Gesierich Benno, Opherk Christian, Rosand Jonathan, Gonik Mariya, Malik Rainer, Jouvent Eric, Hervé Dominique, Adib-Samii Poneh, Bevan Steve, Pianese Luigi, Silvestri Serena, Dotti Maria T, De Stefano Nicola, van der Grond Jeroen, Boon Elles M J, Pescini Francesca, Rost Natalia, Pantoni Leonardo, Oberstein Saskia A Lesnik, Federico Antonio, Ragno Michele, Markus Hugh S, Tournier-Lasserve Elisabeth, Chabriat Hugues, Dichgans Martin, Duering Marco, Ewers Michael
J Cereb Blood Flow Metab. 2016 Jan;36(1):199-203. doi: 10.1038/jcbfm.2015.85.
Apolipoprotein E (APOE) increases the risk for Alzheimer’s disease (ɛ4 allele) and cerebral amyloid angiopathy (ɛ2 and ɛ4), but its role in small vessel disease (SVD) is debated. Here we studied the effects of APOE on white matter hyperintensity volume (WMHV) in CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy), a nonamyloidogenic angiopathy and inherited early-onset form of pure SVD. Four hundred and eighty-eight subjects were recruited through a multicenter consortium. Compared with APOE ɛ3/ɛ3, WMHV was increased in APOE ɛ2 (P = 0.02) but not APOE ɛ4. The results remained significant when controlled for genome-wide genetic background variation. Our findings suggest a modifying influence of APOE ɛ2 on WMHV caused by pure SVD.
载脂蛋白E(APOE)会增加患阿尔茨海默病(ɛ4等位基因)和脑淀粉样血管病(ɛ2和ɛ4)的风险,但其在小血管疾病(SVD)中的作用仍存在争议。在此,我们研究了APOE对伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)中白质高信号体积(WMHV)的影响,CADASIL是一种非淀粉样血管病,也是遗传性早发型纯SVD。通过一个多中心联盟招募了488名受试者。与APOEɛ3/ɛ3相比,APOEɛ2的WMHV增加(P = 0.02),而APOEɛ4则没有。在控制全基因组遗传背景变异后,结果仍然显著。我们的研究结果表明,APOEɛ2对纯SVD引起的WMHV有修饰作用。