Circulating soluble CD36 is a novel marker of liver injury in subjects with altered glucose tolerance

被引:28
作者
Fernandez-Real, Jose-Manuel [1 ,2 ]
Handberg, Aase [4 ]
Ortega, Francisco [1 ,2 ]
Hojlund, Kurt [4 ]
Vendrell, Joan [3 ]
Ricart, Wifredo [1 ,2 ]
机构
[1] Hosp Girona Dr Josep Trueta, Unit Diabet Endocrinol & Nutr, Girona 17007, Spain
[2] CIBER Pathophysiol Obes 06 03 0010, Girona, Spain
[3] Hosp Tarragona, Unit Diabet Endocrinol & Nutr, Tarragona, Spain
[4] Aarhus Univ Hosp, Dept Clin Biochem, DK-8000 Aarhus, Denmark
关键词
Liver enzymes; Inflammation; Insulin resistance; NONALCOHOLIC FATTY LIVER; INSULIN-RESISTANCE; ALANINE AMINOTRANSFERASE; PLASMA ADIPONECTIN; RECEPTOR; ACIDS; DISEASE; RAT; DIFFERENTIATION; STEATOHEPATITIS;
D O I
10.1016/j.jnutbio.2008.05.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Liver injury linked to insulin resistance is characterized by mild to moderate increases in aminotransferase activity. A soluble form of CD36 (sCD36) was recently identified in human plasma. The aim of this study was to evaluate the relationships among plasma sCD36, insulin sensitivity (SI) and indicators of liver health. We evaluated a cohort of men from the general population (n=117). As expected, serum (ALT), aspartate aminotransferase (AST) and gamma-glutamyltransferase (GGT) were associated positively with body mass index (BMI) and age and negatively with SI (minimal model method). Circulating sCD36 was positively associated with ALT, AST and GGT in subjects with altered glucose tolerance, but not in those with normal glucose tolerance. The difference in the slope of the relationships was significant (P=.01). Age, BMI and triglycerides (but not sCD36) contributed independently to 29% of ALT variance in subjects with normal glucose tolerance. In contrast, SI and sCD36 contributed independently to 39% of ALT variance in subjects with altered glucose tolerance. The correlation between ALT activity and sCD36 was confirmed in an independent, replication study. In summary, circulating sCD36 could represent a novel marker of liver injury in subjects with altered glucose tolerance. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:477 / 484
页数:8
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