Department of Neurology, Danish Multiple Sclerosis Center, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Faculty of Health Sciences, Section for Metabolic Genetics, Novo Nordisk Foundation Centre for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.
Acta Neurol Scand. 2019 Mar;139(3):208-219. doi: 10.1111/ane.13045. Epub 2018 Dec 3.
Multiple Sclerosis (MS) is a chronic immune-mediated neurological disease of the central nervous system with a complex and still not fully understood aetiology. In recent years, the gut microbiota and fermentative metabolites like short-chain fatty acids (SCFAs) have received increased attention in relation to the development and disease course of MS. This systematic review highlights and summarizes the existing literature within this field.
A systematic search in PubMed was conducted on 12 October 2017, to find published original studies on SCFAs and their impact on MS and the animal model of MS experimental autoimmune encephalomyelitis (EAE). Furthermore, all studies analysing the gut microbiota in MS patients were included. A total of 14 studies were eligible for this review.
Short-chain fatty acids have been shown to ameliorate the disease course in EAE, but no studies specifically addressing the role of SCFAs in human MS patients were identified. However, some investigations have shown that the microbiota of MS patients is characterized by a reduction in SCFA-producing bacteria.
Studies of EAE in mice suggest that SCFAs may play a role in the development and progression of EAE, but so far this has not been confirmed in humans. An aberrant gut microbiota in MS patients has been reported to be differentially abundant compared with healthy controls, although with little consistency in the bacterial taxa. Further investigations are required to elucidate the involvement of the gut microbiota and its metabolites, including potential beneficial effects of SCFAs, in the development and course of MS.
多发性硬化症(MS)是一种中枢神经系统的慢性免疫介导性疾病,病因复杂,目前尚未完全阐明。近年来,肠道微生物群及其发酵代谢产物(如短链脂肪酸(SCFAs))在多发性硬化症的发生和病程中受到越来越多的关注。本系统综述强调并总结了该领域的现有文献。
于 2017 年 10 月 12 日在 PubMed 上进行了系统检索,以查找关于 SCFAs 及其对多发性硬化症和实验性自身免疫性脑脊髓炎(EAE)动物模型的影响的已发表原始研究。此外,还纳入了所有分析多发性硬化症患者肠道微生物群的研究。共有 14 项研究符合本综述的纳入标准。
短链脂肪酸已被证明可改善 EAE 的病程,但未发现专门研究 SCFAs 在人类多发性硬化症患者中的作用的研究。然而,一些研究表明,多发性硬化症患者的微生物群中 SCFA 产生菌减少。
在小鼠 EAE 中的研究表明,SCFAs 可能在 EAE 的发生和进展中发挥作用,但到目前为止,这在人类中尚未得到证实。与健康对照组相比,多发性硬化症患者的肠道微生物群存在差异,尽管细菌分类群的一致性较差。需要进一步研究来阐明肠道微生物群及其代谢产物(包括 SCFAs 的潜在有益作用)在多发性硬化症的发生和病程中的作用。