Association of common genetic variants with brain microbleeds: a genome-wide association study

Knol, M.J.; Lu, D.W.; Traylor, M.; Adams, H.H.H.; Romero, J.R.J.; Smith, A.V.; ... ; Markus, H.S. (2020)

Article / Letter to editor

ObjectiveTo identify common genetic variants associated with the presence of brain microbleeds (BMBs).MethodsWe performed genome-wide association studies in 11 population-based cohort studies and 3 case-control or case-only stroke cohorts. Genotypes were imputed to the Haplotype Reference Consortium or 1000 Genomes reference panel. BMBs were rated on susceptibility-weighted or T2*-weighted gradient echo MRI sequences, and further classified as lobar or mixed (including strictly deep and infratentorial, possibly with lobar BMB). In a subset, we assessed the effects of APOE epsilon 2 and epsilon 4 alleles on BMB counts. We also related previously identified cerebral small vessel disease variants to BMBs.ResultsBMBs were detected in 3,556 of the 25,862 participants, of which 2,179 were strictly lobar and 1,293 mixed. One locus in the APOE region reached genome-wide significance for its association with BMB (lead single nucleotide polymorphism rs769449; odds ratio [OR](any BMB) [95% confidence interval (CI)] 1.33 [1.21-1.45]; p = 2.5 x 10(-10)). APOE epsilon 4 alleles were associated with strictly lobar (OR [95% CI] 1.34 [1.19-1.50]; p = 1.0 x 10(-6)) but not with mixed BMB counts (OR [95% CI] 1.04 [0.86-1.25]; p = 0.68). APOE epsilon 2 alleles did not show associations with BMB counts. Variants previously related to deep intracerebral hemorrhage and lacunar stroke, and a risk score of cerebral white matter hyperintensity variants, were associated with BMB.ConclusionsGenetic variants in the APOE region are associated with the presence of BMB, most likely due to the APOE epsilon 4 allele count related to a higher number of strictly lobar BMBs. Genetic predisposition to small vessel disease confers risk of BMB, indicating genetic overlap with other cerebral small vessel disease markers.

• All authors: Knol, M.J.; Lu, D.W.; Traylor, M.; Adams, H.H.H.; Romero, J.R.J.; Smith, A.V.; Fornage, M.; Hofer, E.; Liu, J.F.; Hostettler, I.C.; Luciano, M.; Trompet, S.; Giese, A.K.; Hilal, S.; Akker, E.B. van den; Vojinovic, D.; Li, S.; Sigurdsson, S.; Lee, S.J. van der; Jack, C.R.; Wilson, D.; Yilmaz, P.; Satizabal, C.L.; Liewald, D.C.M.; Grond, J. van der; Chen, C.; Saba, Y.; Lugt, A. van der; Bastin, M.E.; Windham, B.G.; Cheng, C.Y.; Pirpamer, L.; Kantarci, K.; Himali, J.J.; Yang, Q.; Morris, Z.; Beiser, A.S.; Tozer, D.J.; Vernooij, M.W.; Amin, N.; Beekman, M.; Koh, J.Y.; Stott, D.J.; Houlden, H.; Schmidt, R.; Gottesman, R.F.; MacKinnon, A.D.; DeCarli, C.; Gudnason, V.; Deary, I.J.; Duijn, C.M. van; Slagboom, P.E.; Wong, T.Y.; Rost, N.S.; Jukema, J.W.; Mosley, T.H.; Werring, D.J.; Schmidt, H.; Wardlaw, J.M.; Ikram, M.A.; Seshadri, S.; Launer, L.J.; Markus, H.S.
• Date: 2020-12-15
• Journal: Neurology
• Volume: 95
• Issue: 24
• Pages: E3331 - E3343
• DOI: doi:10.1212/WNL.0000000000010852
• Link: https://n.neurology.org/content/95/24/e3331