Imperial College London

Dr Fu Siong Ng

Faculty of MedicineNational Heart & Lung Institute

Reader in Cardiac Electrophysiology
 
 
 
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Contact

 

+44 (0)20 7594 3614f.ng Website

 
 
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Location

 

430ICTEM buildingHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Ardissino:2023:10.1161/JAHA.122.027933,
author = {Ardissino, M and Slob, EAW and Carter, P and Rogne, T and Girling, J and Burgess, S and Ng, FS},
doi = {10.1161/JAHA.122.027933},
journal = {Journal of the American Heart Association},
pages = {1--73},
title = {Sex-specific reproductive factors augment cardiovascular disease risk in females: a Mendelian randomization study},
url = {http://dx.doi.org/10.1161/JAHA.122.027933},
volume = {12},
year = {2023}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Background: Cardiovascular disease is a major cause of morbidity and mortality in women. Observational studies suggest that reproductive factors are associated with cardiovascular disease risk, but these are liable to influence by residual confounding. This study aims to explore the causal role of reproductive factors on cardiovascular disease in women using Mendelian randomisation and explore potentially modifiable mediating pathways amenable to intervention.Methods and results: Uncorrelated (r2<0.001), genome-wide significant (p<5x10 -8) SNPs were extracted from sex-specific genome-wide association studies of age at first birth, number of live births, age at menarche and age at menopause. Inverse-variance weighted Mendelian randomisation was utilised for primary analyses on outcomes of atrial fibrillation, coronary artery disease, heart failure, ischaemic stroke, and stroke. Earlier genetically-predicted age at first birth increased risk of coronary artery disease (OR per 1-year lower 1.49, 95%CI 1.28-1.74, p=3.72x10 -7 ), heart failure (OR 1.27, 95%CI 1.06-1.53, p=0.009) and stroke (OR 1.25, 95%CI 1.00-1.56, p=0.048), with partial mediation through body mass index, type 2 diabetes, blood pressure and cholesterol traits. Higher genetically-predicted number of live births increased risk of atrial fibrillation (OR per category increase <2 vs 2 vs>2 live births 2.91, 95%CI 1.16-7.29, p=0.023), heart failure (OR 1.90, 95%CI 1.28-2.82, p=0.001), ischaemic stroke (OR 1.86, 95%CI 1.03-3.37, p=0.039) and stroke (OR 2.07, 95%CI 1.22-3.52, p=0.007). Earlier genetically-predicted age at menarche increased risk of coronary artery disease (OR per 1-year lower 1.10, 95%CI 1.06-1.14, p=1.68 x10 -6) and heart failure (OR 1.12, 95%CI 1.07-1.17, p=5.06x10 -7), and both associations were at least partly mediated by body mass index.Conclusion: These results support a causal role of a number of reproductive factors on cardiovascular disease in women, and identify multiple
AU - Ardissino,M
AU - Slob,EAW
AU - Carter,P
AU - Rogne,T
AU - Girling,J
AU - Burgess,S
AU - Ng,FS
DO - 10.1161/JAHA.122.027933
EP - 73
PY - 2023///
SN - 2047-9980
SP - 1
TI - Sex-specific reproductive factors augment cardiovascular disease risk in females: a Mendelian randomization study
T2 - Journal of the American Heart Association
UR - http://dx.doi.org/10.1161/JAHA.122.027933
UR - https://www.ahajournals.org/doi/10.1161/JAHA.122.027933
UR - http://hdl.handle.net/10044/1/101985
VL - 12
ER -