Tschiderer Lena, Bakker Mark K, Gill Dipender, Burgess Stephen, Willeit Peter, Ruigrok Ynte M, Peters Sanne Ae
Institute of Health Economics, Medical University of Innsbruck, Innsbruck, Austria.
Department of Neurology and Neurosurgery, University Medical Center Utrecht Brain Center, Utrecht University, The Netherlands.
Eur Stroke J. 2024 Jul 30;10(1):216-224. doi: 10.1177/23969873241265224. eCollection 2025 Mar.
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.
The aim of this study was to determine sex differences in causal relationships between cardiometabolic and lifestyle factors and risk of aSAH and IA.
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.
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 (-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 (-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 (-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.
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.
颅内动脉瘤(IA)的患病率和动脉瘤性蛛网膜下腔出血(aSAH)的发病率女性高于男性。尽管一些心脏代谢和生活方式因素与IA或aSAH的风险有关,但尚不清楚这些风险因素的因果关系中是否存在性别差异。
本研究的目的是确定心脏代谢和生活方式因素与aSAH和IA风险之间因果关系的性别差异。
我们使用全基因组关联研究的汇总水平数据进行了一项性别特异性的两样本孟德尔随机化研究。我们分析了低密度脂蛋白胆固醇、高密度脂蛋白胆固醇[HDL-C]、甘油三酯、非HDL-C、总胆固醇、空腹血糖、收缩压和舒张压、开始吸烟和饮酒作为暴露因素,以及aSAH和IA(即aSAH和未破裂IA合并)作为结局。
我们发现,在基因代理的非HDL-C与aSAH风险之间的关系上存在统计学上显著的性别差异,女性的比值比(OR)为0.72(95%置信区间0.58,0.88),男性为1.01(0.77,1.31)(性别差异P值为0.044)。此外,与女性相比,男性开始吸烟的遗传易感性与aSAH的统计学显著更高风险相关(性别差异P值为0.007),OR分别为3.81(1.93,7.52)和1.12(0.63,1.99),并且与男性相比,男性开始吸烟的遗传易感性与IA的统计学显著更高风险相关(性别差异P值为0.036),OR分别为3.58(2.04,6.27)和1.61(0.98,2.64)。此外,基因代理的收缩压和舒张压升高与女性和男性的aSAH和IA风险升高均相关。
与男性相比,基因代理的较高非HDL-C与女性较低的aSAH风险相关。此外,与女性相比,男性开始吸烟的遗传易感性与aSAH和IA的较高风险相关。这些发现可能有助于增进对aSAH和IA发生发展中性别差异的理解。