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四名进行性核上性麻痹帕金森变异型患者肠内左旋多巴输注治疗的真实获益:1 年随访数据报告。

Real-life benefits of intrajejunal levodopa infusion therapy in four patients with the parkinsonian variant of progressive supranuclear palsy: A 1-year follow-up data report.

机构信息

Department of Basic and Clinical Neurosciences, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.

Parkinson's Foundation Centre of Excellence, King's College Hospital, London, UK.

出版信息

Brain Behav. 2022 Sep;12(9):e2547. doi: 10.1002/brb3.2547. Epub 2022 Aug 9.

Abstract

BACKGROUND

Progressive supranuclear palsy (PSP) is a progressive neurodegenerative condition presenting with different clinical endophenotypes. The parkinsonian variant of PSP (PSP-P) is characterised by early but fading responsiveness to high-dose levodopa therapy; however, high-dose oral therapy is often associated with intolerance due to dopaminergic side effects and so doses may have to be capped despite clinical benefits. Evidence from animal models and real-life registries suggest far higher doses of levodopa can be tolerated if given in a continuous drug delivery (CDD) manner. We investigated tolerance and possible clinical benefits in patients with PSP-P still responsive to levodopa after initiating CDD in the form of intrajejunal levodopa infusion (IJLI) therapy as part of a compassionate usage program (CU).

METHODS

This is an observational clinical data report from the IJLI implementation program undertaken in regional tertiary referral Parkinson's centres in India and at King's College Hospital London, Dubai as part of a CU. Four patients with PSP-P receiving IJLI as a part of a CU underwent evaluations of liver and renal function, motor and nonmotor function, quality of life, sleep dysfunction, fatigue, anxiety and depression, and cognitive impairment at baseline and 6 and 12 months post-IJLI initiation.

RESULTS

In total, three out of four patients successfully completed 12 months of treatment (6 months in one patient). All four patients showed good tolerability to IJLI even at higher doses (1400 and 1960 mg at 6 and 12 months, respectively) when compared to oral levodopa (812.5 ± 103 levodopa equivalent daily dose [LEDD]) and presented with overall persistent improvements in motor and nonmotor scores and quality-of-life scores at 6 and 12 months post-IJLI. All patients showed improvement in estimated glomerular filtration rate (43.50 ml/min/1.73 m to 67.5 ml/min/1.73 m and 79.5 ml/min/1.73 m at 6 and 12 months, respectively).

CONCLUSIONS

IJLI led to persistent beneficial effects on motor and some nonmotor aspects in patients with PSP-P at up to 12 months after treatment with associated improvement in overall renal function.

摘要

背景

进行性核上性麻痹(PSP)是一种进行性神经退行性疾病,表现出不同的临床表型。PSP 的帕金森变体(PSP-P)的特点是对高剂量左旋多巴治疗的早期但逐渐减弱的反应;然而,由于多巴胺能副作用,高剂量口服治疗通常会引起不耐受,因此尽管有临床益处,但可能不得不限制剂量。来自动物模型和真实世界登记处的证据表明,如果以连续药物输送(CDD)的方式给予更高剂量的左旋多巴,患者可以更好地耐受。我们调查了在启动肠内左旋多巴输注(IJLI)治疗作为同情使用计划(CU)的一部分后,对仍对左旋多巴有反应的 PSP-P 患者的耐受性和可能的临床益处。

方法

这是一项来自 IJLI 实施计划的观察性临床数据报告,该计划在印度的区域三级转诊帕金森氏症中心和伦敦国王学院医院迪拜进行,作为 CU 的一部分。四名接受 IJLI 治疗的 PSP-P 患者在 IJLI 开始后 6 个月和 12 个月进行了肝肾功能、运动和非运动功能、生活质量、睡眠功能障碍、疲劳、焦虑和抑郁以及认知障碍的评估。

结果

总共有四名患者中的三名成功完成了 12 个月的治疗(一名患者为 6 个月)。与口服左旋多巴(812.5±103 左旋多巴等效日剂量[LEDD])相比,所有四名患者均对 IJLI 表现出良好的耐受性,即使在更高剂量(6 个月时为 1400 毫克和 1960 毫克,12 个月时为 1400 毫克和 1960 毫克)时也是如此,并且在 IJLI 开始后 6 个月和 12 个月时,运动和非运动评分以及生活质量评分均持续改善。所有患者的估算肾小球滤过率(43.50 ml/min/1.73 m 至 67.5 ml/min/1.73 m 和 79.5 ml/min/1.73 m,分别在 6 个月和 12 个月时)均有所改善。

结论

在接受 IJLI 治疗长达 12 个月后,PSP-P 患者的运动和一些非运动方面持续受益,整体肾功能也有所改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30fd/9480946/438bf67b1d99/BRB3-12-e2547-g001.jpg

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