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Genetics of impulse control disorders in Parkinson’s disease: a case control study

J.-C. Corvol, F. Cormier-Dequaire, S. Bekadar, S. Prud'hon, M. Anheim, J.-P. Azulay, F. Durif, J.-L. Houeto, A. Destée, K. Tahiri, G. Mangone, L. Lacomblez, P. Krack, P. Krystkowiak, D. Maltête, O. Rascol, C. Tranchant, M. Vidailhet, A. Brice, S. Tezenas duMontcel (Paris, France)

Meeting: 2017 International Congress

Abstract Number: 1075

Keywords: Dopamine agonists, Dopamine dysregulation syndrome, Obsessive-compulsive behavior/disorder

Session Information

Date: Wednesday, June 7, 2017

Session Title: Parkinson's Disease: Psychiatric Manifestations

Session Time: 1:15pm-2:45pm

Location: Exhibit Hall C

Objective: To investigate the association between candidate genes and impulse control disorders (ICD) in patients with Parkinson’s disease.

Background: ICD are frequently associated with dopaminergic therapy in Parkinson’s disease (PD). Genetic studies have suggested a high heritability of ICD in the general population and in PD. 

Methods: We performed a multicenter genetic case-control study in PD patients with ICD or without ICD related to dopamine therapy, receiving a treatment with dopamine agonist for at least 12 months at 300 mg equivalent daily dose. Cases and controls were matched for age, sex, and disease duration. Patients were assessed during a face-to-face interview with the French Behavioral Scale for PD. Presence of ICD was defined as 1 severe (score > 3) or 2 moderate (score > 2) hyperdopaminergic behaviors. Patients were considered without ICD if hyperdopaminergic behaviors were absent. The study was powered to investigate 50 polymorphisms preselected from 24 candidate genes. We performed a multivariate logistic regression analysis with a discovery step in 33% random samples, a replication step in the 66% leftover samples, and a pooled analysis, taking into account multiple testing.

Results: We enrolled 176 PD patients with ICD and 136 PD patients without ICD. Patients with ICD were younger (59 +/- 8 versus 62 +/- 7, p<0.001), and had a higher family history of pathological gambling (11% versus 4%, p = 0.04). ICD were pathological gambling (31%), pathological shopping (38%), binge eating (58%), and hypersexuality (43%). At the discovery step, polymorphisms in the DRD2, GRIN2B, OPRM1, CA12, and C8B genes were significantly associated with ICD. The μ opioid receptor gene (OPRM1) polymorphism rs1799971 was replicated in the leftover sample (OR [CI95%] = 0.48 [0.27 – 0.84], p=0.01), and remained significant in the pooled analysis (OR = 0.45 [0.29 – 0.69], p=0.0003).

Conclusions: In PD patients treated with dopamine agonists, we found a significant association between ICD and rs1799971, a functional variant of OPRM1 previously associated with a decreased sensitivity to morphine, and drug or alcohol addiction. Our results suggest an involvement of the opioid system in the behavioral response to dopaminergic therapy in PD.

To cite this abstract in AMA style:

J.-C. Corvol, F. Cormier-Dequaire, S. Bekadar, S. Prud'hon, M. Anheim, J.-P. Azulay, F. Durif, J.-L. Houeto, A. Destée, K. Tahiri, G. Mangone, L. Lacomblez, P. Krack, P. Krystkowiak, D. Maltête, O. Rascol, C. Tranchant, M. Vidailhet, A. Brice, S. Tezenas duMontcel. Genetics of impulse control disorders in Parkinson’s disease: a case control study [abstract]. Mov Disord. 2017; 32 (suppl 2). https://www.mdsabstracts.org/abstract/genetics-of-impulse-control-disorders-in-parkinsons-disease-a-case-control-study/. Accessed June 15, 2025.
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