Impulse Control Disorders in Dopamine Agonist-Treated Hyperprolactinemia: Prevalence and Risk Factors

Author:

De Sousa Sunita M C1234ORCID,Baranoff John56,Rushworth R Louise7,Butler Jessica1,Sorbello Jane8,Vorster Juanita8,Thompson Tanya9,McCormack Ann I910,Inder Warrick J811,Torpy David J14

Affiliation:

1. Endocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, Australia

2. Department of Genetics and Molecular Pathology, Centre for Cancer Biology, an SA Pathology and University of South Australia alliance, Adelaide, Australia

3. Adult Genetics Unit, Royal Adelaide Hospital, Adelaide, Australia

4. School of Medicine, University of Adelaide, Adelaide, Australia

5. Centre for Treatment of Anxiety and Depression, Mental Health Directorate, Central Adelaide Local Health Network, Adelaide, Australia

6. School of Psychology, University of Adelaide, Adelaide, Australia

7. School of Medicine, Sydney, University of Notre Dame, Australia

8. Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Brisbane, Australia

9. Hormones and Cancer, Garvan Institute of Medical Research, Sydney, Australia

10. St Vincent’s Clinical School, Faculty of Medicine, UNSW Sydney, Sydney, Australia

11. Princess Alexandra-Southside Clinical Unit, University of Queensland, Brisbane, Australia

Abstract

Abstract Context There are growing reports of dopamine agonist (DA)-induced impulse control disorders (ICDs) in hyperprolactinemic patients. However, the magnitude of this risk and predictive factors remain uncertain. Objective To determine ICD prevalence and risk factors in DA-treated hyperprolactinemic patients compared to community controls. Design, Setting and Participants Multicenter cross-sectional analysis of 113 patients and 99 healthy controls. Main Outcome Measures Participants completed a neuropsychological questionnaire consisting of the Depression Anxiety Stress Scale (DASS21), Questionnaire for Impulsive-Compulsive Disorders in Parkinson’s Disease (QUIP-S), Hypersexual Behavior Inventory (HBI), Hypersexual Behavior Consequences Scale and Social Desirability Response Set Scale. Demographic and clinical data were collated to determine ICD risk factors. Patients testing positive for an ICD were offered a semistructured psychological interview. Results Patients were more likely than controls to test positive by QUIP-S for any ICD (61.1 vs 42.4%, P = .01), hypersexuality (22.1 vs 8.1%, P = .009), compulsive buying (15.9 vs 6.1%, P = .041) and punding (18.6 vs 6.1%, P = 0.012), and by HBI for hypersexuality (8.0 vs 0.0%, P = 0.004). Independent risk factors were male sex (odds ratio [OR] 13.85), eugonadism (OR 7.85), Hardy’s tumor score and psychiatric comorbidity (OR 6.86) for hypersexuality, and age (OR 0.95) for compulsive buying. DASS21 subset scores were higher in patients vs controls and in patients with vs without different ICDs. Only 19/51 (37.3%) interviewed patients were aware of the relationship between DAs and ICDs before the study. Conclusions DA therapy poses a high, previously underestimated risk of ICDs, especially in the form of hypersexuality in eugonadal men.

Funder

Royal Adelaide Hospital A. R. Clarkson Scholarship

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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