Sex differences in risk factor relationships with subarachnoid haemorrhage and intracranial aneurysms: A Mendelian randomization study

被引:1
|
作者
Tschiderer, Lena [1 ]
Bakker, Mark K. [2 ]
Gill, Dipender [3 ]
Burgess, Stephen [4 ,5 ,6 ]
Willeit, Peter [1 ,4 ]
Ruigrok, Ynte M. [2 ]
Peters, Sanne A. E. [7 ,8 ,9 ]
机构
[1] Med Univ Innsbruck, Inst Hlth Econ, Innsbruck, Austria
[2] Univ Utrecht, Univ Med Ctr Utrecht, Brain Ctr, Dept Neurol & Neurosurg, Utrecht, Netherlands
[3] Imperial Coll London, Sch Publ Hlth, Dept Epidemiol & Biostat, London, England
[4] Univ Cambridge, Dept Publ Hlth & Primary Care, Cambridge, England
[5] Univ Cambridge, Heart & Lung Res Inst, Cambridge, England
[6] Univ Cambridge, Sch Clin Med, MRC Biostat Unit, Cambridge, England
[7] Univ Utrecht, Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[8] Imperial Coll London, Sch Publ Hlth, George Inst Global Hlth, London, England
[9] Univ New South Wales, George Inst Global Hlth, Sydney, NSW, Australia
基金
欧洲研究理事会; 奥地利科学基金会; 英国医学研究理事会; 英国惠康基金;
关键词
Aneurysmal subarachnoid haemorrhage; intracranial aneurysm; sex differences; Mendelian randomization; RUPTURE; STROKE; WOMEN;
D O I
10.1177/23969873241265224
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The prevalence of intracranial aneurysms (IAs) and incidence of aneurysmal subarachnoid haemorrhage (aSAH) is higher in women than in men. Although several cardiometabolic and lifestyle factors have been related to the risk of IAs or aSAH, it is unclear whether there are sex differences in causal relationships of these risk factors.Aims: The aim of this study was to determine sex differences in causal relationships between cardiometabolic and lifestyle factors and risk of aSAH and IA.Methods: We conducted a sex-specific two-sample Mendelian randomization study using summary-level data from genome-wide association studies. We analysed low-density lipoprotein cholesterol, high-density lipoprotein cholesterol [HDL-C], triglycerides, non-HDL-C, total cholesterol, fasting glucose, systolic and diastolic blood pressure, smoking initiation, and alcohol use as exposures, and aSAH and IA (i.e. aSAH and unruptured IA combined) as outcomes.Results: We found statistically significant sex differences in the relationship between genetically proxied non-HDL-C and aSAH risk, with odds ratios (ORs) of 0.72 (95% confidence interval 0.58, 0.88) in women and 1.01 (0.77, 1.31) in men (p-value for sex difference 0.044). Moreover, genetic liability to smoking initiation was related to a statistically significantly higher risk of aSAH in men compared to women (p-value for sex difference 0.007) with ORs of 3.81 (1.93, 7.52) and 1.12 (0.63, 1.99), respectively, and to a statistically significantly higher IA risk in men compared to women (p-value for sex difference 0.036) with ORs of 3.58 (2.04, 6.27) and 1.61 (0.98, 2.64), respectively. In addition, higher genetically proxied systolic and diastolic blood pressure were related to a higher risk of aSAH and IA in both women and men.Conclusions: Higher genetically proxied non-HDL-C was related to a lower risk of aSAH in women compared to men. Moreover, genetic liability to smoking initiation was associated with a higher risk for aSAH and IA in men compared to women. These findings may help improve understanding of sex differences in the development of aSAH and IA. Graphical abstract
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页数:9
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