Unravelling shared mechanisms: insights from recent ME/CFS research to illuminate long COVID pathologies

被引:15
作者
Annesley, Sarah J. [1 ]
Missailidis, Daniel [1 ]
Heng, Benjamin [2 ]
Josev, Elisha K. [3 ,4 ,5 ]
Armstrong, Christopher W. [6 ]
机构
[1] La Trobe Univ, Dept Microbiol Anat Physiol & Pharmacol, Bundoora, Vic, Australia
[2] Macquarie Univ, Fac Med Human & Hlth Sci, Macquarie Med Sch, Sydney, NSW, Australia
[3] Murdoch Childrens Res Inst, Neurodisabil & Rehabil, Clin Sci, Parkville, Vic, Australia
[4] Univ Melbourne, Royal Childrens Hosp, Dept Paediat, Parkville, Vic, Australia
[5] Mercy Hosp Women, Heidelberg, Vic, Australia
[6] Univ Melbourne, Bio21 Mol Sci & Biotechnol Inst, Dept Biochem & Pharmacol, Parkville, Vic, Australia
关键词
ENCEPHALOMYELITIS/CHRONIC FATIGUE SYNDROME; GUT MICROBIOME; SEVERITY; SYMPTOMS; SEQUELAE; MODEL;
D O I
10.1016/j.molmed.2024.02.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a debilitating chronic illness often triggered by an initiating acute event, mainly viral infections. The transition from acute to chronic disease remains unknown, but interest in this phenomenon has escalated since the COVID-19 pandemic and the post-COVID19 illness, termed 'long COVID' (LC). Both ME/CFS and LC share many clinical similarities. Here, we present recent findings in ME/CFS research focussing on proposed disease pathologies shared with LC. Understanding these disease pathologies and how they influence each other is key to developing effective therapeutics and diagnostic tests. Given that ME/CFS typically has a longer disease duration compared with LC, with symptoms and pathologies evolving over time, ME/CFS may provide insights into the future progression of LC.
引用
收藏
页码:443 / 458
页数:16
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