Elevated serum γ-glutamyltransferase levels are independently associated with insulin resistance in non-diabetic subjects

Abstract We investigated the associations of γ-glutamyltransferase (GGT) with visceral obesity, adiponectin and retinol binding protein 4 (RBP4), and insulin resistance (IR) and compared these associations with other liver enzymes in non-diabetes. We enrolled 94 healthy subjects 30–69 years old. Cli...

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Veröffentlicht in:Diabetes research and clinical practice 2009-05, Vol.84 (2), p.152-157
Hauptverfasser: Shin, Jang Yel, Chang, Sei Jin, Shin, Young Goo, Seo, Kwang-Seok, Chung, Choon Hee
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Sprache:eng
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Zusammenfassung:Abstract We investigated the associations of γ-glutamyltransferase (GGT) with visceral obesity, adiponectin and retinol binding protein 4 (RBP4), and insulin resistance (IR) and compared these associations with other liver enzymes in non-diabetes. We enrolled 94 healthy subjects 30–69 years old. Clinical and biochemical metabolic parameters were measured. Adiponectin and RBP4 were determined by ELISA. IR was examined by HOMA-IR. Visceral fat was determined by computed tomography scan. GGT and alanine aminotransferase (ALT) were positively correlated with waist circumference (WC), waist-to-hip ratio (WHR), visceral fat area (VFA), visceral-to-subcutaneous fat area ratio (VSR), HOMA-IR, and RBP4, but was negatively correlated with adiponectin ( p < 0.05). In multivariate regression, GGT was associated with male sex, HOMA-IR, and RBP4 ( R2 = 0.48, p < 0.05) and ALT was associated with HOMA-IR ( R2 = 0.22, p < 0.05). By logistic regression after adjusted for age and sex, the odds ratio (OR) for IR in the highest tertile of sex-specific GGT and ALT were significantly increased compared to those in the lowest [OR (95% CI); 6.90 (2.08–22.82), 3.38 (1.08–10.57), respectively]. However, these relationships after further adjustments for RBP4, adiponectin, VFA, VSR, WHR, WC, TG, and HDL remained significant in only GGT. In conclusions, GGT may be a useful marker of IR in non-diabetes.
ISSN:0168-8227
1872-8227
DOI:10.1016/j.diabres.2009.02.004