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Ethnicity-dependent genetic association of ABCA2 with sporadic Alzheimer's disease.
Authors:M Axel Wollmer  Elisabeth Kapaki  Martin Hersberger  J?rg Muntwyler  Fabienne Brunner  Magdalini Tsolaki  Hiroyasu Akatsu  Kenji Kosaka  Makoto Michikawa  Dimitra Molyva  Giorgos P Paraskevas  Dieter Lütjohann  Arnold von Eckardstein  Christoph Hock  Roger M Nitsch  Andreas Papassotiropoulos
Affiliation:Division of Psychiatry Research, University of Zürich, Switzerland. awollmer@bli.unizh.ch
Abstract:A recent study demonstrated a significant genetic association between the ATP-binding cassette transporter A2 (ABCA2) and the risk for Alzheimer's disease (AD) in a large Caucasian sample. The rare T allele of the synonymous exonic single nucleotide polymorphism (SNP) rs908832 was overrepresented in early-onset AD patients as compared to cognitively healthy controls. Here we confirm the association of rs908832 with AD in a Western European population (n = 291, P = 0.008). In a second sample from Southern Europe, rs908832 was not associated with AD. Interestingly, rs908832 was not polymorphic in a Japanese sample. Furthermore, rs908832 was not associated with either serum cholesterol levels or with the risk for coronary artery disease, but seemed to be related to cholesterol levels in the cerebrospinal fluid. These data suggest that ABCA2 may exert population-dependent effects on the genetic risk for sporadic AD and support a role of ABC lipid transporters in the pathogenesis of this disease.
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