Evidence map›Paper›PMID 26141511›Full record

Trial reportEuropean neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology2015

An analysis of moderators in the COMBINE study: Identifying subgroups of patients who benefit from acamprosate.

Ralitza Gueorguieva, Ran Wu, Wan-Min Tsai, Patrick G O'Connor, Lisa Fucito, Heping Zhang, Stephanie S O'Malley

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Ralitza GueorguievaDepartment of Biostatistics, Yale University School of Public Health and School of Medicine, New Haven, CT 06520, USA. Electronic address: ralitza.gueorguieva@yale.edu.
Ran WuDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT 06519, USA.
Wan-Min TsaiDepartment of Biostatistics, Yale University School of Public Health and School of Medicine, New Haven, CT 06520, USA.
Patrick G O'ConnorDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT 06519, USA.
Lisa FucitoDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT 06519, USA.
Heping ZhangDepartment of Biostatistics, Yale University School of Public Health and School of Medicine, New Haven, CT 06520, USA.
Stephanie S O'MalleyDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT 06519, USA.
Yale University · US

Funding

Translational Technologies CoreP50AA012870 · NIAAA · YALE UNIVERSITY · PI John H. Krystal · 2001 to 2026
$43.7M
Statistical Methods in Genetic Studies of Substance UseR01DA016750 · NIDA · YALE UNIVERSITY · PI ZHANG, HEPING · 2004 to 2016
$3.3M
Improving Alcoholism TreatmentK05AA014715 · NIAAA · YALE UNIVERSITY · PI O'MALLEY, STEPHANIE S · 2004 to 2013
$2.1M
Trajectories of Drinking and Compliance in the COMBINE StudyR01AA017173 · NIAAA · YALE UNIVERSITY · PI GUEORGUIEVA, RALITZA, O'MALLEY, STEPHANIE S · 2008 to 2013
$981k
New Approaches to Smoking Cessation in Heavy DrinkersK23AA020000 · NIAAA · YALE UNIVERSITY · PI FUCITO, LISA M · 2011 to 2016
$755k
NIAAA NIH HHS K05 AA014715NIAAA NIH HHS K05AA014715NIAAA NIH HHS K23 AA020000NIAAA NIH HHS K23AA020000NIAAA NIH HHS P50 AA012870NIAAA NIH HHS P50AA012870NIAAA NIH HHS R01 AA017173NIAAA NIH HHS R01AA017173NIDA NIH HHS R01 DA016750
6 · The paper itself

Abstract

The goal of the current study was to use tree-based methods to identify moderators of acamprosate effect on abstinence from heavy drinking in COMBINE, the largest study of pharmacotherapy for alcoholism in the United States to date. We used three different tree-based methods for identification of subgroups with enhanced treatment response on acamprosate based on over 100 predictors measured at baseline in COMBINE. No heavy drinking during the last two months of treatment was the considered outcome. All three methods identified consecutive days of abstinence prior to treatment as the most important moderator of treatment effect. Acamprosate was beneficial for participants with shorter abstinence (1 week or less) especially when body mass index was low or normal. In this group, 46% of participants receiving active acamprosate abstained from heavy drinking compared to 23% of those receiving placebo acamprosate. Prior treatment, age, drinking goal and cognitive inefficiency were identified as moderators of acamprosate effects by one of the three methods. In conclusion, acamprosate may be beneficial for participants with shorter abstinence who are not overweight or obese. One hypothesis for this finding is that this subgroup may have greater glutamatergic hyperactivity, a target of acamprosate, and may achieve better drug plasma levels based on their lower BMI. In contrast, those with extended pretreatment abstinence who have an otherwise good prognosis did not benefit from acamprosate. Further validation of the results in independent data sets is necessary.

Indexed as

AcamprosateAdultAlcohol DeterrentsAlcoholismBody Mass IndexDecision TreesDouble-Blind MethodHumansMiddle AgedTaurineTreatment OutcomeUnited StatesAcamprosateAlcohol DeterrentsTaurineAlcohol dependenceClassification and regression treesClinical trialsModerator effectsSubgroups with enhanced treatment effect

Identifiers

PMID26141511
PMCPMC4600651
OpenAlexW2097388609

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.