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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.
Afiliação
  • Wadon ME; Neuroscience and Mental Health Research Institute, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Maindy Road, Cardiff, CF24 4HQ, UK.
  • Bailey GA; Neuroscience and Mental Health Research Institute, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Maindy Road, Cardiff, CF24 4HQ, UK.
  • Yilmaz Z; Neuroscience and Mental Health Research Institute, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Maindy Road, Cardiff, CF24 4HQ, UK.
  • Hubbard E; Institute of Neurology, University College London, Queen Square, London, WC1N 3BG, UK.
  • AlSaeed M; School of Medicine, Cardiff University, Heath Park Campus, Cardiff, CF14 4YS, UK.
  • Robinson A; School of Medicine, Cardiff University, Heath Park Campus, Cardiff, CF14 4YS, UK.
  • McLauchlan D; Division of Neurology, University of British Columbia, Wesbrook Mall, Vancouver, British Columbia, V6T 2B5, Canada.
  • Barbano RL; School of Medicine, Cardiff University, Heath Park Campus, Cardiff, CF14 4YS, UK.
  • Marsh L; Neuroscience and Mental Health Research Institute, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Maindy Road, Cardiff, CF24 4HQ, UK.
  • Factor SA; Department of Neurology, University of Rochester, Elmwood Avenue, Rochester, New York, NY 14642, USA.
  • Fox SH; Menninger Department of Psychiatry, Baylor College of Medicine, Butler Boulevard, Houston, Texas, 77030, USA.
  • Adler CH; Departments of Neurology & Human Genetics, Emory University, Woodruff Circle, Atlanta, Georgia, 30322, USA.
  • Rodriguez RL; Edmond J Safra Program in Parkinson Disease, Movement Disorder Clinic, Toronto Western Hospital, Bathurst Street, Toronto, Ontario, M5T 2S8, Canada.
  • Comella CL; Department of Medicine, University of Toronto, Queen's Park Crescent West, Toronto, Ontario, M5S 3H2, Canada.
  • Reich SG; The Parkinson's Disease and Movement Disorders Center, Mayo Clinic, Department of Neurology, East Shea Boulevard, Scottsdale, Arizona, 85259, USA.
  • Severt WL; Department of Neurology, University of Florida, Newell Drive, Gainesville, Florida, 32611, USA.
  • Goetz CG; Department of Neurological Sciences, Rush University Medical Center, West Harrison Street, Chicago, Illinois, 60612, USA.
  • Perlmutter JS; Department of Neurology, University of Maryland School of Medicine, south Paca Street, Baltimore, Maryland, 21201, USA.
  • Jinnah HA; Beth Israel Medical Center, First Avenue, New York, New York, 10003, USA.
  • Harding KE; Department of Neurological Sciences, Rush University Medical Center, West Harrison Street, Chicago, Illinois, 60612, USA.
  • Sandor C; Neurology, Radiology, Neuroscience, Physical Therapy and Occupational Therapy, Washington University School of Medicine, South Euclid Avenue, St. Louis, Missouri, 63110, USA.
  • Peall KJ; Departments of Neurology & Human Genetics, Emory University, Woodruff Circle, Atlanta, Georgia, 30322, USA.
Brain Behav ; 11(8): e2292, 2021 08.
Article em En | MEDLINE | ID: mdl-34291595
ABSTRACT

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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Torcicolo / Distúrbios Distônicos Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Torcicolo / Distúrbios Distônicos Idioma: En Ano de publicação: 2021 Tipo de documento: Article