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多发性硬化症患者的痴呆症:系统评价与荟萃分析

Dementia in People With Multiple Sclerosis: A Systematic Review and Meta-Analysis.

作者信息

Mirmosayyeb Omid, Dehghani Firouzabadi Danial, Oraee Soroush, Alinejadfard Mohammadreza, Yazdan Panah Mohammad, Vaheb Saeed, Ghoshouni Hamed, Shaygannejad Vahid

机构信息

Isfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

Department of Neurology, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Brain Behav. 2025 Jun;15(6):e70588. doi: 10.1002/brb3.70588.


DOI:10.1002/brb3.70588
PMID:40443354
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12123099/
Abstract

INTRODUCTION: Multiple sclerosis (MS), as an autoimmune demyelinating disorder, is associated with cognitive dysfunction. Dementia can result from severe cognitive dysfunction or other pathways in MS, but the exact mechanisms and prevalence are unknown. OBJECTIVE: This review aimed to determine the pooled prevalence and risk of dementia in people with MS (PwMS). DESIGN: This meta-analysis was performed in accordance with the guidelines established by the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA). METHODS: Embase, PubMed, Web of Science, and Scopus were comprehensively searched up to August 29, 2024, to identify observational studies that examined the prevalence or hazard ratio (HR) of dementia among PwMS. This meta-analysis used a random-effects model to calculate the pooled prevalence and risk of dementia among PwMS, where the prevalence rate and HR were the main metrics for effect size. RESULTS: Ten studies, including a total of 37,831 PwMS, estimated the prevalence of dementia in PwMS to be 5.31% (I = 99.2%, 95% CI: 2.25%-11.98%). In addition, a meta-analysis of four studies assessed the HR of dementia among PwMS, revealing a pooled HR of 1.67 (p < 0.01, I = 73.5%, 95% CI: 1.31-2.13). CONCLUSION: While dementia is not a common feature of MS, PwMS still have a significantly higher risk of developing it, compared to healthy indiviuals. However, the considerable variability across studies indicates that these estimates should be interpreted with caution, as inconsistencies in research approaches may have influenced the results. These findings warrant further validation.

摘要

引言:多发性硬化症(MS)作为一种自身免疫性脱髓鞘疾病,与认知功能障碍有关。痴呆可能由MS中的严重认知功能障碍或其他途径引起,但其确切机制和患病率尚不清楚。 目的:本综述旨在确定MS患者(PwMS)中痴呆的合并患病率和风险。 设计:本荟萃分析按照系统评价和荟萃分析的首选报告项目(PRISMA)制定的指南进行。 方法:全面检索截至2024年8月29日的Embase、PubMed、科学网和Scopus,以识别研究PwMS中痴呆患病率或风险比(HR)的观察性研究。本荟萃分析使用随机效应模型计算PwMS中痴呆的合并患病率和风险,其中患病率和HR是效应大小的主要指标。 结果:10项研究,共纳入37831例PwMS,估计PwMS中痴呆的患病率为5.31%(I = 99.2%,95%CI:2.25%-11.98%)。此外,对4项研究的荟萃分析评估了PwMS中痴呆的HR,显示合并HR为1.67(p < 0.01,I = 73.5%,95%CI:1.31-2.13)。 结论:虽然痴呆不是MS的常见特征,但与健康个体相比,PwMS患痴呆的风险仍然显著更高。然而,各研究之间存在相当大的变异性,这表明这些估计结果应谨慎解释,因为研究方法的不一致可能影响了结果。这些发现值得进一步验证。

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本文引用的文献

[1]
Effects of intensive lifestyle changes on the progression of mild cognitive impairment or early dementia due to Alzheimer's disease: a randomized, controlled clinical trial.

Alzheimers Res Ther. 2024-6-7

[2]
Social determinants of health but not global genetic ancestry predict dementia prevalence in Latin America.

Alzheimers Dement. 2024-7

[3]
Cognitive dysfunction characteristics of multiple sclerosis with aging.

Mult Scler Relat Disord. 2024-7

[4]
Risk of dementia in older veterans with multiple sclerosis.

Mult Scler Relat Disord. 2024-2

[5]
Multiple sclerosis in the elderly: a retrospective cohort study.

J Neurol. 2024-2

[6]
The impact of disease modifying therapies on cognitive functions typically impaired in multiple sclerosis patients: a clinician's review.

Front Neurol. 2023-7-12

[7]
The risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder.

Front Neurosci. 2023-6-15

[8]
Microglia in Alzheimer's disease: pathogenesis, mechanisms, and therapeutic potentials.

Front Aging Neurosci. 2023-6-15

[9]
Alzheimer's disease and multiple sclerosis: a possible connection through the viral demyelinating neurodegenerative trigger (vDENT).

Front Aging Neurosci. 2023-6-15

[10]
Cognitive rehabilitation for people with mild to moderate dementia.

Cochrane Database Syst Rev. 2023-6-29

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