Evidence map›Paper›PMID 24084072›Full record

Trial reportThe Journal of allergy and clinical immunology2013

Predictors of response to tiotropium versus salmeterol in asthmatic adults.

Stephen P Peters, Eugene R Bleecker, Susan J Kunselman, Nikolina Icitovic, Wendy C Moore, Rodolfo Pascual, Bill T Ameredes, Homer A Boushey, William J Calhoun, Mario Castro and 21 more

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00565266 (Asthma Clinical Research Network), which is not on this map. Cited by 36 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 4 pooled it
8.3field-weighted citation impact, top 2% 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.

NCT00565266 phase3completednot on this map

Asthma Clinical Research Network (ACRN) Trial - Tiotropium Bromide as an Alternative to Increased Inhaled Corticosteroid in Patients Inadequately Controlled on a Lower Dose of Inhaled Corticosteroid (TALC)

TypeinterventionalSponsorMilton S. Hershey Medical CenterRan2008 to 2010Enrolled210ConditionsAsthmaArmstiotropium bromide, salmeterol xinafoate, beclomethasone dipropionate
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 4 syntheses or guidelines pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Dysanapsis and the Spirometric Response to Inhaled Bronchodilators.American journal of respiratory and critical care medicine · 2021
    Trial
  7. Trial
  8. Trial
  9. Review
  10. Improving asthma outcomes: Clinicians' perspectives on peripheral airways.The journal of allergy and clinical immunology. Global · 2024
    Article
  11. Effect of Hyssop (Tanaffos · 2024
    Article
  12. Heterogeneity of Treatment Response to Asthma.Advances in experimental medicine and biology · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. NHLBI ASTHMA NETWORKS: IMPROVING PATIENT CARE, MOVING TOWARD PERSONALIZED MEDICINE.Transactions of the American Clinical and Climatological Association · 2022
    Article
  17. Exacerbation-Prone Asthma.The journal of allergy and clinical immunology. In practice · 2020
    Article
  18. Article
  19. Airway Innervation and Plasticity in Asthma.Physiology (Bethesda, Md.) · 2019
    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

31 authors at 12 institutions in 1 country.

Stephen P PetersWake Forest School of Medicine, Winston-Salem, NC. Electronic address: sppeters@wakehealth.edu.
Eugene R Bleecker
Susan J Kunselman
Nikolina Icitovic
Wendy C Moore
Rodolfo Pascual
Bill T Ameredes
Homer A Boushey
William J Calhoun
Mario Castro
Reuben M Cherniack
Timothy Craig
Loren C Denlinger
Linda L Engle
Emily A Dimango
Elliot Israel
Monica Kraft
Stephen C Lazarus
Robert F Lemanske
Njira Lugogo
Richard J Martin
Deborah A Meyers
Joe Ramsdell
Christine A Sorkness
E Rand Sutherland
Stephen I Wasserman
Michael J Walter
Michael E Wechsler
Vernon M Chinchilli
Stanley J Szefler
National Heart, Lung, and Blood Institute's Asthma Clinical Research Network
Pennsylvania State University · USWake Forest University · USNational Jewish Health · USUniversity of Wisconsin–Madison · USDuke University · USThe University of Texas Medical Branch at Galveston · USUniversity of California, San Diego · USUniversity of California, San Francisco · USWashington University in St. Louis · USBrigham and Women's Hospital · USColumbia University · USUniversity of Colorado Denver · US

