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首页> 外文期刊>Clinical chemistry and laboratory medicine: CCLM >Elevated plasma homocysteine levels in L-dopa-treated Parkinson's disease patients with dyskinesias.
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Elevated plasma homocysteine levels in L-dopa-treated Parkinson's disease patients with dyskinesias.

机译:左旋多巴治疗的帕金森氏病运动障碍患者血浆同型半胱氨酸水平升高。

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BACKGROUND: Elevated plasma homocysteine (Hcy) concentrations are associated with increased risk of systemic vascular diseases, Alzheimer's disease and vascular dementia. Several cross-sectional reports and two prospective clinical studies have recently reported elevated plasma Hcy levels in L-dopa-treated Parkinson's disease (PD) patients and Hcy has been proposed as a possible mediator for the development of long-term L-dopa motor complications (such as wearing off and on-off phenomena, and dyskinesias). The aim of the study was to elucidate a possible role of L-dopa-related hyperhomocysteinemia in the development of dyskinesias. METHODS: In this cross-sectional study we compared Hcy, B(12) and folate levels in 53 PD patients treated with L-dopa (29 with dyskinesias, 24 without dyskinesias). RESULTS: Mean plasma Hcy levels were higher in the group of PD patients with dyskinesias (19 vs. 15.4 micromol/L; T: 2.12; p=0.04). After taking into account potential confounding factors, analysis of the data revealed that the occurrence of dyskinesias progressively increased with plasma Hcy levels (relative risk 1.2, 95% CI 1.015-1.4; p=0.03). CONCLUSIONS: Our results raise the possibility that Hcy plays a role in the development of dyskinesias, through its toxic effects on both dopaminergic neurons and non-substantia nigra, non-dopaminergic neurons.
机译:背景:血浆高半胱氨酸(Hcy)浓度升高与全身性血管疾病,阿尔茨海默氏病和血管性痴呆的风险增加相关。最近有几项横断面报告和两项前瞻性临床研究报道了左旋多巴治疗的帕金森氏病(PD)患者血浆Hcy水平升高,并且已提议Hcy作为长期左旋多巴运动并发症发展的可能介质(例如疲倦和通断现象,以及运动障碍)。该研究的目的是阐明L-多巴相关的高同型半胱氨酸血症在运动障碍发展中的可能作用。方法:在这项横断面研究中,我们比较了接受L-多巴治疗的53例PD患者的Hcy,B(12)和叶酸水平(29例患有运动障碍,24例没有运动障碍)。结果:运动障碍PD患者组的平均血浆Hcy水平较高(19 vs. 15.4 micromol / L; T:2.12; p = 0.04)。考虑到潜在的混杂因素后,数据分析表明,运动障碍的发生随着血浆Hcy水平的升高而逐渐增加(相对危险度1.2,95%CI 1.015-1.4; p = 0.03)。结论:我们的结果提出了Hcy通过对多巴胺能神经元和非黑质,非多巴胺能神经元的毒性作用而在运动障碍发展中起作用的可能性。

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