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Genetic variants associated with acamprosate treatment response in alcohol use disorder patients: A multiple omics study.
Ho, Ming-Fen; Zhang, Cheng; Wei, Lixuan; Zhang, Lingxin; Moon, Irene; Geske, Jennifer R; Skime, Michelle K; Choi, Doo-Sup; Biernacka, Joanna M; Oesterle, Tyler S; Frye, Mark A; Seppala, Marvin D; Karpyak, Victor M; Li, Hu; Weinshilboum, Richard M.
Affiliation
  • Ho MF; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.
  • Zhang C; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.
  • Wei L; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.
  • Zhang L; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.
  • Moon I; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.
  • Geske JR; Department of Health Sciences Research, Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota, USA.
  • Skime MK; Department of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota, USA.
  • Choi DS; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.
  • Biernacka JM; Department of Health Sciences Research, Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota, USA.
  • Oesterle TS; Department of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota, USA.
  • Frye MA; Department of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota, USA.
  • Seppala MD; Department of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota, USA.
  • Karpyak VM; Hazelden Betty Ford Foundation, Center City, Minnesota, USA.
  • Li H; Department of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota, USA.
  • Weinshilboum RM; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.
Br J Pharmacol ; 179(13): 3330-3345, 2022 07.
Article in En | MEDLINE | ID: mdl-35016259
ABSTRACT
BACKGROUND AND

PURPOSE:

Acamprosate is an anti-craving drug used for the pharmacotherapy of alcohol use disorder (AUD). However, only some patients achieve optimal therapeutic outcomes. This study was designed to explore differences in metabolomic profiles between patients who maintained sobriety and those who relapsed, to determine whether those differences provide insight into variation in acamprosate treatment response phenotypes. EXPERIMENTAL

APPROACH:

We previously conducted an acamprosate trial involving 442 AUD patients, and 267 of these subjects presented themselves for a 3-month follow-up. The primary outcome was abstinence. Clinical information, genomic data and metabolomics data were collected. Baseline plasma samples were assayed using targeted metabolomics. KEY

RESULTS:

Baseline plasma arginine, threonine, α-aminoadipic acid and ethanolamine concentrations were associated with acamprosate treatment outcomes and baseline craving intensity, a measure that has been associated with acamprosate treatment response. We next applied a pharmacometabolomics-informed genome-wide association study (GWAS) strategy to identify genetic variants that might contribute to variations in plasma metabolomic profiles that were associated with craving and/or acamprosate treatment outcome. Gene expression data for induced pluripotent stem cell-derived forebrain astrocytes showed that a series of genes identified during the metabolomics-informed GWAS were ethanol responsive. Furthermore, a large number of those genes could be regulated by acamprosate. Finally, we identified a series of single nucleotide polymorphisms that were associated with acamprosate treatment outcomes. CONCLUSION AND IMPLICATIONS These results serve as an important step towards advancing our understanding of disease pathophysiology and drug action responsible for variation in acamprosate response and alcohol craving in AUD patients.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alcohol Deterrents / Alcoholism Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Br J Pharmacol Year: 2022 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alcohol Deterrents / Alcoholism Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Br J Pharmacol Year: 2022 Document type: Article Affiliation country: United States