Evidence map›Paper›PMID 33788425›Full record

Observational studyCancer reports (Hoboken, N.J.)2021

Genetic polymorphisms of metabolic enzyme genes associated with leukocyte mitochondrial DNA copy number in PAHs exposure workers.

Xinling Li, Xiaoran Duan, Hui Zhang, Mingcui Ding, Yanbin Wang, Yongli Yang, Wu Yao, Xiaoshan Zhou, Wei Wang

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Cancer reports (Hoboken, N.J.), 2021. 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
0.3field-weighted citation impact, top 54% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
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

9 authors at 2 institutions in 1 country.

Xinling LiDepartment of Occupational Health and Occupational Diseases, College of Public Health, Zhengzhou University, Zhengzhou, China.
Xiaoran DuanDepartment of Occupational Health and Occupational Diseases, College of Public Health, Zhengzhou University, Zhengzhou, China.
Hui ZhangDepartment of Occupational Health and Occupational Diseases, College of Public Health, Zhengzhou University, Zhengzhou, China.
Mingcui DingDepartment of Occupational Health and Occupational Diseases, College of Public Health, Zhengzhou University, Zhengzhou, China.
Yanbin WangSafety Management Department of Anyang Iron and Steel Group Company, Anyang, China.
Yongli YangDepartment of Epidemiology and Biostatistics, College of Public Health, Zhengzhou University, Zhengzhou, China.ORCID 0000-0002-5361-5733
Wu YaoDepartment of Occupational Health and Occupational Diseases, College of Public Health, Zhengzhou University, Zhengzhou, China.
Xiaoshan ZhouDepartment of Occupational Health and Occupational Diseases, College of Public Health, Zhengzhou University, Zhengzhou, China.
Wei WangDepartment of Occupational Health and Occupational Diseases, College of Public Health, Zhengzhou University, Zhengzhou, China.ORCID 0000-0001-7492-6795
Zhengzhou University · CNTaiyuan Iron and Steel Group (China) · CN

Funding

National Natural Science Foundation of China 81872597The Outstanding Youth Grant of Zhengzhou University 1521329035The Programs for Science and Technology Development of Zhengzhou 121PPTGG503-2
6 · The paper itself

Abstract

backgroundPolycyclic aromatic hydrocarbons (PAHs) exposure had been reported to be a risk factor of mtDNAcn in our early study. However, the effect of metabolic enzymes' genetic polymorphisms on mtDNAcn in PAHs-Exposure workers has not been fully evaluated.

aimThe aim of the study was to explore the effect of metabolic enzymes' genetic polymorphisms on mtDNAcn in PAHs-Exposure. METHODS AND

resultsWe investigated the effects of metabolic enzymes' genetic polymorphisms on mtDNAcn among 544 coke oven workers and 238 office staffs. The mtDNAcn of peripheral blood leukocytes was measured using the Real-time quantitative polymerase chain reaction (PCR) method. PCR and restriction fragment length was used to detect five polymorphisms in GSTT1, GSTM1, GSTP1 rs1695, CYP2E1 rs6413432, and CYP2E1 rs3813867. The mtDNAcn in peripheral blood leukocytes was significantly lower in the exposure group than that in the control group (p < .001). The 1-OHPYR had an increasing trend with the genotypes AA→AG → GG of GSTP1 rs1695 in the control group. Generalized linear model indicated that the influencing factors of mtDNAcn were PAHs-exposure [β (95% CI) = -0.420 (-0.469, -0.372), p < .001], male [β (95% CI) = -0.058 (-0.103, -0.012), p = .013], and AA genotype for GSTP1 rs1695 [β (95% CI) = -0.051 (-0.095, -0.008), p = .020].

conclusionThe individuals carrying the AA genotype of GSTP1 rs1695 may have a lower mtDNAcn due to their weaker detoxification of PAHs.

Indexed as

AdolescentAdultCase-Control StudiesChinaCokeCytochrome P-450 CYP2E1DNA Copy Number VariationsDNA, MitochondrialFemaleGlutathione S-Transferase piGlutathione TransferaseHealthy VolunteersHumansLeukocytesMaleMiddle AgedCokeCytochrome P-450 CYP2E1DNA, MitochondrialGlutathione S-Transferase piglutathione S-transferase T1Glutathione TransferaseGSTP1 protein, humanPolycyclic Aromatic Hydrocarbons1-OHPYRCOEsgene polymorphismsGSTP1 rs1695mtDNAcn

Identifiers

PMID33788425
PMCPMC8388165
OpenAlexW3141992279

What OpenQuestion holds

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LicenceCC BY
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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.