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蛋白质组学揭示了持续体重减轻对人体血浆蛋白质组的影响。

Proteomics reveals the effects of sustained weight loss on the human plasma proteome.

作者信息

Geyer Philipp E, Wewer Albrechtsen Nicolai J, Tyanova Stefka, Grassl Niklas, Iepsen Eva W, Lundgren Julie, Madsbad Sten, Holst Jens J, Torekov Signe S, Mann Matthias

机构信息

Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany.

NNF Center for Protein Research, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

Mol Syst Biol. 2016 Dec 22;12(12):901. doi: 10.15252/msb.20167357.

Abstract

Sustained weight loss is a preferred intervention in a wide range of metabolic conditions, but the effects on an individual's health state remain ill-defined. Here, we investigate the plasma proteomes of a cohort of 43 obese individuals that had undergone 8 weeks of 12% body weight loss followed by a year of weight maintenance. Using mass spectrometry-based plasma proteome profiling, we measured 1,294 plasma proteomes. Longitudinal monitoring of the cohort revealed individual-specific protein levels with wide-ranging effects of losing weight on the plasma proteome reflected in 93 significantly affected proteins. The adipocyte-secreted SERPINF1 and apolipoprotein APOF1 were most significantly regulated with fold changes of -16% and +37%, respectively (P < 10), and the entire apolipoprotein family showed characteristic differential regulation. Clinical laboratory parameters are reflected in the plasma proteome, and eight plasma proteins correlated better with insulin resistance than the known marker adiponectin. Nearly all study participants benefited from weight loss regarding a ten-protein inflammation panel defined from the proteomics data. We conclude that plasma proteome profiling broadly evaluates and monitors intervention in metabolic diseases.

摘要

持续体重减轻是多种代谢疾病的首选干预措施,但对个体健康状况的影响仍不明确。在此,我们对一组43名肥胖个体的血浆蛋白质组进行了研究,这些个体经历了8周体重减轻12%,随后进行了一年的体重维持。使用基于质谱的血浆蛋白质组分析,我们测量了1294种血浆蛋白质。对该队列的纵向监测揭示了个体特异性蛋白质水平,体重减轻对血浆蛋白质组具有广泛影响,93种蛋白质受到显著影响。脂肪细胞分泌的丝氨酸蛋白酶抑制剂F1(SERPINF1)和载脂蛋白APOF1的调节最为显著,倍数变化分别为-16%和+37%(P < 10),整个载脂蛋白家族呈现出特征性的差异调节。临床实验室参数反映在血浆蛋白质组中,八种血浆蛋白与胰岛素抵抗的相关性优于已知标志物脂联素。根据蛋白质组学数据定义的十种蛋白质炎症指标来看,几乎所有研究参与者都从体重减轻中获益。我们得出结论,血浆蛋白质组分析广泛评估和监测代谢疾病的干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/494b/5199119/d17769800357/MSB-12-901-g002.jpg

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