Harada Tomohiro, Imai Yasushi, Nojiri Takefumi, Morita Hiroyuki, Hayashi Doubun, Maemura Koji, Fukino Keiko, Kawanami Daiji, Nishimura Go, Tsushima Kensuke, Monzen Koshiro, Yamazaki Tadashi, Mitsuyama Satoshi, Shintani Takahiko, Watanabe Narimasa, Seto Kumiko, Sugiyama Takao, Nakamura Fumitaka, Ohno Minoru, Hirata Yasunobu, Yamazaki Tsutomu, Nagai Ryozo
Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
Atherosclerosis. 2003 Jul;169(1):105-12. doi: 10.1016/s0021-9150(03)00135-7.
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.
最近,在白种人中,ATP结合盒转运蛋白A1(ABCA1)的变异被证明与高密度脂蛋白胆固醇(HDL-C)水平升高及冠状动脉疾病(CAD)风险降低有关。然而,由于种族或环境差异,这并不普遍适用。在此背景下,为阐明ABCA1在日本人中的作用,我们评估了I/M 823和R/K 219变异对我院招募的410例患者血浆HDL-C水平的表型影响。携带M 823等位基因的受试者的HDL-C水平显著高于未携带M823等位基因的受试者(分别为49.0±15.1与44.9±11.5mg/dl,P<0.05)。即使经过多元回归分析,这种统计学显著性也没有改变。相比之下,R/K 219多态性的不同基因型之间的HDL-C水平没有差异。此外,在我们的研究人群中,HDL-C水平与CAD发病率之间呈负相关。然而,未观察到这些变异与CAD易感性之间存在正相关。在本研究中,我们提供证据表明,ABCA1中的I/M 823变异而非R/K 变异是HDL-C水平的决定因素之一,这表明该基因在日本人脂质代谢中的重要性。