Impulse control disorders, dopamine dysregulation syndrome and sex dysfunction in Parkinson's disease

Int Rev Neurobiol. 2022:162:117-134. doi: 10.1016/bs.irn.2021.12.008. Epub 2022 Mar 24.

Abstract

Hypersexuality (HS), characterized by an aberrant, compulsive and inappropriate sexual drive, is an underreported and undermanaged complication of the treatment with dopamine agonists in patients with Parkinson's disease (PD). HS is part of the spectrum of impulse control disorders (ICDs). The failure to control these addictive behaviors is distressing for the patient and it is associated with important consequences. Reports of the prevalence of HS showed different results, due to the lack of standardized diagnostic criteria, but also due to the embarrassment or guilt feelings that patients experience regarding their sexual behaviors. Overall, it is considered that HS may occur in 1.92-22.8% of PD patients and the main risk factors involved could be male sex and genetic susceptibility. The pathophysiology of HS is unknown, but several degenerative mechanisms were proposed, involving dopaminergic, serotoninergic and noradrenergic pathways in cerebral regions responsive for planning and rewarding. There are no standardized tools for the assessment of HS in PD patients; however, several scales and questionnaires were developed with the aim of screening and rating the severity of ICDs, including HS. The management of HS is challenging. Discontinuation or reducing the dopaminergic treatment was effective in some cases, but it might lead to worsening of the motor function. A multidisciplinary approach is mandatory to manage the other associated aspects, such as psychological and social consequences of HS.

Keywords: Dopamine dysregulation syndrome; Hypersexuality; Impulse control disorders; Parkinson's disease.

MeSH terms

  • Disruptive, Impulse Control, and Conduct Disorders* / chemically induced
  • Dopamine / metabolism
  • Dopamine Agonists / adverse effects
  • Humans
  • Male
  • Parkinson Disease* / complications
  • Parkinson Disease* / drug therapy
  • Parkinson Disease* / metabolism
  • Syndrome

Substances

  • Dopamine Agonists
  • Dopamine