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Chunk #33 — RESULTS — Medication by OPRM1 genotype — Alcohol induced craving (AUQ), high (SHAS)

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Naltrexone modification of drinking effects in a subacute treatment and bar-lab paradigm: influence of OPRM1 and dopamine transporter (SLC6A3) genes.
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There were no significant main effects or interactions of medication group and OPRM1 genotype on alcohol-induced craving (p values > 0.3 for main effects and interaction) or high (p values > 0.4 for main effects and interaction) after the priming drink. Peak blood alcohol level as a covariate had no material effect on these analyzes.