relatively high prevalence of GDM in Bangladeshi women and suggests screening for glucose intolerance in pregnancy should be considered as part of routine antenatal care. This information is also important in order to develop effective and targeted preventive approaches to complications associated with GDM in both the mothers and their offspring and to formulate new policies or strategies to increase awareness, prevention, and management of diabetes among pregnant women in Bangladesh.

      Conflict of interest

      The authors declare that they had no conflict of interest.

      Author contributions

      SJ wrote the report and overall conducted this research. SA analyzed the data and contributed to potential scientific discussion. MMI contributed to the epidemiological survey. HA, OO, MM, SK and TM contributed to scientific supervision of this work and contributed to discussion. All authors read and approve the final version.

      Acknowledgments

      This work was supported by Grant-in-Aid for Scientific Research (overseas academic) from the Ministry of Education, Culture, Sports, Science and Technology of Japan ( 23406037 , 23406016 , 23406029 , 24406026 , 25305034 ), and Japan Society for the promotion of Science . Current project (WDF11-610) on gestational diabetes from World Diabetes Foundation (WDF), Denmark to HDRCRP has also supported a part of this work.

      References

        • American Diabetes Association
        Diagnosis and classification of diabetes mellitus.
        Diabetes Care. 2012; 35: S64-S71
        • Sullivan S.D.
        • Umans J.G.
        • Ratner R.
        Gestational diabetes: implications for cardiovascular health.
        Curr Diab Rep. 2012; 12: 43-52
        • Krishnaveni G.V.
        • Veena S.R.
        • Hill J.C.
        • Kehoe S.
        • Karat S.C.
        • Fall C.H.
        Intrauterine exposure to maternal diabetes is associated with higher adiposity and insulin resistance and clustering of cardiovascular risk markers in Indian children.
        Diabetes Care. 2010; 33: 402-404
        • Xiang A.H.
        • Li B.H.
        • Black M.H.
        • Sacks D.A.
        • Buchanan T.A.
        • Jacobsen S.J.
        • et al.
        Racial and ethnic disparities in diabetes risk after gestational diabetes mellitus.
        Diabetologia. 2011; 54: 3016-3021
        • Dabelea D.
        • Mayer-Davis E.J.
        • Lamichhane A.P.
        • D’Agostino Jr., R.B.
        • Liese A.D.
        • Vehik K.S.
        • et al.
        Association of intrauterine exposure to maternal diabetes and obesity with type 2 diabetes in youth: the SEARCH Case-Control Study.
        Diabetes Care. 2008; 31: 1422-1426
        • Gujral U.P.
        • Pradeepa R.
        • Weber M.B.
        • Narayan K.M.
        • Mohan V.
        Type 2 diabetes in South Asians: similarities and differences with White Caucasian and other populations.
        Ann N Y Acad Sci. 2013; 1281: 51-63
        • Zargar A.H.
        • Sheikh M.I.
        • Bashir M.I.
        • Masoodi S.R.
        • Laway B.A.
        • Wani A.I.
        • et al.
        Prevalence of gestational diabetes mellitus in Kashmiri women from the Indian sub continent.
        Diabetes Res Clin Pract. 2004; 66: 139-145
        • Di Cianni G.
        • Volpe L.
        • Lencioni C.
        • Miccoli R.
        • Cuccuru I.
        • Ghio A.
        • et al.
        Prevalence and risk factors for gestational diabetes assessed by universal screening.
        Diabetes Res Clin Pract. 2003; 62: 131-137
        • Seshiah V.
        • Balaji V.
        • Balaji M.S.
        • Sanjeevi C.B.
        • Green A.
        Gestational diabetes mellitus in India.
        J Assoc Physicians India. 2004; 52: 707-711
        • Yang H.
        • Wei Y.
        • Gao X.
        • Xu X.
        • Fan L.
        • He J.
        • et al.
        Risk factors for gestational diabetes mellitus in Chinese women: a prospective study of 16,286 pregnant women in China.
        Diabet Med. 2009; 26: 1099-1104
        • Zhang F.
        • Dong L.
        • Zhang C.P.
        • Li B.
        • Wen J.
        • Gao W.
        • et al.
        Increasing prevalence of gestational diabetes mellitus in Chinese women from 1999 to 2008.
        Diabet Med. 2011; 28: 652-657
        • Dahanayaka N.J.
        • Agampodi S.B.
