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Multiple system atrophy pathology is associated with primary Sjögren’s syndrome
BACKGROUND: Our objective was to investigate whether primary Sjögren’s syndrome (pSS) is associated with multiple system atrophy (MSA). METHODS: We performed a retrospective cohort study assessing (a) rates of MSA in a cohort of patients with pSS and (b) rates of pSS in a cohort of patients with MSA...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455075/ https://www.ncbi.nlm.nih.gov/pubmed/32644976 http://dx.doi.org/10.1172/jci.insight.138619 |
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author | Conway, Kyle S. Camelo-Piragua, Sandra Fisher-Hubbard, Amanda Perry, William R. Shakkottai, Vikram G. Venneti, Sriram |
author_facet | Conway, Kyle S. Camelo-Piragua, Sandra Fisher-Hubbard, Amanda Perry, William R. Shakkottai, Vikram G. Venneti, Sriram |
author_sort | Conway, Kyle S. |
collection | PubMed |
description | BACKGROUND: Our objective was to investigate whether primary Sjögren’s syndrome (pSS) is associated with multiple system atrophy (MSA). METHODS: We performed a retrospective cohort study assessing (a) rates of MSA in a cohort of patients with pSS and (b) rates of pSS in a cohort of patients with MSA. These data were compared with rates in respective control groups. We additionally reviewed the neuropathologic findings in 2 patients with pSS, cerebellar degeneration, parkinsonism, and autonomic dysfunction. RESULTS: Our cohort of 308 patients with pSS had a greater incidence of MSA compared with 4 large population-based studies and had a significantly higher prevalence of at least probable MSA (1% vs. 0%, P = 0.02) compared with 776 patients in a control cohort of patients with other autoimmune disorders. Our cohort of 26 autopsy-proven patients with MSA had a significantly higher prevalence of pSS compared with a cohort of 115 patients with other autopsy-proven neurodegenerative disorders (8% vs. 0%, P = 0.03). The 2 patients we described with pSS and progressive neurodegenerative disease showed classic MSA pathology at autopsy. CONCLUSION: Our findings provide evidence for an association between MSA and pSS that is specific to both pSS, among autoimmune disorders, and MSA, among neurodegenerative disorders. The 2 cases we describe of autopsy-proven MSA support that MSA pathology can explain neurologic disease in a subset of patients with pSS. These findings together support the hypothesis that systemic autoimmune disease plays a role in neurodegeneration. FUNDING: The Michigan Brain Bank is supported in part through NIH grant P30AG053760. |
format | Online Article Text |
id | pubmed-7455075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-74550752020-09-01 Multiple system atrophy pathology is associated with primary Sjögren’s syndrome Conway, Kyle S. Camelo-Piragua, Sandra Fisher-Hubbard, Amanda Perry, William R. Shakkottai, Vikram G. Venneti, Sriram JCI Insight Clinical Medicine BACKGROUND: Our objective was to investigate whether primary Sjögren’s syndrome (pSS) is associated with multiple system atrophy (MSA). METHODS: We performed a retrospective cohort study assessing (a) rates of MSA in a cohort of patients with pSS and (b) rates of pSS in a cohort of patients with MSA. These data were compared with rates in respective control groups. We additionally reviewed the neuropathologic findings in 2 patients with pSS, cerebellar degeneration, parkinsonism, and autonomic dysfunction. RESULTS: Our cohort of 308 patients with pSS had a greater incidence of MSA compared with 4 large population-based studies and had a significantly higher prevalence of at least probable MSA (1% vs. 0%, P = 0.02) compared with 776 patients in a control cohort of patients with other autoimmune disorders. Our cohort of 26 autopsy-proven patients with MSA had a significantly higher prevalence of pSS compared with a cohort of 115 patients with other autopsy-proven neurodegenerative disorders (8% vs. 0%, P = 0.03). The 2 patients we described with pSS and progressive neurodegenerative disease showed classic MSA pathology at autopsy. CONCLUSION: Our findings provide evidence for an association between MSA and pSS that is specific to both pSS, among autoimmune disorders, and MSA, among neurodegenerative disorders. The 2 cases we describe of autopsy-proven MSA support that MSA pathology can explain neurologic disease in a subset of patients with pSS. These findings together support the hypothesis that systemic autoimmune disease plays a role in neurodegeneration. FUNDING: The Michigan Brain Bank is supported in part through NIH grant P30AG053760. American Society for Clinical Investigation 2020-08-06 /pmc/articles/PMC7455075/ /pubmed/32644976 http://dx.doi.org/10.1172/jci.insight.138619 Text en © 2020 Conway et al. http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Medicine Conway, Kyle S. Camelo-Piragua, Sandra Fisher-Hubbard, Amanda Perry, William R. Shakkottai, Vikram G. Venneti, Sriram Multiple system atrophy pathology is associated with primary Sjögren’s syndrome |
title | Multiple system atrophy pathology is associated with primary Sjögren’s syndrome |
title_full | Multiple system atrophy pathology is associated with primary Sjögren’s syndrome |
title_fullStr | Multiple system atrophy pathology is associated with primary Sjögren’s syndrome |
title_full_unstemmed | Multiple system atrophy pathology is associated with primary Sjögren’s syndrome |
title_short | Multiple system atrophy pathology is associated with primary Sjögren’s syndrome |
title_sort | multiple system atrophy pathology is associated with primary sjögren’s syndrome |
topic | Clinical Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455075/ https://www.ncbi.nlm.nih.gov/pubmed/32644976 http://dx.doi.org/10.1172/jci.insight.138619 |
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