Glucagon-Like Peptide-2 as a Potential Biomarker for Nonalcoholic Fatty Liver Disease in Children with Obesity: Preliminary Assessment of Metabolic Associations and Underlying Mechanisms.

IF 3 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Shu-Juan Zhang, Ke Xu, Feng Zhu, Yi-Qun Teng, Yan-Fei Tang, Hong-Wei Xu
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引用次数: 0

Abstract

Objective: This study aimed to investigate the effects of glucagon-like peptide-2 (GLP-2) on insulin resistance and lipid metabolism, as well as potential mechanisms contributing to the development of non-alcoholic fatty liver disease (NAFLD) in children with obesity.

Methods: A cross-sectional study was conducted involving 107 children with obesity, aged between 5 and 15 years, including 55 with NAFLD and 52 without NAFLD. Anthropometric assessments and fasting blood samples were collected to evaluate GLP-2, plasma glucose, insulin (INS), lipids, leptin (LEP), and adiponectin (ADPN). Correlation and logistic regression analyses were performed to evaluate associations between GLP-2 and metabolic parameters.

Results: Children with NAFLD exhibited significantly higher levels of GLP-2, LEP, total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-C), fasting blood glucose (FPG), INS, and the homeostasis model assessment of insulin resistance index (HOMA-IR) (all p<0.05), along with significantly lower levels of ADPN and high-density lipoprotein cholesterol (HDL-C) compared with those without NAFLD (p<0.05). GLP-2 concentrations correlated positively with TC (r=0.42), TG (r=0.51), LDL-C (r=0.38), FPG (r=0.61), INS (r=0.58), HOMA-IR (r=0.61), and LEP (r=0.42), and negatively with ADPN (r=-0.53; all p<0.01). In univariate analysis, GLP-2 was identified as a risk factor for NAFLD (odds ratio [OR]=1.225, 95% confidence interval [CI]: 1.001-1.499, p<0.05); however, the association was attenuated after adjustment for body mass index (OR=1.112, p=0.102). ADPN retained a protective association (OR=0.771, p<0.05).

Conclusion: GLP-2 may contribute to the pathophysiology of insulin resistance and dyslipidemia in pediatric NAFLD, potentially via modulation of adipokine activity. These findings suggest GLP-2 as a candidate biomarker and possible therapeutic target in this population.

胰高血糖素样肽-2作为肥胖儿童非酒精性脂肪性肝病的潜在生物标志物:代谢关联和潜在机制的初步评估
目的:本研究旨在探讨胰高血糖素样肽-2 (GLP-2)对肥胖儿童胰岛素抵抗和脂质代谢的影响,以及促进非酒精性脂肪性肝病(NAFLD)发展的潜在机制。方法:对107例5 ~ 15岁肥胖儿童进行横断面研究,其中55例合并NAFLD, 52例非NAFLD。采集人体测量和空腹血液样本,评估GLP-2、血糖、胰岛素(INS)、脂质、瘦素(LEP)和脂联素(ADPN)。通过相关和逻辑回归分析来评估GLP-2与代谢参数之间的关系。结果:NAFLD患儿GLP-2、LEP、总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)、空腹血糖(FPG)、INS以及胰岛素抵抗指数(HOMA-IR)(所有ppr=0.42)、TG (r=0.51)、LDL-C (r=0.38)、FPG (r=0.61)、INS (r=0.58)、HOMA-IR (r=0.61)、LEP (r=0.42)等稳态模型评估水平均显著升高,ADPN呈负相关(r=-0.53;所有ppp=0.102)。结论:GLP-2可能通过调节脂肪因子活性参与儿童NAFLD胰岛素抵抗和血脂异常的病理生理过程。这些发现表明GLP-2是该人群的候选生物标志物和可能的治疗靶点。
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来源期刊
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.90
自引率
6.10%
发文量
431
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal. The journal is committed to the rapid publication of the latest laboratory and clinical findings in the fields of diabetes, metabolic syndrome and obesity research. Original research, review, case reports, hypothesis formation, expert opinion and commentaries are all considered for publication.
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