Myalgic encephalomyelitis/chronic fatigue syndrome: From pathophysiological insights to novel therapeutic opportunities

被引:27
|
作者
Morris, Gerwyn [1 ]
Puri, Basant K. [2 ]
Walker, Adam J. [1 ]
Maes, Michael [1 ]
Carvalho, Andre F. [5 ,6 ]
Walder, Ken [3 ]
Mazza, Catherine [1 ]
Berk, Michael [1 ,3 ,4 ,7 ,8 ]
机构
[1] Deakin Univ, Sch Med, IMPACT Strateg Res Ctr, Geelong, Vic, Australia
[2] Imperial Coll London, Hammersmith Hosp, Dept Med, London, England
[3] Deakin Univ, Sch Med, CMMR Strateg Res Ctr, Geelong, Vic, Australia
[4] Natl Ctr Excellence Youth Mental Hlth, Orygen, Melbourne, Vic, Australia
[5] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[6] CAMH, Toronto, ON, Canada
[7] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia
[8] Univ Melbourne, Dept Psychiat, Parkville, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Chronic fatigue syndrome; Myalgic encephalomyelitis; Oxidative stress; Inflammation; Mitochondrial dysfunction; HYDROGEN-RICH SALINE; HEART-RATE-VARIABILITY; NF-KAPPA-B; INDUCED OXIDATIVE STRESS; STATE FUNCTIONAL CONNECTIVITY; COGNITIVE-BEHAVIORAL THERAPY; PRO-INFLAMMATORY CYTOKINES; TRAUMATIC BRAIN-INJURY; NITRIC-OXIDE SYNTHASE; MAGNETIC-RESONANCE-SPECTROSCOPY;
D O I
10.1016/j.phrs.2019.104450
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Myalgic encephalomyelitis (ME) or chronic fatigue syndrome (CFS) is a common and disabling condition with a paucity of effective and evidence-based therapies, reflecting a major unmet need. Cognitive behavioural therapy and graded exercise are of modest benefit for only some ME/CFS patients, and many sufferers report aggravation of symptoms of fatigue with exercise. The presence of a multiplicity of pathophysiological abnormalities in at least the subgroup of people with ME/CFS diagnosed with the current international consensus "Fukuda" criteria, points to numerous potential therapeutic targets. Such abnormalities include extensive data showing that at least a subgroup has a pro-inflammatory state, increased oxidative and nitrosative stress, disruption of gut mucosal barriers and mitochondrial dysfunction together with dysregulated bioenergetics. In this paper, these pathways are summarised, and data regarding promising therapeutic options that target these pathways are highlighted; they include coenzyme Q(10), melatonin, curcumin, molecular hydrogen and N-acetylcysteine. These data are promising yet preliminary, suggesting hopeful avenues to address this major unmet burden of illness.
引用
收藏
页数:20
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