Andreadou Elisabeth, Nikolaou Chryssoula, Gournaras Filippos, Rentzos Michael, Boufidou Fotini, Tsoutsou Anthoussa, Zournas Christos, Zissimopoulos Vassilis, Vassilopoulos Demetrios
Department of Neurology A, Athens National and Kapodistrian University, Aeginition Hospital, 74, 11528 Athens, Greece.
Clin Neurol Neurosurg. 2009 Nov;111(9):724-8. doi: 10.1016/j.clineuro.2009.06.012. Epub 2009 Jul 24.
There is evidence to support that oxidative stress is increased in Parkinson's disease (PD) and contributes to degeneration of dopaminergic neurons. Uric acid (UA), a natural antioxidant in blood and brain tissue, scavenging superoxide, peroxynitrite and hydroxyl radical, was found reduced in the serum of PD patients. In addition low plasma uric acid (UA) levels have been associated with an increased risk of PD.
The aim of our study was to investigate serum UA levels in PD patients compared with age-matched healthy controls and their possible relationship with several clinical parameters of PD and pharmaceutical treatment.
We measured serum UA levels in 43 PD patients and 47 healthy volunteers, age and sex-matched. UA levels were correlated with disease duration, severity and treatment.
Low UA levels were observed in PD patients compared with controls (p=0.009). Age, Body Mass Index (BMI) and UPDRS III score did not significantly affect serum UA concentrations, whereas gender was found to contribute significantly to UA level (p<0.000). Strong and significant inverse correlations of UA with disease duration (R(s)=-0.397, p=0.009) and daily levodopa dosage (R(p)=-0.498, p=0.026) were observed. These associations were significant for men (R(s)=-0.441, p=0.04 and R(s)=-0.717, p=0.03 respectively), but not for women (R(s)=-0.221, p=0.337 and R(s)=-0.17, p=0.966 respectively).
Our results suggest that there may be increased consumption of UA as a scavenger in PD, possibly heightened by dopaminergic drug treatment. Given the antioxidant properties of UA, manipulation of its concentrations should be investigated for potential therapeutic strategies of the disease.
有证据支持帕金森病(PD)中氧化应激增加,并导致多巴胺能神经元变性。尿酸(UA)是血液和脑组织中的一种天然抗氧化剂,可清除超氧化物、过氧亚硝酸盐和羟自由基,在PD患者血清中含量降低。此外,低血浆尿酸(UA)水平与PD风险增加有关。
本研究旨在比较PD患者与年龄匹配的健康对照者的血清UA水平,以及其与PD若干临床参数和药物治疗的可能关系。
我们测量了43例PD患者和47例年龄和性别匹配的健康志愿者的血清UA水平。UA水平与病程、严重程度和治疗相关。
与对照组相比,PD患者的UA水平较低(p = 0.009)。年龄、体重指数(BMI)和统一帕金森病评定量表(UPDRS)III评分对血清UA浓度无显著影响,而性别对UA水平有显著影响(p < 0.000)。观察到UA与病程(R(s)= -0.397,p = 0.009)和每日左旋多巴剂量(R(p)= -0.498,p = 0.026)呈强且显著的负相关。这些关联在男性中显著(分别为R(s)= -0.441,p = 0.04和R(s)= -0.717,p = 0.03),但在女性中不显著(分别为R(s)= -0.221,p = 0.337和R(s)= -0.17,p = 0.966)。
我们的结果表明,在PD中,作为清除剂可能存在UA消耗增加的情况,多巴胺能药物治疗可能会加剧这种情况。鉴于UA的抗氧化特性,应研究调节其浓度以寻找该疾病的潜在治疗策略。