Macleod Angus D, Counsell Carl E
Institute of Applied Health Sciences, University of Aberdeen Aberdeen United Kingdom.
Mov Disord Clin Pract. 2019 Nov 21;7(1):45-51. doi: 10.1002/mdc3.12856. eCollection 2020 Jan.
Treatment response in PD is important clinically and for research diagnostic criteria, but few objective data show treatment-responsiveness of PD motor features.
To evaluate the treatment response of motor features to moderate treatment doses in a "real-world" PD cohort.
We analyzed data from a community-based incident cohort of PD in North-East Scotland (PINE study). We assessed change in the UPDRS motor scale and its individual items over a period of up to 13 months comparing (1) patients with an increase of at least 300 mg of levodopa-equivalent dose (LED) and (2) patients without treatment change, matched for age, sex, and disease duration.
We identified 101 matched pairs of patients with and without a treatment increase. LED increases were mostly 300 to 375 mg/day. Forty-two percent with treatment increase had ≥30% improvement in overall UPDRS motor score, a further 35% had substantial subjective improvement, but only 1 had an objective excellent (>70%) treatment response. Women responded better than men by 5.4 points (95% confidence interval [CI]: 2.7-8.1). All motor features improved with treatment, but after adjustment for age, sex, and initial score, only rest tremor ( < 0.001), rigidity ( = 0.01), bradykinesia (<0.001), posture ( = 0.01), and gait ( = 0.03) had significant improvements, compared to those with no treatment change. Dopa-less-responsive motor items, taken together, had small statistically significant relative improvements (1.1-point difference [95% CI: 0.4-1.8]; = 0.004).
Motor items sometimes previously considered dopa unresponsive have small improvements with moderate LED increases. Women respond better than men. Excellent treatment responses are uncommon. These data can inform clinical decisions about treatment.
帕金森病(PD)的治疗反应在临床及研究诊断标准方面都很重要,但很少有客观数据显示PD运动特征的治疗反应性。
在一个“真实世界”的PD队列中评估运动特征对中等治疗剂量的治疗反应。
我们分析了苏格兰东北部一个基于社区的PD新发队列(PINE研究)的数据。我们比较了(1)左旋多巴等效剂量(LED)增加至少300mg的患者和(2)未改变治疗的患者在长达13个月的时间里统一帕金森病评定量表(UPDRS)运动量表及其各个项目的变化,两组患者在年龄、性别和病程方面相匹配。
我们确定了101对分别有和没有增加治疗的匹配患者对。LED增加量大多为300至375mg/天。治疗增加的患者中,42%的整体UPDRS运动评分改善≥30%,另有35%有明显的主观改善,但只有1例有客观的优异(>70%)治疗反应。女性比男性反应好5.4分(95%置信区间[CI]:2.7 - 8.1)。所有运动特征经治疗均有改善,但在对年龄、性别和初始评分进行调整后,与未改变治疗的患者相比,只有静止性震颤(P < 0.001)、强直(P = 0.01)、运动迟缓(P < 0.001)、姿势(P = 0.01)和步态(P = 0.03)有显著改善。总体而言,对多巴反应不佳的运动项目有小的统计学显著相对改善(差异1.1分[95%CI:0.4 - 1.8];P = 0.004)。
一些以前被认为对多巴无反应的运动项目在中等程度增加LED时会有小的改善。女性比男性反应更好。优异的治疗反应并不常见。这些数据可为治疗的临床决策提供参考。