TY - JOUR
T1 - Psychiatric associations of adult-onset focal dystonia phenotypes
AU - Berman, Brian D.
AU - Junker, Johanna
AU - Shelton, Erika
AU - Sillau, Stefan H.
AU - Jinnah, H. A.
AU - Perlmutter, Joel S.
AU - Espay, Alberto J.
AU - Jankovic, Joseph
AU - Vidailhet, Marie
AU - Bonnet, Cecilia
AU - Ondo, William G.
AU - Malaty, Irene A.
AU - Rodríguez, Ramón
AU - McDonald, William M.
AU - Marsh, Laura
AU - Zurowski, Mateusz
AU - Bäumer, Tobias
AU - Brüggemann, Norbert
N1 - Funding Information:
Funding This work was supported in part by grants to the Dystonia coalition (U54Ns065701/TR001456), a consortium of the Rare Diseases clinical Research Network (RDcRN) that is supported by the Office of Rare Diseases Research (ORDR) at the National center for advancing clinical and Translational studies (NcaTs) in collaboration with the National Institute for Neurological Diseases and stroke (NINDs). Competing interests None declared. Patient consent all patients consent with local IRB-approved consent forms.
Funding Information:
1Department of Neurology, University of colorado anschutz Medical campus, aurora, colorado, Usa 2Neurology section, Va eastern colorado health care system, Denver, colorado, Usa 3Institute of Neurogenetics, University of Luebeck, Luebeck, Germany 4Department of Neurology, University of Luebeck, Luebeck, Germany 5Department of Neurology, emory University, atlanta, Georgia, Usa 6Departments of Neurology, Radiology, Neuroscience, physical Therapy and Occupational Therapy, Washington University in saint Louis school of Medicine, saint Louis, Missouri, Usa 7Department of Neurology, University of cincinnati, cincinnati, Ohio, Usa 8Department of Neurology, Baylor college of Medicine, houston, Texas, Usa 9Département de neurologie, hôpital pitié-salpêtrière, assistance publique - hopitaux de paris, paris, France 10UpMc Univ paris 06, Inserm U1127, cNRs UMR 7225, UM 75, IcM, F-75013, sorbonne Universites, paris, France 11Department of Neurology, houston Methodist, houston, Texas, Usa 12Department of Neurology, center for Movement Disorders and Neurorestoration, University of Florida, Gainesville, Florida, Usa 13Department of Internal Medicine, University of central Florida, Orlando, Florida, Usa 14Department of psychiatry and Behavioral sciences, emory University, atlanta, Georgia, Usa 15Menninger Department of psychiatry, Baylor college of Medicine, houston, Texas, Usa 16Department of psychiatry, University of Toronto, Toronto, Ontario, canada 17Department of paediatric and adult Movement Disorders and Neuropsychiatry, Institute of Neurogenetics, Lübeck, Germany Acknowledgements This study was supported by a grant from the National Institutes of health (Dystonia coalition U54 Ns065701). We would like to thank Laura J Wright, Ma, for her assistance with accessing the Dystonia coalition database and ami R Rosen, Ms, for providing organisational support for the Dystonia coalition.
Publisher Copyright:
© article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. all rights reserved.
PY - 2017/7
Y1 - 2017/7
N2 - Background Depression and anxiety frequently accompany the motor manifestations of isolated adult-onset focal dystonias. Whether the body region affected when this type of dystonia first presents is associated with the severity of these neuropsychiatric symptoms is unknown. Objectives The aim of this study was to determine whether depression, anxiety and social anxiety vary by dystonia onset site and evaluate whether pain and dystonia severity account for any differences. Methods patients with isolated focal dystonia evaluated within 5 years from symptom onset, enrolled in the Natural history project of the Dystonia coalition, were included in the analysis. Individual onset sites were grouped into five body regions: cervical, laryngeal, limb, lower cranial and upper cranial. Neuropsychiatric symptoms were rated using the Beck Depression Inventory, hospital anxiety and Depression scale and Liebowitz social anxiety scale. pain was estimated using the 36-Item short Form survey. results Four hundred and seventy-eight subjects met our inclusion criteria. high levels of depression, anxiety and social anxiety occurred in all groups; however, the severity of anxiety and social anxiety symptoms varied by onset site group. The most pronounced differences were higher anxiety in cervical and laryngeal, lower anxiety in upper cranial and higher social anxiety in laryngeal. Increases in pain were associated with worse neuropsychiatric symptom scores within all groups. higher anxiety and social anxiety in laryngeal and lower anxiety in upper cranial persisted after correcting for pain and dystonia severity. Conclusion anxiety and social anxiety severity vary by onset site of focal dystonia, and this variation is not explained by differences in pain and dystonia severity.
AB - Background Depression and anxiety frequently accompany the motor manifestations of isolated adult-onset focal dystonias. Whether the body region affected when this type of dystonia first presents is associated with the severity of these neuropsychiatric symptoms is unknown. Objectives The aim of this study was to determine whether depression, anxiety and social anxiety vary by dystonia onset site and evaluate whether pain and dystonia severity account for any differences. Methods patients with isolated focal dystonia evaluated within 5 years from symptom onset, enrolled in the Natural history project of the Dystonia coalition, were included in the analysis. Individual onset sites were grouped into five body regions: cervical, laryngeal, limb, lower cranial and upper cranial. Neuropsychiatric symptoms were rated using the Beck Depression Inventory, hospital anxiety and Depression scale and Liebowitz social anxiety scale. pain was estimated using the 36-Item short Form survey. results Four hundred and seventy-eight subjects met our inclusion criteria. high levels of depression, anxiety and social anxiety occurred in all groups; however, the severity of anxiety and social anxiety symptoms varied by onset site group. The most pronounced differences were higher anxiety in cervical and laryngeal, lower anxiety in upper cranial and higher social anxiety in laryngeal. Increases in pain were associated with worse neuropsychiatric symptom scores within all groups. higher anxiety and social anxiety in laryngeal and lower anxiety in upper cranial persisted after correcting for pain and dystonia severity. Conclusion anxiety and social anxiety severity vary by onset site of focal dystonia, and this variation is not explained by differences in pain and dystonia severity.
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U2 - 10.1136/jnnp-2016-315461
DO - 10.1136/jnnp-2016-315461
M3 - Article
C2 - 28438790
AN - SCOPUS:85028947908
SN - 0022-3050
VL - 88
SP - 595
EP - 602
JO - Journal of Neurology, Neurosurgery and Psychiatry
JF - Journal of Neurology, Neurosurgery and Psychiatry
IS - 7
ER -