Clinical and demographic characteristics related to onset site and spread of cervical dystonia

ABSTRACT Background Clinical characteristics of isolated idiopathic cervical dystonia such as onset site and spread to and from additional body regions have been addressed in single‐site studies with limited data and incomplete or variable dissociation of focal and segmental subtypes. The objectives...

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Published inMovement disorders Vol. 31; no. 12; pp. 1874 - 1882
Main Authors Norris, Scott A., Jinnah, H. A., Espay, Alberto J., Klein, Christine, Brüggemann, Norbert, Barbano, Richard L., Malaty, Irene Andonia C., Rodriguez, Ramon L., Vidailhet, Marie, Roze, Emmanuel, Reich, Stephen G., Berman, Brian D., LeDoux, Mark S., Richardson, Sarah Pirio, Agarwal, Pinky, Mari, Zoltan, Ondo, William G., Shih, Ludy C., Fox, Susan H., Berardelli, Alfredo, Testa, Claudia M., Cheng, Florence Ching-Fen, Truong, Daniel, Nahab, Fatta B., Xie, Tao, Hallett, Mark, Rosen, Ami R., Wright, Laura J., Perlmutter, Joel S.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.12.2016
Wiley Subscription Services, Inc
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Summary:ABSTRACT Background Clinical characteristics of isolated idiopathic cervical dystonia such as onset site and spread to and from additional body regions have been addressed in single‐site studies with limited data and incomplete or variable dissociation of focal and segmental subtypes. The objectives of this study were to characterize the clinical characteristics and demographics of isolated idiopathic cervical dystonia in the largest standardized multicenter cohort. Methods The Dystonia Coalition, through a consortium of 37 recruiting sites in North America, Europe, and Australia, recruited 1477 participants with focal (60.7%) or segmental (39.3%) cervical dystonia on examination. Clinical and demographic characteristics were evaluated in terms of the body region of dystonia onset and spread. Results Site of dystonia onset was: (1) focal neck only (78.5%), (2) focal onset elsewhere with later segmental spread to neck (13.3%), and (3) segmental onset with initial neck involvement (8.2%). Frequency of spread from focal cervical to segmental dystonia (22.8%) was consistent with prior reports, but frequency of segmental onset with initial neck involvement was substantially higher than the 3% previously reported. Cervical dystonia with focal neck onset, more than other subtypes, was associated with spread and tremor of any type. Sensory tricks were less frequent in cervical dystonia with segmental components, and segmental cervical onset occurred at an older age. Conclusions Subgroups had modest but significant differences in the clinical characteristics that may represent different clinical entities or pathophysiologic subtypes. These findings are critical for design and implementation of studies to describe, treat, or modify disease progression in idiopathic isolated cervical dystonia. © 2016 International Parkinson and Movement Disorder Society.
Bibliography:NCATS
ark:/67375/WNG-FGRHC180-R
Rare Diseases Research (ORDR)
istex:9C8CA6938C1E471BC6375434350AEBA4F752FEF8
American Parkinson Disease Association (APDA) Center for Advanced PD Research at Washington University
ArticleID:MDS26817
Rare Diseases Clinical Research Network (RDCRN)
NIH NINDS - No. NS065701; No. NS058714; No. NS41509; No. NS075321
Barnes-Jewish Hospital Foundation (Elliot Stein Family Fund and the Parkinson Disease Research Fund)
National Institute of Neurological Diseases and Stroke (NINDS)
Greater St. Louis Chapter of the APDA, McDonnell Center for Higher Brain Function
Dystonia Coalition - No. U54NS065701; No. U54TR001456
Dystonia Coalition (U54NS065701 and U54TR001456), a part of the Rare Diseases Clinical Research Network (RDCRN), an initiative of the Office of Rare Diseases Research (ORDR), NCATS. The Dystonia Coalition is funded through collaboration between NCATS and the National Institute of Neurological Diseases and Stroke (NINDS). The study was also supported by grants from the NIH NINDS (NS065701, NS058714, NS41509, NS075321), Murphy Fund, American Parkinson Disease Association (APDA) Center for Advanced PD Research at Washington University; Greater St. Louis Chapter of the APDA, McDonnell Center for Higher Brain Function; and the Barnes‐Jewish Hospital Foundation (Elliot Stein Family Fund and the Parkinson Disease Research Fund).
This article was published online on 18 October 2016. An error in the affiliation is subsequently identified and corrected. This notice is included in the online and print versions to indicate that both have been corrected on 16 November 2016.
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SourceType-Scholarly Journals-1
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ISSN:0885-3185
1531-8257
DOI:10.1002/mds.26817