Evidence map›Paper›PMID 25356156›Full record

ArticleInternational journal of clinical and experimental medicine2014

Association between MTHFR gene polymorphism and NTDs in Chinese Han population.

Yang Yu, Fang Wang, Yihua Bao, Xiaolin Lu, Li Quan, Ping Lu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2014. 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
0.5field-weighted citation impact, top 30% 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, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Perspectives on urological care in spina bifida patients.Intractable & rare diseases research · 2021
    Review
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

6 authors at 1 institution in 1 country.

Yang YuScientific Research Administration, Capital Institute of Pediatrics 2 Yabao Road, Chaoyang District, Beijing 100020, China.
Fang WangBeijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics 2 Yabao Road, Chaoyang District, Beijing 100020, China.
Yihua BaoBeijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics 2 Yabao Road, Chaoyang District, Beijing 100020, China.
Xiaolin LuBeijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics 2 Yabao Road, Chaoyang District, Beijing 100020, China.
Li QuanBeijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics 2 Yabao Road, Chaoyang District, Beijing 100020, China.
Ping LuBeijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics 2 Yabao Road, Chaoyang District, Beijing 100020, China.
Capital Institute of Pediatrics · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aims to investigate the single nucleotide polymorphisms (SNPs) of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene and neural tube defects (NTDs) in Chinese population.

methodA total of 271 NTDs cases and 192 healthy controls were used in this study. Fifty-two selected single nucleotide polymorphism (SNP) sites in the MTHFR gene were analyzed with next-generation sequencing method. A series of statistical methods were carried out to investigate the correlation between the SNPs and the patient susceptibility to NTDs.

resultsStatistical analysis showed a significant correlation between the SNP sites rs1801133 in MTHFR gene and NTDs. The GG genotype, G allele of rs1801133 in MTHFR significantly decreased the incidence of NTDs (OR = 0.449, 95% CI: 0.255-0.789 with genotype, and OR = 0.669, 95% CI: 0.508-0.881 with allele).

conclusionsThe gene polymorphism loci rs1801133 in MTHFR gene maybe potential risk factors for NTD in Chinese population.

Indexed as

10-methylenetetrahydrofolate reductase (MTHFR)5Neural tube defects (NTDs)single nucleotide polymorphisms (SNPs)

Identifiers

PMID25356156
PMCPMC4211806
OpenAlexW2260281857

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.