Evidence map›Paper›PMID 18617639›Full record

ArticleAmerican journal of respiratory and critical care medicine2008

ARG1 is a novel bronchodilator response gene: screening and replication in four asthma cohorts.

Augusto A Litonjua, Jessica Lasky-Su, Kady Schneiter, Kelan G Tantisira, Ross Lazarus, Barbara Klanderman, John J Lima, Charles G Irvin, Stephen P Peters, John P Hanrahan and 6 more

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory and critical care medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 2 pooled it
6.4field-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

60 citing papers in PubMed, 2 syntheses or guidelines pooled it, 130 citations in OpenAlex.

  1. Pooled it
  2. ST13 polymorphisms and their effect on exacerbations in steroid-treated asthmatic children and young adults.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2015
    Pooled it
  3. Regulatory haplotypes in ARG1 are associated with altered bronchodilator response.American journal of respiratory and critical care medicine · 2011
    Trial
  4. IL-9R/Arg1 pathway promotes polyamine metabolism in human airway macrophages.The Journal of allergy and clinical immunology · 2026
    Article
  5. Article
  6. 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. Article
  14. Article
  15. Pharmacogenetics of Bronchodilator Response: Future Directions.Current allergy and asthma reports · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

16 authors at 8 institutions in 1 country.

Augusto A LitonjuaChanning Laboratory, Pulmonary Division, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA. augusto.litonjua@channing.harvard.edu
Jessica Lasky-Su
Kady Schneiter
Kelan G Tantisira
Ross Lazarus
Barbara Klanderman
John J Lima
Charles G Irvin
Stephen P Peters
John P Hanrahan
Stephen B Liggett
Gregory A Hawkins
Deborah A Meyers
Eugene R Bleecker
Christoph Lange
Scott T Weiss
Brigham and Women's Hospital · USWake Forest University · USHarvard University · USNemours Children's Clinic · USSunovion (United States) · USUniversity of Maryland, Baltimore · USUniversity of Vermont · USUtah State 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
PHARMACOGENETICS OF ASTHMA MONOTHERAPYR01HL074755 · NHLBI · NEMOURS CHILDREN'S CLINIC · PI LIMA, JOHN J · 2003 to 2005
$1.6M
CLINICAL CENTER FOR CAMPN01HR016049 · HR · BRIGHAM AND WOMEN'S HOSPITAL · PI WEISS, SCOTT T · 1991 to 2000
$1.0M
CLINICAL COORDINATING CENTER FOR CAMPN01HR016044 · HR · JOHNS HOPKINS UNIVERSITY · PI TONASCIA, JAMES A · 1991 to 2006
$729k
LEUKOTRIENE POLYMORPHISMS &MONTELUKAST RESPONSER01HL071394 · NHLBI · NEMOURS CHILDREN'S CLINIC · PI LIMA, JOHN J · 2002 to 2003
$352k
CLINICAL CENTER FOR CAMPN01HR016047 · HR · HOSPITAL FOR SICK CHLDRN (TORONTO) · PI MACLUSKY, IAN B · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016050 · HR · ASTHMA, INC. · PI SHAPIRO, GAIL G · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016051 · HR · WASHINGTON UNIVERSITY · PI STRUNK, ROBERT C · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016052 · HR · JOHNS HOPKINS UNIVERSITY · PI ADKINSON, N FRANKLIN · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016046 · HR · UNIVERSITY OF NEW MEXICO · PI KELLY, H W · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016048 · HR · NATIONAL JEWISH HEALTH · PI SZEFLER, STANLEY J · 1991 to 2000
$0k
CLINICAL CENTER FOR CAMPN01HR016045 · HR · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI ZEIGER, ROBERT S · 1991 to 2001
$0k
NHLBI NIH HHS HL071394NHLBI NIH HHS HL074755NHLBI NIH HHS HR16045NHLBI NIH HHS HR16046NHLBI NIH HHS HR16047NHLBI NIH HHS HR16048NHLBI NIH HHS HR16049NHLBI NIH HHS HR16050NHLBI NIH HHS HR16051NHLBI NIH HHS HR16052NHLBI NIH HHS N01-HR16044NHLBI NIH HHS N01-HR16049NHLBI NIH HHS U01 HL065899NHLBI NIH HHS U01 HL65899
6 · The paper itself

Abstract

rationaleInhaled beta-agonists are one of the most widely used classes of drugs for the treatment of asthma. However, a substantial proportion of patients with asthma do not have a favorable response to these drugs, and identifying genetic determinants of drug response may aid in tailoring treatment for individual patients.

objectivesTo screen variants in candidate genes in the steroid and beta-adrenergic pathways for association with response to inhaled beta-agonists.

methodsWe genotyped 844 single nucleotide polymorphisms (SNPs) in 111 candidate genes in 209 children and their parents participating in the Childhood Asthma Management Program. We screened the association of these SNPs with acute response to inhaled beta-agonists (bronchodilator response [BDR]) using a novel algorithm implemented in a family-based association test that ranked SNPs in order of statistical power. Genes that had SNPs with median power in the highest quartile were then taken for replication analyses in three other asthma cohorts. MEASUREMENTS AND MAIN

resultsWe identified 17 genes from the screening algorithm and genotyped 99 SNPs from these genes in a second population of patients with asthma. We then genotyped 63 SNPs from four genes with significant associations with BDR, for replication in a third and fourth population of patients with asthma. Evidence for association from the four asthma cohorts was combined, and SNPs from ARG1 were significantly associated with BDR. SNP rs2781659 survived Bonferroni correction for multiple testing (combined P value = 0.00048, adjusted P value = 0.047).

conclusionsThese findings identify ARG1 as a novel gene for acute BDR in both children and adults with asthma.

Indexed as

AdolescentAdrenergic beta-AgonistsAdultArginaseAsthmaBronchodilator AgentsChildFemaleHumansLinkage DisequilibriumMaleMiddle AgedPharmacogeneticsPolymorphism, Single NucleotideAdrenergic beta-AgonistsArginaseBronchodilator Agents

Identifiers

PMID18617639
PMCPMC2556451
OpenAlexW2087574085

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.