Department of Rehabilitation, Shenzhen Longhua District Central Hospital, 518000 Shenzhen, Guangdong, China.
Department of Neurology, Shenzhen Longhua District Central Hospital, 518000 Shenzhen, Guangdong, China.
J Integr Neurosci. 2024 Jul 9;23(7):127. doi: 10.31083/j.jin2307127.
This meta-analysis explores alterations in the gut microbiota of patients with Multiple Sclerosis (MS) using 16S ribosomal RNA (rRNA) gene sequencing.
Adhering to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, our comprehensive review spanned major databases, including PubMed, Web of Science, Embase, Cochrane, and Ovid, targeting observational studies that implemented 16S rRNA gene sequencing on fecal specimens. The quality of these studies was meticulously evaluated using the Newcastle-Ottawa scale.
Our search yielded 26 relevant studies conducted between 2015-2022, encompassing 2885 participants. No significant differences were observed in alpha diversity indices (Shannon, Chao1, Operational Taxonomic Units (OTU), and Simpson) between MS patients and controls in general. Nonetheless, subgroup analyses according to disease activity using the Shannon index highlighted a significant decrease in microbial diversity during MS's active phase. Similarly, an evaluation focusing on MS phenotype revealed diminished diversity in individuals with relapsing-remitting MS (RRMS). Microbial composition analysis revealed no consistent increase in pro-inflammatory or decrease in anti-inflammatory within the MS cohort.
The gut microbiome's role in MS presents a complex panorama, where alterations in microbial composition might hold greater significance to disease mechanisms than diversity changes. The impact of clinical factors such as disease activity and phenotype are moderately significant, underscoring the need for further research to elucidate these relationships. Prospective research should employ longitudinal methodologies to elucidate the chronological interplay among gut microbiota, disease evolution, and therapeutic strategies.
本荟萃分析使用 16S 核糖体 RNA(rRNA)基因测序探索多发性硬化症(MS)患者肠道微生物组的变化。
我们遵循系统评价和荟萃分析的首选报告项目(PRISMA)指南,全面检索了主要数据库,包括 PubMed、Web of Science、Embase、Cochrane 和 Ovid,针对使用粪便标本进行 16S rRNA 基因测序的观察性研究。使用纽卡斯尔-渥太华量表(Newcastle-Ottawa scale)仔细评估了这些研究的质量。
我们的搜索产生了 2015 年至 2022 年间进行的 26 项相关研究,共纳入 2885 名参与者。一般来说,MS 患者和对照组之间的 alpha 多样性指数(Shannon、Chao1、操作分类单元(OTU)和 Simpson)没有显著差异。然而,根据 Shannon 指数的疾病活动进行亚组分析表明,MS 活跃期微生物多样性显著下降。同样,对 MS 表型的评估表明,缓解复发型 MS(RRMS)患者的多样性降低。微生物组成分析未显示 MS 队列中促炎菌的一致增加或抗炎菌的减少。
肠道微生物组在 MS 中的作用呈现出复杂的局面,微生物组成的变化可能比多样性变化对疾病机制更有意义。临床因素(如疾病活动和表型)的影响适度显著,这突出表明需要进一步研究以阐明这些关系。前瞻性研究应采用纵向方法学来阐明肠道微生物群、疾病演变和治疗策略之间的时间顺序相互作用。