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A promoter SNP (-1323T>C) in G-substrate gene (GSBS) correlates with hypercholesterolemia
Authors:Ono Shuji  Ezura Yoichi  Emi Mitsuru  Fujita Yuko  Takada Daisuke  Sato Keiko  Ishigami Tomoaki  Umemura Satoshi  Takahashi Kaneo  Kamimura Kouhei  Bujo Hideaki  Saito Yasushi
Affiliation:(1) Department of Molecular Biology, Institute of Gerontology, Nippon Medical School, 1-396 Kosugi-cho, Nakahara-ku, Kawasaki 211-8533, Japan;(2) Second Department of Internal Medicine, Yokohama City University School of Medicine, Yokohama, Japan;(3) Awa Medical Association Hospital, Chiba, Japan;(4) Department of Genome Research and Clinical Application, Chiba University Graduate School, Chiba, Japan;(5) Department of Clinical Cell Biology, Chiba University Graduate School, Chiba, Japan
Abstract:
Factors predisposing to the phenotypic features of higher total cholesterol (TC) have not been clearly defined. Here we report an association between a promoter SNP (–1323T>C) in G-substrate gene (GSBS) and TC levels in 368 adult individuals from an east-central area of Japan. Age and gender-adjusted levels of LDL-cholesterol, TG, TC, and HDL-cholesterol were analyzed. When we separate the subjects into two genotypic groups regarding T allele, those who bear the T allele had significantly higher plasma TC levels than the others who lack the T allele (mean; 239.6 mg/dl vs. 210.6 mg/dl; p=0.003; Mann–Whitney test). Of the 341 individuals with the T allele, approximately 80% individuals presented with hypercholesterolemia, whereas only 44% were hypercholesterolemic among the 27 individuals without the T allele (p=0.0001). These results indicate a significant elevating effect of plasma TC levels by a SNP in the putative regulatory region of the G-substrate gene in our studied population. These data suggest that genetic variation at the G-substrate gene may be one of the determinants for plasma lipoprotein levels.
Keywords:G-substrate gene  Plasma total cholesterol (TC)  Single nucleotide polymorphism (SNP)  Modifier gene
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