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血清羧酸酯酶-1 水平升高与肥胖儿童代谢相关脂肪性肝病和代谢综合征相关的代谢功能障碍有关。

Increased serum carboxylesterase-1 levels are associated with metabolic dysfunction associated steatotic liver disease and metabolic syndrome in children with obesity.

机构信息

Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Hubei Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Wuhan, China.

出版信息

Ital J Pediatr. 2024 Sep 4;50(1):162. doi: 10.1186/s13052-024-01733-7.

Abstract

BACKGROUND

Carboxylesterase 1(CES1) is expressed mainly in the liver and adipose tissue and is highly hypothesized to play an essential role in metabolism. Our study aimed to investigate the association between CES1 and metabolic syndrome (MetS) and metabolic dysfunction associated steatotic liver disease (MASLD) in children with obesity in China.

METHODS

This study included 72 children with obesity aged 6-13years (including 25(35%) diagnosed as MetS and 36(50%) diagnosed as MASLD). All subjects were measured in anthropometry, serum level of biochemical parameters related to obesity, circumstance levels of insulin-like growth factor1, adipokines (adiponectin, leptin and growth differentiation factor 15) and CES1.

RESULTS

Higher serum CES1 level were found in the MetS group (P = 0.004) and the MASLD group (P < 0.001) of children with obesity. Serum CES1 levels were positively correlated with alanine aminotransferase, aspartate aminotransferase, triglyceride, cholesterol, low-density lipoprotein cholesterol, GDF15, Leptin and negatively correlated with high-density lipoprotein cholesterol, adiponectin and IGF1. We also found a multivariable logistic regression analysis of MASLD and MetS predicted by CES1 significantly (MASLD P < 0.01, MetS P < 0.05). The combination of CES1, sex, age and BMI Z-score showed a sensitivity and specificity of 92.7% for the identification of MASLD and 78.6% for the identification of MetS. The cutoff for CES1 of MASLD is 56.30 ng/mL and of MetS is 97.79 ng/mL.

CONCLUSIONS

CES1 is associated with an increasing risk of MetS and MASLD and can be established as a biomarker for metabolic syndrome and MASLD of children with obesity.

摘要

背景

羧酸酯酶 1(CES1)主要在肝脏和脂肪组织中表达,高度假设其在代谢中发挥重要作用。我们的研究旨在调查中国肥胖儿童中 CES1 与代谢综合征(MetS)和代谢相关脂肪性肝病(MASLD)的关系。

方法

本研究纳入 72 名 6-13 岁肥胖儿童(包括 25 名(35%)诊断为 MetS 和 36 名(50%)诊断为 MASLD)。所有受试者均进行了人体测量学、与肥胖相关的生化参数血清水平、胰岛素样生长因子 1(IGF1)、脂肪因子(脂联素、瘦素和生长分化因子 15)和 CES1 的环境水平测量。

结果

肥胖儿童的 MetS 组(P=0.004)和 MASLD 组(P<0.001)血清 CES1 水平较高。血清 CES1 水平与丙氨酸氨基转移酶、天冬氨酸氨基转移酶、甘油三酯、胆固醇、低密度脂蛋白胆固醇、GDF15、瘦素呈正相关,与高密度脂蛋白胆固醇、脂联素和 IGF1 呈负相关。我们还发现 CES1 显著预测 MASLD 和 MetS 的多变量逻辑回归分析(MASLD P<0.01,MetS P<0.05)。CES1、性别、年龄和 BMI Z 评分的组合对 MASLD 的识别具有 92.7%的敏感性和特异性,对 MetS 的识别具有 78.6%的敏感性和特异性。CES1 对 MASLD 的截断值为 56.30ng/mL,对 MetS 的截断值为 97.79ng/mL。

结论

CES1 与 MetS 和 MASLD 的风险增加相关,可作为肥胖儿童代谢综合征和 MASLD 的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c403/11373257/eafd5d98bf2d/13052_2024_1733_Fig1_HTML.jpg

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