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Prevalence of gestational diabetes mellitus in India: The ICMR-INDIAB national study (ICMR-INDIAB-24)
#ICMR-INDIAB Collaborative Study Group: Project national coordinator, coinvestigators, and project staff: V. Mohan (National study Coordinator & Principal Investigator), R.M. Anjana, R. Unnikrishnan, R. Pradeepa, M. Deepa, V. Sudha, (National Co-Principal Investigator), E. Nirmal (Project Coordinator), R. Subashini, & U. Venkatesan (Biostatisticians) (Madras Diabetes Research Foundation, Chennai).
Expert group: L.M. Nath (Community Medicine, New Delhi), R. Lakshmy, N. Tandon (All India Institute of Medical Sciences, New Delhi), J. Mahanta (Regional Medical Research Centre, Dibrugarh), S.V. Madhu (University College of Medical Sciences and Guru Teg Bahadur Hospital, New Delhi), A.K. Das (Pondicherry Institute of Medical Sciences, Puducherry), A. Pandey, R.S. Dhaliwal, & T. Kaur (Indian Council of Medical Research, New Delhi)
State principal investigators and Co-Investigators: Andhra Pradesh (undivided)- P.V. Rao (State PI), M.N. Rao (State Co-I) (Nizam’s Institute of Medical Sciences, Hyderabad); Arunachal Pradesh- L. Jampa (State PI); T. Kaki (State Co-I) (Directorate of Health Services, Naharlagun); Assam- H.K. Das, P.K. Borah (Regional Medical Research Centre, Dibrugarh); Bihar- A. Kumar (State PI), S. Sharma (State Co-I) (Diabetes Care and Research Centre, Patna); Chandigarh- A. Bhansali (State PI) (Post-Graduate Institute of Medical Education and Research), Chhattisgarh- K. Dash (State PI), V.K. Shrivas (State Co-I) (Apollo Hospitals, Bilaspur); NCT Delhi- N. Tandon (State PI), A. Krishnan (State Co-I) (All India Institute of Medical Sciences, New Delhi); Goa- A. Desai (State PI), A. Dias (State Co-I) (Goa Medical College, Bambolim); Gujarat- B. Saboo (State PI), J.M. Padhiyar (State Co-I) (Dia Care, Ahmedabad); Haryana- S. Kalra (State PI), B. Kalra (State Co-I) (Bharti Hospital, Karnal); Himachal Pradesh- J.K. Moktha (State PI), R. Gulepa (State Co-I) (Indira Gandhi Medical College, Shimla); Jharkhand- V.K. Dhandhania (State PI) (Diabetes Care Centre, Ranchi); Karnataka- P. Adhikari (State PI) (Department of Epidemiology, Yenepoya Medical college, Yenepoya University Campus, Deralakatte, Karnataka), B.S. Rao (State Co-I) (Kasturba Medical College, Mangalore); Kerala- P.K. Jabbar (State PI), C. Jayakumari (State Co-I) (Government Medical College, Trivandrum); Madhya Pradesh- S.M. Jain (State PI), G. Gupta (State Co-I) (TOTALL Diabetes Thyroid Hormone Research Institute, Indore); Maharashtra- S. Joshi (State PI) (Lilavati Hospital and Research Centre, Mumbai), C. Yajnik (King Edward Memorial Hospital, Pune), P.P. Joshi (Department of General Medicine, All India Institute of Medical Sciences, Nagpur) (State PI); Manipur- S. Ningombam (State PI), T.B. Singh (State Co-I) (Directorate of Health Services, Imphal); Meghalaya- R.O. Budnah (State PI), M.R. Basaiawmoit (State Co-I) (Directorate of Health Services, Shillong); Mizoram- Rosangluaia (State PI), P.C. Lalramenga (State Co-I) (Civil Hospital, Aizawl); Nagaland- V. Suokhrie (State PI), S. Tunyi (State Co-I) (Directorate of Health and Family Welfare, Kohima); Odisha- S.K. Tripathy (State PI), Sarita Behera, N.C. Sahu (State Co-Is) (SCB Medical College & Hospital, Cuttack), Puducherry- A.J. Purty (State PI) (Pondicherry Institute