Serum uric acid levels in patients with myasthenia gravis are inversely correlated with disability

被引:9
作者
Yang, Dehao [1 ]
Weng, Yiyun [1 ]
Lin, Haihua [2 ]
Xie, Feiyan [3 ]
Yin, Fang [5 ]
Lou, Kangliang [5 ]
Zhou, Xuan [5 ]
Han, Yixiang [4 ]
Li, Xiang [1 ]
Zhang, Xu [1 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 1, Dept Neurol, Wenzhou 325000, Peoples R China
[2] Wenzhou Med Univ, Affiliated Hosp 1, Dept Gastroenterol, Wenzhou 325000, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp 1, Dept Surg Oncol, Wenzhou 325000, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 1, Dept Lab Internal Med, Wenzhou 325000, Peoples R China
[5] Wenzhou Med Univ, Sch Clin Med Sci 1, Wenzhou 325000, Peoples R China
关键词
disability; myasthenia gravis; uric acid; MULTIPLE-SCLEROSIS; OXIDATIVE STRESS; PEROXYNITRITE; SCAVENGER; DISEASES; THERAPY; DAMAGE;
D O I
10.1097/WNR.0000000000000535
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Uric acid (UA), the final product of purine metabolism, has been reported to be reduced in patients with various neurological disorders and is considered to be a possible indicator for monitoring the disability and progression of multiple sclerosis. However, it remains unclear whether there is a close relationship between UA and myasthenia gravis (MG), or whether UA is primarily deficient or secondarily reduced because of its peroxynitrite scavenging activity. We investigated the correlation between serum UA levels and the clinical characteristics of MG. We assessed 338 serum UA levels obtained in 135 patients with MG, 47 patients with multiple sclerosis, and 156 healthy controls. In addition, we compared serum UA levels when MG patients were stratified according to disease activity and classifications performed by the Myasthenia Gravis Foundation of America, age of onset, duration, and thymus histology (by means of MRI or computed tomography). MG patients had significantly lower serum UA levels than the controls (P<0.001). Moreover, UA levels in patients with MG were inversely correlated with disease activity and disease progression (P=0.013). However, UA levels did not correlate significantly with disease duration, age of onset, and thymus histology. Our findings suggest that serum level of UA was reduced in patients with MG and serum UA might be considered a surrogate biomarker of MG disability and progression.
引用
收藏
页码:301 / 305
页数:5
相关论文
共 23 条
[1]  
[Anonymous], INDIAN J PHARM
[2]   Hispidin produced from Phellinus linteus protects against peroxynitrite-mediated DNA damage and hydroxyl radical generation [J].
Chen, Wei ;
Feng, Lina ;
Huang, Zhaoyi ;
Su, Hongming .
CHEMICO-BIOLOGICAL INTERACTIONS, 2012, 199 (03) :137-142
[3]   URIC-ACID IRON-ION COMPLEXES - A NEW ASPECT OF THE ANTIOXIDANT FUNCTIONS OF URIC-ACID [J].
DAVIES, KJA ;
SEVANIAN, A ;
MUAKKASSAHKELLY, SF ;
HOCHSTEIN, P .
BIOCHEMICAL JOURNAL, 1986, 235 (03) :747-754
[4]   MEDICAL PROGRESS - MYASTHENIA-GRAVIS [J].
DRACHMAN, DB .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (25) :1797-1810
[5]   Uric acid and oxidative stress [J].
Glantzounis, GK ;
Tsimoyiannis, EC ;
Kappas, AM ;
Galaris, DA .
CURRENT PHARMACEUTICAL DESIGN, 2005, 11 (32) :4145-4151
[6]   Uric acid, a natural scavenger of peroxynitrite, in experimental allergic encephalomyelitis and multiple sclerosis [J].
Hooper, DC ;
Spitsin, S ;
Kean, RB ;
Champion, JM ;
Dickson, GM ;
Chaudhry, I ;
Koprowski, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (02) :675-680
[7]   Uric acid, a peroxynitrite scavenger, inhibits CNS inflammation, blood-CNS barrier permeability changes, and tissue damage in a mouse model of multiple sclerosis [J].
Hooper, DC ;
Scott, GS ;
Zborek, A ;
Mikheeva, T ;
Kean, RB ;
Koprowski, H ;
Spitsin, SV .
FASEB JOURNAL, 2000, 14 (05) :691-698
[8]   Myasthenia gravis: Recommendations for clinical research standards (Reprinted from Neurology, vol 55, pg 16-23, 2000) [J].
Jaretzki, A ;
Barohn, RJ ;
Ernstoff, RM ;
Kaminski, HJ ;
Keesey, JC ;
Penn, AS ;
Sanders, DB .
ANNALS OF THORACIC SURGERY, 2000, 70 (01) :327-334
[9]  
Koprowski H, 2001, ANN NEUROL, V49, P139, DOI 10.1002/1531-8249(200101)49:1<139::AID-ANA28>3.0.CO
[10]  
2-A