Elevated cerebrospinal fluid uric acid during relapse of neuromyelitis optica spectrum disorders

被引:16
|
作者
Shu, Yaqing [1 ]
Li, Haiyan [1 ]
Zhang, Lei [2 ]
Wang, Yuge [1 ]
Long, Youming [1 ,3 ]
Li, Rui [1 ]
Qiu, Wei [1 ]
Lu, Zhengqi [1 ]
Hu, Xueqiang [1 ]
Peng, Fuhua [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Neurol, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Neurol, Zhuhai, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 2, Dept Neurol, Guangzhou, Guangdong, Peoples R China
来源
BRAIN AND BEHAVIOR | 2017年 / 7卷 / 01期
基金
中国国家自然科学基金;
关键词
metabolism; excitotoxicity; neuroimmunology; MULTIPLE-SCLEROSIS; OXIDATIVE STRESS; NEUROLOGICAL DISEASES; ASCORBIC-ACID; DANGER SIGNAL; HYPOXANTHINE; XANTHINE; BLOOD; EXCITOTOXICITY; ANTIOXIDANT;
D O I
10.1002/brb3.584
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
IntroductionPrevious studies have shown that serum uric acid (UA) modulates outcomes of neurological diseases, although little is known about cerebrospinal fluid (CSF) UA levels in neuromyelitis optica spectrum disorders (NMOSDs). MethodsCerebrospinal fluid and serum UA levels were measured in samples from 68 patients, including NMOSDs during relapse (n=38) and controls with noninflammatory and non-neurodegenerative diseases (CTLs, n=30). Correlation analysis was performed between CSF UA and clinical characteristics, serum UA, and blood-brain barrier integrity in NMOSDs. ResultsCerebrospinal fluid UA levels in NMOSDs were significantly higher than in CTLs (p=.002), while serum UA differences between NMOSDs and CTLs were not statistically significant. In NMOSDs, CSF UA levels were significantly higher in patients with an impaired blood-brain barrier than in patients with an intact one (p<.001), and significantly higher in longer disease duration than in shorter disease duration patients (p=.002). CSF UA levels were also significantly higher in active patients upon MRI than in inactive patients (p<.001), and significantly higher in patients with brain lesions than without brain lesions (p=.024). CSF UA was significantly associated with the serum UA levels (r=.454, p=.002), disease duration (r=.383, p=.018), and blood-brain barrier index (r=.805, p<.001), but did not correlate with age, gender, annualized relapse rate, duration, or severity of NMOSD. Multiple regression analysis demonstrated that CSF UA was independent of the blood-brain barrier index (=.765, p<.001) and serum UA levels (=.01, p=.019) in NMOSDs. ConclusionsCerebrospinal fluid UA levels were elevated in NMOSD patients during relapse, and were likely modified by serum UA levels and blood-brain barrier integrity.
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页数:7
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