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
. 2024 Aug 1;37(4):400-408.
doi: 10.1097/WCO.0000000000001285. Epub 2024 Jun 3.

An update on multiple system atrophy

Affiliations
Review

An update on multiple system atrophy

Iva Stankovic et al. Curr Opin Neurol. .

Abstract

Purpose of review: Multiple system atrophy (MSA) is a rapidly progressive synucleinopathy characterized by autonomic failure, parkinsonism, and cerebellar ataxia. Here, we provide an update on α-synuclein's role in MSA pathophysiology and review the new Movement Disorders Society (MDS) diagnostic criteria and the utility of α-synuclein-based biomarkers. We also highlight ongoing efforts toward clinical trial readiness and review potential disease-modifying therapies undergoing clinical trials.

Recent findings: A role of urinary tract infections in triggering α-synuclein aggregation and contribution of genes implicated in oligodendroglial development have been suggested in the MSA pathophysiology. The clinically probable MSA category of the new diagnostic criteria shows improved accuracy in early disease stages. Predictors of phenoconversion from pure autonomic failure to MSA are now better defined. Alpha-synuclein strains in CSF and serum, phosphorylated α-synuclein deposits in the skin, and brain α-synuclein pathology visualized using PET ligand [18F]ACI-12589 are emerging as valuable diagnostic tools. Clinical trials in MSA investigate drugs targeting α-synuclein aggregation or preventing α-synuclein expression, along with stem cell and gene therapies to halt disease progression.

Summary: New MSA diagnostic criteria and α-synuclein-based biomarkers may enhance diagnostic accuracy while promising therapies are in development to address disease progression.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest

I. S. has nothing to disclose.

M. K. and H.K. receive research support from NIH-NINDS (U01NS122419).

Figures

Figure 1.
Figure 1.
Predictors of phenoconversion of pure autonomic failure to MSA bpm: beats per minute, CSF: cerebrospinal fluid, HR: heart rate, NE: norepinephrine, NfL: neurofilament light chain, pg/ml: picograms per milliliter, ThT: thioflavin

References

    1. Fanciulli A, Wenning GK. Multiple-system atrophy. N Engl J Med. 2015;372(3):249–63. - PubMed
    1. Lin CR, Viswanathan A, Chen TX, et al. Clinicopathological correlates of pyramidal signs in multiple system atrophy. Ann Clin Transl Neurol. 2022;9(7):988–94. - PMC - PubMed
    1. Poewe W, Stankovic I, Halliday G, et al. Multiple system atrophy. Nat Rev Dis Primers. 2022;8(1):56. - PubMed
    1. Fanciulli A, Leys F, Lehner F, et al. A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson’s disease with dementia. Brain Commun. 2022;4(4):fcac175. - PMC - PubMed
    1. Multiple-System Atrophy Research C Mutations in COQ2 in familial and sporadic multiple-system atrophy. N Engl J Med. 2013;369(3):233–44. - PubMed

MeSH terms