of Medical Sciences, Kalapet), A.K. Das (State Co-I) (Department of Medicine, Mahatma Gandhi Medical College and Research Institute, SBV); Punjab- A. Bhansali (State PI), M. John (State Co-I) (Post-Graduate Institute of Medical Education and Research, Chandigarh), Rajasthan- A. Gupta (State PI), B.L. Gupta, S.K. Shrivastava (State Co-Is) (Jaipur Diabetes Research Centre, Jaipur), Sikkim- K.J. Tobgay (State PI), T.T. Kaleon (State Co-I) (Human Services and Family Welfare, Gangtok); Tamil Nadu- V. Mohan (National Co-ordinator & State PI), R.M. Anjana, R. Unnikrishnan, R. Pradeepa, M. Deepa, V. Sudha (State Co-Is) (Madras Diabetes Research Foundation, Chennai); Tripura- T. Reang (State PI), S.K. Das (State Co-I) (Government Medical College, Agartala), Uttar Pradesh- S. Bajaj (State PI), M.K. Mathur (State Co-I) (Moti Lal Nehru Medical College, Prayagraj), Uttarakhand- S. Modi (State PI), R. Kakkar (State Co-I) (Himalayan Institute of Medical Sciences, Dehradun); West Bengal- S. Chowdhury (State PI), & S. Ghosh (State Co-I) (Institute of Post-Graduate Medical Education and Research and Seth Sukhlal Karnani Memorial Hospital, Kolkata); Jammu- Rajiv Kumar Gupta (State PI), Suman Kotwal (State Co-I) (Government Medical College, GMC); Kashmir and Ladakh: Mohd. Ashraf Ganie (State PI), Shariq Masoodi (State Co-I) (Sher-i-Kashmir Institute of Medical Sciences (SKIMS), Srinagar), Ghulam Hussain Bardi (State Co-I) (District Hospital, Kargil, Ladakh)
For correspondence: Dr Viswanathan Mohan, Madras Diabetes Research Foundation (ICMR-Collaborating Centre of Excellence) & Dr Mohan’s Diabetes Specialities Centre, (IDF Centre of Excellence in Diabetes Care) Chennai 600 086, Tamil Nadu, India e-mail: drmohans@diabetes.ind.in
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Received: ,
Accepted: ,
Abstract
Background & objectives
The prevalence of gestational diabetes mellitus (GDM) is known to be high among South Asians. However, there is no national study on prevalence of GDM in India and few data comparing prevalence of GDM in early pregnancy (Early GDM) and late pregnancy (Late GDM).
Methods
This is an analysis of pregnant women who participated in the nationally representative Indian Council of Medical Research-India Diabetes (ICMR-INDIAB) study. Of the 1,206 pregnant women 1,032 who underwent oral glucose tolerance test (OGTT) or had fasting blood glucose measurement and did not have overt diabetes, were included in this study. GDM was diagnosed using the NICE criteria. GDM was classified as Early GDM if diagnosed before 20 wk of gestation and Late GDM if diagnosed ≥ 20 wk of gestation,
Results
The weighted national prevalence of GDM in India was 22.4 per cent (95% CI: 16.7-28%) with no significant urban rural differences (24.2% vs. 21.6%, NS). The prevalence of Early GDM and Late GDM were 19.2 per cent (9.8-28.7%) and 23.4 per cent (16.7-30.2%), respectively. Central India had the highest prevalence of GDM at 32.9 per cent (17.9-48%), and West India, the lowest at 16 per cent (3.1-29.3%). High systolic blood pressure and family history of diabetes were independently associated with risk of GDM.
Interpretation & conclusions
Nearly one in four pregnant women in India have GDM with regional variability. The prevalence of Early GDM is also high. Thus, there is a need for screening of all pregnant women for GDM starting in early pregnancy.
