Implication of Circulating Irisin Levels with Brown Adipose Tissue and Sarcopenia in Humans

被引:68
作者
Choi, Hae Yoon [1 ]
Kim, Sungeun [2 ]
Park, Ji Woo [3 ]
Lee, Nam Seok [3 ]
Hwang, Soon Young [4 ]
Huh, Joo Young [5 ]
Hong, Ho Cheol [1 ]
Yoo, Hye Jin [1 ]
Baik, Sei Hyun [1 ]
Youn, Byung-Soo [3 ]
Mantzoros, Christos S. [5 ]
Choi, Kyung Mook [1 ]
机构
[1] Korea Univ, Coll Med, Dept Internal Med, Div Endocrinol & Metab, Seoul 136701, South Korea
[2] Korea Univ, Coll Med, Dept Nucl Med, Seoul 136701, South Korea
[3] AdipoGen Inc, Inchon 406840, South Korea
[4] Korea Univ, Coll Med, Dept Biostat, Seoul 136701, South Korea
[5] Harvard Univ, Sch Med, VA Boston Healthcare Syst, Endocrinol Sect, Boston, MA 02130 USA
基金
新加坡国家研究基金会;
关键词
FNDC5; GENE-EXPRESSION; SKELETAL-MUSCLE MASS; PREDICTING MORTALITY; PHYSICAL-ACTIVITY; ADULT HUMANS; EXERCISE; OBESITY; FAT; THERMOGENESIS; PGC-1-ALPHA;
D O I
10.1210/jc.2014-1195
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Irisin is an exercise-induced novel myokine that drives brown-fat-like conversion of white adipose tissue and has been suggested to be a promising target for the treatment of obesity-related metabolic disorders. Objective: To assess the association of circulating irisin concentrations with brown adipose tissue (BAT) and/or sarcopenia in humans. Setting and Design: We examined irisin levels in 40 BAT-positive and 40 BAT-negative women detected by F-18-fluorodeoxyglucose positron emission tomography ((18)FDG-PET). In a separate study, we also examined 401 subjects with or without sarcopenia defined by skeletal muscle mass index (SMMI) and appendicular skeletal muscle (ASM)/height(2) using dual-energy x-ray absorptiometry. Results: Among 6877 consecutive 18FDG-PET scans in 4736 subjects, 146 subjects (3.1%) had positive BAT scans. The BAT-detectable group and the matched BAT-undetectable group did not differ in circulating irisin levels measured using two different ELISA kits (P = .747 and P = .160, respectively). Serum irisin levels were not different between individuals with sarcopenia and those without sarcopenia using either kit (P = .305 and P = .569, respectively). Also, serum irisin levels were not different between groups defined by ASM/height(2) using either kit (P = .352 and P = .134, respectively). Although visceral fat area and skeletal muscle mass showed significant difference according to tertiles of SMMI levels, irisin concentrations did not differ. Conclusions: Circulating irisin levels were not different in individuals with detectable BAT or those with sarcopenia compared with control subjects and were not correlated with SMMI.
引用
收藏
页码:2778 / 2785
页数:8
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