Suppr超能文献

肌痛性脑脊髓炎/慢性疲劳综合征的病理机制

Pathological Mechanisms Underlying Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

作者信息

Missailidis Daniel, Annesley Sarah J, Fisher Paul R

机构信息

Department of Physiology Anatomy and Microbiology, La Trobe University, VIC 3086, Australia.

出版信息

Diagnostics (Basel). 2019 Jul 20;9(3):80. doi: 10.3390/diagnostics9030080.

Abstract

The underlying molecular basis of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is not well understood. Characterized by chronic, unexplained fatigue, a disabling payback following exertion ("post-exertional malaise"), and variably presenting multi-system symptoms, ME/CFS is a complex disease, which demands a concerted biomedical investigation from disparate fields of expertise. ME/CFS research and patient treatment have been challenged by the lack of diagnostic biomarkers and finding these is a prominent direction of current work. Despite these challenges, modern research demonstrates a tangible biomedical basis for the disorder across many body systems. This evidence is mostly comprised of disturbances to immunological and inflammatory pathways, autonomic and neurological dysfunction, abnormalities in muscle and mitochondrial function, shifts in metabolism, and gut physiology or gut microbiota disturbances. It is possible that these threads are together entangled as parts of an underlying molecular pathology reflecting a far-reaching homeostatic shift. Due to the variability of non-overlapping symptom presentation or precipitating events, such as infection or other bodily stresses, the initiation of body-wide pathological cascades with similar outcomes stemming from different causes may be implicated in the condition. Patient stratification to account for this heterogeneity is therefore one important consideration during exploration of potential diagnostic developments.

摘要

肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)的潜在分子基础尚未完全明确。ME/CFS以慢性、不明原因的疲劳、劳累后出现使人衰弱的疲劳恢复(“劳累后不适”)以及多系统症状的不同表现为特征,是一种复杂的疾病,需要来自不同专业领域的协同生物医学研究。缺乏诊断生物标志物给ME/CFS的研究和患者治疗带来了挑战,寻找这些标志物是当前工作的一个突出方向。尽管存在这些挑战,但现代研究表明该疾病在许多身体系统中都有切实的生物医学基础。这些证据主要包括免疫和炎症途径的紊乱、自主神经和神经功能障碍、肌肉和线粒体功能异常、代谢变化以及肠道生理或肠道微生物群紊乱。这些线索可能共同交织在一起,作为潜在分子病理学的一部分,反映了深远的体内平衡变化。由于非重叠症状表现或促发事件(如感染或其他身体应激)的变异性,由不同原因引发的具有相似结果的全身病理级联反应可能与该病症有关。因此,在探索潜在的诊断进展时,考虑患者分层以解释这种异质性是一个重要因素。

相似文献

引用本文的文献

8
Regulation of nitric oxide generation and consumption.一氧化氮生成与消耗的调节
Int J Biol Sci. 2025 Jan 13;21(3):1097-1109. doi: 10.7150/ijbs.105016. eCollection 2025.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验