<i>COL4A2</i> is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls.

Abstract

To determine whether common variants in familial cerebral small vessel disease (SVD) genes confer risk of sporadic cerebral SVD. We meta-analyzed genotype data from individuals of European ancestry to determine associations of common single nucleotide polymorphisms (SNPs) in 6 familial cerebral SVD genes (<i>COL4A1</i>, <i>COL4A2</i>, <i>NOTCH3</i>, <i>HTRA1</i>, <i>TREX1</i>, and <i>CECR1</i>) with intracerebral hemorrhage (ICH) (deep, lobar, all; 1,878 cases, 2,830 controls) and ischemic stroke (IS) (lacunar, cardioembolic, large vessel disease, all; 19,569 cases, 37,853 controls). We applied data quality filters and set statistical significance thresholds accounting for linkage disequilibrium and multiple testing. A locus in <i>COL4A2</i> was associated (significance threshold <i>p</i> < 3.5 × 10^-4) with both lacunar IS (lead SNP rs9515201: odds ratio [OR] 1.17, 95% confidence interval [CI] 1.11-1.24, <i>p</i> = 6.62 × 10^-8) and deep ICH (lead SNP rs4771674: OR 1.28, 95% CI 1.13-1.44, <i>p</i> = 5.76 × 10^-5). A SNP in <i>HTRA1</i> was associated (significance threshold <i>p</i> < 5.5 × 10^-4) with lacunar IS (rs79043147: OR 1.23, 95% CI 1.10-1.37, <i>p</i> = 1.90 × 10^-4) and less robustly with deep ICH. There was no clear evidence for association of common variants in either <i>COL4A2</i> or <i>HTRA1</i> with non-SVD strokes or in any of the other genes with any stroke phenotype. These results provide evidence of shared genetic determinants and suggest common pathophysiologic mechanisms of distinct ischemic and hemorrhagic cerebral SVD stroke phenotypes, offering new insights into the causal mechanisms of cerebral SVD.