Genetic aetiology of blood pressure relates to aortic stiffness with bi-directional causality: evidence from heritability, blood pressure polymorphisms, and Mendelian randomization

被引:29
|
作者
Cecelja, Marina [1 ]
Keehn, Louise [1 ]
Ye, Li [1 ]
Spector, Tim D. [2 ]
Hughes, Alun D. [3 ]
Chowienczyk, Phil [1 ]
机构
[1] Kings Coll London, Dept Clin Pharmacol, Cardiovasc Div, British Heart Fdn Ctr,St Thomas Hosp, Westminster Bridge Rd, London SE1 7EH, England
[2] Kings Coll London, Dept Twin Res & Genet Epidemiol, St Thomas Hosp, Westminster Bridge Rd, London SE1 7EH, England
[3] UCL, Inst Cardiovasc Sci, Dept Populat Sci & Expt Med, 69 Chenies Mews, London W1T 7HA, England
基金
英国惠康基金;
关键词
Blood pressure; Genes; Haemodynamics; Arterial stiffness; Mendelian randomization; ARTERIAL STIFFNESS; RISK; DISEASE; BIAS; HYPERTENSION; INSTRUMENTS; VARIANTS;
D O I
10.1093/eurheartj/ehaa238
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Haemodynamic determinants of blood pressure (BP) include cardiac output (CO), systemic vascular resistance (SVR), and arterial stiffness. We investigated the heritability of these phenotypes, their association with BP-related single-nucleotide polymorphisms (SNPs), and the causal association between BP and arterial stiffness. Methods and results We assessed BP, central BP components, and haemodynamic properties (during a single visit) including CO, SVR, and pulse wave velocity (PWV, measure of arterial stiffness) in 3531 (1934 monozygotic, 1586 dizygotic) female TwinsUK participants. Heritability was estimated using structural equation modelling. Association with 984 BP-associated SNP was examined using least absolute shrinkage and selection operator (LASSO) and generalized estimating equation regression. One and two-sample Mendelian randomization (MR) was used to estimate the causal direction between BP and arterial stiffness including data on 436 419 UK Biobank participants. We found high heritability for systolic and pulsatile components of BP (>50%) and PWV (65%) with overlapping genes accounting for >50% of their observed correlation. Environmental factors explained most of the variability of CO and SVR (>80%). Regression identified SNPs (n = 5) known to be associated with BP to also be associated with PWV. One-sample MR showed evidence of bi-directional causal association between BP and PWV in TwinsUK participants. Two-sample MR, confirmed a bi-directional causal effect of PWV on BP (inverse variance weighted (IVW) beta = 0.11, P < 0.02) and BP on arterial stiffness (IVW beta = 0.004, P < 0.0001). Conclusion The genetic basis of BP is mediated not only by genes regulating BP but also by genes that influence arterial stiffness. Mendelian randomization indicates a bi-directional causal association between BP and arterial stiffness.
引用
收藏
页码:3314 / +
页数:10
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