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儿童肥胖症血清代谢特征的非靶向代谢组学分析。

Untargeted Metabolomics Analysis of the Serum Metabolic Signature of Childhood Obesity.

机构信息

Department of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Sklodowskiej-Curie 24A, 15-276 Bialystok, Poland.

Clinical Research Centre, Medical University of Bialystok, Sklodowskiej-Curie 24A, 15-276 Bialystok, Poland.

出版信息

Nutrients. 2022 Jan 4;14(1):214. doi: 10.3390/nu14010214.

Abstract

Obesity rates among children are growing rapidly worldwide, placing massive pressure on healthcare systems. Untargeted metabolomics can expand our understanding of the pathogenesis of obesity and elucidate mechanisms related to its symptoms. However, the metabolic signatures of obesity in children have not been thoroughly investigated. Herein, we explored metabolites associated with obesity development in childhood. Untargeted metabolomic profiling was performed on fasting serum samples from 27 obese Caucasian children and adolescents and 15 sex- and age-matched normal-weight children. Three metabolomic assays were combined and yielded 726 unique identified metabolites: gas chromatography-mass spectrometry (GC-MS), hydrophilic interaction liquid chromatography coupled to mass spectrometry (HILIC LC-MS/MS), and lipidomics. Univariate and multivariate analyses showed clear discrimination between the untargeted metabolomes of obese and normal-weight children, with 162 significantly differentially expressed metabolites between groups. Children with obesity had higher concentrations of branch-chained amino acids and various lipid metabolites, including phosphatidylcholines, cholesteryl esters, triglycerides. Thus, an early manifestation of obesity pathogenesis and its metabolic consequences in the serum metabolome are correlated with altered lipid metabolism. Obesity metabolite patterns in the adult population were very similar to the metabolic signature of childhood obesity. Identified metabolites could be potential biomarkers and used to study obesity pathomechanisms.

摘要

儿童肥胖率在全球范围内迅速增长,给医疗保健系统带来了巨大压力。非靶向代谢组学可以扩展我们对肥胖发病机制的理解,并阐明与肥胖症状相关的机制。然而,儿童肥胖的代谢特征尚未得到彻底研究。在此,我们探讨了与儿童肥胖发展相关的代谢物。对 27 名肥胖白种人儿童和青少年以及 15 名性别和年龄匹配的正常体重儿童的空腹血清样本进行了非靶向代谢组学分析。将三种代谢组学分析方法相结合,得到了 726 种独特的鉴定代谢物:气相色谱-质谱法(GC-MS)、亲水相互作用液相色谱-质谱法(HILIC LC-MS/MS)和脂质组学。单变量和多变量分析表明,肥胖和正常体重儿童的非靶向代谢组之间存在明显的区分,两组之间有 162 种差异表达的代谢物。肥胖儿童的支链氨基酸和各种脂质代谢物,包括磷脂、胆固醇酯、甘油三酯的浓度更高。因此,肥胖发病机制的早期表现及其在血清代谢组中的代谢后果与脂质代谢的改变相关。成年人的肥胖代谢物模式与儿童肥胖的代谢特征非常相似。鉴定出的代谢物可能是潜在的生物标志物,可用于研究肥胖的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90fc/8747180/4a40fb671585/nutrients-14-00214-g001.jpg

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