Evidence map›Paper›PMID 28157160›Full record

ArticleInternational journal of molecular sciences2017

Embryological Results of Couples Undergoing ICSI-ET Treatments with Males Carrying the Single Nucleotide Polymorphism rs175080 of the MLH3 Gene.

George Anifandis, Ourania Markandona, Konstantinos Dafopoulos, Christina Messini, Aspasia Tsezou, Marina Dimitraki, Panagiotis Georgoulias, Alexandros Daponte, Ioannis Messinis

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Paternal factors contributing to embryo quality.Journal of assisted reproduction and genetics · 2018
    Review
  4. Age-Related Loss of Cohesion: Causes and Effects.International journal of molecular sciences · 2017
    Review
  5. De Novo Paternal FBN1 Mutation Detected in Embryos Before Implantation.Medical science monitor : international medical journal of experimental and clinical research · 2017
    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

9 authors at 1 institution in 1 country.

George AnifandisUniversity of Thessaly, Department of Obstetrics and Gynaecology, ART Unit, School of Health Sciences, Faculty of Medicine, Larissa 41110, Greece. ganif@med.uth.gr.
Ourania MarkandonaUniversity of Thessaly, Department of Obstetrics and Gynaecology, ART Unit, School of Health Sciences, Faculty of Medicine, Larissa 41110, Greece. ranja@hotmail.com.
Konstantinos DafopoulosUniversity of Thessaly, Department of Obstetrics and Gynaecology, ART Unit, School of Health Sciences, Faculty of Medicine, Larissa 41110, Greece. kdafop@med.uth.gr.
Christina MessiniUniversity of Thessaly, Department of Obstetrics and Gynaecology, ART Unit, School of Health Sciences, Faculty of Medicine, Larissa 41110, Greece. pireaschristina@gmail.com.
Aspasia TsezouUniversity of Thessaly, Department of Molecular Genetics and Cytogenetics, School of Health Sciences, Faculty of Medicine, Larissa 41110, Greece. atsezou@med.uth.gr.
Marina DimitrakiUniversity of Thessaly, Department of Obstetrics and Gynaecology, ART Unit, School of Health Sciences, Faculty of Medicine, Larissa 41110, Greece. dimitrakimarina@yahoo.com.
Panagiotis GeorgouliasUniversity of Thessaly, Department of Nuclear Medicine, School of Health Sciences, Faculty of Medicine, Larissa 41110, Greece. pgeorgoul@med.uth.gr.
Alexandros DaponteUniversity of Thessaly, Department of Obstetrics and Gynaecology, ART Unit, School of Health Sciences, Faculty of Medicine, Larissa 41110, Greece. dapontea@otenet.gr.
Ioannis MessinisUniversity of Thessaly, Department of Obstetrics and Gynaecology, ART Unit, School of Health Sciences, Faculty of Medicine, Larissa 41110, Greece. messinis@uth.gr.
University of Thessaly · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human MLH3 (hMLH3) gene has been suggested to play a role in the DNA mismatch repair mechanism, while it may also be associated with abnormal spermatogenesis and subsequently male infertility. The aim of the present study was to investigate possible relationships between the single nucleotide polymorphism (SNP) rs175080 in the MLH3 gene of males and the embryological results in couples undergoing intracytoplasmatic sperm injection-embryo transfer (ICSI-ET) treatments. A total of 132 men volunteered for the study and gave written informed consent. All couples were subjected to ICSI-ET treatments in the years 2010 to 2012. The couples were divided into three groups according to the genotype of their husbands: the wild type GG (n = 28), the heterozygotic type GA (n = 72) and the mutant type AA (n = 32). Significantly lower sperm concentration and progressive motility were observed in the AA group as compared to the other two groups (Concentration: 14.57 ± 4.9 mil/mL in AA, 38.3 ± 5.4 mil/mL in GA and 41.03 ± 6.8 mil/mL in GG, p < 0.05, mean ± standard error of the mean-SEM). However, significantly better embryological results (mean score of embryo quality-MSEQ) were found in the AA (8.12 ± 0.5) and the GA group (7.36 ± 0.4) as compared to the GG group (5.82 ± 0.7), (p < 0.05). Clinical pregnancy rate was significantly higher in the AA genotype group (43.8%) and the GA group (30.6%) than in the GG group (14.3%), (p < 0.05). Live birth rate was not different. It is suggested for the first time that the deteriorating effect of the mutant type on sperm characteristics does not impact on embryo development after fertilization in vitro.

Indexed as

Embryo TransferPolymorphism, Single NucleotideSperm Injections, IntracytoplasmicAdultAllelesFemaleFertilization in VitroGenotypeHumansMaleMutL ProteinsPregnancyPregnancy RateSemen AnalysisMLH3 protein, humanMutL Proteinsembryologyembryo qualitypolymorphismpregnancy ratessperm parameters.

Identifiers

PMID28157160
PMCPMC5343850
OpenAlexW2585012348

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.