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Non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia

Background: Non‐motor symptoms are well established phenotypic components of adult‐onset idiopathic, isolated, focal cervical dystonia (AOIFCD). However, improved understanding of their clinical heterogeneity is needed to better target therapeutic intervention. Here, we examine non‐motor phenotypic...

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Autores principales: Wadon, Megan E., Bailey, Grace A., Yilmaz, Zehra, Hubbard, Emily, AlSaeed, Meshari, Robinson, Amy, McLauchlan, Duncan, Barbano, Richard L., Marsh, Laura, Factor, Stewart A., Fox, Susan H., Adler, Charles H., Rodriguez, Ramon L., Comella, Cynthia L., Reich, Stephen G., Severt, William L., Goetz, Christopher G., Perlmutter, Joel S., Jinnah, Hyder A., Harding, Katharine E., Sandor, Cynthia, Peall, Kathryn J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413761/
https://www.ncbi.nlm.nih.gov/pubmed/34291595
http://dx.doi.org/10.1002/brb3.2292
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author Wadon, Megan E.
Bailey, Grace A.
Yilmaz, Zehra
Hubbard, Emily
AlSaeed, Meshari
Robinson, Amy
McLauchlan, Duncan
Barbano, Richard L.
Marsh, Laura
Factor, Stewart A.
Fox, Susan H.
Adler, Charles H.
Rodriguez, Ramon L.
Comella, Cynthia L.
Reich, Stephen G.
Severt, William L.
Goetz, Christopher G.
Perlmutter, Joel S.
Jinnah, Hyder A.
Harding, Katharine E.
Sandor, Cynthia
Peall, Kathryn J.
author_facet Wadon, Megan E.
Bailey, Grace A.
Yilmaz, Zehra
Hubbard, Emily
AlSaeed, Meshari
Robinson, Amy
McLauchlan, Duncan
Barbano, Richard L.
Marsh, Laura
Factor, Stewart A.
Fox, Susan H.
Adler, Charles H.
Rodriguez, Ramon L.
Comella, Cynthia L.
Reich, Stephen G.
Severt, William L.
Goetz, Christopher G.
Perlmutter, Joel S.
Jinnah, Hyder A.
Harding, Katharine E.
Sandor, Cynthia
Peall, Kathryn J.
author_sort Wadon, Megan E.
collection PubMed
description Background: Non‐motor symptoms are well established phenotypic components of adult‐onset idiopathic, isolated, focal cervical dystonia (AOIFCD). However, improved understanding of their clinical heterogeneity is needed to better target therapeutic intervention. Here, we examine non‐motor phenotypic features to identify possible AOIFCD subgroups. Methods: Participants diagnosed with AOIFCD were recruited via specialist neurology clinics (dystonia wales: n = 114, dystonia coalition: n = 183). Non‐motor assessment included psychiatric symptoms, pain, sleep disturbance, and quality of life, assessed using self‐completed questionnaires or face‐to‐face assessment. Both cohorts were analyzed independently using Cluster, and Bayesian multiple mixed model phenotype analyses to investigate the relationship between non‐motor symptoms and determine evidence of phenotypic subgroups. Results: Independent cluster analysis of the two cohorts suggests two predominant phenotypic subgroups, one consisting of approximately a third of participants in both cohorts, experiencing increased levels of depression, anxiety, sleep impairment, and pain catastrophizing, as well as, decreased quality of life. The Bayesian approach reinforced this with the primary axis, which explained the majority of the variance, in each cohort being associated with psychiatric symptomology, and also sleep impairment and pain catastrophizing in the Dystonia Wales cohort. Conclusions: Non‐motor symptoms accompanying AOIFCD parse into two predominant phenotypic sub‐groups, with differences in psychiatric symptoms, pain catastrophizing, sleep quality, and quality of life. Improved understanding of these symptom groups will enable better targeted pathophysiological investigation and future therapeutic intervention.
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spelling pubmed-84137612021-09-07 Non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia Wadon, Megan E. Bailey, Grace A. Yilmaz, Zehra Hubbard, Emily AlSaeed, Meshari Robinson, Amy McLauchlan, Duncan Barbano, Richard L. Marsh, Laura Factor, Stewart A. Fox, Susan H. Adler, Charles H. Rodriguez, Ramon L. Comella, Cynthia L. Reich, Stephen G. Severt, William L. Goetz, Christopher G. Perlmutter, Joel S. Jinnah, Hyder A. Harding, Katharine E. Sandor, Cynthia Peall, Kathryn J. Brain Behav Original Research Background: Non‐motor symptoms are well established phenotypic components of adult‐onset idiopathic, isolated, focal cervical dystonia (AOIFCD). However, improved understanding of their clinical heterogeneity is needed to better target therapeutic intervention. Here, we examine non‐motor phenotypic features to identify possible AOIFCD subgroups. Methods: Participants diagnosed with AOIFCD were recruited via specialist neurology clinics (dystonia wales: n = 114, dystonia coalition: n = 183). Non‐motor assessment included psychiatric symptoms, pain, sleep disturbance, and quality of life, assessed using self‐completed questionnaires or face‐to‐face assessment. Both cohorts were analyzed independently using Cluster, and Bayesian multiple mixed model phenotype analyses to investigate the relationship between non‐motor symptoms and determine evidence of phenotypic subgroups. Results: Independent cluster analysis of the two cohorts suggests two predominant phenotypic subgroups, one consisting of approximately a third of participants in both cohorts, experiencing increased levels of depression, anxiety, sleep impairment, and pain catastrophizing, as well as, decreased quality of life. The Bayesian approach reinforced this with the primary axis, which explained the majority of the variance, in each cohort being associated with psychiatric symptomology, and also sleep impairment and pain catastrophizing in the Dystonia Wales cohort. Conclusions: Non‐motor symptoms accompanying AOIFCD parse into two predominant phenotypic sub‐groups, with differences in psychiatric symptoms, pain catastrophizing, sleep quality, and quality of life. Improved understanding of these symptom groups will enable better targeted pathophysiological investigation and future therapeutic intervention. John Wiley and Sons Inc. 2021-07-21 /pmc/articles/PMC8413761/ /pubmed/34291595 http://dx.doi.org/10.1002/brb3.2292 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Wadon, Megan E.
Bailey, Grace A.
Yilmaz, Zehra
Hubbard, Emily
AlSaeed, Meshari
Robinson, Amy
McLauchlan, Duncan
Barbano, Richard L.
Marsh, Laura
Factor, Stewart A.
Fox, Susan H.
Adler, Charles H.
Rodriguez, Ramon L.
Comella, Cynthia L.
Reich, Stephen G.
Severt, William L.
Goetz, Christopher G.
Perlmutter, Joel S.
Jinnah, Hyder A.
Harding, Katharine E.
Sandor, Cynthia
Peall, Kathryn J.
Non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia
title Non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia
title_full Non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia
title_fullStr Non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia
title_full_unstemmed Non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia
title_short Non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia
title_sort non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413761/
https://www.ncbi.nlm.nih.gov/pubmed/34291595
http://dx.doi.org/10.1002/brb3.2292
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