Cargando…

Sex differences in brain atrophy in multiple sclerosis

BACKGROUND: Women are more susceptible to multiple sclerosis (MS) than men by a ratio of approximately 3:1. However, being male is a risk factor for worse disability progression. Inflammatory genes have been linked to susceptibility, while neurodegeneration underlies disability progression. Thus, th...

Descripción completa

Detalles Bibliográficos
Autores principales: Voskuhl, Rhonda R., Patel, Kevin, Paul, Friedemann, Gold, Stefan M., Scheel, Michael, Kuchling, Joseph, Cooper, Graham, Asseyer, Susanna, Chien, Claudia, Brandt, Alexander U., Meyer, Cassandra Eve, MacKenzie-Graham, Allan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7456053/
https://www.ncbi.nlm.nih.gov/pubmed/32859258
http://dx.doi.org/10.1186/s13293-020-00326-3
_version_ 1783575744629178368
author Voskuhl, Rhonda R.
Patel, Kevin
Paul, Friedemann
Gold, Stefan M.
Scheel, Michael
Kuchling, Joseph
Cooper, Graham
Asseyer, Susanna
Chien, Claudia
Brandt, Alexander U.
Meyer, Cassandra Eve
MacKenzie-Graham, Allan
author_facet Voskuhl, Rhonda R.
Patel, Kevin
Paul, Friedemann
Gold, Stefan M.
Scheel, Michael
Kuchling, Joseph
Cooper, Graham
Asseyer, Susanna
Chien, Claudia
Brandt, Alexander U.
Meyer, Cassandra Eve
MacKenzie-Graham, Allan
author_sort Voskuhl, Rhonda R.
collection PubMed
description BACKGROUND: Women are more susceptible to multiple sclerosis (MS) than men by a ratio of approximately 3:1. However, being male is a risk factor for worse disability progression. Inflammatory genes have been linked to susceptibility, while neurodegeneration underlies disability progression. Thus, there appears to be a differential effect of sex on inflammation versus neurodegeneration. Further, gray matter (GM) atrophy is not uniform across the brain in MS, but instead shows regional variation. Here, we study sex differences in neurodegeneration by comparing regional GM atrophy in a cohort of men and women with MS versus their respective age- and sex-matched healthy controls. METHODS: Voxel-based morphometry (VBM), deep GM substructure volumetry, and cortical thinning were used to examine regional GM atrophy. RESULTS: VBM analysis showed deep GM atrophy in the thalamic area in both men and women with MS, whereas men had additional atrophy in the putamen as well as in localized cortical regions. Volumetry confirmed deep GM loss, while localized cortical thinning confirmed GM loss in the cerebral cortex. Further, MS males exhibited worse performance on the 9-hole peg test (9HPT) than MS females. We observed a strong correlation between thalamic volume and 9HPT performance in MS males, but not in MS females. CONCLUSION: More regional GM atrophy was observed in men with MS than women with MS, consistent with previous observations that male sex is a risk factor for worse disease progression.
format Online
Article
Text
id pubmed-7456053
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-74560532020-08-31 Sex differences in brain atrophy in multiple sclerosis Voskuhl, Rhonda R. Patel, Kevin Paul, Friedemann Gold, Stefan M. Scheel, Michael Kuchling, Joseph Cooper, Graham Asseyer, Susanna Chien, Claudia Brandt, Alexander U. Meyer, Cassandra Eve MacKenzie-Graham, Allan Biol Sex Differ Research BACKGROUND: Women are more susceptible to multiple sclerosis (MS) than men by a ratio of approximately 3:1. However, being male is a risk factor for worse disability progression. Inflammatory genes have been linked to susceptibility, while neurodegeneration underlies disability progression. Thus, there appears to be a differential effect of sex on inflammation versus neurodegeneration. Further, gray matter (GM) atrophy is not uniform across the brain in MS, but instead shows regional variation. Here, we study sex differences in neurodegeneration by comparing regional GM atrophy in a cohort of men and women with MS versus their respective age- and sex-matched healthy controls. METHODS: Voxel-based morphometry (VBM), deep GM substructure volumetry, and cortical thinning were used to examine regional GM atrophy. RESULTS: VBM analysis showed deep GM atrophy in the thalamic area in both men and women with MS, whereas men had additional atrophy in the putamen as well as in localized cortical regions. Volumetry confirmed deep GM loss, while localized cortical thinning confirmed GM loss in the cerebral cortex. Further, MS males exhibited worse performance on the 9-hole peg test (9HPT) than MS females. We observed a strong correlation between thalamic volume and 9HPT performance in MS males, but not in MS females. CONCLUSION: More regional GM atrophy was observed in men with MS than women with MS, consistent with previous observations that male sex is a risk factor for worse disease progression. BioMed Central 2020-08-28 /pmc/articles/PMC7456053/ /pubmed/32859258 http://dx.doi.org/10.1186/s13293-020-00326-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Voskuhl, Rhonda R.
Patel, Kevin
Paul, Friedemann
Gold, Stefan M.
Scheel, Michael
Kuchling, Joseph
Cooper, Graham
Asseyer, Susanna
Chien, Claudia
Brandt, Alexander U.
Meyer, Cassandra Eve
MacKenzie-Graham, Allan
Sex differences in brain atrophy in multiple sclerosis
title Sex differences in brain atrophy in multiple sclerosis
title_full Sex differences in brain atrophy in multiple sclerosis
title_fullStr Sex differences in brain atrophy in multiple sclerosis
title_full_unstemmed Sex differences in brain atrophy in multiple sclerosis
title_short Sex differences in brain atrophy in multiple sclerosis
title_sort sex differences in brain atrophy in multiple sclerosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7456053/
https://www.ncbi.nlm.nih.gov/pubmed/32859258
http://dx.doi.org/10.1186/s13293-020-00326-3
work_keys_str_mv AT voskuhlrhondar sexdifferencesinbrainatrophyinmultiplesclerosis
AT patelkevin sexdifferencesinbrainatrophyinmultiplesclerosis
AT paulfriedemann sexdifferencesinbrainatrophyinmultiplesclerosis
AT goldstefanm sexdifferencesinbrainatrophyinmultiplesclerosis
AT scheelmichael sexdifferencesinbrainatrophyinmultiplesclerosis
AT kuchlingjoseph sexdifferencesinbrainatrophyinmultiplesclerosis
AT coopergraham sexdifferencesinbrainatrophyinmultiplesclerosis
AT asseyersusanna sexdifferencesinbrainatrophyinmultiplesclerosis
AT chienclaudia sexdifferencesinbrainatrophyinmultiplesclerosis
AT brandtalexanderu sexdifferencesinbrainatrophyinmultiplesclerosis
AT meyercassandraeve sexdifferencesinbrainatrophyinmultiplesclerosis
AT mackenziegrahamallan sexdifferencesinbrainatrophyinmultiplesclerosis