Evidence map›Paper›PMID 36371490›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2023

Low 15d-PGJ2 status is associated with oxidative stress in chronic obstructive pulmonary disease patients.

Shi-Xue Ma, Guo-Fang Xie, Pu Fang, Min-Min Tang, You-Peng Deng, Yu-Jin Lu, Wei Cao, Lin Fu

Abstract read
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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 28% of its field
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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. SYVN1-provoked RASA1 ubiquitination promotes pulmonary inflammation in chronic obstructive pulmonary disease.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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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 at 2 institutions in 1 country.

Shi-Xue Ma *Thoracic Surgery Department, Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, Anhui, China.
Guo-Fang Xie *Department of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, Anhui, China.
Pu FangDepartment of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, Anhui, China.
Min-Min TangDepartment of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, Anhui, China.
You-Peng DengDepartment of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, Anhui, China.
Yu-Jin LuDepartment of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, Anhui, China. luyougolden@hotmail.com.
Wei CaoThoracic Surgery Department, Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, Anhui, China. 13514964858@qq.com.
Lin FuDepartment of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, Anhui, China. fulindev@126.com.
Anhui Medical University · CNSecond Hospital of Anhui Medical University · CN

Funding

Incubation Program of National Natural Science Foundation of The Second Affiliated Hospital of Anhui Medical University No.2020GQFY05National Natural Science Foundation of China No.82100078Natural Science Foundation of Anhui Province No.2008085QH400Scientific Research Program of Anhui Provincial Health Commission No.AHWJ2021B091
6 · The paper itself

Abstract

backgroundPeroxisome proliferator-activated receptor γ (PPARγ) is a ligand-dependent nuclear receptor and highly expressed in human and rodent lungs. 15-Deoxy-delta-

methodsAll 130 fasting blood samples and 40 lung specimens were obtained from COPD patients and control subjects. Serum 15d-PGJ2 was detected by ELISA. The expressions of oxidative stress indicators were measured using western blotting and PPARγ nuclei were evaluated with immunohistochemistry in lungs. The associations among serum 15d-PGJ2, pulmonary PPARγ and oxidative stress indicators, and COPD were estimated.

resultsSerum 15d-PGJ2 was reduced in COPD patients compared with healthy volunteers. Linear and logistic regression analysis indicated that serum 15d-PGJ2 was positively associated with pulmonary function in COPD patients. In addition, PPARγ-positive nuclei were reduced and oxidative stress indicators, included HO-1 and NOX-4, were increased in lungs of COPD patients. Further correlative analysis suggested that pulmonary function parameters was positively correlated with serum 15d-PGJ2 and pulmonary PPARγ-positive nuclei, inversely related to oxidative stress indicators in lungs of COPD patients. Pretreatment with 15d-PGJ2 obviously attenuated TNFα-induced oxidative stress in BEAS-2B cells.

conclusionsSerum 15d-PGJ2 and pulmonary PPARγ are reduced, and oxidative stress is elevated in COPD patients. Serum 15d-PGJ2 is inversely associated with oxidative stress in COPD patients.

Indexed as

PPAR gammaPulmonary Disease, Chronic ObstructiveHumansLigandsOxidative StressProstaglandin D215-deoxyprostaglandin J2LigandsPPAR gammaProstaglandin D215d-PGJ2COPDOxidative stressPPARγPulmonary function

Identifiers

PMID36371490
OpenAlexW4308890918

What OpenQuestion 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 OpenQuestion graph.