Evidence map›Paper›PMID 40798880›Full record

ArticleHGG advances2026

Overlap between COPD genetic association results and transcriptional quantitative trait loci.

Aabida Saferali, Wonji Kim, Robert P Chase, NHLBI TransOmics in Precision Medicine (TOPMed), Christopher Vollmers, Edwin K Silverman, Michael H Cho, Peter J Castaldi, Craig P Hersh

Abstract read
In one paragraph

Article in HGG advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. Characterisation of a COPD-associated nephronectin (The European respiratory journal · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Aabida SaferaliChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA. Electronic address: aabida.saferali@channing.harvard.edu.
Wonji KimChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Robert P ChaseChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA.
NHLBI TransOmics in Precision Medicine (TOPMed)
Christopher VollmersDepartment of Biomolecular Engineering, Cellular, Cellular, and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA, USA.
Edwin K SilvermanChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA; Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Michael H ChoChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA; Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Peter J CastaldiChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA; Division of General Medicine and Primary Care, Brigham and Women's Hospital, Boston, MA, USA.
Craig P HershChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA; Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, MA, USA.

Funding

Genetic Epidemiology of COPDU01HL089897 · NHLBI · NATIONAL JEWISH HEALTH · PI CRAPO, JAMES D · 2007 to 2021
$56.9M
GENETIC EPIDEMIOLOGY OF COPD (COPD GENE) TASK A: STUDY VISIT 4, COLLECTION OF COPDGENE STUDY DATA ANDBIOSPECIMENS AND OVERSIGHT OF THE COPDGENE STUDY75N92023D00011 · NHLBI · NATIONAL JEWISH HEALTH · PI NEWMAN, LEE S · 2023 to 2025
$29.6M
Genetic Epidemiology of COPDU01HL089856 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SILVERMAN, EDWIN K · 2007 to 2021
$20.7M
Studies of Rare Genetic Variation in the Isolated Population of SardiniaR01HL117626 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ABECASIS, GONCALO · 2013 to 2016
$10.5M
Rare variants and NHLBI traits in deeply phenotyped cohortsR01HL120393 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M, RICE, KENNETH M. · 2014 to 2016
$8.9M
Using Integrative Genomics To Identify and Characterize Emphysema-Associated eQTLR01HL124233 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI CASTALDI, PETER · 2014 to 2024
$7.1M
Rare variants and NHLBI traits in deeply phenotyped cohortsU01HL120393 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M, RICE, KENNETH M. · 2017 to 2018
$5.6M
Genetic variants that affect the airway epithelium to drive obstructive lung diseaseR01HL166992 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Peter Castaldi, Yohannes Tesfaigzi · 2024 to 2026
$2.6M
COPD GWAS Functional Variant Identification in Airway Epithelial Cells using Deep Learning Splicing ModelsR01HL171213 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Peter Castaldi, Yohannes Tesfaigzi · 2024 to 2026
$2.3M
Variant induced RNA structure change in human genetic diseaseR35GM140844 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LAEDERACH, ALAIN T · 2021 to 2025
$2.1M
Integrative 'Omics of Transcriptome Complexity in COPDK01HL157613 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SAFERALI, AABIDA · 2021 to 2025
$944k
NHLBI NIH HHS 75N92023D00011NHLBI NIH HHS HHSN268201800001CNHLBI NIH HHS K01 HL157613NHLBI NIH HHS R01 HL117626NHLBI NIH HHS R01 HL120393NHLBI NIH HHS R01 HL124233NHLBI NIH HHS R01 HL166992NHLBI NIH HHS R01 HL171213NHLBI NIH HHS U01 HL089856NHLBI NIH HHS U01 HL089897NHLBI NIH HHS U01 HL120393NIEHS NIH HHS HHSN268201600032CNIGMS NIH HHS R35 GM140844
6 · The paper itself

Abstract

Genome-wide association studies (GWASs) have identified multiple genetic loci associated with chronic obstructive pulmonary disease (COPD). Here, we identify SNPs that are associated with alternative splicing (splicing quantitative trait loci [sQTLs]) and gene expression (expression QTLs [eQTLs]) to identify functions for COPD-associated genetic variants. RNA sequencing on whole blood from 3,743 subjects in the COPDGene Study and from lung tissue of 1,241 subjects from the Lung Tissue Research Consortium (LTRC) was analyzed. Associations between all SNPs within 1,000 kb of a gene (cis-) and splice and gene expression quantifications were tested using tensorQTL. We assessed colocalization with COPD-associated SNPs from a published GWAS. After adjustment for multiple statistical testing, we identified 28,110 splice sites corresponding to 3,889 unique genes that were significantly associated with genotype in COPDGene whole blood and 58,258 splice sites corresponding to 10,307 unique genes associated with genotype in LTRC lung tissue. To determine what proportion of COPD-associated SNPs were associated with transcriptional splicing, we performed colocalization analysis between COPD GWAS and sQTL data and found that 38 genomic windows, corresponding to 33 COPD GWAS loci, had evidence of colocalization between QTLs and COPD. The top five colocalizations between COPD and lung sQTLs include Nephronectin (NPNT), F box protein 38 (FBXO38), Hedgehog interacting protein (HHIP), Netrin 4 (NTN4), and Betacellulin (BTC). Overall, a total of 38 COPD GWAS loci contain evidence of sQTLs, suggesting that analysis of sQTLs in whole blood and lung tissue can provide insights into disease mechanisms.

Indexed as

Genetic Predisposition to DiseasePulmonary Disease, Chronic ObstructiveQuantitative Trait LociAgedAlternative SplicingFemaleGenome-Wide Association StudyHumansMalePolymorphism, Single Nucleotidechronic obstructive pulmonary diseasegenetic colocalizationquantitative trait locisplicing

Identifiers

PMID40798880
PMCPMC12481885

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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.