Evidence map›Paper›PMID 30197492›Full record

ArticleJournal of developmental and physical disabilities2018

Testing genetic modifiers of behavior and response to atomoxetine in autism spectrum disorder with ADHD.

Elizabeth S Barrie, Julia K Pinsonneault, Wolfgang Sadee, Jill A Hollway, Benjamin L Handen, Tristram Smith, L Eugene Arnold, Eric Butter, Emily Hansen-Kiss, Gail E Herman and 1 more

Abstract read
In one paragraph

Article in Journal of developmental and physical disabilities, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Article
  3. The Role of GCH1 Deficiency and Tetrahydrobiopterin in Mental Health.International journal of molecular sciences · 2025
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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

11 authors at 4 institutions in 1 country.

Elizabeth S BarrieThe Ohio State University.
Julia K PinsonneaultThe Ohio State University.
Wolfgang SadeeThe Ohio State University.
Jill A HollwayThe Ohio State University.
Benjamin L HandenDepartments of Psychiatry and Pediatrics, University of Pittsburgh School of Medicine.
Tristram SmithDepartment of Pediatrics, University of Rochester Medical Center.
L Eugene ArnoldThe Ohio State University.
Eric ButterThe Ohio State University.
Emily Hansen-KissInstitute for Genomic Medicine, Nationwide Children's Hospital.
Gail E HermanThe Ohio State University.
Michael G AmanThe Ohio State University.
The Ohio State University · USNationwide Children's Hospital · USUniversity of Pittsburgh · USUniversity of Rochester Medical Center · US

Funding

UNIVERSITY OF ROCHESTER'S RESEARCH ASSOCIATE ORGANIZATIONUL1RR024160 · NCRR · UNIVERSITY OF ROCHESTER · PI PEARSON, THOMAS ARTHUR · 2006 to 2011
$38.7M
University of Iowa Clinical and Translational Science Program (TL1)UL1RR025755 · NCRR · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2008 to 2011
$26.3M
The Ohio State University Center for clinical and Translational ScienceUL1TR001070 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$22.6M
Expression Genetics in Drug TherapyU01GM092655 · NIGMS · OHIO STATE UNIVERSITY · PI SADEE, WOLFGANG · 2010 to 2014
$8.6M
2/3-Atomoxetine Placebo and Parent Training in AutismR01MH079080 · NIMH · OHIO STATE UNIVERSITY · PI AMAN, MICHAEL GEORGE · 2008 to 2012
$1.8M
3/3-Atomoxetine Placebo and Parent Training in AutismR01MH083247 · NIMH · UNIVERSITY OF ROCHESTER · PI SMITH, TRISTRAM H · 2008 to 2012
$1.4M
1/3-Atomoxetine Placebo and Parent Training in AutismR01MH079082 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HANDEN, BENJAMIN L · 2008 to 2012
$1.4M
NCATS NIH HHS UL1 TR001070NCRR NIH HHS UL1 RR024160NCRR NIH HHS UL1 RR025755NIGMS NIH HHS U01 GM092655NIMH NIH HHS R01 MH079080NIMH NIH HHS R01 MH079082NIMH NIH HHS R01 MH083247
6 · The paper itself

Abstract

backgroundFrequent non-pathogenic genetic variants may act as moderators of phenotypic severity for complex disorders such as autism spectrum disorder (ASD). We previously identified polymorphisms affecting mRNA expression of candidate genes, including tryptophan hydroxylase 2 (

methodWe compare genotypes and (1) clinical response to atomoxetine, (2) scores from the Autism Diagnostic Interview-Revised (ADI-R), and (3) severity of Attention Deficit Hyperactivity Disorder (ADHD) symptoms in a cohort of patients with ASD from multiple study sites.

resultsThere was no association between CYP2D6 metabolizer status and atomoxetine response.

conclusionsWe find associations between ASD phenotypes and regulatory variants in catecholamine biosynthesis genes. This work may help guide future genetics studies related to ASD.

Indexed as

atomoxetine (Strattera)attention deficit/hyperactivity disorder (ADHD)autism spectrum disorder (ASD)dopamine transporter (DAT, SLC6A3)geneticsrestrictive and repetitive behaviortryptophan hydroxylase 2 (TPH2)

Identifiers

PMID30197492
PMCPMC6128165
OpenAlexW2793195116

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.