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Prognostic Role of Serum Levels of Uric Acid in Amyotrophic Lateral Sclerosisopen access

Authors
Oh, Seong-ilBaek, SoojeongPark, Jin-SeokPiao, LiyingOh, Ki-WookKim, Seung Hyun
Issue Date
Oct-2015
Publisher
KOREAN NEUROLOGICAL ASSOC
Keywords
amyotrophic lateral sclerosis; uric acid; survival; oxidative stress; prognosis
Citation
JOURNAL OF CLINICAL NEUROLOGY, v.11, no.4, pp.376 - 382
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF CLINICAL NEUROLOGY
Volume
11
Number
4
Start Page
376
End Page
382
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/156245
DOI
10.3988/jcn.2015.11.4.376
ISSN
1738-6586
Abstract
Background and Purpose It has been suggested that oxidative stress is one of the pathomechanisms underlying amyotrophic lateral sclerosis (ALS), and thus antioxidants such as uric acid (UA) that could reduce oxidative stress might be beneficial in the prevention or treatment of this disease. The objective of this study was to prospectively investigate serum UA levels in Korean ALS patients and to relate them to disease progression. Methods ALS patients and healthy controls who were individually well-matched for sex, age, and body mass index (BMI) underwent blood testing for serum UA levels, and analyzed whether UA levels were correlated with the disease status of the patients, as defined by the ALS Functional Rating Scale-Revised (ALSFRS-R). Results The study included 136 ALS patients and 136 matched controls. The UA level was lower in the ALS patients (4.50 +/- 1.17 mg/dL, mean +/- SD) than in the controls (5.51 +/- 1.22 mg/dL; p<0.001). Among the ALS patients, the level of UA acid was inversely correlated with the rate of disease progression (decrease in ALSFRS-R score). Kaplan-Meier analysis revealed that a better survival rate was more strongly correlated with top-tertile levels of serum UA than with bottom-tertile levels (log-rank test: p=0.035). Conclusions ALS patients had lower serum UA levels than did healthy individuals. UA levels in ALS were negatively correlated with the rate of disease progression and positively associated with survival, suggesting that UA levels contribute to the progression of ALS. UA levels could be considered a biomarker of disease progression in the early phase in ALS patients.
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