Irisin as a predictor of glucose metabolism in children: sexually dimorphic effects. (6th December 2013)

• Record Type: Journal Article
• Authors: Al‐Daghri, Nasser M.; Alkharfy, Khalid M.; Rahman, Shakilur; Amer, Osama E.; Vinodson, Benjamin; Sabico, Shaun; Piya, Milan K.; Harte, Alison L.; McTernan, Philip G.; Alokail, Majed S.; Chrousos, George P.
• Is Part Of: European journal of clinical investigation. Volume 44:Number 2(2014:Feb.)
• Page Start: 119
• Page End: 124
• Publication Date: 2013-12-06
• Subjects: Pathology -- Periodicals; Medical research -- Periodicals; 616.075
• DOI: 10.1111/eci.12196
• Languages: English
• ISSNs: 0014-2972

Abstract

<abstract abstract-type="main" id="eci12196-abs-0001"> <title>Abstract</title> <sec id="eci12196-sec-0001" sec-type="section"> <title>Background</title> <p>Irisin, a novel myokine, increases energy expenditure and glucose tolerance and, thus, improves carbohydrate homeostasis in humans. This hormone has potential therapeutic applications for weight loss and improvement in insulin resistance in subjects with obesity and diabetes mellitus type 2 (T2DM). In this cross‐sectional study, we aimed to associate circulating levels of irisin and several anthropometric and metabolic parameters among Arab children.</p> </sec> <sec id="eci12196-sec-0002" sec-type="section"> <title>Methods</title> <p>A cohort of 153 Saudi children, 81 boys [age: 12·4 ± 3·2 years; BMI: 19·5 ± 5·9 kg/m<sup>2</sup>] and 72 girls: [age: 12·9 ± 3·2 years; BMI: 20·6 ± 5·2], were examined. Anthropometry was obtained, and fasted bloods were collected for biochemical analyses. Irisin was assessed by a specific enzyme‐linked immunosorbent assay (ELISA).</p> </sec> <sec id="eci12196-sec-0003" sec-type="section"> <title>Results</title> <p>Girls had higher circulating irisin levels than boys (<italic>P </italic>=<italic> </italic>0·04). There were several significant correlations between circulating irisin and fasting blood glucose (FBG) (<italic>r</italic> = −0·35, <italic>P </italic><<italic> </italic>0·001), sagittal abdominal diameter (SAD) (<italic>r</italic> = −0·34, <italic>P </italic><<italic> </italic>0·001) and HDL cholesterol (<italic>r</italic> = 0·17, <italic>P </italic>=<italic> </italic>0·04) across the entire cohort studied. Notably in girls, but not in boys, HOMA‐IR correlated negatively with irisin levels (<italic>r</italic> = −0·32, <italic>P </italic>=<italic> </italic>0·02), as previously noted in adults. FBG was a significant predictor of circulating irisin (<italic>R</italic><sup>2</sup> = 0·16) followed by SAD. In multivariate linear regression analysis, after controlling for potential confounders such as gender, age and BMI, irisin levels were independently associated with FBG (β = −0·34, <italic>P </italic>=<italic> </italic>0·01), particularly in girls.</p> </sec> <sec id="eci12196-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Serum irisin levels were higher in girls than in boys and correlated negatively with HOMA‐IR. They were also independently associated with FBG predominantly in girls, suggesting that this hormone may play a crucial role in glucose metabolism from an early age.</p> </sec> </abstract>