Evidence map›Paper›PMID 28842818›Full record

ArticleJournal of assisted reproduction and genetics2017

Association between the MTHFR-C677T isoform and structure of sperm DNA.

Dominique Cornet, Marc Cohen, Arthur Clement, Edouard Amar, Laetitia Fournols, Patrice Clement, Paul Neveux, Yves Ménézo

Open access · greenAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The Study ofInternational journal of fertility & sterility · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. C677T polymorphism increases the risk of early spontaneous abortion.Journal of assisted reproduction and genetics · 2019
    Article
  8. Article
  9. Article
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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 4 institutions in 1 country.

Dominique CornetClinique de La Muette, 75016, Paris, France.
Marc CohenClinique Natecia, 69008, Lyon, France.
Arthur ClementLaboratoire Clement, Avenue d'Eylau, 75016, Paris, France.
Edouard AmarAmerican Hospital, 92200, Neuilly sur Seine, France.
Laetitia FournolsClinique de La Muette, 75016, Paris, France.
Patrice ClementLaboratoire Clement, Avenue d'Eylau, 75016, Paris, France.
Paul NeveuxCentre Hospitalo Univesitaire d'Angers, 49000, Angers, France.
Yves MénézoLaboratoire Clement, Avenue d'Eylau, 75016, Paris, France. yves.menezo@gmail.com.
Chimie Moléculaire, Macromoléculaire, Matériaux · FRHôpital américain de paris · FRCentre Hospitalier Universitaire d'Angers · FRClinique Ambroise Paré · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of this study is to evaluate whether the MTHFR contribution to male decreased fertility can be attributable to anomalies in sperm nucleus DNA structure in relation to defective methylation.

methodsThe presence of MTHFR C677T, contributing at most for male infertility, was determined from a venous blood sample, using real-time polymerase chain reaction (PCR). Sperm DNA fragmentation (SDF) and sperm nucleus decondensation index (SDI) measurements were performed using acridine orange and flow cytometry. SDF and SDI of men MTHFR C677T heterozygous or homozygous were compared to a general population of hypo-fertile patients

resultsSDF is not increased either in homozygous or heterozygous carriers of MTHFR C677T. In contrast, SDI is increased with a higher incidence in homozygous (p = 0.0006) than in heterozygous (p = 0.029) patients when compared with the control population. Using a critical threshold of 20% for either SDI or SDF assayed with our technique, the percentage of patients with results higher than this value is not significant with respect to fragmentation (0.128), but is significantly increased for decondensation (0.0003).

conclusionsDefective methylation linked to MTHFR may contribute to sperm pathogenesis via increased SDI. After DNA structure analysis, especially SDI, treatment with 5-methyl tetrahydrofolate (MTHF), the metabolite downstream from the action of MTHFR, should be recommended as a therapeutic approach. Patients with a high SDI should be tested for MTHFR isoforms as part of a healthcare policy.

Indexed as

Case-Control StudiesDNADNA FragmentationHeterozygoteHomozygoteHumansInfertility, MaleIsoenzymesMaleMethylenetetrahydrofolate Reductase (NADPH2)Polymorphism, Single NucleotideSemen AnalysisSpermatozoaDNAIsoenzymesMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanDNA fragmentationMTHFR isoform C677TNucleus decondensationSperm

Identifiers

PMID28842818
PMCPMC5633564
OpenAlexW2748598625

What OpenQuestion holds

Textmetadata
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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.