Keywords
Asian Indians
early GDM
gestational diabetes
late GDM
prevalence
South Asians
Gestational diabetes mellitus (GDM) refers to glucose intolerance i.e., elevated blood glucose levels first detected during pregnancy. GDM increases the risk of adverse pregnancy outcomes both for the mother and the foetus. It is also associated with increased risk of developing type 2 diabetes (T2D) and cardiovascular disease in the future. The current global prevalence of GDM is reported to be 15.6 per cent, according to the International Diabetes Federation1. South Asians (including Asian Indians) have a higher prevalence of GDM compared to other ethnic groups2-4. It is also well-documented that Asian Indians also have a unique predisposition to develop T2D at younger ages and at a lower body mass index (BMI) compared to other populations5,6, translating to increased risk of T2D in the reproductive age group. The aetiology of GDM is multifactorial, with family history of diabetes, obesity, excessive weight gain during pregnancy and physical inactivity being important risk factors. The prevalence of GDM varies greatly depending on screening methods (e.g. universal vs. selective screening) and the diagnostic criteria used. There is no community-based national data on prevalence of GDM in India as most studies are from hospitals and clinics, which are subject to referral bias. In this paper, we utilised data on pregnant women from the nationally representative Indian Council of Medical Research-India Diabetes (ICMR-INDIAB) study on diabetes and prediabetes, to report on the national prevalence of GDM in India using a uniform screening protocol and to look for regional difference in prevalence of GDM. In addition, we also report the first national data in India on prevalence of Early GDM diagnosed before 20 wk of pregnancy and Late GDM diagnosed after 20 wk of gestation.
Materials & Methods
The ICMR-INDIAB study is a nationwide, cross-sectional survey assessing metabolic non communicable diseases (NCDs) in a representative Indian sample7-14. The study methodology of this cross-sectional study is provided elsewhere in detailed. Ethical approval was obtained from the Institutional Ethics Committee of the coordinating centre and the respective Ethics Committees of the nodal institutions implementing the ICMR-INDIAB study across different States. All participants provided written informed consent. The study was also registered with the Clinical Trials Registry of India (CTRI/2019/03/018095).
Study design and participants information
The study methodology is reported in detail elsewhere7. It used stratified multistage sampling to select 113,043 participants (33,537 urban, 79,506 rural) from 31 States/UTs, conducted in five phases between 2008 and 2024. Phases covered different regions: Phase 1 (Chandigarh, Jharkhand, Maharashtra, Tamil Nadu), Phase 2 [undivided Andhra Pradesh (later split into Andhra Pradesh and Telangana), Gujarat, Karnataka, Bihar, Punjab], Northeast Phase (Assam and other NE States), Phase 3 (Delhi, Madhya Pradesh, Rajasthan, Uttar Pradesh), Phase 4 (Chhattisgarh, Goa, Kerala, Puducherry, Haryana), and Phase 5 (Odisha, Himachal Pradesh, Uttarakhand, West Bengal). Sampling details are published7,15 and provided in the supplementary material.
The study sampled 4,000 individuals per State/Union Territory (1,200 urban, 2,800 rural). Of 119,022 invited from 31 States/UTs, 113,043 participated (95% response). A three-tier stratification based on population size, geography, and socioeconomic status ensured national representativeness. Villages were the primary sampling units in rural areas, and census enumeration blocks in urban areas. Systematic sampling selected 24 urban and 56 rural households per area, with one individual chosen per household using World Health Organization (WHO) method16 to avoid selection bias. A standardised, structured, interviewer administered questionnaire was used to gather data on the medical history, family history of diabetes, physical activity, smoking, alcohol consumption and socioeconomic status in all participants. Pregnant women were included if selected, with all ICMR-INDIAB procedures except for body weight measurement.
Study methods
Standardised methods were used to measure blood pressure and height17. Blood pressure was recorded on the right arm with an electronic sphygmomanometer (Omron HEM-7101, Omron Corporation, Tokyo, Japan) in a seated position, averaging two readings taken 5 min apart. Technicians’ interobserver and intraobserver coefficients of variation was under 5 per cent. Identical equipment were used throughout for quality control. Capillary blood glucose was measured after overnight fasting using a one touch ultra glucose meter (LifeScan, Johnson & Johnson, Milpitas, California). An 82.5 g oral glucose load (equivalent to 75 g anhydrous glucose) was given to women without self-reported diabetes, with capillary blood collected after two hours for glucose levels. Those with self-reported diabetes had only fasting glucose measured.
Definitions
Self-reported GDM was defined based on physician diagnosis, which was validated by comparing it to medical records or prescriptions. Women with fasting blood glucose (FBG)≥126 mg/dl (7 mmol/L) or 2-h glucose ≥200 mg/dL (11.1 mmol/L) on 75-g OGTT, or HbA1c≥6.5 per cent were classified as having overt diabetes as per WHO criteria and excluded from the study18. GDM was diagnosed if the fasting blood glucose (FBG) was 100-125 mg/dL (5.6-6.9 mmol/L) and/or 2-h glucose (2HrPG) was 140-199 mg/dL (7.8-11.1 mmol/L) as per the National Institute for Health and Care Excellence (NICE), UK criteria19. If GDM was diagnosed before 20 wk of gestation, it was called Early GDM and if it was diagnosed ≥20 wk, it was called Late GDM.
