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Cited 2 time in webofscience Cited 2 time in scopus
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Hereditary Spastic Paraplegia in Koreans: Clinical Characteristics and Factors Influencing the Disease Severityopen access

Authors
Do, JG[Do, Jong Geol]Kim, BJ[Kim, Byoung Joon]Kim, NS[Kim, Nam-Soon]Sung, DH[Sung, Duk Hyun]
Issue Date
May-2022
Publisher
KOREAN NEUROLOGICAL ASSOC
Keywords
hereditary spastic paraplegia; spastic paraplegia; locomotion; Korea
Citation
JOURNAL OF CLINICAL NEUROLOGY, v.18, no.3, pp.343 - 350
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF CLINICAL NEUROLOGY
Volume
18
Number
3
Start Page
343
End Page
350
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/97751
DOI
10.3988/jcn.2022.18.3.343
ISSN
1738-6586
Abstract
Background and Purpose Hereditary spastic paraplegia (HSP) progresses over time and is associated with locomotive dysfunction. Understanding the factors affecting disease severity and locomotive function is important in HSP. This study investigated the factors influencing disease severity and ambulation status of HSP. Methods We consecutively enrolled 109 Korean patients (64 males, and 45 females)from 84 families with a clinical diagnosis of HSP. HSP was primarily diagnosed based on clinical criteria including clinical findings, family history, and supported by genetic studies. Epidemiological and clinical features of the patients were analyzed, and the Spastic Paraplegia Rating Scale (SPRS) score and ambulatory status were used to evaluate disease severity. Results Ninety-two (84.4%) patients had pure HSP, and 55 (50.4%) had a dominant family history. Thirty-one (28.4%) patients required a mobility aid for locomotion. A Kaplan-Meier analysis showed that HSP patients lost their independent gait ability after a median disease duration of 34 years. Those with an age at onset of <= 18 years had a longer median independent walking time. Pure HSP is characterized by predominant bilateral lower extremity weakness and spasticity, whereas complicated HSP presents more complex neurological findings such as ocular and bulbar symptoms, ataxia, and cognitive impairment. Complicated HSP was significantly correlated with the SPRS mobility score (beta=3.70, 95% confidence interval=0.45-6.94). The age at onset and disease duration were significantly correlated with disease severity, and they were significant predictors of the use of a mobility aid (p<0.05). Conclusions These findings suggest that a later age at onset and longer disease duration are significant factors affecting the disease severity and ambulatory function in patients with HSP. These findings can help clinicians to identify subjects at risk of locomotive impairment.
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