Evidence mapPaperPMID 40655182Full record

ArticleInternational journal of chronic obstructive pulmonary disease2025

The Crucial Role of the PPAR Signaling Pathway in the Diagnosis and Treatment of Chronic Obstructive Pulmonary Disease: An Analysis of Gene Expression and Macrophage Polarization.

Ling Zhang, Rong Guo, Haixia Wu, Abula Abudusalamu, Wei Ding, Dewei Li, Xuemei Wei, Lin Niu

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Article in International journal of chronic obstructive pulmonary disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Review
  2. International journal of chronic obstructive pulmonary disease · 2026
    Article
  3. Review
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.

Ling Zhang *Department of Respiratory and Critical Care Medicine, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, 830001, People's Republic of China.ORCID 0000-0001-5850-6811
Rong Guo *Department of Respiratory and Critical Care Medicine, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, 830001, People's Republic of China.ORCID 0000-0002-0548-9218
Haixia WuDepartment of Respiratory and Critical Care Medicine, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, 830001, People's Republic of China.
Abula AbudusalamuDepartment of Respiratory and Critical Care Medicine, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, 830001, People's Republic of China.
Wei DingDepartment of Respiratory and Critical Care Medicine, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, 830001, People's Republic of China.
Dewei LiDepartment of Respiratory and Critical Care Medicine, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, 830001, People's Republic of China.ORCID 0000-0002-9429-3881
Xuemei WeiDepartment of Respiratory and Critical Care Medicine, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, 830001, People's Republic of China.
Lin NiuDepartment of Respiratory and Critical Care Medicine, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, 830001, People's Republic of China.

Funding

Tianchi Talent Program (TCYCQNBS)Tianshan Talents Program of the Xinjiang Uygur Autonomous Region PROJECT NO. TSYC202301A029
6 · The paper itself

Abstract

Purpose: To explore the role of the peroxisome proliferator-activated receptor (PPAR) signaling pathway in chronic obstructive pulmonary disease (COPD) and identify potential biomarkers and therapeutic targets, given that COPD is a major global health burden and the specific molecular mechanisms of the PPAR pathway in COPD are not fully understood. Patients and Methods: Gene expression data from the GEO database were analyzed to identify key genes and immune cells related to COPD. Peripheral blood samples were collected from COPD patients and healthy controls. Key genes were confirmed by PCR, and immune cells were characterized using flow cytometry. Results: Eight core genes associated with the PPAR signaling pathway were identified. NCOA1 and PPARGC1A were downregulated in COPD patients, while NCOR1, NRIP1, and SLC27A5 were upregulated. Receiver operating characteristic (ROC) curve analysis showed that NCOA1, NCOR1, and SLC27A5 have potential for COPD diagnosis. There was a significant increase in the proportion of M2 macrophages in COPD patients, indicating a shift in macrophage polarization towards the M2 phenotype. Genes within the PPAR signaling pathway were closely associated with macrophage polarization state. Conclusion: The research findings provide new biomarkers and potential therapeutic targets for the early diagnosis and personalized treatment of COPD, emphasizing the significant role of the PPAR signaling pathway in the pathogenesis of COPD. Clinical Trial Registry: The population study involved in this research has been registered under the (chictr.org.cn). Registry identifier: ChiCTR2400086268.

Indexed as

Macrophage ActivationMacrophagesPeroxisome Proliferator-Activated ReceptorsPulmonary Disease, Chronic ObstructiveAgedCase-Control StudiesDatabases, GeneticFemaleGene Expression ProfilingHumansMaleMiddle AgedNuclear Receptor Coactivator 1Nuclear Receptor Co-Repressor 1Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPhenotypeNCOR1 protein, humanNuclear Receptor Coactivator 1Nuclear Receptor Co-Repressor 1Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPeroxisome Proliferator-Activated ReceptorsPPARGC1A protein, humanCOPDdiagnosis biomarkermacrophage polarizationPPAR signaling pathway

Identifiers

PMID40655182
PMCPMC12248238

What Socratic holds

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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 Socratic graph.