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ABSTRACT: Background and aims
There is wide inter-individual variability in response to the treatment of alcohol use disorder (AUD) with the opioid receptor antagonist naltrexone. To identify patients who may be most responsive to naltrexone treatment, studies have examined the moderating effect of rs1799971, a single nucleotide polymorphism (SNP) that encodes a non-synonymous substitution (Asn40Asp) in the mu-opioid receptor gene, OPRM1. The aims of this study were to: (1) conduct a systematic review of randomized clinical trials (RCTs); (2) assess the bias of the available studies and gauge publication bias; and (3) meta-analyze the interaction effect of the Asn40Asp SNP on the response to naltrexone treatment.Methods
We searched for placebo-controlled RCTs that examined the effect
SUBMITTER: Hartwell EE
PROVIDER: S-EPMC7340566 | biostudies-literature | 2020 Aug
REPOSITORIES: biostudies-literature