肥胖儿童的室管结素相关蛋白1水平升高,并与代谢紊乱相关

Chunfeng Mou, Sha Liu, Yetao Luo, Yu Xue, Jia Liu, Dapeng Chen, Xiaoqiang Li, Han Wang
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引用次数: 0

摘要

EPDR1在脂肪细胞的分泌体中被发现,它在脂质结合、运输和分解代谢中起作用。本研究的目的是调查肥胖儿童和正常体重儿童的血清EPDR1水平,并比较肥胖、伴和不伴代谢相关脂肪肝(MAFLD)儿童的EPDR1水平。34名体重正常的儿童和49名肥胖儿童(其中15名患有MAFLD)被纳入研究。采用酶联免疫吸附法测定循环EPDR1、IL - 1β和TNF - α。对所有参与者进行了与肥胖、血脂和胰岛素抵抗相关的人体测量和生化测量。肥胖患儿血清EPDR1水平明显高于对照组。EPDR1水平在患有和未患有MAFLD的患者之间没有差异。循环EPDR1与体重指数(BMI)、BMI z评分、胰岛素、葡萄糖、稳态模型评估胰岛素抵抗指数(HOMA‐IR)、甘油三酯、白细胞和中性粒细胞呈正相关。二元logistic回归分析显示,随着EPDR1水平的升高,肥胖的比值比显著增加。EPDR1与肥胖密切相关,也可能与代谢紊乱有关。该试验注册号为ChiCTR2300070951。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ependymin‐related protein 1 levels are elevated in children with obesity and correlated with metabolic disorders
Ependymin‐related protein 1 (EPDR1) has been found in the secretory body of adipocytes where it plays a role in lipid binding, transportation, and catabolism. The aim of this study was to investigate serum EPDR1 levels in children with obesity and normal‐weight children and to compare the levels of EPDR1 between children with obesity, with and without metabolic‐associated fatty liver disease (MAFLD). Thirty‐four normal‐weight children and 49 children with obesity (15 with MAFLD) were included in the study. Circulating EPDR1, IL‐1β, and TNF‐α were measured using enzyme‐linked immunosorbent assays. Anthropometric and biochemical measurements related to obesity, blood lipids, and insulin resistance were performed on all participants. The serum EPDR1 levels of children with obesity were significantly higher than those of the control group. There was no difference in EPDR1 levels between the patients with and without MAFLD. Circulating EPDR1 was positively correlated with body mass index (BMI), BMI z‐score, insulin, glucose, homeostatic model assessment insulin resistance index (HOMA‐IR), triglycerides, white blood cells, and neutrophils. Binary logistic regression analysis showed a significant increase in the odds ratio of obesity with increasing EPDR1 levels. EPDR1 is strongly associated with obesity and may also be associated with metabolic disorders. This trial is registered with ChiCTR2300070951.
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