Department of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
SC Neurologia 2U, AOU City of Health and Science, Turin, Italy.
Eur J Neurol. 2023 Jan;30(1):96-106. doi: 10.1111/ene.15558. Epub 2022 Oct 12.
Treatment of freezing of gait (FoG) and other Parkinson disease (PD) axial symptoms is challenging. Systematic assessments of axial symptoms at progressively increasing levodopa doses are lacking. We sought to analyze the resistance to high levodopa doses of FoG, posture, speech, and altered gait features presenting in daily-ON therapeutic condition.
We performed a pre-/postinterventional study including patients treated with levodopa/carbidopa intestinal gel infusion (LCIG) with disabling FoG in daily-ON condition. Patients were evaluated at their usual LCIG infusion rate (T1), and 1 h after 1.5× (T2) and 2× (T3) increase of the LCIG infusion rate by quantitative outcome measures. The number of FoG episodes (primary outcome), posture, speech, and gait features were objectively quantified during a standardized test by a blinded rater. Changes in motor symptoms, dyskinesia, and plasma levodopa concentrations were also analyzed.
We evaluated 16 patients with a mean age of 69 ± 9.4 years and treated with LCIG for a mean of 2.2 ± 2.1 years. FoG improved in 83.3% of patients by increasing the levodopa doses. The number of FoG episodes significantly decreased (mean = 2.3 at T1, 1.7 at T2, 1.2 at T3; p = 0.013). Posture and speech features did not show significant changes, whereas stride length (p = 0.049), turn duration (p = 0.001), and turn velocity (p = 0.024) significantly improved on doubling the levodopa infusion rate.
In a short-term evaluation, the increase of LCIG dose can improve "dopa-resistant" FoG and gait issues in most advanced PD patients with overall good control of motor symptoms in the absence of clinically significant dyskinesia.
治疗冻结步态(FoG)和其他帕金森病(PD)的轴性症状具有挑战性。缺乏对轴性症状进行逐渐增加左旋多巴剂量的系统评估。我们旨在分析在日常开处方左旋多巴治疗条件下,FoG、姿势、言语和步态改变特征对高剂量左旋多巴的抵抗情况。
我们进行了一项预/后干预研究,包括在日常开处方左旋多巴/卡比多巴肠内凝胶输注(LCIG)治疗下出现严重 FoG 的患者。患者在其常规 LCIG 输注率(T1)时进行评估,在 LCIG 输注率增加 1.5 倍(T2)和 2 倍(T3)后 1 小时进行评估,通过定量评估方法评估运动症状、运动障碍和血浆左旋多巴浓度的变化。通过盲法评估者在标准化测试中客观地量化 FoG 发作次数(主要结局)、姿势、言语和步态特征。
我们评估了 16 名年龄 69±9.4 岁的患者,使用 LCIG 治疗的平均时间为 2.2±2.1 年。通过增加左旋多巴剂量,83.3%的患者 FoG 得到改善。FoG 发作次数明显减少(T1 时平均为 2.3 次,T2 时为 1.7 次,T3 时为 1.2 次;p=0.013)。姿势和言语特征无显著变化,而步幅(p=0.049)、转身时间(p=0.001)和转身速度(p=0.024)在 LCIG 剂量加倍时显著改善。
在短期评估中,增加 LCIG 剂量可以改善大多数晚期 PD 患者的“抗多巴”FoG 和步态问题,同时在没有明显运动障碍的情况下,很好地控制运动症状。