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肌痛性脑脊髓炎/慢性疲劳综合征血浆代谢组学的前瞻性生物标志物表明氧化还原失衡与疾病症状有关。

Prospective Biomarkers from Plasma Metabolomics of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Implicate Redox Imbalance in Disease Symptomatology.

作者信息

Germain Arnaud, Ruppert David, Levine Susan M, Hanson Maureen R

机构信息

Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.

Department of Statistical Science and School of Operations Research and Information Engineering, Cornell University, Ithaca, NY 14853, USA.

出版信息

Metabolites. 2018 Dec 6;8(4):90. doi: 10.3390/metabo8040090.

Abstract

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a disease of enigmatic origin with no established cure. Its constellation of symptoms has silently ruined the lives of millions of people around the world. A plethora of hypotheses have been vainly investigated over the past few decades, so that the biological basis of this debilitating condition remains a mystery. In this study, we investigate whether there is a disturbance in homeostasis of metabolic networks in the plasma of a female 32-patient cohort compared to 19 healthy female controls. Extensive analysis of the 832-metabolite dataset generated by Metabolon, covering eight biological classes, generated important insight into metabolic disruptions that occur in ME/CFS. We report on 14 metabolites with differences in abundance, allowing us to develop a theory of broad redox imbalance in ME/CFS patients, which is consistent with findings of prior work in the ME/CFS field. Moreover, exploration of enrichment analysis using www.MetaboAnalyst.ca provides information concerning similarities between metabolite disruptions in ME/CFS and those that occur in other diseases, while its biomarker analysis unit yielded prospective plasma biomarkers for ME/CFS. This work contributes key elements to the development of ME/CFS diagnostics, a crucial step required for discovering a therapy for any disease of unknown origin.

摘要

肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)是一种病因不明且尚无公认治愈方法的疾病。其一系列症状悄然毁掉了全球数百万人的生活。在过去几十年里,大量假说都经过了徒劳的研究,以至于这种使人衰弱的病症的生物学基础仍是个谜。在本研究中,我们调查了与19名健康女性对照相比,32名女性患者队列的血浆中代谢网络的内稳态是否存在紊乱。对Metabolon生成的涵盖八个生物类别的832种代谢物数据集进行的广泛分析,为ME/CFS中发生的代谢紊乱提供了重要见解。我们报告了14种丰度存在差异的代谢物,这使我们能够提出ME/CFS患者存在广泛氧化还原失衡的理论,这与ME/CFS领域先前的研究结果一致。此外,使用www.MetaboAnalyst.ca进行富集分析的探索提供了有关ME/CFS中代谢物紊乱与其他疾病中代谢物紊乱之间相似性的信息,而其生物标志物分析单元产生了ME/CFS的潜在血浆生物标志物。这项工作为ME/CFS诊断方法的开发提供了关键要素,这是为任何病因不明的疾病找到治疗方法所需的关键一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/6315598/316a1013f347/metabolites-08-00090-g001.jpg

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