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Naltrexone in Compulsive Sexual Behavior Disorder: A Feasibility Study of Twenty Men
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk vetenskap, Psykiatri. Anova, Karolinska University Hospital, Stockholm, Sweden.ORCID-id: 0000-0002-0140-4109
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk vetenskap, Psykiatri. Medical School, University of Cyprus, Nicosia, Cyprus.ORCID-id: 0000-0002-6635-9564
Visa övriga samt affilieringar
2020 (Engelska)Ingår i: Journal of Sexual Medicine, ISSN 1743-6095, E-ISSN 1743-6109, Vol. 17, nr 8, s. 1544-1552Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Background: Compulsive sexual behavior disorder (CSBD) is a common disorder affecting different areas of life, although studies focusing on pharmacological treatment are sparse.

Aim: To investigate whether the opioid receptor antagonist naltrexone is feasible and tolerable and can provide symptom reduction in CSBD.

Methods: Twenty men aged 27-60 years (mean = 38.8 years, standard deviation = 10.3) with CSBD seeking treatment in an outpatient nonforensic clinic received four weeks of naltrexone 25-50 mg. Measurements were made before, during, and four weeks after treatment.

Outcomes: The self-assessment Hypersexual Disorder: Current Assessment Scale (HD: CAS) score was the primary outcome measure, and secondary outcomes were the Hypersexual Behavior Inventory (HBI) score, reported adverse effects, adherence to treatment, and dropouts.

Results: There was significant decrease on both HD: CAS and HBI scores during treatment with naltrexone. Even though some of the effects remained after treatment, the increased scores on HD: CAS indicated worsening of CSBD symptoms. The most reported side effects were fatigue (55%), nausea (30%), vertigo (30%), and abdominal pain (30%). However, there were no serious adverse effects leading to discontinuation of naltrexone.

Clinical Implications: Despite side effects being common, naltrexone seems to be feasible in the treatment of CSBD.

Strengths & Limitations: Being the first nonforensic prospective trial on naltrexone in CSBD, this study provides novel insights on a pharmacological intervention. However, owing to the small sample size and the lack of a control group, conclusions of effectiveness should be interpreted with caution.

Conclusion: Naltrexone is feasible and tolerable and may reduce symptoms of CSBD; nevertheless, future studies should ensure a randomized controlled procedure to evaluate possible effectiveness.

Ort, förlag, år, upplaga, sidor
Elsevier, 2020. Vol. 17, nr 8, s. 1544-1552
Nyckelord [en]
Compulsive sexual behavior disorder, Naltrexone, Hypersexual disorder, Sexual addiction
Nationell ämneskategori
Farmakologi och toxikologi Psykiatri
Identifikatorer
URN: urn:nbn:se:umu:diva-174027DOI: 10.1016/j.jsxm.2020.04.318ISI: 000552729900017PubMedID: 32532705Scopus ID: 2-s2.0-85086166963OAI: oai:DiVA.org:umu-174027DiVA, id: diva2:1458820
Tillgänglig från: 2020-08-18 Skapad: 2020-08-18 Senast uppdaterad: 2023-03-24Bibliografiskt granskad
Ingår i avhandling
1. Compulsive sexual behavior disorder: clinical characteristics and treatment with Naltrexone
Öppna denna publikation i ny flik eller fönster >>Compulsive sexual behavior disorder: clinical characteristics and treatment with Naltrexone
2021 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Background: Compulsive Sexual Behavior Disorder (CSBD) is characterized by sexual preoccupation and loss of control of sexual behaviors causing distress, negative consequences, and impairment. Despite its high prevalence, the condition is understudied in terms of background factors and treatment. 

Aims: The overall aim of this thesis is to investigate clinical characteristics with a specific focus on self-reported experience of interpersonal violence and various dimensions of impulsivity, and to evaluate treatment with naltrexone in help-seeking men with CSBD. 

Methods: In Study I, 67 men with CSBD were compared with 40 healthy, age-matched controls concerning interpersonal violence measured with the Karolinska Interpersonal Violence Scale (KIVS). In Study II, clinical, neurocognitive, and self-reported measures of impulsivity were compared between men with CSBD (n=20), a clinical control cohort with pedophilic disorder (n=55), and a healthy male control cohort (n=57). In Study III, 20 men with CSBD received four weeks of treatment with the opioid antagonist naltrexone, followed by a four-week follow-up phase. Adverse effects, adherence to treatment, and changes in compulsive sexual behavior were assessed. Study IV is an ongoing randomized controlled trial in which 80 individuals with CSBD receive either naltrexone or the selective serotonin reuptake inhibitor (SSRI) fluoxetine for eight weeks, followed by a six-week follow-up phase. The primary outcome measure is Hypersexual Disorder: Current Assessment Scale (HD:CAS), also used in Study III.

Results: In Study I, men with CSBD had higher scores on self-reports of exposure to violence in childhood and use of violence as adults, as well as higher KIVS total scores compared with healthy controls. Those who had made a suicide attempt (n=8, 12%) reported higher scores of sexual abuse in childhood as well as the highest value of total experience of interpersonal violence. In Study II, neurodevelopmental disorders were common in both clinical cohorts, both of which also reported more compulsive sexuality and attentional impulsivity than controls. Self-reported attentional impulsivity was the only independent positive predictor of compulsive sexual behavior. In Study III, despite initial adverse effects being common, naltrexone was found tolerable and the study procedures were feasible. Self-reported measures of compulsive sexual behavior decreased during treatment with naltrexone. 

Conclusion: Interpersonal violence may be related to suicidal behavior in CSBD; and attentional impulsivity is linked to the level of compulsive sexual behavior. Screening for interpersonal violence and neurodevelopmental disorders should be part of routine assessment in disorders of problematic sexuality. Treatment with naltrexone was tolerable and might be a suitable option for treatment in CSBD if found efficacious in the ongoing randomized controlled trial.

Ort, förlag, år, upplaga, sidor
Umeå: Umeå universitetet, 2021. s. 67
Serie
Umeå University medical dissertations, ISSN 0346-6612 ; 2149
Nyckelord
compulsive sexual behavior disorder, Naltrexone, Fluoxetine, hypersexual disorder, sexual addiction, interpersonal violence, suicidal behavior, impulsivity, treatment
Nationell ämneskategori
Psykiatri
Forskningsämne
psykiatri
Identifikatorer
urn:nbn:se:umu:diva-186811 (URN)978-91-7855-611-3 (ISBN)978-91-7855-612-0 (ISBN)
Disputation
2021-10-08, Psykiatrins sal A, Målpunkt F, plan o, Norrlands universitetssjukhus, Umeå, 09:00 (Engelska)
Opponent
Handledare
Tillgänglig från: 2021-09-17 Skapad: 2021-09-02 Senast uppdaterad: 2021-09-02Bibliografiskt granskad

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