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Volume 169, Issue 1, Pages 105-112 (July 2003)


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A common Ile 823 Met variant of ATP-binding cassette transporter A1 gene (ABCA1) alters high density lipoprotein cholesterol level in Japanese population

Tomohiro Haradaa, Yasushi Imaiab, Takefumi Nojiria, Hiroyuki Moritaa, Doubun Hayashic, Koji Maemuraa, Keiko Fukinoa, Daiji Kawanamia, Go Nishimuraa, Kensuke Tsushimaa, Koshiro Monzenab, Tadashi Yamazakiab, Satoshi Mitsuyamad, Takahiko Shintanid, Narimasa Watanabed, Kumiko Setod, Takao Sugiyamae, Fumitaka Nakamuraa, Minoru Ohnoa, Yasunobu Hirataa, Tsutomu Yamazakibc, Ryozo NagaiaCorresponding Author Informationemail address

Received 18 November 2002; received in revised form 13 March 2003; accepted 24 March 2003.

Abstract 

Recently, variants in ATP-binding cassette transporter A1 (ABCA1) were demonstrated to be associated with increased level of high density lipoprotein cholesterol (HDL-C) and decreased risk of coronary artery disease (CAD) in Caucasians. However, this is not universally applicable due to the ethnic or environmental differences. In this context, to clarify the effect of ABCA1 in Japanese, we evaluated the phenotypic effects of I/M 823 and R/K 219 variants on the plasma level of HDL-C in 410 patients recruited in our hospital. Subjects with M 823 allele had significantly higher level of HDL-C than those without M823 allele (49.0±15.1 vs. 44.9±11.5 mg/dl, respectively, P<0.05). This statistical significance did not change even after multiple regression analysis. In contrast, there was no difference in HDL-C level among the genotypes in R/K 219 polymorphism. Further, in our study population an inverse relationship was shown to exist between HDL-C level and incidence of CAD. However, no positive association was observed between those variants and susceptibility to CAD. In this study, we provide evidence that I/M 823 variant, not R/K 219 variant, in ABCA1 is one of the determinants of HDL-C level, suggesting the importance of this gene on lipid metabolism in Japanese.

a Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan

b Department of Clinical Bioinformatics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

c Department of Pharmacoepidemiology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

d Hitachi Ltd., Tokyo, Japan

e Institute for Adult Diseases, Asahi Life Foundation, Tokyo, Japan

Corresponding Author InformationCorresponding author. Tel.: +81-3-5800-6519; fax: +81-3-3815-2087

PII: S0021-9150(03)00135-7

doi:10.1016/S0021-9150(03)00135-7


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