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本文引用的文献

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Microbial regulation of organismal energy homeostasis.微生物对机体能量稳态的调节。
Nat Metab. 2019 Jan;1(1):34-46. doi: 10.1038/s42255-018-0017-4. Epub 2019 Jan 7.
2
From Association to Causality: the Role of the Gut Microbiota and Its Functional Products on Host Metabolism.从关联到因果关系:肠道微生物群及其功能产物对宿主代谢的作用。
Mol Cell. 2020 May 21;78(4):584-596. doi: 10.1016/j.molcel.2020.03.005. Epub 2020 Mar 31.
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Change in obesity-related metabolic abnormalities associated with body mass index improvement through life-style intervention: A meta-regression.生活方式干预对肥胖相关代谢异常的影响与体重指数改善的关系:一项荟萃回归分析。
Pediatr Diabetes. 2020 Mar;21(2):173-193. doi: 10.1111/pedi.12955. Epub 2019 Dec 27.
4
Author Correction: Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2.作者更正:使用QIIME 2进行可重复、交互式、可扩展和可延伸的微生物组数据科学研究。
Nat Biotechnol. 2019 Sep;37(9):1091. doi: 10.1038/s41587-019-0252-6.
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Gut microbiota phenotypes of obesity.肥胖的肠道微生物组表型。
NPJ Biofilms Microbiomes. 2019 Jul 1;5(1):18. doi: 10.1038/s41522-019-0091-8. eCollection 2019.
6
Are we close to defining a metabolomic signature of human obesity? A systematic review of metabolomics studies.我们是否即将定义人类肥胖的代谢组学特征?代谢组学研究的系统评价。
Metabolomics. 2019 Jun 13;15(6):93. doi: 10.1007/s11306-019-1553-y.
7
Heterogeneity in Response to Treatment of Adolescents with Severe Obesity: The Need for Precision Obesity Medicine.青少年重度肥胖治疗反应的异质性:精准肥胖医学的需求。
Obesity (Silver Spring). 2019 Feb;27(2):288-294. doi: 10.1002/oby.22369.
8
Life course trajectories of cardiovascular risk: Impact on atherosclerotic and metabolic indicators.心血管风险的生命轨迹:对动脉粥样硬化和代谢指标的影响。
Atherosclerosis. 2019 Jan;280:21-27. doi: 10.1016/j.atherosclerosis.2018.11.008. Epub 2018 Nov 8.
9
The Gut Microbiome Profile in Obesity: A Systematic Review.肥胖中的肠道微生物群概况:一项系统综述。
Int J Endocrinol. 2018 Mar 22;2018:4095789. doi: 10.1155/2018/4095789. eCollection 2018.
10
Prevalence of Obesity and Severe Obesity in US Children, 1999-2016.美国儿童肥胖和重度肥胖的患病率,1999-2016 年。
Pediatrics. 2018 Mar;141(3). doi: 10.1542/peds.2017-3459.

儿科肥胖微生物组与代谢研究(POMMS):方法、基线数据和早期见解。

The Pediatric Obesity Microbiome and Metabolism Study (POMMS): Methods, Baseline Data, and Early Insights.

机构信息

Department of Molecular Genetics and Microbiology, Duke University, Durham, North Carolina, USA.

Duke Molecular Physiology Institute and Sarah W. Stedman Nutrition and Metabolism Center, Duke University, Durham, North Carolina, USA.

出版信息

Obesity (Silver Spring). 2021 Mar;29(3):569-578. doi: 10.1002/oby.23081.

DOI:10.1002/oby.23081
PMID:33624438
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7927749/
Abstract

OBJECTIVE

The purpose of this study was to establish a biorepository of clinical, metabolomic, and microbiome samples from adolescents with obesity as they undergo lifestyle modification.

METHODS

A total of 223 adolescents aged 10 to 18 years with BMI ≥95th percentile were enrolled, along with 71 healthy weight participants. Clinical data, fasting serum, and fecal samples were collected at repeated intervals over 6 months. Herein, the study design, data collection methods, and interim analysis-including targeted serum metabolite measurements and fecal 16S ribosomal RNA gene amplicon sequencing among adolescents with obesity (n = 27) and healthy weight controls (n = 27)-are presented.

RESULTS

Adolescents with obesity have higher serum alanine aminotransferase, C-reactive protein, and glycated hemoglobin, and they have lower high-density lipoprotein cholesterol when compared with healthy weight controls. Metabolomics revealed differences in branched-chain amino acid-related metabolites. Also observed was a differential abundance of specific microbial taxa and lower species diversity among adolescents with obesity when compared with the healthy weight group.

CONCLUSIONS

The Pediatric Metabolism and Microbiome Study (POMMS) biorepository is available as a shared resource. Early findings suggest evidence of a metabolic signature of obesity unique to adolescents, along with confirmation of previously reported findings that describe metabolic and microbiome markers of obesity.

摘要

目的

本研究旨在建立一个临床、代谢组学和微生物组样本的生物库,用于研究肥胖青少年在进行生活方式改变时的情况。

方法

共纳入 223 名年龄在 10 至 18 岁、BMI≥第 95 百分位数的青少年肥胖患者,以及 71 名健康体重参与者。在 6 个月的时间内,反复采集临床数据、空腹血清和粪便样本。本文介绍了研究设计、数据收集方法和中期分析,包括对肥胖青少年(n=27)和健康体重对照组(n=27)进行靶向血清代谢物测量和粪便 16S 核糖体 RNA 基因扩增子测序。

结果

与健康体重对照组相比,肥胖青少年的血清丙氨酸氨基转移酶、C 反应蛋白和糖化血红蛋白水平较高,而高密度脂蛋白胆固醇水平较低。代谢组学显示出与支链氨基酸相关代谢物的差异。还观察到肥胖青少年特定微生物类群的丰度差异和物种多样性降低。

结论

儿科代谢和微生物组研究(POMMS)生物库可作为共享资源。早期发现表明,肥胖青少年存在独特的代谢特征证据,同时也证实了先前报道的描述肥胖代谢和微生物组标志物的发现。