Premium
Adiponectin Oligomers and Ectopic Fat in Liver and Skeletal Muscle in Humans
Author(s) -
Kantartzis Konstantinos,
Staiger Harald,
Machann Jürgen,
Schick Fritz,
Claussen Claus D.,
Machicao Fausto,
Fritsche Andreas,
Häring HansUlrich,
Stefan Norbert
Publication year - 2009
Publication title -
obesity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.438
H-Index - 199
eISSN - 1930-739X
pISSN - 1930-7381
DOI - 10.1038/oby.2008.487
Subject(s) - adiponectin , endocrinology , medicine , adipokine , skeletal muscle , chemistry , fatty liver , diabetes mellitus , insulin resistance , disease
We aimed at determining which circulating forms of the adipokine adiponectin that increases lipid oxidation in liver and skeletal muscle are related to ectopic fat in these depots in humans. Plasma total‐, high‐molecular weight (HMW)‐, middle‐molecular weight (MMW)‐, and low‐molecular weight (LMW) adiponectin were quantified by an enzyme‐linked immunosorbent assay. Their relationships with liver‐ and intramyocellular fat, measured using 1 H magnetic resonance spectroscopy, were investigated in 54 whites without type 2 diabetes. Liver fat, adjusted for gender, age, and total body fat, was associated only with HMW adiponectin ( r = −0.35, P = 0.012), but not with total‐, MMW‐, or LMW adiponectin. In addition, subjects with fatty liver (liver fat ≥5.56%, n = 15) had significantly lower HMW‐ ( P = 0.04), but not total‐, MMW‐, or LMW adiponectin levels, compared to controls ( n = 39). Similarly, intramyocellular fat correlated only with HMW ( r = −0.32, P = 0.039), but not with the other circulating forms of adiponectin. These data indicate that, among circulating forms of adiponectin, HMW is strongly related to ectopic fat, thus possibly representing the form of adiponectin regulating lipid oxidation in liver and skeletal muscle.