Botulinum toxin for hereditary spastic paraplegia: effects on motor and non-motor manifestations
ABSTRACT Motor and non-motor manifestations are common and disabling features of hereditary spastic paraplegia (HSP). Botulinum toxin type A (Btx-A) is considered effective for spasticity and may improve gait in these patients. Little is known about the effects of Btx-A on non-motor symptoms in HSP...
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Published in: | Arquivos de neuro-psiquiatria Vol. 76; no. 3; pp. 183 - 188 |
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Main Authors: | , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
Thieme Revinter Publicações Ltda
01-03-2018
Arquivos de Neuro-Psiquiatria Academia Brasileira de Neurologia - ABNEURO Academia Brasileira de Neurologia (ABNEURO) |
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Online Access: | Get full text |
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Summary: | ABSTRACT
Motor and non-motor manifestations are common and disabling features of hereditary spastic paraplegia (HSP). Botulinum toxin type A (Btx-A) is considered effective for spasticity and may improve gait in these patients. Little is known about the effects of Btx-A on non-motor symptoms in HSP patients.
Objective
To assess the efficacy of Btx-A on motor and non-motor manifestations in HSP patients.
Methods
Thirty-three adult patients with a clinical and molecular diagnosis of HSP were evaluated before and after Btx-A injections.
Results
Mean age was 41.7 ± 13.6 years and there were 18 women. Most patients had a pure phenotype and
SPG4
was the most frequent genotype. The Btx-A injections resulted in a decrease in spasticity at the adductor muscles, and no other motor measure was significantly modified. In contrast, fatigue scores were significantly reduced after Btx-A injections.
Conclusion
Btx-A injections resulted in no significant functional motor improvement for HSP, but fatigue improved after treatment. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0004-282X 1678-4227 1678-4227 |
DOI: | 10.1590/0004-282X20180013 |