St Clair D, Rennie M, Slorach E, Norrman J, Yates C, Carothers A
MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
J Med Genet. 1995 Aug;32(8):642-4. doi: 10.1136/jmg.32.8.642.
While apoliprotein E (ApoE) epsilon 4 allele is now a well established risk factor for familial and sporadic senile Alzheimer's disease (AD), its role in the development of the rarer presenile or early onset type is controversial. Early studies showed no association; later ones found enrichment for the epsilon 4 allele in familial or sporadic types or both. We have ApoE genotyped a series of Scottish people (n = 85) with early onset AD. We find highly significant enrichment for both homozygote and heterozygote ApoE epsilon 4 allele carriers in familial and sporadic early onset AD with a pattern closely resembling that in late onset AD.
虽然载脂蛋白E(ApoE)ε4等位基因现在是家族性和散发性老年痴呆症(AD)的一个公认的危险因素,但其在较罕见的早老性或早发型类型发展中的作用仍存在争议。早期研究未发现关联;后来的研究发现ε4等位基因在家族性或散发性类型或两者中均有富集。我们对一系列患有早发性AD的苏格兰人(n = 85)进行了ApoE基因分型。我们发现,在家族性和散发性早发性AD中,纯合子和杂合子ApoE ε4等位基因携带者均有高度显著的富集,其模式与晚发性AD非常相似。