Evidence map›Paper›PMID 38410140›Full record

ArticleInternational journal of chronic obstructive pulmonary disease2024

GSTP1 rs4147581 C>G and NLRP3 rs3806265 T>C as Risk Factors for Chronic Obstructive Pulmonary Disease: A Case-Control Study.

Honge Li, Raorao Wang, Xueyan Wei, Chunyan Zhang, Wenhui Pei, Xuhui Zhang, Zhen Yang, Zhi Li, Yuhuan Zhang, Yanli Shi and 2 more

Abstract read
In one paragraph

Article in International journal of chronic obstructive pulmonary disease, 2024. 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

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

1 citing paper in PubMed.

  1. International journal of chronic obstructive pulmonary disease · 2026
    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

12 authors.

Honge Li *Institute of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Raorao Wang *Institute of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Xueyan Wei *Institute of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Chunyan ZhangInstitute of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Wenhui PeiInstitute of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Xuhui ZhangDepartment of Respiratory Medicine, Affiliated Hospital of Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Zhen YangInstitute of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Zhi LiThe State Key Laboratory of Respiratory Disease, The First Affiliated Hospital, Institute of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, People's Republic of China.
Yuhuan ZhangInstitute of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Yanli ShiInstitute of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Yunchao WangInstitute of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.
Xinhua WangInstitute of Public Health, Gansu University of Chinese Medicine, Lanzhou, Gansu, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic obstructive pulmonary disease (COPD) is a chronic respiratory ailment influenced by a blend of genetic and environmental factors. Inflammatory response and an imbalance in oxidative-antioxidant mechanisms constitute the primary pathogenesis of COPD. Glutathione S-transferase P1(GSTP1) plays a pivotal role as an antioxidant enzyme in regulating oxidative-antioxidant responses in the pulmonary system. The activation of the NOD-like receptor thermal protein domain (NLRP3) inflammatory vesicle can trigger an inflammatory response. Several investigations have implicated GSTP1 and NLRP3 in the progression of COPD; nonetheless, there remains debate regarding this mechanism. Methods: Employing a case-control study design, 312 individuals diagnosed with COPD and 314 healthy controls were recruited from Gansu Province to evaluate the correlation between GSTP1 (rs4147581C>G and rs1695A>G) and NLRP3 (rs3806265T>C and rs10754558G>C) polymorphisms and the susceptibility to COPD. Results: The presence of the GSTP1 rs4147581G allele substantially elevated the susceptibility to COPD (CGvs.CC:OR=3.11,95% CI=1.961-4.935, Conclusion: In summary, this study ascertained that the GSTP1 rs4147581C>G polymorphism is associated with increased COPD susceptibility, with the G allele elevating the risk of COPD. Similarly, the NLRP3 rs3806265T>C polymorphism is linked to elevated COPD susceptibility, with the T allele heightening the risk of COPD.

Indexed as

Pulmonary Disease, Chronic ObstructiveAntioxidantsCase-Control StudiesGenetic Predisposition to DiseaseGenotypeGlutathione S-Transferase piHumansNLR Family, Pyrin Domain-Containing 3 ProteinPolymorphism, Single NucleotideRisk FactorsAntioxidantsGlutathione S-Transferase piGSTP1 protein, humanNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanchronic obstructive pulmonary diseaseGSTP1NLRP3polymorphism

Identifiers

PMID38410140
PMCPMC10896110

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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.