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Published on: January 26, 2024
Hypertensive disorders of pregnancy and cardiovascular disease risk: A Mendelian Randomisation study
Lena Tschiderer1,2, 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, associated with higher blood pressure and earlier hypertension diagnosis. These links suggest a causal relationship between HDPs and later life CVD.
Area of Science:
- Cardiovascular Science
- Genetics
- Obstetrics & Gynecology
Background:
- Hypertensive disorders of pregnancy (HDPs) are linked to adverse maternal cardiovascular disease (CVD) risk profiles post-pregnancy.
- Understanding the genetic underpinnings of HDPs and their association with CVD is crucial for risk prediction and prevention.
Purpose of the Study:
- To investigate the association between genetic liability to pre-eclampsia/eclampsia and gestational hypertension with CVD risk factors and events.
- To determine if genetic predisposition to HDPs causally influences later-life CVD risk.
Main Methods:
- Utilized genome-wide association study data for HDPs and UK Biobank individual-participant data for CVD risk factors and events.
- Employed Mendelian Randomisation analysis in 221,155 ever pregnant women, with sensitivity analyses in men and nulligravidae.
Main Results:
- Genetic liability to HDPs showed increased odds of CVD (OR 1.20-1.24 per unit increase).
- Associated with higher systolic/diastolic blood pressure and earlier hypertension diagnosis.
- Sensitivity analyses in men and nulligravidae corroborated findings, indicating no significant differences.
Conclusions:
- Genetic liability to HDPs is causally linked to increased CVD risk, higher blood pressure, and earlier hypertension onset.
- The findings suggest shared biological mechanisms between HDPs and cardiovascular risk across different populations.
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]) with available genetic data. Odds ratios for CVD were 1.20 (1.02-1.41) and 1.24 (1.12-1.38) 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 to 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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