DSpace university logo mark
詳細検索
Japanese | English 

NAOSITE : Nagasaki University's Academic Output SITE > 030 医学部 > 030 紀要 > Acta Medica Nagasakiensia > Volume 55, No. 2 >

The evidence of polymorphisms of the liver X receptor gene as a DNA-based biomarker for susceptibility to coronary artery disease in a Japanese population


ファイル 記述 サイズフォーマット
ActMed55_69.pdf152.85 kBAdobe PDF本文ファイル

タイトル: The evidence of polymorphisms of the liver X receptor gene as a DNA-based biomarker for susceptibility to coronary artery disease in a Japanese population
著者: Fukae, Atsuki / Ikeda, Satoshi / Inoue, Mariko / Tachibana, Toshiko / Inamine, Tatsuo / Kondo, Shinji / Miyahara, Yoshiyuki / Maemura, Koji / Kohno, Shigeru / Tsukamoto, Kazuhiro
発行日: 2011年 3月
出版者: Nagasaki University School of Medicine / 長崎大学医学部
引用: Acta Medica Nagasakiensia, 55(2), pp.69-76; 2011
抄録: Coronary artery disease (CAD) is a multifactorial and polygenic disorder, which arises due to atherosclerosis of the coronary arteries. Both numerous genetic factors and environmental risk factors may contribute to the pathogenesis of atherosclerosis. Thus, in order to identify the genetic determinants of CAD, an association of genetic polymorphisms of the liver X receptoralpha (NR1H3) and -beta (NR1H2) genes with susceptibility to CAD was examined in a Japanese population. Eight tag single nucleotide polymorphisms (SNPs) in NR1H3 and NR1H2 were analyzed by PCR-restriction fragment length polymorphism or PCR-direct DNA sequencing method in 143 Japanese patients with CAD and 164 healthy control subjects with normal coronary arteries. Subsequently, haplotypes composed of the two tag SNPs in NR1H2 were constructed. Significant differences in the clinical risk factors, dyscholesteremia and diabetes mellitus, were observed between CAD patients and controls (P = 0.040 and P = 0.005, respectively). The frequencies of a C allele in the multiplicative model and its homozygous C/C genotype in the recessive model at rs2279238 in NR1H3 were significantly higher in CAD patients as compared to those in controls (P = 0.039 and P = 0.016, respectively). Furthermore, the frequency of a Hap 4/any diplotype of NR1H2 was significantly higher in CAD patients in comparison to controls (P = <0.0001, OR = 17.16). Multivariate logistic regression analysis revealed that these polymorphisms, dyscholesteremia, and diabetes mellitus independently contributed to susceptibility to CAD. In conclusion, NR1H3 and NR1H2 appears to be the genetic determinants of CAD. Furthermore, the genetic polymorphisms of NR1H3 and NR1H2 may be useful as new DNA-based diagnostic biomarkers for identifying high-risk individuals susceptible to CAD.
キーワード: single nucleotide polymorphism / liver X receptor gene / coronary artery disease / dyscholesteremia
URI: http://hdl.handle.net/10069/24845
ISSN: 00016055
関連リンク : http://hdl.handle.net/10069/26724
資料タイプ: Departmental Bulletin Paper
原稿種類: publisher
出現コレクション:Volume 55, No. 2

引用URI : http://hdl.handle.net/10069/24845

このリポジトリに保管されている文献はすべて著作権により保護されています。
印刷やダウンロード等データの複製は、調査研究・教育または学習を目的とする場合に限定されます。

 

Valid XHTML 1.0! Copyright © 2006-2015 長崎大学附属図書館 - お問い合わせ Powerd by DSpace