Evidence map›Paper›PMID 31209737›Full record

ArticleJournal of assisted reproduction and genetics2019

C677T polymorphism increases the risk of early spontaneous abortion.

Yongjie Liu, Fan Zhang, Liang Dai

Open access · hybridAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-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

6 citing papers in PubMed, 14 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Yongjie LiuDepartment of Reproductive Center, Yinchuan Maternal and Child Health Hospital, No. 56, Culture West Street, Xingqing District, Yinchuan, 750001, Ningxia, China. lyj1722006@126.com.ORCID http://orcid.org/0000-0003-1428-3753
Fan ZhangDepartment of Reproductive Center, Yinchuan Maternal and Child Health Hospital, No. 56, Culture West Street, Xingqing District, Yinchuan, 750001, Ningxia, China.
Liang DaiDepartment of Reproductive Center, Yinchuan Maternal and Child Health Hospital, No. 56, Culture West Street, Xingqing District, Yinchuan, 750001, Ningxia, China.
Yinchuan First People's Hospital · CN

Funding

the Ningxia Natural Science Foundation Funded Project 17242
6 · The paper itself

Abstract

purposeTo investigate the relationship of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism in male population having spouses with early spontaneous abortion.

methodsA total of 345 males whose spouses had at least one early spontaneous abortion were included in the study group, and 145 males who planned to have a second child were included in the control group. Semen was collected in a sterile cup by masturbation. After liquefaction, the sperm concentration and forward motility sperm rate (PR) were obtained. The genomic DNA was extracted from peripheral vein, followed by MTHFR C677T polymorphism detection through PCR-gold magnetic nanoparticle chromatography.

resultsThe numbers of alleles and genotypes of MTHFR in the case group were 303 (C), 387 (T), 64 (CC), 175 (CT), and 106 (TT) cases, respectively. The numbers of allele and genotype of MTHFR in the control group were 167 (C), 123 (T), 145 (CC), 65 (CT), and 29 (TT) cases. There were significant differences in the distribution frequency of genotypes (χ

conclusionsMTHFR could affect sperm DNA integrity through affecting DNA methylation, which led to an increase in the rate of early spontaneous abortion in spouses.

Indexed as

Polymorphism, Single NucleotideAbortion, SpontaneousAdultCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMethylenetetrahydrofolate Reductase (NADPH2)PregnancyRisk FactorsYoung AdultMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanEarly spontaneous abortionMaleMTHFR C677T polymorphism

Identifiers

PMID31209737
PMCPMC6707973
OpenAlexW2949972707

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.