Evidence map›Paper›PMID 41721757›Full record

ArticleAnnals of the American Thoracic Society2026

Real-world effectiveness of asthma biologics by age of initiation and early-childhood risk factors.

Arthur H Owora, Kirsten Kloepfer, Robert Tepper, Nadia Krupp, Samantha H Averill, Ryan C Unruh, Bowen Jiang, Yash Shah, Benjamin Gaston, Erick Forno

Abstract read
In one paragraph

Article in Annals of the American Thoracic Society, 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

10 authors.

Arthur H OworaDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.ORCID 0000-0002-4580-7428
Kirsten KloepferDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Robert TepperDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Nadia KruppDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Samantha H AverillDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Ryan C UnruhDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Bowen JiangDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Yash ShahDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Benjamin GastonDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Erick FornoDivision of Pediatric Pulmonology, Allergy/Immunology and Sleep Medicine, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.

Funding

S-nitrosylation signaling in asthmaP01HL158507 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI GASTON, BENJAMIN · 2021 to 2025
$12.0M
Advancing telemedicine in pulmonology: acoustic-waveform respiratory evaluation (AWARE) via sensing and machine learning on smartphonesR01HL170368 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI Erick Forno, Wei Gao · 2024 to 2026
$1.9M
Developing a Childhood Asthma Risk Passive Digital MarkerK01HL166436 · NHLBI · TRUSTEES OF INDIANA UNIVERSITY · PI OWORA, ARTHUR HAMIE · 2023 to 2024
$324k
AHRQ HHS R03 HS029088National Heart, Lung, and Blood Institute and Agency for Healthcare Research and Quality K01HL166436National Heart, Lung, and Blood Institute and Agency for Healthcare Research and Quality P01HL158507National Heart, Lung, and Blood Institute and Agency for Healthcare Research and Quality R01HL170368National Heart, Lung, and Blood Institute and Agency for Healthcare Research and Quality R03HS029088NHLBI NIH HHS K01 HL166436NHLBI NIH HHS P01 HL158507NHLBI NIH HHS R01 HL170368NIH HHS
6 · The paper itself

Abstract

backgroundWhile several biologics are approved in the United States for the treatment of severe asthma in children aged ≥6 years, important knowledge gaps persist regarding their real-world effectiveness. Here, we examine their real-world effectiveness and whether it differs by age of treatment initiation, biologic agent, or early-childhood asthma risk factors and characteristics.

methodsRetrospective cohort of 122 children with moderate/severe asthma treated with a biologic by pediatric subspecialists between December 2019 and December 2024. Piecewise generalized linear mixed-effects models were used to examine biologic clinical benefit, defined as the change in the odds of severe asthma exacerbations before versus after treatment initiation.

resultsThe cohort (52% female, 59% African American, mean age 10 ± 4 years at biologic initiation) was prescribed dupilumab (64%), omalizumab (29%), or mepolizumab (8%) and had 10 years median follow-up. Biologics led to significant reductions in severe exacerbations (adjusted OR = 0.47 [95% CI = 0.28, 0.80]); this benefit was more pronounced with younger age at initiation: aOR = 0.46 [95% CI = 0.26, 0.80] in ≤11-year olds, vs aOR = 0.56 [95% CI: 0.27, 1.89] in those ≥12 years. Similarly, benefit was more pronounced among patients with early-childhood polysensitization (aOR = 0.32 [95% CI = 0.14, 0.74]) than those without (aOR = 0.59 [95% CI = 0.30, 1.19]) and patients with a moderate/high burden of early-childhood asthma risk factors (aOR = 0.39 [95% CI = 0.21, 0.70]) than those with low burden (aOR = 0.90 [95% CI = 0.32, 2.57]). We found no significant differences by biologic agent.

conclusionBiologics may be more effective with earlier treatment initiation, especially among children with early polysensitization or multiple early-childhood risk factors. Screening for these risk factors may help inform targeted early initiation of biologics for asthma.

Indexed as

Anti-Asthmatic AgentsAsthmaBiological ProductsAdolescentAge FactorsAntibodies, Monoclonal, HumanizedChildChild, PreschoolFemaleHumansMaleOmalizumabRetrospective StudiesRisk FactorsSeverity of Illness IndexTreatment OutcomeAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedBiological ProductsdupilumabmepolizumabOmalizumabbiologic therapyearly-life risk factorspediatric asthmareal-world effectivenesssevere asthma

Identifiers

PMID41721757
PMCPMC13152658

What OpenQuestion holds

Textmetadata
LicenceTDM
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.