Evidence map›Paper›PMID 19264973›Full record

Trial reportAmerican journal of respiratory and critical care medicine2009

Assessing the reproducibility of asthma candidate gene associations, using genome-wide data.

Angela J Rogers, Benjamin A Raby, Jessica A Lasky-Su, Amy Murphy, Ross Lazarus, Barbara J Klanderman, Jody S Sylvia, John P Ziniti, Christoph Lange, Juan C Celedón and 2 more

Open access · greenAbstract readClinical TrialComparative StudyMulticenter Study
In one paragraph

Trial report in American journal of respiratory and critical care medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
9.8field-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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 105 citations in OpenAlex.

  1. Pooled it
  2. Identification of ATPAF1 as a novel candidate gene for asthma in children.The Journal of allergy and clinical immunology · 2011
    Trial
  3. The interaction of glutathione S-transferase M1-null variants with tobacco smoke exposure and the development of childhood asthma.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2009
    Trial
  4. Article
  5. Article
  6. Asthma Susceptibility GeneAmerican journal of respiratory cell and molecular biology · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Epistatic effects of multiple receptor genes on pathophysiology of asthma - its limits and potential for clinical application.Medical science monitor : international medical journal of experimental and clinical research · 2014
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Copy number variation prevalence in known asthma genes and their impact on asthma susceptibility.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2013
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Angela J RogersChanning Laboratory, Brigham and Women's Hospital, Harvard Medical School, 181 Longwood Avenue, Boston, MA 02115, USA. reajr@channing.harvard.edu
Benjamin A Raby
Jessica A Lasky-Su
Amy Murphy
Ross Lazarus
Barbara J Klanderman
Jody S Sylvia
John P Ziniti
Christoph Lange
Juan C Celedón
Edwin K Silverman
Scott T Weiss
Brigham and Women's Hospital · USHarvard University · US

Funding

THE PHARMACOGENETICS OF ASTHMA TREATMENTU01HL065899 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI TANTISIRA, KELAN G, WEISS, SCOTT T · 2000 to 2014
$38.5M
SYSTEMS APPROACHES TO THE EPIDEMIOLOGY, GENETICS AND GENOMICS OF LUNG DISEASEST32HL007427 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI DAWN L DEMEO, Edwin K Silverman · 1985 to 2026
$13.6M
Statistical GeneticsP01HL083069 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI WEISS, SCOTT T · 2007 to 2011
$12.2M
CAMP Continuation Study/Phase 3U01HL075419 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI FUHLBRIGGE, ANNE L · 2003 to 2010
$2.0M
CLINICAL CENTER FOR CAMPN01HR016049 · HR · BRIGHAM AND WOMEN'S HOSPITAL · PI WEISS, SCOTT T · 1991 to 2000
$1.0M
Fine mapping of an Asthma Locus of Chromosome 12qK08HL074193 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI RABY, BENJAMIN ALEXANDER · 2003 to 2007
$670k
NHLBI NIH HHS K08 HL074193NHLBI NIH HHS N01 HR16049NHLBI NIH HHS P01 HL083069NHLBI NIH HHS T32 HL07427NHLBI NIH HHS U01 HL065899NHLBI NIH HHS U01 HL075419
6 · The paper itself

Abstract

rationaleAssociation studies have implicated many genes in asthma pathogenesis, with replicated associations between single-nucleotide polymorphisms (SNPs) and asthma reported for more than 30 genes. Genome-wide genotyping enables simultaneous evaluation of most of this variation, and facilitates more comprehensive analysis of other common genetic variation around these candidate genes for association with asthma.

objectivesTo use available genome-wide genotypic data to assess the reproducibility of previously reported associations with asthma and to evaluate the contribution of additional common genetic variation surrounding these loci to asthma susceptibility.

methodsIllumina Human Hap 550Kv3 BeadChip (Illumina, San Diego, CA) SNP arrays were genotyped in 422 nuclear families participating in the Childhood Asthma Management Program. Genes with at least one SNP demonstrating prior association with asthma in two or more populations were tested for evidence of association with asthma, using family-based association testing. MEASUREMENTS AND MAIN

resultsWe identified 39 candidate genes from the literature, using prespecified criteria. Of the 160 SNPs previously genotyped in these 39 genes, 10 SNPs in 6 genes were significantly associated with asthma (including the first independent replication for asthma-associated integrin beta(3) [ITGB3]). Evaluation of 619 additional common variants included in the Illumina 550K array revealed additional evidence of asthma association for 15 genes, although none were significant after adjustment for multiple comparisons.

conclusionsWe replicated asthma associations for a minority of candidate genes. Pooling genome-wide association study results from multiple studies will increase the power to appreciate marginal effects of genes and further clarify which candidates are true "asthma genes."

Indexed as

Genome, HumanPolymorphism, GeneticAdministration, InhalationAllelesAnti-Inflammatory AgentsAsthmaChildDNAFemaleFollow-Up StudiesGenetic Predisposition to DiseaseGenotypeHumansIntegrin beta3Interleukin-1 Receptor-Associated KinasesMaleAnti-Inflammatory AgentsDNAIntegrin beta3Interleukin-1 Receptor-Associated KinasesITGB3 protein, humanMembrane ProteinsORMDL3 protein, human

Identifiers

PMID19264973
PMCPMC2695495
OpenAlexW2106852187

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.