Evidence map›Paper›PMID 26835343›Full record

ArticleTranslational pediatrics2014

Association of folate metabolism genes MTHFR and MTRR with multiple complex congenital malformation risk in Chinese population of Shanxi.

Qin Zhang, Baoling Bai, Xiaozhen Liu, Chunyue Miao, Huili Li

Open access · greenAbstract read
In one paragraph

Article in Translational pediatrics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 95% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 1 institution in 1 country.

Qin ZhangBeijing Municipal Key Laboratory of Child Development Nutrigenomics, Capital Institute of Pediatrics, Beijing 100020, China.
Baoling BaiBeijing Municipal Key Laboratory of Child Development Nutrigenomics, Capital Institute of Pediatrics, Beijing 100020, China.
Xiaozhen LiuBeijing Municipal Key Laboratory of Child Development Nutrigenomics, Capital Institute of Pediatrics, Beijing 100020, China.
Chunyue MiaoBeijing Municipal Key Laboratory of Child Development Nutrigenomics, Capital Institute of Pediatrics, Beijing 100020, China.
Huili LiBeijing Municipal Key Laboratory of Child Development Nutrigenomics, Capital Institute of Pediatrics, Beijing 100020, China.
Capital Institute of Pediatrics · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Birth defects are common, serious malformations with a complex etiology that suggests involvement of both genetic and environmental factors. Low dietary folate and polymorphisms in genes of folate metabolism can influence risk for birth defects. In the present study 250 Chinese birth defects cases who suffered 1-8 types of birth defect disease phenotypes were subjected and two genetic variants in two folate metabolism key enzymes, rs1801394 of methionine synthase reductase (MTRR) and rs1801133 of methylenetetrahydrofolate reductase (MTHFR) were genotyped by using SNaPshot method. The results indicated that rs1801394 and rs1801133 were associated with multiple birth defects. According to homology of organogenesis, the disease phenotypes were classified into ectoderm-, mesoderm-, and endoderm-developed groups. Genetic analysis results displayed that as protective factors, genetic variants of rs1801133 and rs1801394 were associated with the risk of ectoderm-, and endoderm-developed malformations, but only the variant of rs1801394 was associated with the risk of mesoderm-developed malformations. Our present study first related nutrition metabolism related gene variants to germ layers and provided a novel understanding of an implication of earlier causation of birth defects pathogenesis in humans.

Indexed as

Birth defectsmethionine synthase reductase (MTRR)methylenetetrahydrofolate reductase (MTHFR)multiple complex congenital malformationsingle nucleotide olymorphism (SNP)

Identifiers

PMID26835343
PMCPMC4729852
OpenAlexW1866831042

What OpenQuestion holds

Textmetadata
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.