Genetically determined blood pressure, antihypertensive medications, and risk of intracranial aneurysms and aneurysmal subarachnoid hemorrhage: A Mendelian randomization study

Author:

Liu Hanchen1ORCID,Zuo Huiqin2,Johanna Ospel3,Zhao Rui1,Yang Pengfei1,Chen Weixing4,Li Qiang1,Lin Xiaolei5,Zhou Yu1,Liu Jianmin1

Affiliation:

1. Neurovascular Center, Naval Medical University Changhai Hospital, Shanghai, China

2. Huamu Community Center of Pudong, Shanghai, China

3. Department of Radiology, University Hospital Basel, Basel, Switzerland

4. Luoping People’s Hospital, Yun’nan, China

5. School of Data Science, Fudan University, Shanghai, China

Abstract

Introduction: Observational studies suggest that different classes of antihypertensive drugs may have different effects on the occurrence of intracranial aneurysms (IA) and subarachnoid hemorrhage (SAH). However, the reported results in previous studies are inconsistent, and randomized data are absent. We performed a two-sample Mendelian randomization (MR) analysis to study the causal effects of genetically determined blood pressure (BP) and genetic proxies for antihypertensive drug classes on the risk of IA and SAH. Materials and methods: Genetic instruments and outcome data were obtained from independent genome-wide association studies (GWAS) or published data, which were exclusively restricted to European ancestry. Causal relationships were identified using inverse-variance weighted MR analyses and a series of statistical sensitivity analyses. The FinnGen consortium was used for repeated analysis to verify results obtained from the above GWAS. Results: Two-sample MR analysis showed that genetically determined Systolic BP, Dystolic BP, and Pulse Pressure were related to a higher risk of IA and SAH. Based on identified single nucleotide polymorphisms (SNPs) that influence the effect of calcium channel blockers (CCB, 42 SNPs), beta-blockers (BB, 8 SNPs), angiotensin-converting enzyme inhibitors (ACEI, 2 SNPs), angiotensin receptor blockers (ARB, 1 SNPs), and thiazides (5 SNPs), genetically determined effect of CCBs was associated with a higher risk of IA (OR, 1.07 [95% CI, 1.03–1.10], p = 5.02 × 10−5) and SAH (OR, 1.06 [95% CI, 1.03–1.09], p = 1.84 × 10−3). No associations were found between other antihypertensive drugs and the risk of IA or SAH. The effect of CCBs on SAH was confirmed in FinnGenconsortium samples (OR, 1.04 [95% CI, 1.00–1.08], p = 0.042). Discussion and conclusion: This MR analysis supports the role of elevated blood pressure in the occurrence of intracranial aneurysms and subarachnoid hemorrhage. However, genetic proxies for calcium channel blockers were associated with an increased risk of intracranial aneurysms and subarachnoid hemorrhage. Further studies are required to confirm these findings and investigate the underlying mechanisms.

Funder

National Natural Science Foundation of China

SanHang Program of the Naval Medical University

Climbing’ program of Changhai Hospital

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical)

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