Evidence map›Paper›PMID 40118907›Full record

ArticleScientific reports2025

Genome wide interaction study of genetic variants associated with lung function decline.

Chi Young Kim, Boram Park, Ji Ye Jung, Je Hyeong Kim, Chung Mo Nam, Jaehoon An, Sungho Won, Young Sam Kim

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

8 authors.

Chi Young KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.
Boram ParkDepartment of Public Health Sciences, School of Public Health, Seoul National University, Kwanak-Ro Kwanak-Gu, Seoul, 151-742, South Korea.
Ji Ye JungDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.
Je Hyeong KimDivision of Pulmonology, Department of Internal Medicine, Korea University Ansan Hospital, Korea University College of Medicine, Ansan, Republic of Korea.
Chung Mo NamDepartment of Preventive Medicine and Public Health, Yonsei University College of Medicine, Seoul, Korea.
Jaehoon AnDepartment of Public Health Sciences, School of Public Health, Seoul National University, Kwanak-Ro Kwanak-Gu, Seoul, 151-742, South Korea.
Sungho WonDepartment of Public Health Sciences, School of Public Health, Seoul National University, Kwanak-Ro Kwanak-Gu, Seoul, 151-742, South Korea. won1@snu.ac.kr.
Young Sam KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea. ysamkim@yuhs.ac.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some genetic variants are associated with lung function decline and chronic obstructive pulmonary disease (COPD), but functional studies are necessary to confirm causality. We investigated the genetic susceptibility-associated lung function decline with or without COPD, using data from a community-based cohort (N = 8554). A genome-wide interaction study was conducted to identify the association between genetic variants and pulmonary function, and the way variants relate to lung impairment in accordance with smoking status and amount was examined. We further used a linear mixed model to examine the association and interaction to time effect. We found annual mean FEV

Indexed as

Genome-Wide Association StudyLungPolymorphism, Single NucleotidePulmonary Disease, Chronic ObstructiveAgedFemaleForced Expiratory VolumeGene FrequencyGenetic Predisposition to DiseaseGTPase-Activating ProteinsHumansMaleMiddle AgedRespiratory Function TestsSmokingFAM13A protein, humanGTPase-Activating ProteinsAADAT geneAirflow obstructionChronic obstructive pulmonary diseaseDNAH11 geneFAM13A geneGenome-wide association studySingle nucleotide polymorphism

Identifiers

PMID40118907
PMCPMC11928451

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.