In addition, GDM was also defined using three additional criteria for comparison purposes: (i) International Association of the Diabetes and Pregnancy Study Groups (IADPSG) criteria as FBG 92-125 mg/dL and/or 2HrPG 153-199 mg/dL, (ii) Treatment of Booking Gestational Diabetes Mellitus (TOBOGM) high glycemic band criteria i.e., FBG 95-125 mg/dL and/or 2HrPG 162-199 mg/dL and (iii) The Diabetes in Pregnancy Study Groups of India (DIPSI) criteria of 2h value ≥140 mg/dL after 75 g of glucose load.
Statistical analysis
The PROC SURVEY (frequency/mean) procedure was employed to analyse data from the complex survey design, ensuring that the statistical analyses and resulting inferences were both accurate and reflective of the target population. This method is specifically designed for survey data that incorporates stratification, clustering, and sampling weights. In this context, the PSU was treated as a cluster, while the State and study weight were accounted for as clusters and weights, respectively. To take into consideration sampling at various levels within each State, the sampling weights were computed (Supplementary Material). From the NFHS-5 study20, weights for pregnant women were calculated for subgroups defined by 10-yr age intervals, in accordance with the complex survey design. Each subgroup’s weight, as provided in the NFHS-5 dataset20, was multiplied by the weighted prevalence of GDM within that subgroup. The overall regional prevalence of GDM was then derived by summing the re-weighted prevalence estimates across all subgroups. Continuous variables were summarized as mean with either 95 per cent confidence intervals (95% CI) or standard error (SE), while categorical variables were presented as proportions with 95 per cent CI. Variables found significant in univariate analyses were entered into a multivariable logistic regression model to assess risk factors for GDM, including age, blood pressure, family history of diabetes and area of residence. Assumptions of linearity in the logit, multicollinearity, and outliers were evaluated prior to analysis to ensure the validity of the logistic regression model. A significance level (α) of 0.05 was used to determine statistical significance. All analyses were performed using statistical analysis software (SAS), version 9.4 (SAS Institute, Cary, NC, USA).
Results
Figure 1 shows the disposition of individuals in the study. The ICMR-INDIAB study included 113,043 adults, of whom 53.5 per cent were women. Of the women surveyed, 70 per cent were in the reproductive age group (20-49 yr) of whom 1,206 (2.9%) were pregnant at the time of survey. OGTT results (i.e., fasting and/or 2-h glucose measurements) were available for 1,032 pregnant women, excluding those with overt diabetes. The pregnant women studied were spread across all three trimesters. None of the pregnant women had pre-pregnancy diabetes, and only one woman reported pre-pregnancy hypertension. Supplementary table I compares the characteristics of pregnant women from the ICMR-INDIAB study with those from the NFHS-5 survey. No significant differences were observed in urban-rural distribution, literacy levels, socio-economic status, or trimester of pregnancy between the ICMR-INDIAB study and the NFHS-5 survey, confirming the representativeness of this subsample of the INDIAB survey.

- Flowchart depicting the participant recruitment in the Indian Council of Medical Research-India Diabetes (ICMR-INDIAB) Survey.
Table I presents the prevalence (crude and weighted) of GDM in the Indian population. The weighted prevalence was 22.4 per cent, including 2.5 per cent self-reported GDM and 19.8 per cent, newly diagnosed GDM. Urban women had a slightly higher prevalence of GDM than rural women, but the difference was not statistically significant. Early GDM was diagnosed in 19.2 per cent and late GDM, in 23.4 per cent.
