Evidence map›Paper›PMID 20421847›Full record

ArticlePsychiatric genetics2010

Using trajectory analyses to refine phenotype for genetic association: conduct problems and the serotonin transporter (5HTTLPR).

Joseph T Sakai, Jason D Boardman, Heather L Gelhorn, Andrew Smolen, Robin P Corley, David Huizinga, Scott Menard, John K Hewitt, Michael C Stallings

Abstract read
In one paragraph

Article in Psychiatric genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Bringing a developmental perspective to anxiety genetics.Development and psychopathology · 2012
    Review
  7. Article
  8. Article
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.

Joseph T SakaiUniversity of Colorado Denver, Aurora, Colorado, USA. joseph.sakai@ucdenver.edu
Jason D Boardman
Heather L Gelhorn
Andrew Smolen
Robin P Corley
David Huizinga
Scott Menard
John K Hewitt
Michael C Stallings

Funding

Twin StudyP60DA011015 · NIDA · UNIVERSITY OF COLORADO DENVER · PI HEWITT, JOHN K. · 1997 to 2013
$22.5M
NYS FAMILY STUDY: PROBLEM ALCOHOL USE &PROBLEM BEHAVIORR01AA011949 · NIAAA · UNIVERSITY OF COLORADO AT BOULDER · PI MENARD, SCOTT W · 2000 to 2004
$6.9M
Asian Teens, substance dependence and conduct disorderK08DA016314 · NIDA · UNIVERSITY OF COLORADO DENVER · PI SAKAI, JOSEPH T · 2004 to 2008
$892k
THE SOCIAL DETERMINANTS OF GENETIC EXPRESSION: A LIFE-COURSE PERSPECTIVEK01HD050336 · NICHD · UNIVERSITY OF COLORADO AT BOULDER · PI BOARDMAN, JASON D · 2005 to 2009
$602k
Integrating Genetics and Social Sciences Annual ConferenceR13HD078100 · NICHD · UNIVERSITY OF COLORADO · PI BOARDMAN, JASON D · 2013 to 2017
$60k
NIAAA NIH HHS AA011949NIAAA NIH HHS R01 AA011949NICHD NIH HHS HD050336NICHD NIH HHS K01 HD050336NICHD NIH HHS R13 HD078100NIDA NIH HHS DA011015NIDA NIH HHS DA016314NIDA NIH HHS K08 DA016314NIDA NIH HHS P60 DA011015
6 · The paper itself

Abstract

backgroundConduct disorder is a serious, relatively common disorder of childhood and adolescence. Findings from genetic association studies searching for genetic determinants of the liability toward such behaviors have been inconsistent. One possible explanation for differential results is that most studies define phenotype from a single assessment; for many adolescents conduct problems decrease in severity over time, whereas for others such behaviors persist. Therefore, longitudinal datasets offer the opportunity to refine phenotype.

methodsWe used Caucasians that were first assessed during adolescence from the National Youth Survey Family Study. Nine waves of data were used to create latent growth trajectories and test for associations between trajectory class and 5HTTLPR genotype.

resultsFor the full sample, 5HTTLPR was not associated with conduct problem phenotypes. However, the short (s) allele was associated with chronic conduct problems in females; a nominally significant sex by 5HTTLPR genotype interaction was noted.

conclusionLongitudinal studies provide unique opportunities for phenotypic refinement and such techniques, with large samples, may be useful for phenotypic definition with other study designs, such as whole genome association studies.

Indexed as

AdolescentBase SequenceChildConduct DisorderDNA PrimersFemaleGene FrequencyHumansMalePhenotypeSerotonin Plasma Membrane Transport ProteinsSurveys and QuestionnairesDNA PrimersSerotonin Plasma Membrane Transport Proteins

Identifiers

PMID20421847
PMCPMC2934879

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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.