多巴胺与早期帕金森病

Katarzyna Wize, W. Kozubski, J. Dorszewska
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引用次数: 0

摘要

帕金森病(PD)分为发生在45岁以下的早发性(EOPD)和45岁以上的晚发性(LOPD)。EOPD占所有PD病例的5 - 10%。据认为,这一年龄段的发生与遗传因素有关,例如PRKN、PINK1、DJ-1的突变及其编码蛋白的变化。黑质纹状体系统中多巴胺能神经元的缺失导致多巴胺(DA)浓度下降。致病性PD蛋白可影响DA水平。低水平的DA可能是运动相关症状的原因。eopd的病程进展较慢,病程持续时间较长,但往往比LOPD更早出现运动障碍和运动波动。目前,PD的诊断是基于临床标准,支持MRI或PET等神经影像学。了解EOPD的发病机制可能有助于提高诊断和药物治疗的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dopamine and Early Onset Parkinson’s Disease
Parkinson’s disease (PD) is divided into early-onset (EOPD) occurring at the age of fewer than 45 years of age and late-onset PD (LOPD) above 45 years of age. EOPD accounts for 5– 10% of all the cases with PD. It is thought that occurrence in this age is connected with genetic factors, mutations in e.g. PRKN, PINK1, DJ-1 and changes in proteins it is encoded. The loss of dopaminergic neurons in the nigrostriatal system leads to decreased dopamine (DA) concentrations. Pathogenic PD proteins may affect the DA level. The lower level of DA may be responsible for movement-related symptoms. EOPDs have a slower progression of the disease and a longer disorder duration but tend to develop dyskinesias and motor fluctuations earlier than LOPD. Currently, the diagnosis of PD is based on clinical criteria, supported neuroimaging like MRI or PET. Understanding the pathogenesis of the EOPD may be contributing to improving diagnostics and effectiveness of pharmacotherapy.
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