Evidence map›Paper›PMID 18519826›Full record

Trial reportArchives of general psychiatry2008

Molecular genetics of successful smoking cessation: convergent genome-wide association study results.

George R Uhl, Qing-Rong Liu, Tomas Drgon, Catherine Johnson, Donna Walther, Jed E Rose, Sean P David, Ray Niaura, Caryn Lerman

Open access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Archives of general psychiatry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 156 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
156citing papers in PubMed, 8 pooled it
18.3field-weighted citation impact, top 1% 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

156 citing papers in PubMed, 8 syntheses or guidelines pooled it, 240 citations in OpenAlex.

  1. Pooled it
  2. Antidepressants for smoking cessation.The Cochrane database of systematic reviews · 2020
    Pooled it
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  6. Antidepressants for smoking cessation.The Cochrane database of systematic reviews · 2014
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  9. Organic cation transporter variation and response to smoking cessation therapies.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2014
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  14. Pharmacogenetic smoking cessation intervention in a health care setting: a pilot feasibility study.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2013
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96 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 1 country.

George R UhlMolecular Neurobiology Research Branch, National Institutes of Health-Intramural Research Program, National Institute on Drug Abuse, 333 Cassell Dr, Ste 3510, Baltimore, MD 21224, USA. guhl@intra.nida.nih.gov
Qing-Rong Liu
Tomas Drgon
Catherine Johnson
Donna Walther
Jed E Rose
Sean P David
Ray Niaura
Caryn Lerman
National Institutes of Health · USDuke University · USRhode Island Hospital · US

Funding

TRANSDISCIPLINARY TOBACCO USE RESEARCH CENTERSP50CA084718 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LERMAN, CARYN · 1999 to 2008
$17.8M
Statistical Sciences CoreP50CA084719 · NCI · MIRIAM HOSPITAL · PI PAPANDONATOS, GEORGE DENNIS · 1999 to 2008
$17.8M
BIOBEHAVIORAL LUNG CANCER PREVENTION PROGRAMR01CA063562 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LERMAN, CARYN · 1993 to 2004
$2.7M
Molecular Genetic Bases for Quit SuccessZ01DA000537 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI UHL, GEORGE RICHARD · 2007 to 2008
$1.7M
Psychobiological /Genetic Determinants-Smoking CessationK08DA014276 · NIDA · MEMORIAL HOSPITAL OF RHODE ISLAND · PI DAVID, SEAN P. · 2002 to 2006
$786k
COPING WITH DEPRESSION IN SMOKING CESSATIONR01DA008511 · NIDA · BUTLER HOSPITAL (PROVIDENCE, RI) · PI BROWN, RICHARD A · 1993 to 2000
$342k
PSYCHOSOCIAL STRESSORS, SMOKING CESSATION AND C V RISKR01HL032318 · NHLBI · MIRIAM HOSPITAL · PI NIAURA, RAYMOND S. · 1986 to 2000
$251k
Intramural NIH HHSNCI NIH HHS P50 CA084719NCI NIH HHS P50CA84719NCI NIH HHS P50CA/DA84718NCI NIH HHS R01 CA063562NCI NIH HHS R01CA 63562NHLBI NIH HHS HL32318NIDA NIH HHS 1K08 DA14276-05NIDA NIH HHS DA08511NIDA NIH HHS K08 DA014276
6 · The paper itself

Abstract

contextSmoking remains a major public health problem. Twin studies indicate that the ability to quit smoking is substantially heritable, with genetics that overlap modestly with the genetics of vulnerability to dependence on addictive substances.

objectivesTo identify replicated genes that facilitate smokers' abilities to achieve and sustain abstinence from smoking (herein after referred to as quit-success genes) found in more than 2 genome-wide association (GWA) studies of successful vs unsuccessful abstainers, and, secondarily, to nominate genes for selective involvement in smoking cessation success with bupropion hydrochloride vs nicotine replacement therapy (NRT).

designThe GWA results in subjects from 3 centers, with secondary analyses of NRT vs bupropion responders.

settingOutpatient smoking cessation trial participants from 3 centers.

participantsEuropean American smokers who successfully vs unsuccessfully abstain from smoking with biochemical confirmation in a smoking cessation trial using NRT, bupropion, or placebo (N = 550).

main outcome measuresQuit-success genes, reproducibly identified by clustered nominally positive single-nucleotide polymorphisms (SNPs) in more than 2 independent samples with significant P values based on Monte Carlo simulation trials. The NRT-selective genes were nominated by clustered SNPs that display much larger t values for NRT vs placebo comparisons. The bupropion-selective genes were nominated by bupropion-selective results.

resultsVariants in quit-success genes are likely to alter cell adhesion, enzymatic, transcriptional, structural, and DNA, RNA, and/or protein-handling functions. Quit-success genes are identified by clustered nominally positive SNPs from more than 2 samples and are unlikely to represent chance observations (Monte Carlo P< .0003). These genes display modest overlap with genes identified in GWA studies of dependence on addictive substances and memory.

conclusionsThese results support polygenic genetics for success in abstaining from smoking, overlap with genetics of substance dependence and memory, and nominate gene variants for selective influences on therapeutic responses to bupropion vs NRT. Molecular genetics should help match the types and/or intensity of antismoking treatments with the smokers most likely to benefit from them.

Indexed as

AllelesGenomeSmoking CessationAdultAntidepressive Agents, Second-GenerationBupropionChromosome MappingControlled Clinical Trials as TopicDose-Response Relationship, DrugDouble-Blind MethodFemaleGenetic MarkersGenetic Predisposition to DiseaseGenetic VariationHumansMaleAntidepressive Agents, Second-GenerationBupropionGenetic MarkersNicotineNicotinic Agonists

Identifiers

PMID18519826
PMCPMC2430596
OpenAlexW2077723521

What OpenQuestion holds

Textmetadata
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.