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CD14基因启动子区域的-159C/T多态性与重度饮酒者的晚期肝病及急性期蛋白血清水平升高有关。

The -159C/T polymorphism in the promoter region of the CD14 gene is associated with advanced liver disease and higher serum levels of acute-phase proteins in heavy drinkers.

作者信息

Campos Joaquin, Gonzalez-Quintela Arturo, Quinteiro Celsa, Gude Francisco, Perez Luis-Fernando, Torre Jose-Antonio, Vidal Carmen

机构信息

Department of Internal Medicine, Hospital Clinico Universitario, Fundación Publica Gallega de Medicina Genomica, Santiago de Compostela, Spain.

出版信息

Alcohol Clin Exp Res. 2005 Jul;29(7):1206-13. doi: 10.1097/01.alc.0000171977.25531.7a.

Abstract

BACKGROUND

Innate inflammatory responses to endotoxin (lipopolysaccharide) contribute to the development of alcoholic liver disease (ALD). A single-nucleotide polymorphism (-159C/T) in the promoter region of the gene coding for CD14 (a lipopolysaccharide receptor) could be associated with the development of ALD. We sought too investigate the relationship between the CD14/-159C/T polymorphism and advanced ALD and acute-phase protein levels in heavy drinkers.

METHODS

A total of 138 heavy drinkers consecutively admitted to an Internal Medicine department were genotyped for the CD14/-159C/T polymorphism. Serum samples were analyzed for lipopolysaccharide-binding protein (LBP), soluble CD14 (sCD14), C-reactive protein (CRP), and immunoglobulin (Ig) A, IgG, and IgM. Patients with ascites or liver encephalopathy (n = 35) were classified as having advanced ALD.

RESULTS

After adjusting for potential confounding variables, the CD14/-159TT genotype was positively associated with advanced ALD (odds ratio, 2.99; 95% confidence interval, 1.09-8.24, p = 0.03) and serum LBP (p = 0.01) and sCD14 (p = 0.04) levels. The CD14/-159C/T polymorphism was not associated with serum levels of CRP, IgA, IgG, or IgM.

CONCLUSIONS

Our results support the notion that CD14/-159TT homozygous heavy drinkers have higher levels of the LPS-binding acute-phase proteins (LBP and sCD14) than do carriers of the CD14/-159C allele. Also, the CD14/-159TT genotype may be a risk factor for advanced ALD.

摘要

背景

对内毒素(脂多糖)的先天性炎症反应有助于酒精性肝病(ALD)的发展。编码CD14(一种脂多糖受体)的基因启动子区域的单核苷酸多态性(-159C/T)可能与ALD的发展有关。我们试图研究CD14 / -159C/T多态性与重度饮酒者晚期ALD及急性期蛋白水平之间的关系。

方法

连续入住内科的138名重度饮酒者进行了CD14 / -159C/T多态性基因分型。分析血清样本中的脂多糖结合蛋白(LBP)、可溶性CD14(sCD14)、C反应蛋白(CRP)以及免疫球蛋白(Ig)A、IgG和IgM。有腹水或肝性脑病的患者(n = 35)被归类为晚期ALD。

结果

在调整潜在混杂变量后,CD14 / -159TT基因型与晚期ALD(优势比,2.99;95%置信区间,1.09 - 8.24,p = 0.03)以及血清LBP(p = 0.01)和sCD14(p = 0.04)水平呈正相关。CD14 / -159C/T多态性与血清CRP、IgA、IgG或IgM水平无关。

结论

我们的结果支持以下观点,即与CD14 / -159C等位基因携带者相比,CD14 / -159TT纯合子重度饮酒者具有更高水平的LPS结合急性期蛋白(LBP和sCD14)。此外,CD14 / -159TT基因型可能是晚期ALD的一个危险因素。

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