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补体 C1q/TNF 相关蛋白 13 水平低与儿童肥胖有关,但与暴食障碍无关。

Low Complement C1q/TNF-related Protein-13 Levels are Associated with Childhood Obesity But not Binge Eating Disorder.

机构信息

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

出版信息

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.

Abstract

OBJECTIVE

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).

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e1d/9176081/c46edfb28bdc/JCRPE-14-179-g1.jpg

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