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The chronic use of serotonin norepinephrine reuptake inhibitors facilitates dyskinesia priming in early Parkinson's disease.
Marano, Massimo; Pilotto, Andrea; Padovani, Alessandro; Gupta, Deepak; Vivacqua, Giorgio; Magliozzi, Alessandro; Di Lazzaro, Vincenzo; Carta, Manolo; Meloni, Mario.
Afiliação
  • Marano M; Neurology, Neurophysiology, Neurobiology and Psychiatry Unit, Department of Medicine, Università Campus Bio-Medico di Roma, Via Alvaro del Portillo 200, 00128, Rome, Italy. m.marano@policlinicocampus.it.
  • Pilotto A; Fondazione Policlinico Universitario Campus Bio-Medico, Viale Alvaro del Portillo 200, 00128, Rome, Italy. m.marano@policlinicocampus.it.
  • Padovani A; Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
  • Gupta D; Laboratory of Digital Neurology and Biosensors, University of Brescia, Brescia, Italy.
  • Vivacqua G; Neurology Unit, Department of Continuity of Care and Frailty, ASST Spedali Civili Brescia Hospital, Brescia, Italy.
  • Magliozzi A; Brain Health Center, University of Brescia, Brescia, Italy.
  • Di Lazzaro V; Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
  • Carta M; Laboratory of Digital Neurology and Biosensors, University of Brescia, Brescia, Italy.
  • Meloni M; Neurology Unit, Department of Continuity of Care and Frailty, ASST Spedali Civili Brescia Hospital, Brescia, Italy.
J Neurol ; 271(7): 3711-3720, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38720139
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Levodopa / Discinesia Induzida por Medicamentos / Antiparkinsonianos Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Levodopa / Discinesia Induzida por Medicamentos / Antiparkinsonianos Idioma: En Ano de publicação: 2024 Tipo de documento: Article