| Category | No. of women | Crude prevalence n (%) | Weighted prevalence % (95% CI) |
|---|---|---|---|
| Self-reported GDM (n=1,032) | 27 | 2.6 (1.7-3.6) | 2.5 (0.6-4.5) |
|
Newly diagnosed GDM (n=1,032) (FBG 100-125 mg/dL and/or 2HrPG 140-199 mg/dL) |
205 | 19.9 (17.5-22.2) | 19.8 (14.4-25.3) |
|
Overall GDM (n=1,032) (self-reported + newly diagnosed) |
232 | 22.5 (20-24.9) | 22.4 (16.7-28) |
| By region (n=1,032) | |||
| Urban (n=270) | 62 | 23 (17.9-28) | 24.2 (11.4-37.1) |
| Rural (n=762) | 170 | 22.3 (19.4-25.2) | 21.6 (15.7-27.6) |
| Based on time of gestation (n=1,032) | |||
| Early GDM (<20 wk) (n=270) | 60 | 22.2 (17.4-27) | 19.2 (9.8-28.7) |
| Late GDM (>20 wk) (n=762) | 172 | 22.6 (19.7-25.5) | 23.4 (16.7-30.7) |
Supplementary table II presents the prevalence of GDM by different criteria. Using the IADPSG, TOBOGM (high glycaemic band), DIPSI criteria and NICE criteria, the prevalence rates of GDM were 36.3 per cent, 28.7 per cent, 11.4 per cent and 22.4 per cent, respectively. Trends across urban/rural areas and by Early GDM and Late GDM remained similar, irrespective of diagnostic criteria used.
The characteristics of women without GDM and those with GDM both Early GDM and Late GDM are presented in table II. The average age of the pregnant women was 26.4 yr. Those with GDM were significantly older than those without. The women with GDM were also taller, had better education (14.9% vs. 10.1%), were more professionally accomplished compared to those without GDM. Individuals with GDM had significantly higher blood pressure, glucose levels, and a greater prevalence of family history of diabetes. No significant differences were observed between those with Early GDM and Late GDM within this study population.
| Characteristics | All pregnant women (n=1,032) | Women without GDM (n=800) | Women with GDM (n=232) | Women with early GDM (n=60) | Women with late GDM (n=172) |
|---|---|---|---|---|---|
| Age (yr) | 26.4 (0.2) | 26.1 (0.2) | 27.2 (0.4)* | 27.5 (0.7) | 27.1 (0.5) |
| Age group (yr) | |||||
| 20-24 | 50.9 (47.3-54.5) | 53.6 (49.5-57.6) | 42 (34.6-49.4)* | 40.2 (26.8-53.7) | 42.5 (33.8-51.2) |
| 25-34 | 41.1 (37.6-44.6) | 39.4 (35.4-43.3) | 46.7 (39-54.4) | 47.2 (33.2-61.2) | 46.6 (37.6-55.6) |
| 35+ | 8 (5.9-10.2) | 7 (4.9-9.2) | 11.3 (5.4-17.2) | 12.6 (3.9-21.3) | 10.9 (3.8-18) |
| Place of residence | |||||
| Urban | 26.1 (23.4-28.9) | 77 (72-82.1) | 22.9 (17.9-28) | 5.5 (2.8-8.3) | 17.4 (12.8-22) |
| Rural | 73.8 (70-76.6) | 77.6 (74.7-80.6) | 22.3 (19.3-25.2) | 5.9 (4.2-7.6) | 16.4 (13.8-19) |
| Anthropometry & Clinical | |||||
| Height (cm) | 152.4 (0.2) | 152.1 (0.3) | 153.5 (0.5)* | 153.2 (0.7) | 153.7 (0.6) |
| Systolic BP (mmHg) | 113.8 (0.5) | 112.9 (0.5) | 116.9 (1)** | 118.9 (2.1) | 116.4 (1.2) |
| Diastolic BP (mmHg) | 71.5 (0.3) | 70.8 (0.4) | 74 (0.7)** | 74.6 (1.4) | 73.9 (0.8) |
| Literacy status | |||||
| Illiterate/less than primary school | 24.4 (21.1-27.6) | 24.4 (20.9-27.8) | 24.4 (17.8-30.9) | 19.3 (8.3-30.3) | 25.8 (18-33.5) |
| Middle or high school | 65.5 (62-69) | 66.9 (63.2-70.7) | 60.7 (53-68.4) | 61.5 (47.9-75.1) | 60.5 (51.5-69.5) |
| College or higher | 10.1 (8-12.3) | 8.7 (6.7-10.8) | 14.9 (8.9-21)* | 19.2 (8-30.4) | 13.7 (7-20.5) |
