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Published on: January 26, 2024
Hypertensive disorders of pregnancy and cardiovascular disease risk: a Mendelian randomisation study
Lena Tschiderer1, Yvonne T van der Schouw2, Stephen Burgess3,4,5
1Institute of Health Economics, Medical University of Innsbruck, Innsbruck, Austria.
Insights
Genetic predisposition to hypertensive disorders of pregnancy (HDPs) increases cardiovascular disease (CVD) risk. This genetic liability is linked to higher blood pressure and earlier hypertension diagnosis, suggesting a causal relationship with CVD.
Area of Science:
- Cardiovascular Health
- Genetics
- Obstetrics & Gynecology
Background:
- Hypertensive disorders of pregnancy (HDPs) are linked to adverse maternal cardiovascular disease (CVD) risk profiles.
- Observational studies suggest a connection between HDPs and later-life CVD risk.
Purpose of the Study:
- To investigate the association between genetic liability to HDPs (pre-eclampsia/eclampsia and gestational hypertension) and CVD risk factors.
- To determine if genetic predisposition to HDPs is linked to the occurrence of CVD events like myocardial infarction or stroke.
Main Methods:
- Utilized Mendelian randomization with individual participant data from the UK Biobank.
- Analyzed genetic associations with HDPs from genome-wide association studies.
- Included ever pregnant women in the primary analysis, with sensitivity analyses in nulligravidae and men.
Main Results:
- Genetic liability to HDPs showed increased odds of CVD (ORs 1.20-1.24 per unit increase).
- Associated with higher systolic/diastolic blood pressure and earlier hypertension diagnosis.
- Sensitivity analyses in men and nulligravidae supported these findings.
Conclusions:
- Genetic liability to HDPs is causally related to increased CVD risk.
- Biological mechanisms underlying HDPs appear to contribute to CVD development.
- Findings were consistent across ever pregnant women, nulligravidae, and men.
Objective:
Observational studies show that hypertensive disorders of pregnancy (HDPs) are related to unfavourable maternal cardiovascular disease (CVD) risk profiles later in life. We investigated whether genetic liability to pre-eclampsia/eclampsia and gestational hypertension is associated with CVD risk factors and occurrence of CVD events.
Methods:
We obtained genetic associations with HDPs from a genome-wide association study and used individual participant data from the UK Biobank to obtain genetic associations with CVD risk factors and CVD events (defined as myocardial infarction or stroke). In our primary analysis, we applied Mendelian randomisation using inverse-variance weighted regression analysis in ever pregnant women. In sensitivity analyses, we studied men and nulligravidae to investigate genetic liability to HDPs and CVD risk without the ability to experience the underlying phenotype.
Results:
Our primary analysis included 221 155 ever pregnant women (mean age 56.8 (SD 7.9) years) with available genetic data. ORs for CVD were 1.20 (1.02 to 1.41) and 1.24 (1.12 to 1.38) per unit increase in the log odds of genetic liability to pre-eclampsia/eclampsia and gestational hypertension, respectively. Furthermore, genetic liability to HDPs was associated with higher levels of systolic and diastolic blood pressure and younger age at hypertension diagnosis. Sensitivity analyses revealed no statistically significant differences when comparing the findings with those of nulligravidae and men.
Conclusions:
Genetic liability to HDPs is associated with higher CVD risk, lower blood pressure levels and earlier hypertension diagnosis. Our study suggests similar findings in ever pregnant women, nulligravidae and men, implying biological mechanisms relating to HDPs are causally related to CVD risk.
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