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Implication of circulating irisin levels with brown adipose tissue and sarcopenia in humans. | LitMetric

Implication of circulating irisin levels with brown adipose tissue and sarcopenia in humans.

J Clin Endocrinol Metab

Division of Endocrinology and Metabolism, Department of Internal Medicine, College of Medicine (H.Y.C., H.C.H., H.J.Y., S.Y.B., K.M.C.), Korea University, Seoul 136-701, Korea; Department of Nuclear Medicine, College of Medicine (S.K.), Korea University, Seoul 136-701, Korea; AdipoGen, Inc (J.W.P., N.S.L., B.-S.Y.), Incheon 406-840, Korea; Department of Biostatistics, College of Medicine (S.W.H.), Korea University, Seoul 136-701, Korea; and Section of Endocrinology (J.Y.H., C.S.M.), VA Boston Healthcare System, Harvard Medical School, Boston, Massachusetts 02130.

Published: August 2014

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 (18)F-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 (18)FDG-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.

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Source
http://dx.doi.org/10.1210/jc.2014-1195DOI Listing

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