TY - JOUR
T1 - Low uric acid levels in serum of patients with ALS
T2 - Further evidence for oxidative stress?
AU - Keizman, D.
AU - Ish-Shalom, M.
AU - Berliner, S.
AU - Maimon, N.
AU - Vered, Y.
AU - Artamonov, I.
AU - Tsehori, J.
AU - Nefussy, B.
AU - Drory, V. E.
PY - 2009/10/15
Y1 - 2009/10/15
N2 - Background: The exact cause of amyotrophic lateral sclerosis (ALS) is unknown. Oxidative stress is one of the factors implicated in the etiology of ALS as well as in that of other neurodegenerative diseases. Uric acid is an important natural antioxidant that may reduce oxidative stress. The objective of this study was to prospectively determine the serum uric acid levels in ALS patients and allegedly healthy individuals and to correlate those values with measures of ALS disease progression among the patients. Methods: The ALS patients and well-matched controls underwent blood tests for serum uric acid levels which were then correlated with the patients' disability status, as expressed by the ALS Functional Rating Scale (ALSFRS-R). Results: Eighty-six ALS patients and 86 well-matched controls participated. The ALS patients' mean ± SD uric acid level was significantly lower (4.78 ± 1.3 mg/dl) than that of the controls (5.76 ± 1.26 mg/dl) (p < 0.0001). The findings were similar for a second examination performed after an interval of at least 6 months. There was a correlation between the relative decrease of serum uric acid levels among patients (the difference between the patients' level and the controls' level) and the rate of disease progression (ALSFRS-R decline) (p < 0.0001, r = 0.624). Conclusions: ALS patients had lower serum uric acid levels than healthy individuals. The decreased uric acid levels were correlated to the rate of disease progression (ALSFRS-R decline), further demonstrating the possible role of oxidative stress in the induction and propagation of the disease.
AB - Background: The exact cause of amyotrophic lateral sclerosis (ALS) is unknown. Oxidative stress is one of the factors implicated in the etiology of ALS as well as in that of other neurodegenerative diseases. Uric acid is an important natural antioxidant that may reduce oxidative stress. The objective of this study was to prospectively determine the serum uric acid levels in ALS patients and allegedly healthy individuals and to correlate those values with measures of ALS disease progression among the patients. Methods: The ALS patients and well-matched controls underwent blood tests for serum uric acid levels which were then correlated with the patients' disability status, as expressed by the ALS Functional Rating Scale (ALSFRS-R). Results: Eighty-six ALS patients and 86 well-matched controls participated. The ALS patients' mean ± SD uric acid level was significantly lower (4.78 ± 1.3 mg/dl) than that of the controls (5.76 ± 1.26 mg/dl) (p < 0.0001). The findings were similar for a second examination performed after an interval of at least 6 months. There was a correlation between the relative decrease of serum uric acid levels among patients (the difference between the patients' level and the controls' level) and the rate of disease progression (ALSFRS-R decline) (p < 0.0001, r = 0.624). Conclusions: ALS patients had lower serum uric acid levels than healthy individuals. The decreased uric acid levels were correlated to the rate of disease progression (ALSFRS-R decline), further demonstrating the possible role of oxidative stress in the induction and propagation of the disease.
KW - Amyotrophic lateral sclerosis
KW - Neurodegeneration
KW - Oxidative stress
KW - Uric acid
UR - http://www.scopus.com/inward/record.url?scp=69549116245&partnerID=8YFLogxK
U2 - 10.1016/j.jns.2009.06.002
DO - 10.1016/j.jns.2009.06.002
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C2 - 19552925
AN - SCOPUS:69549116245
VL - 285
SP - 95
EP - 99
JO - Journal of the Neurological Sciences
JF - Journal of the Neurological Sciences
SN - 0022-510X
IS - 1-2
ER -