| Occupational status | |||||
| Professional/Executive/Manager/Big business, Clerical/Medium business | 2.4 (1.3-3.4) | 2.3 (1.2-3.4) | 2.6 (0.3-5) | 2.4 (0-6.9) | 2.7 (0-5.4) |
| Sales, Services, Skilled manuals | 2.5 (1.4-3.5) | 3 (1.7-4.3) | 0.8 (0-1.8)* | 0 | 1 (0-2.3) |
| Agriculture/Self-employed | 5.9 (3.8-7.9) | 5.7 (3.7-7.6) | 6.5 (1.2-11.9) | 2.2 (0-6.2) | 7.8 (1.1-14.4) |
| Household & domestic work Unskilled manuals | 3.3 (2-4.6) | 3.3 (1.9-4.7) | 3.4 (0-6.7) | 4.4 (0-9.6) | 3.1 (0-7.1) |
| Do not work/Unemployed | 86 (83.4-88.6) | 85.8 (83-88.6) | 86.7 (80.3-93.1) | 91.1 (83.3-98.8) | 85.5 (77.6-93.3) |
| Socio-economic status | |||||
| Low (n=258) | 32.4 (28.8-35.8) | 31.7 (28-35.4) | 34.5 (26.7-42.4) | 34.8 (21.4-48.1) | 34.4 (25.3-43.5) |
| Middle (n=359) | 44.6 (41-48) | 41.5 (41.2-48.9) | 42.9(35.4-50.3) | 36.3 (22.6-50) | 44.7 (36.1-53.3) |
| High (n=180) | 23.1 (20-26.1) | 23.2(20-26.5) | 22.6 (15.9-29.2) | 28.8 (16-41.7) | 20.8 (13.2-28.4) |
| Glycaemic parameters | |||||
| Fasting capillary glucose (mg/dL) | 87.3 (0.4) | 83 (0.3) | 101.8 (0.9)** | 102.4 (1.48) | 101.6 (1.1) |
| 2-h post glucose (mg/dL) | 119.8 (0.9) | 103.7 (0.8) | 129.9 (2.3)** | 124 (4.6) | 131.5 (2.6) |
| Family history | |||||
| Family history of diabetes n (%) | 7.8 (6-9.6) | 6.2 (4.4-8) | 13.2 (8-18.4)* | 13.4 (3.7-23.2) | 13.1 (7-19.2) |
| History of GDM (previous pregnancy) | 7.6 (5.5-9.7) | 8 (5.6-10.4) | 6.3 (2.3-10.3) | 2.5 (1.6-6.5) | 7.4 (2.4-12.3) |
| By Trimester of pregnancy | |||||
| I Trimester | 25.4 (22.4-28.4) | 26.5 (23-30) | 21.8 (16.2-27.5) | - | - |
| II Trimester | 38.5 (35-42) | 38.3 (34.6-42) | 39.3 (31.4-47.2) | - | - |
| III Trimester | 36.1 (32.7-39.4) | 35.2 (31.6-38.9) | 38.8 (31.5-46.2) | - | - |
| Primigravida | 31.7 (28.4-35) | 31.7 (28.1-35.3) | 31.8 (24.5-39.1) | 37.3 (24-50.7) | 30.2 (21.8-38.7) |
Values are presented as mean (standard error) or weighted % (95% confidence interval) as appropriate; P *<0.05, **<0.001 compared to women without GDM
Region-wise prevalence of GDM in India is presented in figure 2. The highest prevalence of GDM was observed in central India (n=139, 32.9%), followed by north India (n=223, 31.4%), south India (n=121, 24.2%), east India (n=135, 17.9%), northeast India (n=334, 16.6%) and west India (n=80, 16%). The highest prevalence of Early GDM was reported in central India (34.2%) and the lowest in north India (9.2%), while the highest and lowest prevalence of Late GDM was reported in north India (39%) and northeast India (15.3%), respectively.

- Heatmap showing prevalence of overall gestational diabetes mellitus (GDM) in India by region. Regions details are as follows, North: Chandigarh, Delhi, Haryana, Himachal Pradesh, Punjab, Rajasthan; South: Andhra Pradesh (undivided), Karnataka, Kerala, Puducherry, Tamil Nadu; East: Bihar, Jharkhand, Odisha, West Bengal; West: Goa, Gujarat, Maharashtra; Central: Chhattisgarh, Madhya Pradesh, Uttarakhand, Uttar Pradesh; North East: Arunachal Pradesh, Assam, Manipur, Meghalaya, Mizoram, Nagaland, Sikkim, Tripura. The templates of the maps are constructed using MapChart (https://www.mapchart.net/india.html).
