Is there a link between inflammation and fatigue in multiple sclerosis?

被引:35
作者
Chalah, Moussa A. [1 ,2 ]
Ayache, Samar S. [1 ,2 ,3 ]
机构
[1] Univ Paris Est Creteil, EA 4391, Excitabilite Nerveuse & Therapeut, Creteil, France
[2] Hop Henri Mondor, AP HP, Serv Physiol Explorat Fonct, Creteil, France
[3] Lebanese Amer Univ, Rizk Hosp, Neurol Div, Med Ctr, Beirut, Lebanon
关键词
pathophysiology; cytokines; interleukins; cerebrospinal fluids; inflammatory markers; PITUITARY-ADRENAL AXIS; INTERFERON-BETA; CEREBROSPINAL-FLUID; COGNITIVE DYSFUNCTION; RHEUMATOID-ARTHRITIS; CYTOKINE RESPONSES; HPA AXIS; T-CELLS; OREXIN; NATALIZUMAB;
D O I
10.2147/JIR.S167199
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose: Among autoimmune diseases of the central nervous system stands multiple sclerosis (MS), which is characterized by demyelination, synaptopathy, and neurodegeneration. MS fatigue can affect up to 90% of patients and be very disabling, with a drastic impact on their quality of life. To date, the evaluation of MS fatigue has relied mainly on subjective scales, and actual therapeutic interventions are challenged by modest efficacy and numerous undesirable effects. Therefore, finding biomarkers of MS fatigue might help in optimizing evaluation and treatment strategies. The main objective here was to assess the relationship between MS fatigue and inflammatory or other immunomediated markers. Methods: Research was conducted according to PRISMA guidelines. Computerized databases (ie, PubMed/Medline and Scopus) were consulted till February 2018 aiming to identify articles that addressed inflammation and MS fatigue. Studies in English and French published at any time were considered. Results: A total of 27 studies matched the research criteria. Inconsistency existed regarding the relationship between fatigue and the orexin A system, hypothalamus-pituitary-adrenal axis, and cerebrospinal fluid inflammatory markers. As for peripheral markers, although there was scarcity in the available data, serum proinflammatory cytokines (ie, IL6, TNF alpha, and IFN gamma) seem to be associated with MS fatigue. Finally, no link was found between MS fatigue and T-cell populations (ie, CD3(+) CD4(+) T lymphocytes, regulatory T cells) or other peripheral markers of inflammation (ie, CRP, erythrocyte-sedimentation rate, soluble ICAM1). Conclusion: Future large-scale studies would benefit from comparing the relationship between fatigue and immune measures in patients with different disease phenotypes with and without disease-modifying drugs. With the subjective nature of fatigue scales, finding objective biomarkers for fatigue would be of great help.
引用
收藏
页码:253 / 264
页数:12
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