Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Apr 29:13:874388.
doi: 10.3389/fneur.2022.874388. eCollection 2022.

Cerebellar and/or Brainstem Lesions Indicate Poor Prognosis in Multiple Sclerosis: A Systematic Review

Affiliations
Review

Cerebellar and/or Brainstem Lesions Indicate Poor Prognosis in Multiple Sclerosis: A Systematic Review

Yuyuan Yang et al. Front Neurol. .

Abstract

Multiple sclerosis is a serious neurological disease that affects millions of people worldwide. Cerebellar and brainstem symptoms are common in the course of multiple sclerosis, but their prognostic value is unclear. This systematic review aimed to determine the relationship between the location of lesions in the cerebellum and/or brainstem and the prognosis in multiple sclerosis. In this systematic review, we searched and comprehensively read articles related to this research topic in Chinese and English electronic databases (PubMed, Embase, Cochrane Library, CNKI, and CBM) using search terms "multiple sclerosis," "cerebellum," "brainstem," "prognosis," and others. Cerebellar and brainstem clinically isolated syndromes and clinically definite multiple sclerosis were important predictors of transformation (hazard ratio, 2.58; 95% confidence interval, 1.58-4.22). Cerebellar and/or brainstem lesions indicate a poor overall prognosis in multiple sclerosis, but because of inconsistency, more clinical data are needed.

Keywords: brainstem; cerebellum; disability outcome; multiple sclerosis; predictors.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Preferred Reporting Items for Systematic Reviews and Meta-analyses.
Figure 2
Figure 2
Brainstem and cerebellar lesions predict the risk ratio of conversion of clinically isolated syndromes to clinically definite multiple sclerosis. HR, hazards ratio; CI, confidence interval.

References

    1. Lublin FD, Reingold SC, Cohen JA, Cutter GR, Sørensen PS, Thompson AJ, et al. . Defining the clinical course of multiple sclerosis: the 2013 revisions. Neurology. (2014) 83:278–86. 10.1212/WNL.0000000000000560 - DOI - PMC - PubMed
    1. Poser S, Wikström J, Bauer HJ. Clinical data and the identification of special forms of multiple sclerosis in 1271 cases studied with a standardized documentation system. J Neurol Sci. (1979) 40:159–68. 10.1016/0022-510X(79)90201-6 - DOI - PubMed
    1. Kalincik T, Buzzard K, Jokubaitis V, Trojano M, Duquette P, Izquierdo G, et al. . Risk of relapse phenotype recurrence in multiple sclerosis. Mult Scler. (2014) 20:1511–22. 10.1177/1352458514528762 - DOI - PubMed
    1. Nakashima I, Fujihara K, Okita N, Takase S, Itoyama Y. Clinical and MRI study of brain stem and cerebellar involvement in Japanese patients with multiple sclerosis. J Neurol Neurosurg Psychiatry. (1999) 67:153–7. 10.1136/jnnp.67.2.153 - DOI - PMC - PubMed
    1. Weier K, Banwell B, Cerasa A, Collins DL, Dogonowski AM, Lassmann H, et al. . The role of the cerebellum in multiple sclerosis. Cerebellum. (2015) 14:364–74. 10.1007/s12311-014-0634-8 - DOI - PubMed

LinkOut - more resources