Vieru Eugeniu, Köksal Ayhan, Mutluay Belgin, Dirican Ayten Ceyhan, Altunkaynak Yavuz, Baybas Sevim
Department of Neurology, Ozel Kas Tıp Merkezi, Istanbul, Turkey.
Department of Neurology, Bakirkoy Research and Training Hospital for Neurologic and Psychiatric Diseases, Bakirkoy, 34147, Istanbul, Turkey.
Neurol Sci. 2016 May;37(5):743-7. doi: 10.1007/s10072-015-2471-z. Epub 2016 Jan 11.
In this study, we aimed to investigate the association of the serum uric acid (UA) level with disease progression and L-Dopa treatment in PD (Parkinson's disease) patients. Serum UA levels of 80 consecutive PD patients were measured and were matched according to age and sex with 80 healthy controls. The patients were divided into two subgroups according to the pharmaceutical treatment received. First group consisted of patients treated with L-Dopa and a dopamine agonist and the second group consisted of patients treated only with a dopamine agonist. The patients were divided into two other subgroups according to Hoehn and Yahr scale. First group consisted of patients at the first two stages and the second group included patients at the third and upper stages. PD patients were found to have significantly lower levels of serum UA than controls (p = 0.000). Serum UA levels were lower in the group under L-Dopa + dopamine agonist treatment and in patients at third and upper Hoehn and Yahr stages than the patients under only dopamine agonist treatment and in the patients at the first two stages (p = 0.000 and p = 0.000). Multivariate logistic regression showed that advanced stages (OR 0.65, CI 0.50-0.79, p = 0.000) and L-Dopa treatment (OR 1.08, CI 1.03-1.16, p = 0.001) were independently associated with low UA levels. Our study supports that there is an inverse relation between UA levels and L-Dopa treatment and PD stages, and high serum UA levels may decrease the oxidative stress taking part in the pathogenesis of PD.
在本研究中,我们旨在调查血清尿酸(UA)水平与帕金森病(PD)患者疾病进展及左旋多巴治疗之间的关联。测量了80例连续PD患者的血清UA水平,并根据年龄和性别与80名健康对照进行匹配。根据接受的药物治疗将患者分为两个亚组。第一组由接受左旋多巴和多巴胺激动剂治疗的患者组成,第二组由仅接受多巴胺激动剂治疗的患者组成。根据Hoehn和Yahr量表将患者分为另外两个亚组。第一组由处于前两个阶段的患者组成,第二组包括处于第三及更高阶段的患者。发现PD患者的血清UA水平显著低于对照组(p = 0.000)。与仅接受多巴胺激动剂治疗的患者以及处于前两个阶段的患者相比,接受左旋多巴+多巴胺激动剂治疗的组以及处于Hoehn和Yahr第三及更高阶段的患者的血清UA水平较低(p = 0.000和p = 0.000)。多因素逻辑回归显示,疾病晚期(OR 0.65,CI 0.50 - 0.79,p = 0.000)和左旋多巴治疗(OR 1.08,CI 1.03 - 1.16,p = 0.001)与低UA水平独立相关。我们的研究支持UA水平与左旋多巴治疗及PD分期之间存在负相关关系,且高血清UA水平可能会降低参与PD发病机制的氧化应激。