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慢性使用 5-羟色胺-去甲肾上腺素再摄取抑制剂会促进早期帕金森病运动障碍的形成。

The chronic use of serotonin norepinephrine reuptake inhibitors facilitates dyskinesia priming in early Parkinson's disease.

机构信息

Neurology, Neurophysiology, Neurobiology and Psychiatry Unit, Department of Medicine, Università Campus Bio-Medico di Roma, Via Alvaro del Portillo 200, 00128, Rome, Italy.

Fondazione Policlinico Universitario Campus Bio-Medico, Viale Alvaro del Portillo 200, 00128, Rome, Italy.

出版信息

J Neurol. 2024 Jul;271(7):3711-3720. doi: 10.1007/s00415-024-12400-6. Epub 2024 May 8.

Abstract

BACKGROUND

Parkinson's disease (PD) patients are frequently exposed to antidepressant medications (ADMs). Norepinephrine (NE) and serotonin (5HT) systems have a role in levodopa-induced dyskinesias (LID) pathophysiology.

METHODS

We performed a longitudinal analysis on the PPMI cohort including drug-naïve PD patients, who are progressively exposed to dopamine replacement therapies (DRTs) to test the effect of ADM exposure on LID development by the 4th year of follow-up.

RESULTS

LID prevalence (according to MDS UPDRS score 4.1 ≥ 1) was 16% (42/251); these patients were more likely women (p = 0.01), had higher motor (p < 0.001) and depression scores (p = 0.01) and lower putaminal DAT binding ratio (p = 0.01). LID were associated with the exposure time to L-DOPA (2.2 ± 1.07 vs 2.6 ± 0.9, p = 0.02) and to the exposure to ADMs, in particular to SNRI (4.8% vs 21.4%, p < 0.001). The latter persisted after correcting for significant covariates (e.g., disease duration, cognitive status, motor impairment, depression, dopaminergic denervation). A similar difference in LID prevalence in PD patients exposed vs non-exposed to SNRI was observed on matched data by the real-world TriNetX repository (22% vs 13%, p < 0.001).

DISCUSSION

This study supports the presence of an effect of SNRI on LID priming in patients with early PD. Independent prospective cohort studies are warranted to further verify such association.

摘要

背景

帕金森病(PD)患者经常接触抗抑郁药物(ADM)。去甲肾上腺素(NE)和 5-羟色胺(5HT)系统在左旋多巴诱导的运动障碍(LID)发病机制中起作用。

方法

我们对 PPMI 队列进行了纵向分析,包括药物-naive PD 患者,他们逐渐接受多巴胺替代疗法(DRT),以测试 ADM 暴露对第 4 年随访时 LID 发展的影响。

结果

LID 患病率(根据 MDS UPDRS 评分 4.1≥1)为 16%(42/251);这些患者更可能是女性(p=0.01),运动评分更高(p<0.001)、抑郁评分更高(p=0.01)和纹状体 DAT 结合率更低(p=0.01)。LID 与 L-DOPA 暴露时间(2.2±1.07 与 2.6±0.9,p=0.02)和 ADM 暴露有关,特别是与 SNRIs 有关(4.8%与 21.4%,p<0.001)。在对显著协变量(如疾病持续时间、认知状态、运动障碍、抑郁、多巴胺能神经支配丧失)进行校正后,这种差异仍然存在。在 TriNetX 真实世界数据库中,暴露与未暴露于 SNRIs 的 PD 患者的 LID 患病率存在类似差异(22%与 13%,p<0.001)。

讨论

这项研究支持 SNRIs 对早期 PD 患者 LID 启动的影响。需要进行独立的前瞻性队列研究来进一步验证这种关联。

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