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Expanding clinical profiles and prognostic markers in stiff person syndrome spectrum disorders.
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- Author(s): Wang Y;Wang Y;Wang Y; Hu C; Hu C; Aljarallah S; Aljarallah S; Reyes Mantilla M; Reyes Mantilla M; Mukharesh L; Mukharesh L; Simpson A; Simpson A; Roy S; Roy S; Harrison K; Harrison K; Shoemaker T; Shoemaker T; Comisac M; Comisac M; Balshi A; Balshi A; Obando D; Obando D; Maldonado DAP; Maldonado DAP; Koshorek J; Koshorek J; Snoops S; Snoops S; Fitzgerald KC; Fitzgerald KC; Fitzgerald KC; Newsome SD; Newsome SD
- Source:Journal of neurology [J Neurol] 2024 Apr; Vol. 271 (4), pp. 1861-1872. Date of Electronic Publication: 2023 Dec 11.
- Publication Type:Observational Study; Journal Article
- Language:English
- Additional Information
- Source: Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0423161 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1459 (Electronic) Linking ISSN: 03405354 NLM ISO Abbreviation: J Neurol Subsets: MEDLINE
- Publication Information: Original Publication: Berlin ; New York, Springer-Verlag
- Subject Terms:
- Abstract: Objective: To describe the clinical features of a cohort of individuals with stiff person syndrome spectrum disorders (SPSD) and identify potential early predictors of future disability.
Background: There is a need to better understand the full spectrum of clinical and paraclinical features and long-term impact of SPSD.
Design/methods: Observational study from 1997 to 2022 at Johns Hopkins. Clinical phenotypes included classic SPS, partial SPS (limb or trunk limited), SPS-plus (classic features plus cerebellar/brainstem involvement), and progressive encephalomyelitis with rigidity and myoclonus (PERM). Outcome measures were modified Rankin scale (mRS) and use of assistive device for ambulation. Multivariate logistic regression was used to assess significant predictors of outcomes.
Results: Cohort included 227 individuals with SPSD with mean follow-up of 10 years; 154 classic, 48 SPS-plus, 16 PERM, and 9 partial. Mean age at symptom onset was 42.9 ± 14.1 years, majority were white (69.2%) and female (75.8%). Median time to diagnosis was 36.2 months (longest for SPS-plus and PERM) and 61.2% were initially misdiagnosed. Most had systemic co-morbidities and required assistive devices for ambulation. Female sex (OR 2.08; CI 1.06-4.11) and initial brainstem/cerebellar involvement (OR 4.41; CI 1.63-14.33) predicted worse outcome by mRS. Older age at symptom onset (OR 1.04; CI 1.01-1.06), female sex (OR 1.99; CI 1.01-4.01), Black race (OR 4.14; CI 1.79-10.63), and initial brainstem/cerebellar involvement (OR 2.44; CI 1.04-7.19) predicted worse outcome by use of assistive device. Early implementation of immunotherapy was associated with better outcomes by either mRS (OR 0.45; CI 0.22-0.92) or use of assistive device (OR 0.79; CI 0.66-0.94).
Conclusions: We present the expanding phenotypic variability of this rare spectrum of disorders and highlight potential predictors of future disability.
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- Publication Date: Date Created: 20231211 Date Completed: 20240328 Latest Revision: 20240517
- Publication Date: 20240517
- Accession Number: PMC10973082
- Accession Number: 10.1007/s00415-023-12123-0
- Accession Number: 38078976
- Source:
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