TY - DATA T1 - Supplementary Material for: A Randomised, Double-Blind, Placebo-Controlled Trial of As-Needed Naltrexone in the Treatment of Pathological Gambling PY - 2015/09/05 AU - Kovanen L. AU - Basnet S. AU - Castrén S. AU - Pankakoski M. AU - Saarikoski S.T. AU - Partonen T. AU - Alho H. AU - Lahti T. UR - https://karger.figshare.com/articles/dataset/Supplementary_Material_for_A_Randomised_Double-Blind_Placebo-Controlled_Trial_of_As-Needed_Naltrexone_in_the_Treatment_of_Pathological_Gambling/5128354 DO - 10.6084/m9.figshare.5128354.v1 L4 - https://ndownloader.figshare.com/files/8716507 L4 - https://ndownloader.figshare.com/files/8716510 KW - OPRM1 KW - Randomized controlled trial KW - Pathological gambling KW - Psychosocial support KW - Naltrexone N2 - Background/Aims: Effective treatment strategies are needed for the treatment of pathological gambling (PG). The efficacy of as-needed naltrexone was assessed in a single-centre, randomised, double-blind, placebo-controlled trial. Methods: The participants (n = 101) received either as-needed placebo or naltrexone (50 mg) and psychosocial support for 20 weeks. The primary outcome measure was the severity of PG assessed by the Yale-Brown Obsessive Compulsive Scale adapted for PG (PG-YBOCS). Secondary gambling-related outcome measures included thoughts/urges and behaviour subscales of PG-YBOCS as well as the highest daily expenditure and gambling frequency. In addition, RAND-36 scales of emotional well-being and social functioning were used as outcomes. The results were analysed using the intention-to-treat principle and linear random effects modelling. Results: No significant treatment group differences were found. In an exploratory analysis, emotional well-being increased in a subgroup of participants with AA genotype of opioid receptor, mu 1 (OPRM1) A118G polymorphism (p = 0.02). Conclusion: Overall, the as-needed naltrexone may not provide substantial additional benefit for PG patients receiving psychosocial support. Replication by larger scale studies is warranted to further evaluate naltrexone administration schedules for the treatment of PG and the role of OPRM1. ER -