Funding

ACRN Data Coordinating CenterU10HL074231 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI CHINCHILLI, VERNON M. · 2003 to 2007
$13.3M
Informative Clinical Studies in AsthmaU10HL074227 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ISRAEL, ELLIOT · 2003 to 2007
$5.8M
Treatment of Severe Persistent AsthmaU10HL074212 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI LEMANSKE, ROBERT F · 2003 to 2007
$4.9M
Innovative Investigations and Therapies for AsthmaU10HL074073 · NHLBI · NATIONAL JEWISH HEALTH · PI MARTIN, RICHARD J · 2003 to 2007
$3.9M
Asthma Clinical Research Network Center at UCSFU10HL074204 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOUSHEY, HOMER A · 2003 to 2007
$3.8M
Asthma Clinical Research NetworkU10HL074206 · NHLBI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CALHOUN, WILLIAM J · 2003 to 2008
$3.6M
Asthma Clinical Research Network-Washington UniversityU10HL074208 · NHLBI · WASHINGTON UNIVERSITY · PI CASTRO, MARIO · 2003 to 2007
$3.4M
ASTHMA CLINICAL RESEARCH NETWORKU10HL074218 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WASSERMAN, STEPHEN I · 2003 to 2012
$3.3M
Asthma Clinical Research Network (ACRN)U10HL074225 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERS, STEPHEN P · 2003 to 2007
$3.2M
NHLBI NIH HHS U10 HL074073NHLBI NIH HHS U10 HL074204NHLBI NIH HHS U10 HL074206NHLBI NIH HHS U10 HL074208NHLBI NIH HHS U10 HL074212NHLBI NIH HHS U10 HL074218NHLBI NIH HHS U10 HL074225NHLBI NIH HHS U10 HL074227NHLBI NIH HHS U10 HL074231
6 · The paper itself

Abstract

backgroundTiotropium has activity as an asthma controller. However, predictors of a positive response to tiotropium have not been described.

objectiveWe sought to describe individual and differential responses of asthmatic patients to salmeterol and tiotropium when added to an inhaled corticosteroid, as well as predictors of a positive clinical response.

methodsData from the double-blind, 3-way, crossover National Heart, Lung, and Blood Institute's Asthma Clinical Research Network's Tiotropium Bromide as an Alternative to Increased Inhaled Glucocorticoid in Patients Inadequately Controlled on a Lower Dose of Inhaled Corticosteroid (ClinicalTrials.gov number, NCT00565266) trial were analyzed for individual and differential treatment responses to salmeterol and tiotropium and predictors of a positive response to the end points FEV1, morning peak expiratory flow (PEF), and asthma control days (ACDs).

resultsAlthough approximately equal numbers of patients showed a differential response to salmeterol and tiotropium in terms of morning PEF (n = 90 and 78, respectively) and ACDs (n = 49 and 53, respectively), more showed a differential response to tiotropium for FEV1 (n = 104) than salmeterol (n = 62). An acute response to a short-acting bronchodilator, especially albuterol, predicted a positive clinical response to tiotropium for FEV1 (odds ratio, 4.08; 95% CI, 2.00-8.31; P < .001) and morning PEF (odds ratio, 2.12; 95% CI, 1.12-4.01; P = 0.021), as did a decreased FEV1/forced vital capacity ratio (FEV1 response increased 0.39% of baseline for every 1% decrease in FEV1/forced vital capacity ratio). Higher cholinergic tone was also a predictor, whereas ethnicity, sex, atopy, IgE level, sputum eosinophil count, fraction of exhaled nitric oxide, asthma duration, and body mass index were not.

conclusionAlthough these results require confirmation, predictors of a positive clinical response to tiotropium include a positive response to albuterol and airway obstruction, factors that could help identify appropriate patients for this therapy.

Indexed as

Adrenergic beta-2 Receptor AgonistsAdultAlbuterolAnti-Asthmatic AgentsAsthmaBronchodilator AgentsCross-Over StudiesFemaleHumansMaleMiddle AgedPrognosisSalmeterol XinafoateScopolamine DerivativesTiotropium BromideTreatment OutcomeAdrenergic beta-2 Receptor AgonistsAlbuterolAnti-Asthmatic AgentsBronchodilator AgentsSalmeterol XinafoateScopolamine DerivativesTiotropium BromideACDACRNAsthmaAsthma Clinical Research NetworkAsthma control dayForced vital capacityFVCHFAHydrofluoroalkaneICSInhaled corticosteroidLABALAMALong-acting muscarinic antagonistLong-acting β-agonistNational Heart, Lung, and Blood InstituteNHLBIOdds ratioORPeak expiratory flowPEFpredictor of responseresponder analysissalmeterolTALCtiotropiumTiotropium Bromide as an Alternative to Increased Inhaled Glucocorticoid in Patients Inadequately Controlled on a Lower Dose of Inhaled Corticosteroid (ClinicalTrials.gov number, NCT00565266) trial

Identifiers

PMID24084072
PMCPMC3826080
OpenAlexW2117993701

What OpenQuestion holds

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Registered trials

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.