Evidence map›Paper›PMID 22538805›Full record

Trial reportAmerican journal of respiratory and critical care medicine2012

Genome-wide association identifies the T gene as a novel asthma pharmacogenetic locus.

Kelan G Tantisira, Amy Damask, Stanley J Szefler, Brooke Schuemann, Amy Markezich, Jessica Su, Barbara Klanderman, Jody Sylvia, Rongling Wu, Fernando Martinez and 6 more

Open access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in American journal of respiratory and critical care medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 94 citations in OpenAlex.

  1. Genome-wide association study of inhaled corticosteroid response in admixed children with asthma.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2019
    Trial
  2. Trial
  3. Trial
  4. Trial
  5. Enhancing Asthma Pharmacogenetics Through Subtype-Specific Associations.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2025
    Article
  6. Genes · 2024
    Article
  7. Article
  8. Article
  9. Heterogeneity of Treatment Response to Asthma.Advances in experimental medicine and biology · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Identification ofJournal of personalized medicine · 2021
    Article
  14. Article
  15. Advances in asthma and allergic disease genetics: Is bigger always better?The Journal of allergy and clinical immunology · 2019
    Review
  16. Article
  17. How does race and ethnicity effect the precision treatment of asthma?Expert review of precision medicine and drug development · 2019
    Article
  18. Review
  19. Review
  20. Review
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

16 authors at 8 institutions in 1 country.

Kelan G TantisiraChanning Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, 181 Longwood Avenue, Boston, MA 02115, USA. kelan.tantisira@channing.harvard.edu
Amy Damask
Stanley J Szefler
Brooke Schuemann
Amy Markezich
Jessica Su
Barbara Klanderman
Jody Sylvia
Rongling Wu
Fernando Martinez
Homer A Boushey
Vernon M Chinchilli
Dave Mauger
Scott T Weiss
Elliot Israel
SHARP Investigators
Brigham and Women's Hospital · USPenn State Milton S. Hershey Medical Center · USHarvard University Press · USNational Jewish Health · USNovartis (United States) · USOverlake Hospital Medical Center · USUniversity of Arizona · USUniversity of California, San Francisco · US

