TY - JOUR
T1 - Predictive modeling of spread in adult-onset isolated dystonia
T2 - Key properties and effect of tremor inclusion
AU - Wang, Meng
AU - Sajobi, Tolulope
AU - Morgante, Francesca
AU - Adler, Charles
AU - Agarwal, Pinky
AU - Bäumer, Tobias
AU - Berardelli, Alfredo
AU - Berman, Brian D.
AU - Blumin, Joel
AU - Borsche, Max
AU - Brashear, Allison
AU - Deik, Andres
AU - Duque, Kevin
AU - Espay, Alberto J.
AU - Ferrazzano, Gina
AU - Feuerstein, Jeanne
AU - Fox, Susan
AU - Frank, Samuel
AU - Hallett, Mark
AU - Jankovic, Joseph
AU - LeDoux, Mark S.
AU - Leegwater-Kim, Julie
AU - Mahajan, Abhimanyu
AU - Malaty, Irene A.
AU - Ondo, William
AU - Pantelyat, Alexander
AU - Pirio-Richardson, Sarah
AU - Roze, Emmanuel
AU - Saunders-Pullman, Rachel
AU - Suchowersky, Oksana
AU - Truong, Daniel
AU - Vidailhet, Marie
AU - Shukla, Aparna Wagle
AU - Perlmutter, Joel S.
AU - Jinnah, Hyder A.
AU - Martino, Davide
N1 - Publisher Copyright:
© 2021 European Academy of Neurology
PY - 2021/12
Y1 - 2021/12
N2 - Background and purpose: Several clinical and demographic factors relate to anatomic spread of adult-onset isolated dystonia, but a predictive model is still lacking. The aims of this study were: (i) to develop and validate a predictive model of anatomic spread of adult-onset isolated dystonia; and (ii) to evaluate whether presence of tremor associated with dystonia influences model predictions of spread. Methods: Adult-onset isolated dystonia participants with focal onset from the Dystonia Coalition Natural History Project database were included. We developed two prediction models, one with dystonia as sole disease manifestation (“dystonia-only”) and one accepting dystonia OR tremor in any body part as disease manifestations (“dystonia OR tremor”). Demographic and clinical predictors were selected based on previous evidence, clinical plausibility of association with spread, or both. We used logistic regressions and evaluated model discrimination and calibration. Internal validation was carried out based on bootstrapping. Results: Both predictive models showed an area under the curve of 0.65 (95% confidence intervals 0.62–0.70 and 0.62–0.69, respectively) and good calibration after internal validation. In both models, onset of dystonia in body regions other than the neck, older age, depression and history of neck trauma were predictors of spread. Conclusions: This predictive modeling of spread in adult-onset isolated dystonia based on accessible predictors (demographic and clinical) can be easily implemented to inform individuals’ risk of spread. Because tremor did not influence prediction of spread, our results support the argument that tremor is a part of the dystonia syndrome, and not an independent or coincidental disorder.
AB - Background and purpose: Several clinical and demographic factors relate to anatomic spread of adult-onset isolated dystonia, but a predictive model is still lacking. The aims of this study were: (i) to develop and validate a predictive model of anatomic spread of adult-onset isolated dystonia; and (ii) to evaluate whether presence of tremor associated with dystonia influences model predictions of spread. Methods: Adult-onset isolated dystonia participants with focal onset from the Dystonia Coalition Natural History Project database were included. We developed two prediction models, one with dystonia as sole disease manifestation (“dystonia-only”) and one accepting dystonia OR tremor in any body part as disease manifestations (“dystonia OR tremor”). Demographic and clinical predictors were selected based on previous evidence, clinical plausibility of association with spread, or both. We used logistic regressions and evaluated model discrimination and calibration. Internal validation was carried out based on bootstrapping. Results: Both predictive models showed an area under the curve of 0.65 (95% confidence intervals 0.62–0.70 and 0.62–0.69, respectively) and good calibration after internal validation. In both models, onset of dystonia in body regions other than the neck, older age, depression and history of neck trauma were predictors of spread. Conclusions: This predictive modeling of spread in adult-onset isolated dystonia based on accessible predictors (demographic and clinical) can be easily implemented to inform individuals’ risk of spread. Because tremor did not influence prediction of spread, our results support the argument that tremor is a part of the dystonia syndrome, and not an independent or coincidental disorder.
KW - isolated dystonia
KW - neurological diseases
KW - predictive models
KW - spread
KW - tremor
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U2 - 10.1111/ene.15031
DO - 10.1111/ene.15031
M3 - Article
C2 - 34296504
AN - SCOPUS:85111723355
SN - 1351-5101
VL - 28
SP - 3999
EP - 4009
JO - European Journal of Neurology
JF - European Journal of Neurology
IS - 12
ER -