An increasing trend in the prevalence of GDM was observed over time across the various phases of the ICMR-INDIAB study (Supplementary Table III). The GDM prevalence increased from 13.3 per cent in Phase I (2008-2010) to 30.2 per cent in Phase V (2019-2020) of the ICMR-INDIAB study. Similar pattern of increase in prevalence was observed for Early GDM (12% to 37.6%) and Late GDM (13.8% to 27.2%) over the same period.
Table III shows the multivariate logistic regression analysis of factors contribution to GDM. In the regression analysis, systolic blood pressure and family history of diabetes were found to be associated with higher risk of GDM. No differences were seen between Early and Late GDM.
| Risk factors | Odds Ratio, OR (95% Confidence Interval) | P value |
|---|---|---|
| Age (yr)(every unit increase) | 1.03 (1-1.01) | 0.06 |
| Systolic blood pressure (mmHg)(every unit increase) | 1.24 (1.01-1.04) | <0.001 |
| Family history of diabetes | 2.16 (1.20-3.87) | 0.010 |
| Urban residence | 1.26 (0.81-1.98) | 0.308 |
Discussion
To our knowledge, this is the first nationally representative study assessing the prevalence of GDM in India. It is also the first to report on regional prevalence rates of GDM and also the first to report on prevalence of Early and Late GDM. We report the following findings (i) overall, 22.4 per cent of the pregnant women had GDM in India; (ii) the prevalence of Early GDM was 19.2 per cent and that of Late GDM, 23.4 per cent; (iii) there is heterogeneity in the prevalence of GDM in India with highest prevalence seen in central India and lowest in west India; (iv) there are no significant urban/rural differences in GDM prevalence; (v) during the various phases of the ICMR-INDIAB study done over a period of 12 yr, there appears to be an increase in prevalence of GDM and (vi) higher systolic blood pressure and family history of diabetes were associated with the increased risk of GDM.
The prevalence of GDM varies widely due to different diagnostic criteria, such as those from American Diabetes Association (ADA), WHO, IADPSG, DIPSI, NICE, and others. These criteria use distinct screening methods and thresholds, leading to inconsistent prevalence rates. This inconsistency underscores the need for standardised diagnostic approaches. Analysis of HAPO study centres showed that in Asians (mainly Chinese), NICE criteria detected more GDM, while in Whites, Hispanics, and Blacks, IADPSG identified more cases19. In this study we used NICE criteria as it aligned with OGTT fasting and 2-h glucose measures. However, for comparison, GDM prevalence was also provided using the IADPSG, the TOBOGM high glycaemic band, and the DIPSI criteria. The highest prevalence was with IADPSG (36.3%) vs. NICE (22.4%), consistent with other studies19,21 showing IADPSG increases diagnosis rates by about 75 per cent22. DIPSI showed the lowest prevalence, likely due to lower sensitivity as reported in earlier studies23-25.
A recent systematic review26 of 110 Indian studies reported a pooled GDM prevalence of 13 per cent (urban 12%, rural 10%), but most data were hospital-based. Another review27 showed a wide GDM range (0%-41.9%) with pooled prevalence by IADPSG (19.2%), WHO 1999 (10.1%), and DIPSI (7.4%) criteria. The National Family Health Survey (NFHS-5) (2019-21)28 found weighted GDM prevalence of 4.2 per cent and age-adjusted prevalence of 5.4 per cent, where GDM was defined as elevated random blood glucose (≥200 mg/dL in nonfasting state and ≥92 mg/dL in fasting state). The NFHS survey29 reported self-reported GDM prevalence of 0.53 per cent in 2015-16 and 0.80 per cent in 2019-20, with higher rates in some States like Goa (4.88%) and Kerala (3.06%), indicating regional variability. The stratification of risk of diabetes in early pregnancy (STRiDE)30 study reported 19.2 per cent prevalence by OGTT; women in India with gestational diabetes mellitus strategy (WINGS)4 found to be 18.4 per cent by IADPSG and 14.6 per cent by WHO criteria; REVAMP31 reported 15.2 per cent prevalence by DIPSI. Definitions partly explain differences. Notably, ICMR-INDIAB data show a rise from 13.3 per cent (2008-10) to 30.2 per cent (2019-20), likely driven by maternal age, obesity, urbanisation, and lifestyle, marking GDM as a growing public health concern.
