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血清代谢组学分析显示特发性炎症性肌病患者类固醇激素生物合成紊乱。

Serum metabolomic analysis reveals disorder of steroid hormone biosynthesis in patients with idiopathic inflammatory myopathy.

机构信息

Chinese Academy of Medical Sciences (CAMS) Key Laboratory for T Cell and Immunotherapy, State Key Laboratory of Medical Molecular Biology, Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medicine, Peking Union Medical College, Beijing, China.

Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

Front Immunol. 2023 Jun 12;14:1188257. doi: 10.3389/fimmu.2023.1188257. eCollection 2023.

Abstract

Idiopathic inflammatory myopathy (IIM) is a heterogeneous group of autoimmune diseases with various clinical manifestations, treatment responses, and prognoses. According to the clinical manifestations and presence of different myositis-specific autoantibodies (MSAs), IIM is classified into several major subgroups, including PM, DM, IBM, ASS, IMNM, and CADM. However, the pathogenic mechanisms of these subgroups remain unclear and need to be investigated. Here, we applied MALDI-TOF-MS to examine the serum metabolome of 144 patients with IIM and analyze differentially expressed metabolites among IIM subgroups or MSA groups. The results showed that the DM subgroup had lower activation of the steroid hormone biosynthesis pathway, while the non-MDA5 MSA group had higher activation of the arachidonic acid metabolism pathway. Our study may provide some insights into the heterogeneous mechanisms of IIM subgroups, potential biomarkers, and management of IIM.

摘要

特发性炎性肌病(IIM)是一组具有不同临床表现、治疗反应和预后的自身免疫性疾病。根据临床表现和不同的肌炎特异性自身抗体(MSAs)的存在,IIM 分为几个主要亚组,包括 PM、DM、IBM、ASS、IMNM 和 CADM。然而,这些亚组的发病机制尚不清楚,需要进一步研究。在这里,我们应用 MALDI-TOF-MS 检测了 144 例 IIM 患者的血清代谢组,并分析了 IIM 亚组或 MSA 组之间差异表达的代谢物。结果表明,DM 亚组类固醇激素生物合成途径的激活较低,而非 MDA5 MSA 组花生四烯酸代谢途径的激活较高。我们的研究可能为 IIM 亚组的异质性机制、潜在的生物标志物和 IIM 的管理提供一些见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c0f/10291268/59281442ba79/fimmu-14-1188257-g001.jpg

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