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Visfatin in juvenile obesity – the effect of obesity intervention and sex
Author(s) -
KrzystekKorpacka Malgorzata,
Patryn Eliza,
BednarzMisa Iwona,
Hotowy Katarzyna,
Noczynska Anna
Publication year - 2011
Publication title -
european journal of clinical investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 107
eISSN - 1365-2362
pISSN - 0014-2972
DOI - 10.1111/j.1365-2362.2011.02538.x
Subject(s) - medicine , endocrinology , insulin resistance , overweight , tbars , obesity , waist , hyperinsulinemia , leptin , body mass index , metabolic syndrome , adipokine , insulin , oxidative stress , lipid peroxidation
Eur J Clin Invest 2011; 41 (12): 1284–1291 Abstract Background The association of visfatin, an adipocytokine relevant to the development of inflammation and metabolic disorders, with juvenile obesity needs to be re‐established as previously used tests occurred to be nonspecific. Objective To evaluate visfatin association with a metabolic profile of 88 overweight/obese and 26 lean children/adolescents as well as changes in its levels following weight reduction programme (diet + enhanced physical activity ± metformin). Design A case–control and cohort study. Results Visfatin was higher in obese than lean and overweight individuals (2·07 vs. 1·53 and 1·47 ng mL −1 , P = 0·034). Of metabolic syndrome components, central obesity combined with either insulin resistance (IR) or hyperinsulinemia (HI) was associated with increases in circulating visfatin. In girls, visfatin correlated with leptin ( r = 0·40, P = 0·009) and thiols ( r = −0·36, P = 0·009), which explained 24% in visfatin variability. In boys, visfatin correlated with waist circumference ( r = 0·36, P = 0·036), BMI% ( r = 0·38, P = 0·025), whole body insulin sensitivity index ( r = −0·36, P = 0·036), IL‐6 ( r = 0·38, P = 0·024) and thiobarbituric acid reactive substances (TBARS) ( r = 0·52, P = 0·001), of which IL‐6 and TBARS were independent predictors of visfatin elevation, explaining 42% in data variability. Visfatin was significantly lower following weight reduction programme than at baseline (1·43 vs. 1·83 ng mL −1 , P = 0·033). Visfatin reduction correlated neither with changes in metabolic parameters nor was it affected by metformin. ΔVisfatin correlated exclusively with baseline visfatin ( r = 0·612, P < 0·0001), which explained 38% in data variability. Conclusions Central obesity combined with HI/IR contributes to visfatin elevation. Visfatin association with metabolic/biochemical variables is gender dependent. Diet + enhanced physical activity are effective in visfatin reduction, the degree of which depends on baseline visfatin.