Evidence map›Paper›PMID 28894282›Full record

ArticleScientific reports2017

Idiopathic male infertility and polymorphisms in the DNA methyltransferase genes involved in epigenetic marking.

Qiuqin Tang, Yiqiu Chen, Wei Wu, Hongjuan Ding, Yankai Xia, Daozhen Chen, Xinru Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Unravelling male infertility through epigenetics: present understanding and future challenges.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  3. Review
  4. Review
  5. Review
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  7. Article
  8. Towards a Multi-Omics of Male Infertility.The world journal of men's health · 2023
    Review
  9. Review
  10. Epigenetics of Male Infertility: The Role of DNA Methylation.Frontiers in cell and developmental biology · 2021
    Review
  11. Association of UHRF1 gene polymorphisms with oligospermia in Chinese males.Journal of assisted reproduction and genetics · 2019
    Article
  12. Association of Polymorphisms in Genes Involved in One-Carbon Metabolism withInternational journal of molecular sciences · 2019
    Article
  13. Article
  14. Article
  15. Review
  16. Review
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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

7 authors at 2 institutions in 1 country.

Qiuqin TangState Key Laboratory of Reproductive Medicine, Department of Obstetrics, Nanjing Maternity and Child Health Hospital, Obstetrics and Gynecology Hospital Affiliated to Nanjing Medical University, Nanjing, 210004, China.
Yiqiu ChenState Key Laboratory of Reproductive Medicine, Institute of Applied Toxicology, School of Public Health, Nanjing Medical University, Nanjing, 211166, China.
Wei WuState Key Laboratory of Reproductive Medicine, Institute of Applied Toxicology, School of Public Health, Nanjing Medical University, Nanjing, 211166, China. wwu@njmu.edu.cn.
Hongjuan DingState Key Laboratory of Reproductive Medicine, Department of Obstetrics, Nanjing Maternity and Child Health Hospital, Obstetrics and Gynecology Hospital Affiliated to Nanjing Medical University, Nanjing, 210004, China.
Yankai XiaState Key Laboratory of Reproductive Medicine, Institute of Applied Toxicology, School of Public Health, Nanjing Medical University, Nanjing, 211166, China. yankaixia@njmu.edu.cn.
Daozhen ChenClinical Laboratory, Wuxi Maternity and Child Health Care Hospital Affiliated to Nanjing Medical University, Wuxi, 214002, China.
Xinru WangState Key Laboratory of Reproductive Medicine, Institute of Applied Toxicology, School of Public Health, Nanjing Medical University, Nanjing, 211166, China.
Nanjing Medical University · CNNanjing Maternity and Child Health Care Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study was to investigate the association between male infertility and single-nucleotide polymorphisms (SNPs) of DNA methyltransferases (DNMT) genes (DNMT3B: rs2424909, DNMT1: rs4804490, DNMT3A: rs1550117 and DNMT3L: rs7354779). Eight hundred and thirty three idiopathic infertile males and four hundred and ten fertile controls from the hospitals affiliated to Nanjing Medical University between 2010 and 2012 were recruited in the study. We demonstrated a significantly increased risk of idiopathic infertility with abnormal semen parameters in association with the heterozygous genotype of variant rs4804490. Moreover, the AA genotype of variant rs4804490 was associated with significantly decreased risk for male infertility with abnormal semen parameters. A decreased risk of idiopathic infertility with abnormal semen parameters was associated with the homozygous genotype of variant rs2424909. These results suggested that variants in different DNMT genes have different relationships with idiopathic male infertility, and Chinese men carrying these variants have an increased or decreased risk of abnormal semen parameters.

Indexed as

Epigenesis, GeneticPolymorphism, Single NucleotideDNA Modification MethylasesGenotypeHumansInfertility, MaleMaleSemenDNA Modification Methylases

Identifiers

PMID28894282
PMCPMC5593912
OpenAlexW2750818129

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.