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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.
Affiliation
  • 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 ; 2024 May 08.
Article in 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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Neurol Year: 2024 Document type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Neurol Year: 2024 Document type: Article Affiliation country: Italy
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