Microsornal triglyceride transfer protein 493-T variant is associated with resistin levels and C-reactive protein

被引:4
作者
Gambino, Roberto [1 ]
Bo, Simona [1 ]
Musso, Giovanni [1 ]
Ghione, Federica [1 ]
Guidi, Sabrina [1 ]
Tiozzo, Elisa [1 ]
Chiusano, Valentina [1 ]
Gentile, Luigi [1 ]
Durazzo, Marilena [1 ]
Pagano, Gianfranco [1 ]
Cassader, Maurizio [1 ]
机构
[1] Univ Turin, Dept Internal Med, I-10126 Turin, Italy
关键词
lipids; microsomal triglyceride transfer protein; polymorphism; resistin; hs-C-reactive protein;
D O I
10.1016/j.clinbiochem.2007.07.005
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: The microsomal triglyceride transfer protein (MTP) is a heterodimeric lipid transfer protein that consists of a large unique 97-kDA subunit and protein disulfide isomerase. MTP is involved in the assembly of apoB-containing lipoprotein and enables the secretion of VLDLs by the liver and chylomicrons by the intestine. The MTP gene is highly polymorphic. The less common T variant has been associated with the reduction of plasma LDL-cholesterol levels and with an increased risk in coronary heart disease. We hypothesized that MTP polymorphism could be associated to LDL-cholesterol levels and proinflammatory cytokines, such as resistin. Methods and results: The -493G/T MTP gene polymorphism was investigated in 290 subjects. Subjects carrying the TT genotype had lower level of LDL-cholesterol and higher serum resistin levels than individual carrying one or two copies of the -493G allele. After adjustments for age, BMI, waist circumference, alcohol intake and exercise levels, a significant direct association was evident between hs-CRP and resistin levels and the presence of the TT genotype in a multiple regression model. Conclusion: This study supports the notion that the rare MTP-493T/T genotype is associated both with higher levels of inflammatory parameters and with low levels of LDL-cholesterol. Prospective data are needed to investigate if the association between CVD and the MTP-493T/ T genotype might be due to the increased sub-clinical proinflammatory state associated with this mutation. (C) 2007 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1219 / 1224
页数:6
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