Evidence map›Paper›PMID 24586405›Full record

SynthesisPloS one2014

Association between MTHFR polymorphisms and acute myeloid leukemia risk: a meta-analysis.

Yu-Tao Qin, Yong Zhang, Fang Wu, Yan Su, Ge-Ning Lu, Ren-Sheng Wang

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Children (Basel, Switzerland) · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase, dietary folate intake, and the risk of leukemia in adults.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  8. Article
  9. The methylenetetrahydrofolate reductase (MTHFR) 677 C>T polymorphism increases the risk of developing chronic myeloid leukemia-a case-control study.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  10. 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

6 authors at 1 institution in 1 country.

Yu-Tao QinDepartment of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Yong ZhangDepartment of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Fang WuDepartment of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Yan SuDepartment of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Ge-Ning LuDepartment of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Ren-Sheng WangDepartment of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
First Affiliated Hospital of GuangXi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous observational studies investigating the association between methylenetetrahydrofolate reductase (MTHFR) polymorphisms and acute myeloid leukemia risk (AML) have yielded inconsistent results. The aim of this study is to derive a more precise estimation of the association between MTHFR (C677T and A1298C) polymorphisms and acute myeloid leukemia risk. PubMed and Embase databases were systematically searched to identify relevant studies from their inception to August 2013. Odds ratios (ORs) with 95% confidence intervals (CIs) were the metric of choice. Thirteen studies were selected for C677T polymorphism (1838 cases and 5318 controls) and 9 studies (1335 patients and 4295 controls) for A1298C polymorphism. Overall, pooled results showed that C677T polymorphism was not significant associated with AML risk(OR, 0.98-1.04; 95% CI, 0.86-0.92 to 1.09-1.25). Similar results were observed for the A1298C polymorphism and in subgroup analysis. All comparisons revealed no substantial heterogeneity nor did we detect evidence of publication bias. In summary, this meta-analysis provides evidence that MTHFR polymorphisms were not associated with AML risk. Further investigations are needed to offer better insight into the role of these polymorphisms in AML carcinogenesis.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseHumansLeukemia, Myeloid, AcuteMethylenetetrahydrofolate Reductase (NADPH2)Odds RatioPolymorphism, Single NucleotideMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, human

Identifiers

PMID24586405
PMCPMC3930602
OpenAlexW2053982407

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.