Association of I27L Polymorphism of Hepatocyte Nuclear Factor-1α Gene with High-Density Lipoprotein Cholesterol Level

The serum level of high-density lipoprotein cholesterol (HDL-c), which protects against the development of atherosclerosis, is under genetic control. However, the genetic components responsible for the serum HDL-c level are yet to be determined. A recent knockout mouse study demonstrated that hepato...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2003-06, Vol.88 (6), p.2548-2551
Hauptverfasser: Babaya, Naru, Ikegami, Hiroshi, Fujisawa, Tomomi, Nojima, Koji, Itoi-Babaya, Michiko, Inoue, Kaori, Nakura, Jun, Abe, Michiko, Yamamoto, Miyuki, Jin, Jin Ji, Wu, Zhihong, Miki, Tetsuro, Fukuda, Masakatsu, Ogihara, Toshio
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Sprache:eng
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Zusammenfassung:The serum level of high-density lipoprotein cholesterol (HDL-c), which protects against the development of atherosclerosis, is under genetic control. However, the genetic components responsible for the serum HDL-c level are yet to be determined. A recent knockout mouse study demonstrated that hepatocyte nuclear factor-1α (HNF-1α) is an essential transcriptional regulator of HDL-c metabolism. In this study, the association of an HNF-1α gene polymorphism, isoleucine (Ile) 27 leucine (Leu), with lipid parameters, in particular with serum HDL-c level, was studied in 356 unrelated Japanese men. Though no significant difference was observed in total cholesterol and triglyceride levels among the three genotypes, the serum HDL-c level was significantly associated with the genotype (P < 0.01, trend test). Subjects with the Ile/Ile genotype had low serum HDL-c levels, and those with the Leu/Leu genotype had high serum HDL-c levels. These results demonstrate that the HNF-1α gene locus is associated with serum HDL-c level and suggest that the Ile27 allele is a risk marker for atherosclerosis.
ISSN:0021-972X
1945-7197
DOI:10.1210/jc.2002-021891