학술논문

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Document Type
article
Source
Nature Genetics. 52(12)
Subject
Genetics
Brain Disorders
Human Genome
Clinical Research
Prevention
Stroke
Neurosciences
Aetiology
2.1 Biological and endogenous factors
Cardiovascular
Asian People
Blood Pressure
Case-Control Studies
Endothelial Cells
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Hypertension
Intracranial Aneurysm
Polymorphism
Single Nucleotide
Risk Factors
Smoking
Subarachnoid Hemorrhage
White People
HUNT All-In Stroke
China Kadoorie Biobank Collaborative Group
BioBank Japan Project Consortium
ICAN Study Group
CADISP Group
Genetics and Observational Subarachnoid Haemorrhage (GOSH) Study investigators
International Stroke Genetics Consortium
Biological Sciences
Medical and Health Sciences
Developmental Biology
Language
Abstract
Rupture of an intracranial aneurysm leads to subarachnoid hemorrhage, a severe type of stroke. To discover new risk loci and the genetic architecture of intracranial aneurysms, we performed a cross-ancestry, genome-wide association study in 10,754 cases and 306,882 controls of European and East Asian ancestry. We discovered 17 risk loci, 11 of which are new. We reveal a polygenic architecture and explain over half of the disease heritability. We show a high genetic correlation between ruptured and unruptured intracranial aneurysms. We also find a suggestive role for endothelial cells by using gene mapping and heritability enrichment. Drug-target enrichment shows pleiotropy between intracranial aneurysms and antiepileptic and sex hormone drugs, providing insights into intracranial aneurysm pathophysiology. Finally, genetic risks for smoking and high blood pressure, the two main clinical risk factors, play important roles in intracranial aneurysm risk, and drive most of the genetic correlation between intracranial aneurysms and other cerebrovascular traits.