IntroductionWe evaluated the relationship between adipokine plasma concentrations and
body fat distribution and the metabolic syndrome.MethodsIn a cohort of 1215 patients with clinically manifest vascular disease the
relation between subcutaneous adipose tissue, visceral adipose tissue, waist
circumference, body mass index and plasma concentrations of adipsin,
chemerin, monocyte chemoattractant protein-1, migration inhibitory factor,
nerve growth factor, resistin, plasma amyloid A1, adiponectin, leptin,
plasminogen activator inhibitor-1 and hepatic growth factor were
cross-sectionally assessed with linear regression and adjusted for age and
gender. The relation between adipokines and the metabolic syndrome was
cross-sectionally evaluated using logistic regression. An adipokine profile
was developed to measure the effect of combined rather than single
adipokines.ResultsAdiposity was related to higher nerve growth factor, hepatic growth factor,
migration inhibitory factor, leptin and adipsin and with lower chemerin,
plasminogen activator inhibitor-1, resistin, plasma amyloid A1 and
adiponectin. The strongest positive relations were between body mass index
and adipsin (β 0.247; 95% CI 0.137–0.356) and leptin (β 0.266; 95% CI
0.207–0.324); the strongest negative relations were between body mass index
and plasma amyloid A1 (β –0.266; 95% CI –0.386 to –0.146) and visceral
adipose tissue and adiponectin (β –0.168; 95% CI –0.226 to –0.111). There
was no relation between subcutaneous adipose tissue and adipokines. Odds for
the metabolic syndrome were higher with each 1 SD higher hepatic growth
factor (OR 1.21; 95% CI 1.06–1.38) and leptin (OR 1.26; 95% CI 1.10–1.45)
and lower with each 1 SD higher adiponectin (OR 0.73; 95% CI 0.64–0.83) and
resistin (OR 0.85; 95% CI 0.74–0.97). The adipokine profile was related to
the metabolic syndrome (OR 1.03; 95% CI 1.00–1.06).ConclusionPlasma concentrations of adipokines are related to obesity and body fat
distribution. The relation between adipokine concentrations and the
metabolic syndrome is independent of visceral adipose tissue.