Evidence map›Paper›PMID 35854898›Full record

ArticleInternational journal of chronic obstructive pulmonary disease2022

Serum Derivatives of Reactive Oxygen Metabolites are Associated with Severity of Chronic Obstructive Pulmonary Disease and Affected by a p53 Gene Polymorphism.

Koichi Yamamura, Masafumi Nojiri, Kazuaki Nishiki, Ryo Kato, Shohei Shinomiya, Yutaka Takahara, Taku Oikawa, Takeshi Ishizaki, Hirohisa Toga, Shiro Mizuno

Open access · goldAbstract read
In one paragraph

Article in International journal of chronic obstructive pulmonary disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Knockdown of GNL3L Alleviates the Progression of COPD Through Inhibiting the ATM/p53 Pathway.International journal of chronic obstructive pulmonary disease · 2023
    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

10 authors at 1 institution in 1 country.

Koichi Yamamura *Department of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Masafumi Nojiri *Department of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Kazuaki NishikiDepartment of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Ryo KatoDepartment of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Shohei ShinomiyaDepartment of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Yutaka TakaharaDepartment of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Taku OikawaDepartment of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Takeshi IshizakiDepartment of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Hirohisa TogaDepartment of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Shiro MizunoDepartment of Respiratory Medicine, Kanazawa Medical University, Ishikawa, Japan.
Kanazawa Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Oxidative stress is known to activate tumor suppressor p53, which inhibits cell cycle progression and induces apoptosis. Levels of p53 in lung tissues from patients with chronic obstructive pulmonary disease (COPD) are increased compared with levels in nonsmokers or smokers without emphysema. A polymorphism in p53 codon 72 (rs1042522) is associated with emphysematous changes in patients with COPD. However, whether oxidative stress in the serum is associated with the p53 polymorphism and disease severity in COPD patients is unclear. Patients and Methods: A total of 251 patients with a history of smoking more than 10 pack-years were enrolled in this study, and serum levels of derivatives of reactive oxygen metabolites (d-ROMs), biological antioxidant potential (BAP), and d-ROMs/BAP ratio (oxidative stress index; OSI) were measured. The percent low-attenuation area (LAA%) and cross-sectional area of the erector spinae muscles (ESM Results: In patients carrying the p53 GG genotype, LAA% was significantly higher than in those carrying the CC genotype. d-ROM levels and OSI were associated with COPD severity and correlated with airflow limitation and markers of muscle atrophy (ESM Conclusion: Susceptibility to pulmonary emphysema and responses to oxidative stress may be affected by the p53 gene polymorphism.

Indexed as

EmphysemaPulmonary Disease, Chronic ObstructivePulmonary EmphysemaReactive Oxygen SpeciesHumansPolymorphism, GeneticTumor Suppressor Protein p53Reactive Oxygen SpeciesTP53 protein, humanTumor Suppressor Protein p53low attenuation areaoxidative stresssarcopeniasmoking status

Identifiers

PMID35854898
PMCPMC9289177
OpenAlexW4285097742

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.