Dokuz Eylül University Faculty of Medicine, Department of Pediatric Endocrinology, İzmir, Turkey
Bursa Uludağ University Faculty of Medicine, Department of Child and Adolescent Psychiatry, Bursa, Turkey
J Clin Res Pediatr Endocrinol. 2022 Jun 7;14(2):179-187. doi: 10.4274/jcrpe.galenos.2021.2021-11-1. Epub 2022 Jan 11.
C1q/tumor necrosis factor-related proteins (CTRPs) are recently described members of the adipokine family. CTRP-13, a new member of this family, has been shown to increase insulin sensitivity and had an anorexigenic effect on food intake in experimental studies. The aim was to investigate serum CTRP-13 levels in children with obesity, and its relationship with other adipokines, metabolic parameters, or binge eating disorder (BED).
A cross-sectional study was conducted with 105 pubertal children attending a single center. Clinical (metabolic syndrome, BED) and biochemical (glucose, insulin, lipids, leptin, adiponectin, CTRP-13 levels) parameters were assessed.
Sixty children with obesity [24 males (40%); median age 14.7 (13.0-16.4) years] and 45 healthy controls [15 males (33.3%); median age 15.2 (14.1-16.5) years] were included. Serum adiponectin and CTRP-13 levels were significantly lower in children with obesity than controls (7.1 vs 20.1 μg/mL, p<0.001; 64.7 vs 103.8 ng/mL, p<0.001, respectively). CTRP-13 levels correlated negatively with body mass index (Spearman rho=-0.230, p=0.018) and positively with high-density lipoprotein-cholesterol levels (Spearman rho=0.218, p=0.026). There was no significant difference in serum CTRP-13 concentrations in terms of the presence of metabolic syndrome or BED.
Childhood obesity seems to be causing dysregulation in adipokine production and function, including the down-regulation of CTRP-13. The positive correlation between CTRP-13 and HDL-C levels suggested a possible effect of this adipokine on lipid metabolism. Thus CTRP-13 may be a novel biomarker for dyslipidemia in childhood obesity.
C1q/肿瘤坏死因子相关蛋白(CTRPs)是最近被描述的脂肪因子家族成员。该家族的新成员 CTRP-13 已被证明可增加胰岛素敏感性,并在实验研究中对食物摄入具有厌食作用。本研究旨在探讨肥胖儿童血清 CTRP-13 水平及其与其他脂肪因子、代谢参数或暴食障碍(BED)的关系。
对单一中心的 105 名青春期儿童进行了横断面研究。评估了临床(代谢综合征、BED)和生化(血糖、胰岛素、血脂、瘦素、脂联素、CTRP-13 水平)参数。
共纳入 60 名肥胖儿童[24 名男性(40%);中位年龄 14.7(13.0-16.4)岁]和 45 名健康对照者[15 名男性(33.3%);中位年龄 15.2(14.1-16.5)岁]。肥胖儿童血清脂联素和 CTRP-13 水平明显低于对照组(7.1 与 20.1 μg/mL,p<0.001;64.7 与 103.8 ng/mL,p<0.001)。CTRP-13 水平与体重指数呈负相关(Spearman rho=-0.230,p=0.018),与高密度脂蛋白胆固醇水平呈正相关(Spearman rho=0.218,p=0.026)。代谢综合征或 BED 的存在与否,血清 CTRP-13 浓度无显著差异。
儿童肥胖似乎导致脂肪因子产生和功能失调,包括 CTRP-13 的下调。CTRP-13 与 HDL-C 水平呈正相关提示该脂肪因子可能对脂代谢有一定影响。因此,CTRP-13 可能是儿童肥胖症血脂异常的一种新的生物标志物。