Maternal Diabetes during Pregnancy and Early Onset of Cardiovascular Disease in Offspring: Population Based Cohort Study with 40 Years of Follow-Up
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Objective: To evaluate the associations between maternal diabetes diagnosed before or during pregnancy and early onset cardiovascular disease (CVD) in offspring during their first four decades of life. Design: Population based cohort study. Setting: Danish national health registries. Participants: All 2 432 000 liveborn children without congenital heart disease in Denmark during 1977-2016. Follow-up began at birth and continued until first time diagnosis of CVD, death, emigration, or 31 December 2016, whichever came first. Exposures for observational studies: Pregestational diabetes, including type 1 diabetes (n=22 055) and type 2 diabetes (n=6537), and gestational diabetes (n=26 272). Main outcome measures: The primary outcome was early onset CVD (excluding congenital heart diseases) defined by hospital diagnosis. Associations between maternal diabetes and risks of early onset CVD in offspring were studied. Cox regression was used to assess whether a maternal history of CVD or maternal diabetic complications affected these associations. Adjustments were made for calendar year, sex, singleton status, maternal factors (parity, age, smoking, education, cohabitation, residence at childbirth, history of CVD before childbirth), and paternal history of CVD before childbirth. The cumulative incidence was averaged across all individuals, and factors were adjusted while treating deaths from causes other than CVD as competing events. Results: During up to 40 years of follow-up, 1153 offspring of mothers with diabetes and 91 311 offspring of mothers who did not have diabetes were diagnosed with CVD. Offspring of mothers with diabetes had a 29% increased overall rate of early onset CVD (hazard ratio 1.29 (95% confidence interval 1.21 to 1.37); cumulative incidence among offspring unexposed to maternal diabetes at 40 years of age 13.07% (12.92% to 13.21%), difference in cumulative incidence between exposed and unexposed offspring 4.72% (2.37% to 7.06%)). The sibship design yielded results similar to those of the unpaired design based on the whole cohort. Both pregestational diabetes (1.34 (1.25 to 1.43)) and gestational diabetes (1.19 (1.07 to 1.32)) were associated with increased rates of CVD in offspring. We also observed varied increased rates of specific early onset CVDs, particularly heart failure (1.45 (0.89 to 2.35)), hypertensive disease (1.78 (1.50 to 2.11)), deep vein thrombosis (1.82 (1.38 to 2.41)), and pulmonary embolism (1.91 (1.31 to 2.80)). Increased rates of CVD were seen in different age groups from childhood to early adulthood until age 40 years. The increased rates were more pronounced among offspring of mothers with diabetic complications (1.60 (1.25 to 2.05)). A higher incidence of early onset CVD in offspring of mothers with diabetes and comorbid CVD (1.73 (1.36 to 2.20)) was associated with the added influence of comorbid CVD but not due to the interaction between diabetes and CVD on the multiplicative scale (P value for interaction 0.94). Conclusions: Children of mothers with diabetes, especially those mothers with a history of CVD or diabetic complications, have increased rates of early onset CVD from childhood to early adulthood. If maternal diabetes does have a causal association with increased CVD rate in offspring, the prevention, screening, and treatment of diabetes in women of childbearing age could help to reduce the risk of CVD in the next generation.
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Recent epidemiological studies show a relationship between increased risk of cardiometabolic diseases in adulthood for offspring of women whose pregnancy was complicated by GDM.
“Recent epidemiological studies show a relationship between an increased risk of cardiometabolic diseases in adulthood for offspring of women whose pregnancy has been complicated by GDM.”
From Maternal Overnutrition and Fetal Programming: Long-Term Metabolic, Cognitive, and Epigenetic Consequences (2026) · cites this paper as [62]
The Results (page not provided) report increased early-onset cardiovascular disease among offspring exposed to gestational diabetes, including in early adulthood (ages 20–40). They also report higher rates of metabolic conditions among offspring exposed to maternal diabetes overall, but do not establish those outcomes specifically for gestational diabetes or address adulthood beyond age 40. The claim is therefore broader than this study’s findings. (LLM, conf=0.85)
Experimental — accuracy not yet measuredThe incidence ratio of offspring exposed to every type of maternal diabetes was increased by 29% compared to non-exposed offspring, with increased risk observed in every age group.
“The incidence ratio of offspring exposed to every type of maternal diabetes was increased by 29% compared to non-exposed offspring, and the increase in risk was observed in every age group (<20 years old; >20 years old) [33,62,63,64,65].”
From Maternal Overnutrition and Fetal Programming: Long-Term Metabolic, Cognitive, and Epigenetic Consequences (2026) · cites this paper as [62]
Yu Y. et al. demonstrated an association between gestational diabetes and an increased rate of early-onset cardiovascular diseases (≤40 years old) in offspring.
“A large study conducted by Yu Y. et al. demonstrated an association between gestational diabetes and an increased rate of early-onset cardiovascular diseases (CVD; ≤40 years old) in offspring.”
From Maternal Overnutrition and Fetal Programming: Long-Term Metabolic, Cognitive, and Epigenetic Consequences (2026) · cites this paper as [62]
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- Authors
- Yu, Y., Arah, O. A., Liew, Z., Cnattingius, S., Olsen, J., Sørensen, H. T., Qin, G., & Li, J.
- Affiliations
- University of California, Los Angeles (US)
- Yale University (US)
- Karolinska University Hospital (SE)
- Aarhus University Hospital (DK)
- Fudan University (CN)
- Shanghai Jiao Tong University (CN)
- Corresponding author
- Yu, Yongfu
- Qin, Guoyou
- ORCID
- Venue
- BMJ
- Publisher
- BMJ
- Published
- 2019-12-04
- Volume
- 367
- Pages
- l6398
- ISSN
- 1756-1833 (ISSN-L)
- PMC
- PMC6891797
- OpenAlex
- W2992178815
- Cited by
- 305
- References
- 9
- Citations by year
- 2026: 29 · 2025: 32 · 2024: 54 · 2023: 48 · 2022: 60 · 2021: 47 · 2020: 35
- FWCI
- 38.62
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- BMJ (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by-nc)
- eScholarship (California Digital Library) (submittedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- National Natural Science Foundation of China (11871164)
- Lundbeckfonden (R265-2017–4069, R232-2016-2462 and R265-2017-4069, R232‐2016‐2462)
- Karen Elise Jensens Fond
- Novo Nordisk (NNF18OC0052029)
- Danmarks Frie Forskningsfond (DFF-6110–00019)
- Novo Nordisk Fonden (NNF18OC0052029)
- H. Lundbeck A/S
- National Institutes of Health (UL1TR001881)
- National Institute of Child Health and Human Development
- National Center for Advancing Translational Sciences
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD072296, P2CHD041022)
- Topics
- Health Sciences › Medicine › Obstetrics and Gynecology › Gestational Diabetes Research and Management
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Keywords
- maternal diabetes, gestational diabetes mellitus, pregestational diabetes, type 1 diabetes, type 2 diabetes, early-onset cardiovascular disease, maternal diabetes complications, cumulative incidence
- MeSH terms
- Adult, Cardiovascular Diseases, Denmark, Diabetes Mellitus, Female, Follow-Up Studies, Humans, Male, Pregnancy, Prenatal Exposure Delayed Effects, Diabetes, Gestational, Maternal Exposure, Young Adult
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