He Xiaoqin, Shi Kai, Mo Chengjun, Zhang Yi, Xiao Qin, Yang Xiaodong
Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Geriatrics Health Care Ward, Qingdao Municipal Hospital, University of Health and Rehabilitation Sciences, Qingdao, Shandong, China.
Clin Park Relat Disord. 2025 Apr 20;12:100333. doi: 10.1016/j.prdoa.2025.100333. eCollection 2025.
Levodopa is the mainstay of treatments for Parkinson's disease (PD), but large heterogeneity exists in patient response. Pharmacogenetic studies highlighted that genetic factors may play a relevant influence in this drug response variability.
To explore the relationship between dopaminergic polymorphisms, levodopa treatment response, and drug concentration in Chinese patients with PD.
Acute levodopa challenge test was conducted in 90 PD patients. Each patient underwent comprehensive neurological examination at baseline and after levodopa administration. Plasma levodopa concentrations were measured by liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis. Twelve genetic polymorphisms in genes encoding dopaminergic enzymes (TH, DDC, COMT, MAOB and DBH) were genotyped.
Patients with the TH-rs6356 TT genotype showed higher ΔMDS-UPDRS-III scores compared to those with the CC + CT genotype after adjustment for the levodopa dose in the acute challenge test (P = 0.048). Furthermore, peak plasma levodopa concentration and Δplasma levodopa concentration were significantly higher in the TH-rs6356 TT group compared to the CC + CT group after adjustment (P = 0.007). Patients with the TH-rs6356 TT genotype exhibited a longer time to peak response compared to those with the CC + CT genotype (P = 0.042). However, this difference became non-significant after adjusting for levodopa dose (P = 0.066). The impact of other dopamine-related gene polymorphisms on levodopa efficacy appeared to be minimal in our study.
Our preliminary results from a relatively small patients' sample, may suggest that the rs6356 polymorphism in the TH gene could act as a possible modifier of levodopa response in PD.
左旋多巴是帕金森病(PD)治疗的主要药物,但患者反应存在很大异质性。药物遗传学研究强调,遗传因素可能对这种药物反应变异性产生相关影响。
探讨中国PD患者中多巴胺能基因多态性、左旋多巴治疗反应与药物浓度之间的关系。
对90例PD患者进行急性左旋多巴激发试验。每位患者在基线和服用左旋多巴后均接受全面的神经学检查。采用液相色谱串联质谱(LC-MS/MS)分析法测定血浆左旋多巴浓度。对编码多巴胺能酶(TH、DDC、COMT、MAOB和DBH)的基因中的12个基因多态性进行基因分型。
在急性激发试验中,调整左旋多巴剂量后,与CC + CT基因型患者相比,TH-rs6356 TT基因型患者的ΔMDS-UPDRS-III评分更高(P = 0.048)。此外,调整后,TH-rs6356 TT组的血浆左旋多巴峰值浓度和Δ血浆左旋多巴浓度显著高于CC + CT组(P = 0.007)。与CC + CT基因型患者相比,TH-rs6356 TT基因型患者达到峰值反应的时间更长(P = 0.042)。然而,调整左旋多巴剂量后,这种差异变得不显著(P = 0.066)。在我们的研究中,其他多巴胺相关基因多态性对左旋多巴疗效的影响似乎很小。
我们从相对较小的患者样本中获得的初步结果可能表明,TH基因中的rs6356多态性可能是PD患者左旋多巴反应的一个潜在调节因素。