From the Departments of Neurology (P.T., M.M.M., J.H.B., J.K.C.-G., J.E.A., R.S.), Health Science Research (M.M.M.), and Laboratory Medicine and Pathology (J.E.P.), Mayo Clinic, Rochester, MN.
Neurology. 2018 Dec 11;91(24):e2238-e2243. doi: 10.1212/WNL.0000000000006643. Epub 2018 Nov 7.
To assess dyskinesia frequency in a population-based cohort of patients with Parkinson disease (PD). Dyskinesia complicates levodopa treatment and affects quality of life.
Utilizing the 1991-2010 population-based, parkinsonism-incident cohort of Olmsted County, MN (n = 669), accessed via the Rochester Epidemiology Project, we identified patients with PD and abstracted levodopa-related dyskinesia information.
Of 309 patients with PD (46.2% with parkinsonisms), 279 (90.3%) received levodopa. Most (230/279; 82.4%) had been treated by a Mayo Clinic neurologist. Median age of the 309 patients with PD at the time of diagnosis was 74.1 years (range 33.1-97.8 years). Median-age levodopa initiation in this cohort was 75 years (range 37-98 years), and median-duration levodopa treatment was 6 years (range 2 months to 19.8 years). Dyskinesia was documented in 84 of 279 patients (30.1%). Median time from levodopa initiation to dyskinesia onset was 4 years (range 2 months to 20 years); those with dyskinesia (65.5%; 55/84) developed it within 5 years of levodopa initiation (9 within the first year). Dyskinesia was mild in 57/84 (67.9%), moderate in 16/84 (19.1%), and severe in 9/84 (10.7%); severity was not reported in 2 cases. Dyskinesia severity led to levodopa adjustments or amantadine initiation in 60.7% (51/84 of those with dyskinesia), with improvement in 23/51 (45.1%). Thirteen patients with dyskinesia underwent deep brain stimulation, reporting marked improvement. Postmortem examination confirmed Lewy body disease in 7 autopsied cases.
Levodopa-induced dyskinesia affected 30% of the patients with PD in our cohort. Mayo neurologists favoring levodopa dosage optimization treated most patients. Dyskinesia was severe in 3.2% of all levodopa-treated patients with PD (10.7% of all patients with dyskinesia) with marked improvement among those treated with deep brain stimulation.
评估帕金森病(PD)患者人群中运动障碍的发生频率。运动障碍使左旋多巴的治疗复杂化,并影响生活质量。
利用明尼苏达州奥姆斯特德县的 1991-2010 年基于人群的帕金森症发病队列(n=669),通过罗切斯特流行病学项目获取数据,我们确定了患有 PD 的患者,并提取了与左旋多巴相关的运动障碍信息。
309 名 PD 患者(46.2%患有帕金森症)中,279 名(90.3%)接受了左旋多巴治疗。大多数(230/279;82.4%)由梅奥诊所神经病学家治疗。该队列中 309 名 PD 患者的中位诊断年龄为 74.1 岁(范围 33.1-97.8 岁)。该队列中左旋多巴起始的中位年龄为 75 岁(范围 37-98 岁),左旋多巴治疗的中位持续时间为 6 年(范围 2 个月至 19.8 年)。279 名患者中有 84 名(30.1%)记录了运动障碍。从左旋多巴开始到运动障碍开始的中位时间为 4 年(范围 2 个月至 20 年);84 名中有 55 名(65.5%)在左旋多巴开始后的 5 年内出现运动障碍(9 名在第一年)。84 名中,57 名(67.9%)运动障碍为轻度,16 名(19.1%)为中度,9 名(10.7%)为重度;2 例未报告运动障碍的严重程度。60.7%(84 名中 51 名)出现运动障碍的患者进行了左旋多巴调整或金刚烷胺治疗,23 名(51 名中的 23 名)有所改善。13 名运动障碍患者接受了深部脑刺激治疗,报告症状显著改善。13 例尸检证实存在路易体病。
我们队列中 30%的 PD 患者出现了左旋多巴诱导的运动障碍。倾向于优化左旋多巴剂量的梅奥诊所神经病学家治疗了大多数患者。在所有接受左旋多巴治疗的 PD 患者中,运动障碍的严重程度为 3.2%(所有运动障碍患者中为 10.7%),深部脑刺激治疗的患者症状明显改善。