Parkinson's disease and iatrogenic impulsive-compulsive behaviors: A case/non-case study to build a complete model of individual vulnerability Cover Image

Parkinson's disease and iatrogenic impulsive-compulsive behaviors: A case/non-case study to build a complete model of individual vulnerability
Parkinson's disease and iatrogenic impulsive-compulsive behaviors: A case/non-case study to build a complete model of individual vulnerability

Author(s): Marie Grall-Bronnec, Caroline Victorri-Vigneau, Tiphaine Rouaud, Audrey Verholleman, Benoît Schreck, Juliette Leboucher, Elsa Thiabaud, Fanny Feuillet, Monica Roy, Jean-Benoit Hardouin, Morgane Guillou-Landrea, Pascal Derkinderen, Gaélle Challet-Bouju
Subject(s): Behaviorism
Published by: Akadémiai Kiadó
Keywords: Parkinson's disease; disruptive; impulse control, and conduct disorders; addictive behavior; opioid receptor mu 1; predictive model; vulnerability

Summary/Abstract: Background and aims. Parkinson's disease (PD) is one of the most prevalent neurodegenerative diseases. First-line medications consist of drugs that act by counteracting dopamine deficiency in the basal ganglia. Unfortunately, iatrogenic impulsive-compulsive behaviors (ICBs) can occur in up to 20% of PD patients over the course of their illness. ICBs must be considered multifactorial disorders that reflect the interactions of the medication with an individual's vulnerability and the underlying neurobiology of PD. We aimed to explore the predictive genetic, psychopathological and neurological factors involved in the development of ICBs in PD patients by building a complete model of individual vulnerability. Methods. The PARKADD study was a case/non-case study. A total of 225 patients were enrolled (“ICB” group, N = 75; “no ICB” group, N = 150), and 163 agreed to provide saliva samples for genetic analysis. Sociodemographic, neurological and psychiatric characteristics were assessed, and genotyping for the characterization of polymorphisms related to dopaminergic and opioid systems was performed. Results. Factors associated with “ICBs” were younger age of PD onset, personal history of ICB prior to PD onset and higher scores on the urgency and sensation seeking facets of impulsivity. No gene variant was significantly associated, but the association with the opioid receptor mu 1 (OPRM1) rs1799971 polymorphism was close to significance. Discussion and conclusions. The influence of gene-environment interactions probably exists, and additional studies are needed to decipher the possible role of the opioid system in the development of ICBs in PD patients.

  • Issue Year: 11/2022
  • Issue No: 3
  • Page Range: 766-777
  • Page Count: 12
  • Language: English