Evidence map›Paper›PMID 38164813›Full record

ArticleAllergy2024

Lung function trajectories in a cohort of patients with moderate-to-severe asthma on mepolizumab, omalizumab, or dupilumab.

Tanawin Nopsopon, Nora A Barrett, Wanda Phipatanakul, Tanya M Laidlaw, Scott T Weiss, Ayobami Akenroye

Open access · greenAbstract read
In one paragraph

Article in Allergy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Achieving remission in severe asthma.Chinese medical journal pulmonary and critical care medicine · 2025
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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

6 authors at 2 institutions in 1 country.

Tanawin NopsoponDivision of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts, USA.ORCID 0000-0003-0428-973X
Nora A BarrettDivision of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Wanda PhipatanakulDivision of Immunology, Boston Children's Hospital, Boston, Massachusetts, USA.
Tanya M LaidlawDivision of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Scott T WeissChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Ayobami AkenroyeDivision of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-1909-1470
Brigham and Women's Hospital · USBoston Children's Hospital · US

Funding

Therapeutic Control of Aspirin-Exacerbated Respiratory DiseaseU19AI095219 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Joshua A Boyce · 2011 to 2026
$29.1M
Leveraging Pharmacogenomics in Asthma for Predication, Mechanism and EndotypingR01HL161362 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI EUGENE ROLAND BLEECKER, GEOFFREY L CHUPP · 2022 to 2026
$8.4M
Type 2 Inflammation and Remodeling Elicited Through an LTE4/OXGR1-dependent pathwayR01AI134989 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Nora Amanda Barrett · 2019 to 2026
$5.1M
Synthesizing Trial and Real-world Data on the Use of Biologics in Patients with Severe AsthmaR00MD015767 · NIMHD · BRIGHAM AND WOMEN'S HOSPITAL · PI AKENROYE, AYOBAMI T · 2023 to 2025
$677k
NHLBI NIH HHS L30 HL165481NHLBI NIH HHS R01 HL161362NIAID NIH HHS R01 AI134989NIAID NIH HHS U19 AI095219NIMHD NIH HHS R00 MD015767
6 · The paper itself

Abstract

backgroundLung function is an independent predictor of mortality. We evaluated the lung function trajectories of a cohort of patients with asthma receiving biologic therapy.

methodsWe identified 229 monoclonal antibody-naïve adult patients with moderate-to-severe asthma who initiated omalizumab, mepolizumab, or dupilumab between 2010 and 2022 in a large healthcare system in Boston, MA. Generalized additive mixed models were used to estimate the lung function trajectories during the 156 weeks following biologic initiation. Response was defined as an improvement in FEV

resultsEighty-eight patients initiated mepolizumab, 76 omalizumab, and 65 dupilumab. Baseline eosinophil count was highest in the mepolizumab group (405 cells/mcL) and lowest for omalizumab (250 cells/mcL). Both FEV

conclusionIn this clinical cohort, mepolizumab, omalizumab, and dupilumab had beneficial effects on FEV

Indexed as

Anti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedAsthmaOmalizumabRespiratory Function TestsAdultAgedCohort StudiesFemaleHumansLungMaleMiddle AgedSeverity of Illness IndexTreatment OutcomeAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizeddupilumabmepolizumabOmalizumabasthmabiologicslung functionmonoclonal antibodiestrajectory

Identifiers

PMID38164813
PMCPMC11062846
OpenAlexW4390507494

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.