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Prospective randomized pharmacogenetic study of topiramate for treating alcohol use disorder
by
Hartwell, Emily E
, Kranzler, Henry R
, Pond, Timothy
, Kampman, Kyle M
, Morris, Paige E
, Lynch, Kevin G
, Crist, Richard C
in
Alcohol abuse
/ Alcohol use
/ Alleles
/ Dosage
/ Drinking behavior
/ Gene polymorphism
/ Genotype & phenotype
/ Homozygotes
/ Placebos
/ Single-nucleotide polymorphism
/ Topiramate
/ γ-Glutamyltransferase
2021
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Prospective randomized pharmacogenetic study of topiramate for treating alcohol use disorder
by
Hartwell, Emily E
, Kranzler, Henry R
, Pond, Timothy
, Kampman, Kyle M
, Morris, Paige E
, Lynch, Kevin G
, Crist, Richard C
in
Alcohol abuse
/ Alcohol use
/ Alleles
/ Dosage
/ Drinking behavior
/ Gene polymorphism
/ Genotype & phenotype
/ Homozygotes
/ Placebos
/ Single-nucleotide polymorphism
/ Topiramate
/ γ-Glutamyltransferase
2021
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Prospective randomized pharmacogenetic study of topiramate for treating alcohol use disorder
by
Hartwell, Emily E
, Kranzler, Henry R
, Pond, Timothy
, Kampman, Kyle M
, Morris, Paige E
, Lynch, Kevin G
, Crist, Richard C
in
Alcohol abuse
/ Alcohol use
/ Alleles
/ Dosage
/ Drinking behavior
/ Gene polymorphism
/ Genotype & phenotype
/ Homozygotes
/ Placebos
/ Single-nucleotide polymorphism
/ Topiramate
/ γ-Glutamyltransferase
2021
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Prospective randomized pharmacogenetic study of topiramate for treating alcohol use disorder
Journal Article
Prospective randomized pharmacogenetic study of topiramate for treating alcohol use disorder
2021
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Overview
In a prior study, topiramate reduced heavy drinking among individuals who sought to reduce their drinking, with the effect moderated by a single nucleotide polymorphism (SNP; rs2832407) in GRIK1, which encodes the kainate GluK1 receptor subunit (Kranzler et al. 2014). The present study sought to replicate prospectively the effect of topiramate and rs2832407 in patients with DSM-5 alcohol use disorder (AUD) who sought to reduce or stop their drinking. We stratified the randomization on genotype (rs2832407*C-allele homozygotes vs. A-allele carriers) and assigned 170 European-American participants (71.2% male) to receive 12 weeks of treatment with topiramate (N = 85), at a maximal daily dosage of 200 mg, or matching placebo (N = 85). At each of nine treatment visits participants received brief counseling to reduce drinking and increase abstinent days. We hypothesized that topiramate-treated patients with the rs2832407*CC genotype would reduce heavy drinking days (HDDs) more than the other three groups. The rate of treatment completion was 91.8% in both groups. The mean number of HDDs per week in the placebo group was 1.67 (95% CI = (1.29, 2.16), p = 0.0001) times greater than in the topiramate group, which was confirmed by the topiramate group’s significantly greater reduction in the concentration of the liver enzyme γ-glutamyltransferase and lower alcohol-related problems score. There was no significant difference in topiramate’s effect on HDDs between genotype groups. Although consistent with other studies showing a reduction in heavy drinking with topiramate treatment, the prior finding of a moderating effect of rs2832407 genotype was not replicated in this prospective trial.
Publisher
Nature Publishing Group
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