Evidence map›Paper›PMID 41021275›Full record

ArticleAmerican journal of respiratory cell and molecular biology2026

Functional Variant Discovery Identifies a Novel Genetic Link between SPRY2, Wood Smoke, and Asthma.

Arnav Gupta, Amber Dahlin, Alejandra Macario, Fabienne Gally, Michael R Weaver, Samuel Guarino, Louisa Kahn, Lynn Sanford, Margaret A Gruca, Michael H Cho and 4 more

Abstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 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

14 authors.

Arnav GuptaDepartment of Medicine and.ORCID 0000-0002-7439-8168
Amber DahlinChanning Division of Network Medicine, Harvard Medical School, Boston, Massachusetts.
Alejandra MacarioDepartment of Medicine and.
Fabienne GallyDepartment of Medicine and.
Michael R WeaverDepartment of Medicine and.
Samuel GuarinoDepartment of Medicine and.
Louisa KahnDepartment of Medicine and.
Lynn SanfordBioFrontiers Institute.
Margaret A GrucaBioFrontiers Institute.
Michael H ChoChanning Division of Network Medicine, Harvard Medical School, Boston, Massachusetts.
Robin D DowellBioFrontiers Institute.
Scott T WeissChanning Division of Network Medicine, Harvard Medical School, Boston, Massachusetts.
Sarah K SasseDepartment of Medicine and.
Anthony N GerberDepartment of Medicine and.

Funding

Targeting early events in MUC5B-driven lung injury and fibrosisP01HL162607 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI David Albert Schwartz · 2023 to 2026
$12.4M
Role of FABP5 in COPD ExacerbationsR01HL141264 · NHLBI · NATIONAL JEWISH HEALTH · PI Fabienne Gally · 2019 to 2026
$3.7M
Transcriptional Responses to Wildfire Pollution in Airway Epithelial Cells Identify Genetic Risk Factors and Mechanisms of Asthma ExacerbationsK08ES034820 · NIEHS · NATIONAL JEWISH HEALTH · PI Arnav Gupta · 2023 to 2026
$688k
NHLBI NIH HHS P01 HL162607NHLBI NIH HHS P01HL162607NHLBI NIH HHS R01 HL141264NIEHS NIH HHS 1K08ES034820-01NIEHS NIH HHS K08 ES034820
6 · The paper itself

Abstract

As a consequence of climate change and land-use policies, there has been a historic rise in wildfire smoke across the United States and the world. Although the deleterious effects of wildfire smoke and associated air pollution on asthma outcomes are established epidemiologically, genetic risks and molecular mechanisms of how wildfire smoke affects asthma are unknown. This knowledge gap hinders the identification of high-risk individuals and the creation of targeted therapies or recommendations to protect these individuals. We identified 52 genetic risk variants that colocalized with genomic responses to woodsmoke particles (WSPs), a model of wildfire particulate matter, and associated with asthma in the GERA (Genetic Epidemiology Research on Adult Health and Aging) cohort. We used additional filters to prioritize variants for direct testing of allele-dependent transcriptional regulatory function in plasmid reporters. We found that the rs3861144 variant (odds ratioasthma, 1.036) changes SPRY2 responses to WSPs in airway epithelial cells, which are involved in IL-8 secretion, ERK (extracellular signal-related kinase) activation, and mechanical scratch repair in cell culture. These findings provide insights into the molecular pathways through which WSPs may influence asthma risk and propose genetic candidates that warrant further study for their potential as clinical tools for asthma.

Indexed as

AsthmaIntracellular Signaling Peptides and ProteinsMembrane ProteinsSmokeWoodEpithelial CellsGenetic Predisposition to DiseaseHumansInterleukin-8Particulate MatterPolymorphism, Single NucleotideInterleukin-8Intracellular Signaling Peptides and ProteinsMembrane ProteinsParticulate MatterSmokeSPRY2 protein, humanenvironmental asthmafunctional geneticswildfire smoke

Identifiers

PMID41021275
PMCPMC12560217

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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.