Evidence map›Paper›PMID 41921057›Full record

ArticleAmerican journal of epidemiology2026

Leukotriene-modifying agent chemoprophylaxis for severe influenza illness: a multi-approach study.

Brittney M Snyder, Corinne A Riddell, Tebeb Gebretsadik, Tan Ding, Rees L Lee, William D Dupont, Justin R Ortiz, Veronika Pav, Thomas J Braciale, Pingsheng Wu and 1 more

Abstract read
In one paragraph

Article in American journal of epidemiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Brittney M SnyderDepartment of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, TN, United States.
Corinne A RiddellDivisions of Biostatistics and Epidemiology, School of Public Health, University of California, Berkeley, CA, United States.ORCID 0000-0001-9517-0739
Tebeb GebretsadikDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, United States.
Tan DingDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, United States.
Rees L LeeDepartment of Pediatrics, University of Arizona, College of Medicine, Tucson, AZ, United States.
William D DupontDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, United States.
Justin R OrtizCenter for Vaccine Development & Global Health, University of Maryland School of Medicine, Baltimore, MD, United States.ORCID 0000-0002-3138-5965
Veronika PavKennell and Associates Inc., Falls Church, VA, United States.
Thomas J BracialeDepartment of Pathology and Molecular Medicine, University of Virginia, Charlottesville, VA, United States.
Pingsheng WuDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0003-4947-3063
Tina V HartertDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0001-7470-1166

Funding

Leukotriene modifying agents in the prevention of excess morbidity and mortality from influenzaR01AI136526 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BRACIALE, THOMAS J, HARTERT, TINA V · 2018 to 2020
$2.5M
Identifying molecular pathways in childhood asthma pathogenesis by integrating newborn metabolic profiles and GWAS dataK01HL161257 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Brittney M Snyder · 2022 to 2026
$650k
NHLBI NIH HHS K01 HL161257NIAID NIH HHS R01 AI136526NIH HHS K01 HL161257NIH HHS R01 AI136526
6 · The paper itself

Abstract

Animal and in vitro studies suggest that leukotriene-modifying agents (LMAs) may decrease susceptibility to influenza illness. We estimated the effect of LMAs on severe human influenza illness in a retrospective cohort using three analytic approaches: (1) a marginal structural model, (2) a proportional hazards model, and (3) a case-time-control design. Study populations included individuals with asthma and/or allergic rhinitis for whom LMAs are approved and who were enrolled in Tennessee Medicaid (TennCare) or Department of Defense Military Health System (DoD MHS) from 1995 to 2019. Exposed periods were defined by LMA prescription start dates plus days' supply. Severe influenza illness was defined using previously validated International Classification of Diseases criteria. Montelukast accounted for 99% of LMA prescription fills. Adjusted incidence rate ratios from the marginal structural model and adjusted hazard ratios from the proportional hazards model were 1.26 (95% confidence interval [CI], 0.99-1.59) and 1.14 (95% CI, 0.92-1.41) for TennCare and 1.01 (95% CI, 0.84-1.21) and 0.97 (95% CI, 0.82-1.16) for DoD MHS, respectively. Adjusted odds ratios from the case-time-control were 1.11 (95% CI, 0.74-1.65) for TennCare and 1.91 (95% CI, 1.29-2.84) for DoD MHS. Findings in different populations and designs do not support the use of LMAs for chemoprophylaxis of severe influenza illness. Conclusions regarding LMAs other than montelukast were not possible.

Indexed as

AcetatesInfluenza, HumanLeukotriene AntagonistsQuinolinesAdolescentAdultAsthmaCase-Control StudiesChemopreventionCyclopropanesFemaleHumansMaleMiddle AgedProportional Hazards ModelsRetrospective StudiesAcetatesCyclopropanesLeukotriene AntagonistsmontelukastQuinolinesSulfidescase–time–controlchemoprophylaxisleukotriene-modifying agentsmarginal structural modelpandemic preparednessproportional hazardssevere influenza illness

Identifiers

PMID41921057
PMCPMC13231862

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Registered trials

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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.