Cardiometabolic & kidney

Gestational diabetes and future cardiovascular diseases: associations by sex-specific genetic data

Eur Heart JPublished Mendelian randomisation study

Authors' conclusion

This study demonstrated a suggestive causal relationship between genetic predisposition to gestational diabetes mellitus and the risk of coronary artery disease, which was mainly mediated by Type 2 diabetes and hypertension.

Study context

Population
Ever-pregnant women; GDM GWAS summary statistics from FinnGen, CVD from UK Biobank individual-level genetic data
Comparison
Genetic predisposition to gestational diabetes mellitus and risk of CVD
Outcome
CAD and MI risk per unit increase in log-odds of genetic predisposition to GDM (ever-pregnant women)
Methodological detailssex-specific, two-sample Mendelian randomization, linkage disequilibrium score regression, two-step Mendelian randomization mediation analysis
  • Sex-specific
  • Two-sample Mendelian randomization
  • Linkage disequilibrium score regression
  • Two-step Mendelian randomization mediation analysis

Main finding

As reported in the abstract

Genetic predisposition to gestational diabetes mellitusOdds ratio (95% CI)
CAD, per unit increase in log-odds, ever-pregnant women
1.09(1.01–1.17)
MI, per unit increase in log-odds, ever-pregnant women
1.12(.96-1.31)

Per unit increase in log-odds, as printed

Further findings

Genetic correlation (LD score regression)

Significant genetic correlation of GDM with CAD and MI after Benjamini-Hochberg correction in ever-pregnant women

Mediation of GDM–CAD causality

T2DM and hypertension identified as mediators

Sensitivity analysis: instruments with GDM-predominant effects and CAD

OR direction consistent with primary results in ever-pregnant women, not statistically significant

Parts of this Brief are withheld: the automatic checks could not confirm them against the abstract.

Original publication

Gestational diabetes and future cardiovascular diseases: associations by sex-specific genetic data. Eur Heart J. Published 25 October 2024. doi:10.1093/eurheartj/ehae706

Composed by AI from the published abstract and checked against it. How Briefs are made →

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