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Published on: January 26, 2024
OS050. Genetic variants in pre-eclampsia: a meta-analysis.
A Buurma1, R Turner1, A Driessen2
1Pathology, Leiden University Medical Center, Leiden, Netherlands.
This study identified 8 genetic variants reproducibly associated with preeclampsia, primarily in the renin-angiotensin and coagulation systems. These findings suggest shared genetic risk factors between preeclampsia and cardiovascular disease.
Area of Science:
- Genetics
- Obstetrics
- Cardiovascular Medicine
Background:
- Preeclampsia exhibits a familial component, indicating a potential genetic susceptibility.
- Numerous genetic association studies exist, but replication has been inconsistent.
- This meta-analysis focuses on reproducibly associated genetic variants in preeclampsia.
Purpose of the Study:
- To provide an overview of genetic variants reproducibly linked to preeclampsia.
- To consolidate findings from multiple genetic association studies.
Main Methods:
- A systematic literature search was conducted in PubMed, EMBASE, and Web of Science.
- Genetic variants significantly associated in an initial study and reproduced in at least one other study were selected.
- Pooled odds ratios were calculated at the allele level for the association between variants and preeclampsia.
Main Results:
- 542 genetic association studies on preeclampsia were identified from 2965 citations.
- 23 genetic variants were found to be replicated.
- A random-effects meta-analysis confirmed 8 variants significantly associated with preeclampsia, located in or near ACE, AGT, CTLA4, F2, FV (two variants), LPL, and SERPINE1 genes.
Conclusions:
- Eight genetic variants are associated with preeclampsia, predominantly in the renin-angiotensin and coagulation systems.
- Shared genetic risk factors between preeclampsia and cardiovascular disease are indicated.
- Future research should explore the role of these identified genes in preeclampsia pathogenesis.
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