        • Ranasinghe O.R.
        • Jayaweera P.M.
        • Fernando S.
        Screening for gestational diabetes mellitus in Anuradhapura district.
        Ceylon Med J. 2011; 56: 128-129
        • Agarwal M.M.
        • Dhatt G.S.
        • Zayed R.
        • Bali N.
        Gestational diabetes: relevance of diagnostic criteria and preventive strategies for Type 2 diabetes mellitus.
        Arch Gynecol Obstet. 2007; 276: 237-243
        • Keshavarz M.
        • Cheung N.W.
        • Babaee G.R.
        • Moghadam H.K.
        • Ajami M.E.
        • Shariati M.
        Gestational diabetes in Iran: incidence, risk factors and pregnancy outcomes.
        Diabetes Res Clin Pract. 2005; 69: 279-286
        • Tan P.C.
        • Ling L.P.
        • Omar S.Z.
        Screening for gestational diabetes at antenatal booking in a Malaysian university hospital: the role of risk factors and threshold value for the 50-g glucose challenge test.
        Aust N Z J Obstet Gynaecol. 2007; 47: 191-197
        • Guariguata L.
        • Whiting D.R.
        • Hambleton I.
        • Beagley J.
        • Linnenkamp U.
        • Shaw J.E.
        Global estimates of diabetes prevalence for 2013 and projections for 2035 for the IDF Diabetes Atlas.
        Diabetes Res Clin Pract. 2013; ([in press])
      1. WHO Consultation: definition, diagnosis and classification of diabetes mellitus and its complications: report of a WHO Consultation. Part 1: diagnosis and classification of diabetes mellitus.
        World Health Organization, Geneva, WHO/NCD/NCS/99.21999
        • Metzger B.E.
        • Gabbe S.G.
        • Persson B.
        • Buchanan T.A.
        • Catalano P.A.
        • et al.
        • International Association of Diabetes and Pregnancy Study Groups Consensus Panel
        International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy.
        Diabetes Care. 2010; 33: 676-682
        • Bener A.
        • Saleh N.M.
        • Al-Hamaq A.
        Prevalence of gestational diabetes and associated maternal and neonatal complications in a fast-developing community: global comparisons.
        Int J Womens Health. 2011; 3: 367-373
        • Parhofer K.G.
        • Hasbargen U.
        • Ulugberdiyewa A.
        • Abdullayewa M.
        • Melebayewa B.
        • Annamuhammedov A.
        • et al.
        Gestational diabetes in Turkmenistan: implementation of a screening program and first results.
        Arch Gynecol Obstet. 2013; ([in press])
        • Dabelea D.
        • Snell-Bergeon J.K.
        • Hartsfield C.L.
        • Bischoff K.J.
        • Hamman R.F.
        • McDuffie R.S.
        • et al.
        Increasing prevalence of gestational diabetes mellitus (GDM) over time and by birth cohort: Kaiser Permanente of Colorado GDM Screening Program.
        Diabetes Care. 2005; 28: 579-584
        • Ferrara A.
        • Kahn H.S.
        • Quesenberry C.P.
        • Riley C.
        • Hedderson M.M.
        An increase in the incidence of gestational diabetes mellitus: Northern California, 1991–2000.
        Obstet Gynecol. 2004; 103: 526-533
        • Buckley B.S.
        • Harreiter J.
        • Damm P.
        • Corcoy R.
        • Chico A.
        • Simmons D.
        • et al.
        Gestational diabetes mellitus in Europe: prevalence, current screening practice and barriers to screening. A review.
        Diabet Med. 2012; 29: 844-854
        • Hossein-Nezhad A.
        • Maghbooli Z.
        • Vassigh A.R.
        • Larijani B.
        Prevalence of gestational diabetes mellitus and pregnancy outcomes in Iranian women.
        Taiwan J Obstet Gynecol. 2007; l46: 236-241
        • Hossain P.
        • Kawar B.
        • El Nahas M.
        Obesity and diabetes in the developing world – a growing challenge.
        N Engl J Med. 2007; 356: 213-215
        • Kim S.Y.
        • Saraiva C.
        • Curtis M.
        • Wilson H.G.
        • Troyan J.
        • Sharma A.J.
        Fraction of gestational diabetes mellitus attributable to overweight and obesity by race/ethnicity, California, 2007–2009.
        Am J Public Health. 2013; 103: e65-e72
        • Yang X.
        • Hsu-Hage B.
        • Zhang H.
        • Yu L.
        • Dong L.
        • Li J.
        • et al.
        Gestational diabetes mellitus in women of single gravidity in Tianjin City, China.
        Diabetes Care. 2002; 25: 847-851