Inflammatory Genes in Epicardial Fat Contiguous With Coronary Atherosclerosis in the Metabolic Syndrome and Type 2 Diabetes Changes associated with pioglitazone

被引:102
作者
Sacks, Harold S. [1 ,2 ]
Fain, John N. [3 ]
Cheema, Paramjeet [3 ]
Bahouth, Suleiman W. [4 ]
Garrett, Edward [2 ]
Wolf, Rodney Y. [2 ]
Wolford, David [2 ]
Samaha, Joseph [2 ]
机构
[1] Univ Tennessee, Ctr Hlth Sci, Coll Med, Dept Med, Memphis, TN 38163 USA
[2] Baptist Mem Hosp, Baptist Heart Inst, Memphis, TN 38146 USA
[3] Univ Tennessee, Ctr Hlth Sci, Coll Med, Dept Mol Sci, Memphis, TN 38163 USA
[4] Univ Tennessee, Ctr Hlth Sci, Coll Med, Dept Pharmacol, Memphis, TN 38163 USA
关键词
INTERLEUKIN-1 RECEPTOR ANTAGONIST; ADIPOSE-TISSUE;
D O I
10.2337/dc10-2083
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-To determine changes in gene expression in epicardial adipose tissue (EAT) associated with coronary atherosclerosis (CAD) and effects of pioglitazone therapy. RESEARCH DESIGN AND METHODS-Genes were quantified by RT-PCR in EAT and thoracic subcutaneous adipose tissue (SAT) obtained during surgery in CAD patients with metabolic syndrome (MS) or type 2 diabetes and control subjects with minimal or no CAD and no MS or type 2 diabetes. RESULTS-Increased expression of interleukin-1 receptor antagonist (IL-1Ra) and IL-10, a trend for higher IL-1 beta, and no change in peroxisome proliferator activated receptor-gamma (PPAR gamma) was found in EAT from MS or type 2 diabetes. Only PPAR gamma mRNA was reduced in SAT. Pioglitazone therapy in type 2 diabetes was associated with decreased expression of IL-1 beta, IL-1Ra, and IL-10 in EAT; decreased IL-10 in SAT; and increased PPAR gamma in SAT. CONCLUSIONS-In MS and type 2 diabetes with CAD, proinflammatory and anti-inflammatory genes were differentially increased in EAT and selectively reduced in association with pioglitazone treatment.
引用
收藏
页码:730 / 733
页数:4
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