Funding

Informatics for Integrating Biology/ the Bedside (RMI)U54LM008748 · NLM · BRIGHAM AND WOMEN'S HOSPITAL · PI KOHANE, ISAAC S. · 2004 to 2013
$39.0M
THE PHARMACOGENETICS OF ASTHMA TREATMENTU01HL065899 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI TANTISIRA, KELAN G, WEISS, SCOTT T · 2000 to 2014
$38.5M
PEDIATRIC ASTHMA NETWORK DATA COORDINATING CENTERU10HL064313 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI MAUGER, DAVID T. · 1999 to 2008
$18.3M
ACRN Data Coordinating CenterU10HL074231 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI CHINCHILLI, VERNON M. · 2003 to 2007
$13.3M
CHILDHOOD ASTHMA: EARLY PREVENTION AND PHARMACOGENETICSU10HL064307 · NHLBI · UNIVERSITY OF ARIZONA · PI MARTINEZ, FERNANDO D · 1999 to 2008
$9.0M
EARLY INTERVENTION IN CHILDHOOD ASTHMAU10HL064288 · NHLBI · NATIONAL JEWISH HEALTH · PI SZEFLER, STANLEY J. · 1999 to 2008
$6.7M
CHILDHOOD ASTHMA: INITIATION AND INTERVENTIONU10HL064305 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI LEMANSKE, ROBERT F · 1999 to 2008
$5.8M
PEDIATRIC ASTHMA CLINICAL RESEARCH NETWORK-CLINICAL CTRU10HL064287 · NHLBI · WASHINGTON UNIVERSITY · PI STRUNK, ROBERT · 1999 to 2008
$5.6M
ASTHMA NETWORK DATA COORDINATING CENTERU10HL051845 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI CHINCHILLI, VERNON M. · 1993 to 2002
$5.1M
CAMPCS/3U01HL075408 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI TONASCIA, JAMES A · 2003 to 2010
$4.9M
CHILDHOOD ASTHMA PREVENTION STUDY (CAPS) FOR PACRNU10HL064295 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZEIGER, ROBERT S · 1999 to 2008
$4.4M
INTEGRATIVE PHARMACOGENOMICS OF LEUKOTRIENE INHIBITION IN ASTHMAR01HL092197 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI TANTISIRA, KELAN G · 2009 to 2013
$3.6M
NHLBI NIH HHS R01 HL092197NHLBI NIH HHS U01 HL065899NHLBI NIH HHS U01 HL075232NHLBI NIH HHS U01 HL075408NHLBI NIH HHS U01 HL075409NHLBI NIH HHS U01 HL075415NHLBI NIH HHS U01 HL075416NHLBI NIH HHS U01 HL075417NHLBI NIH HHS U01 HL075419NHLBI NIH HHS U01 HL075420NHLBI NIH HHS U01 HL64313NHLBI NIH HHS U01 HL65899NHLBI NIH HHS U01 HL75232NHLBI NIH HHS U01 HL75408NHLBI NIH HHS U01 HL75409NHLBI NIH HHS U01 HL75415NHLBI NIH HHS U01 HL75416NHLBI NIH HHS U01 HL75417NHLBI NIH HHS U01 HL75419NHLBI NIH HHS U01 HL75420NHLBI NIH HHS U10 HL051823NHLBI NIH HHS U10 HL051831NHLBI NIH HHS U10 HL051834NHLBI NIH HHS U10 HL051843NHLBI NIH HHS U10 HL051845NHLBI NIH HHS U10 HL056443NHLBI NIH HHS U10 HL064287NHLBI NIH HHS U10 HL064288NHLBI NIH HHS U10 HL064295NHLBI NIH HHS U10 HL064305NHLBI NIH HHS U10 HL064307NHLBI NIH HHS U10 HL064313NHLBI NIH HHS U10 HL074231NHLBI NIH HHS U10 HL51810NHLBI NIH HHS U10 HL51823NHLBI NIH HHS U10 HL51831NHLBI NIH HHS U10 HL51834NHLBI NIH HHS U10 HL51843NHLBI NIH HHS U10 HL51845NHLBI NIH HHS U10 HL56443NHLBI NIH HHS U10 HL64287NHLBI NIH HHS U10 HL64288NHLBI NIH HHS U10 HL64295NHLBI NIH HHS U10 HL64305NHLBI NIH HHS U10 HL64307NHLBI NIH HHS U10 HL74231NLM NIH HHS U54 LM008748NLM NIH HHS U54LM8748
6 · The paper itself

Abstract

rationaleTo date, most studies aimed at discovering genetic factors influencing treatment response in asthma have focused on biologic candidate genes. Genome-wide association studies (GWAS) can rapidly identify novel pharmacogenetic loci.

objectivesTo investigate if GWAS can identify novel pharmacogenetic loci in asthma.

methodsUsing phenotypic and GWAS genotype data available through the NHLBI-funded Single-nucleotide polymorphism Health association-Asthma Resource Project, we analyzed differences in FEV(1) in response to inhaled corticosteroids in 418 white subjects with asthma. Of the 444,088 single nucleotide polymorphisms (SNPs) analyzed, the lowest 50 SNPs by P value were genotyped in an independent clinical trial population of 407 subjects with asthma. MEASUREMENTS AND MAIN

resultsThe lowest P value for the GWAS analysis was 2.09 × 10(-6). Of the 47 SNPs successfully genotyped in the replication population, three were associated under the same genetic model in the same direction, including two of the top four SNPs ranked by P value. Combined P values for these SNPs were 1.06 × 10(-5) for rs3127412 and 6.13 × 10(-6) for rs6456042. Although these two were not located within a gene, they were tightly correlated with three variants mapping to potentially functional regions within the T gene. After genotyping, each T gene variant was also associated with lung function response to inhaled corticosteroids in each of the trials associated with rs3127412 and rs6456042 in the initial GWAS analysis. On average, there was a twofold to threefold difference in FEV(1) response for those subjects homozygous for the wild-type versus mutant alleles for each T gene SNP.

conclusionsGenome-wide association has identified the T gene as a novel pharmacogenetic locus for inhaled corticosteroid response in asthma.

Indexed as

AdolescentAdrenal Cortex HormonesAdultAllelesAsthmaBrachyury ProteinChildChild, PreschoolFemaleFetal ProteinsGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansMaleMiddle AgedAdrenal Cortex HormonesBrachyury ProteinFetal ProteinsT-Box Domain Proteins

Identifiers

PMID22538805
PMCPMC3381232
OpenAlexW2109534427

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.