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Sex differences in risk factor relationships with subarachnoid haemorrhage and intracranial aneurysms: A Mendelian Randomisation study.
Tschiderer, Lena; Bakker, Mark K; Gill, Dipender; Burgess, Stephen; Willeit, Peter; Ruigrok, Ynte M; Peters, Sanne Ae.
Affiliation
  • Tschiderer L; Institute of Health Economics; Medical University of Innsbruck, Innsbruck, Austria.
  • Bakker MK; Department of Neurology and Neurosurgery, University Medical Center Utrecht Brain Center, Utrecht University, the Netherlands.
  • Gill D; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, United Kingdom.
  • Burgess S; Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
  • Willeit P; Heart and Lung Research Institute, University of Cambridge, Cambridge, United Kingdom.
  • Ruigrok YM; MRC Biostatistics Unit, School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Peters SA; Institute of Health Economics; Medical University of Innsbruck, Innsbruck, Austria.
Eur J Prev Cardiol ; 31(Suppl 1)2024 Jun 13.
Article in En | MEDLINE | ID: mdl-38989054
ABSTRACT

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 randomisation 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Subarachnoid Hemorrhage / Intracranial Aneurysm / Genome-Wide Association Study / Mendelian Randomization Analysis Limits: Female / Humans / Male Language: En Journal: Eur J Prev Cardiol Year: 2024 Document type: Article Affiliation country: Austria

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Subarachnoid Hemorrhage / Intracranial Aneurysm / Genome-Wide Association Study / Mendelian Randomization Analysis Limits: Female / Humans / Male Language: En Journal: Eur J Prev Cardiol Year: 2024 Document type: Article Affiliation country: Austria