Although urban-rural differences in the prevalence of T2D among non-pregnant women are well-documented, our study found no significant difference in GDM prevalence between urban and rural populations. This finding raises the possibility that pregnancy itself may act as a dominant metabolic influence, potentially overriding the influence of conventional diabetes risk factors, such as lifestyle, diet, and adiposity, typically associated with urbanisation. This convergence in GDM prevalence in urban and rural areas warrants further investigation.
A meta-analysis32 of 84 asian studies identified key GDM risk factors including multiparity (≥2), prior GDM, family diabetes history, stillbirth, congenital anomalies, abortion, macrosomia, preterm birth, pregnancy-induced hypertension, polycystic ovary syndrome, age ≥25 yr, and BMI ≥25, with odds ratios from 1.90 to 8.42. Socioeconomic status also influences GDM risk, with higher prevalence in high SES groups33. Studies like STRiDE30 and WINGS4 have highlighted HbA1c, prior GDM, family history of diabetes, and age as significant predictors of GDM. In our study, only family history and higher systolic blood pressure were associated with increased GDM risk.
Few studies report on prevalence of Early and Late GDM34-36. A global review37 reported Early GDM ranging from 0.7-36.8 per cent. In INDIAB, Early GDM ranged 19.2-34 per cent by different criteria. Our study likely underestimates prevalence due to missing 1-h glucose data per IADPSG criteria. It is known that the pathogenesis of Early GDM differs from that of Late GDM38. Late GDM is more common in Northern India, Early GDM in Central India, possibly reflecting differences in risk factor profiles. The TOBOGM trial39,40 showed early screening (<20 wk) and intervention reduce complications, such as, preterm birth, neonatal hypoglycaemia, macrosomia, and birth trauma. In India, early detection is crucial for reducing maternal, neonatal risks, and future diabetes burden. Incorporating early screening in antenatal care can improve outcomes significantly.
The study’s main strength is its large, nationally representative, community-based sample with standardized cardiometabolic assessments throughout pregnancy, ensuring reliable data and capturing true regional GDM variations. Limitations include its cross-sectional design, preventing causal conclusions or long-term follow up, and missing body weight and BMI data (not collected as per ICMR-INDIAB protocol). Use of capillary blood glucose adds variability compared to venous plasma, though correlation is acceptable41. Conducting even two-sample OGTTs is challenging in large epidemiological studies, as demonstrated by the ICMR-INDIAB experience42.
In conclusion, our findings highlight the high prevalence of GDM among Indians, underscoring the need for monitoring for GDM throughout pregnancy, starting from the first trimester. With nearly one in four pregnant women in India having GDM, this represents a large population at risk of pregnancy complications and future chronic disease, necessitating urgent public health attention and resources. The high prevalence of Early GDM (one-fifth of the pregnant women) underscores the importance of early screening, while the regional differences highlight the need for tailored, region-specific interventions addressing local risk factors and healthcare access. Key risk factors like elevated systolic blood pressure and family diabetes history identify groups needing prioritized screening. Inadequate implementation of the GDM screening protocol during antenatal care can result in missed or delayed diagnosis, preventing timely interventions such as dietary adjustments, glucose monitoring, and medication when necessary. Poor implementation of screening protocols can delay diagnosis and intervention, increasing risks for mother and child. Overall, these findings stress the critical need for standardized, universal GDM screening and effective management integrated into maternal health programmes nationwide.
Acknowledgment
Authors acknowledge ICMR-INDIAB Expert Group for guidance and scientific contributions, ICMR-INDIAB quality managers, quality supervisors, and the field team for execution of the study, as well as to all the participants for their cooperation.
Financial support & sponsorship
This study received support from the Department of Health Research (DHR), Ministry of Health and Family Welfare, Government of India, New Delhi (No. 57/1/VM/INDIAB-DHR/2012-NCD-II) and the Indian Council of Medical Research, New Delhi (No. 55/1/TF/Diab/07-NCD-II).
Conflicts of Interest
None.
Use of Artificial Intelligence (AI)-Assisted Technology for manuscript preparation
The authors confirm that there was no use of AI-assisted technology for assisting in the writing of the manuscript and no images were manipulated using AI.
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