Evidence map›Paper›PMID 32972375›Full record

SynthesisBMC pediatrics2020

Association between MTHFR C677T/A1298C and susceptibility to autism spectrum disorders: a meta-analysis.

Yan Li, Shuang Qiu, Jikang Shi, Yanbo Guo, Zhijun Li, Yi Cheng, Yawen Liu

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in BMC pediatrics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 3 pooled it
5.4field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 3 syntheses or guidelines pooled it, 55 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Natural Molecules for Brain Health and Resilience.International journal of molecular sciences · 2026
    Review
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  16. Frontiers in psychiatry · 2025
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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

7 authors at 1 institution in 1 country.

Yan LiDepartment of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, 130021, China.
Shuang QiuDepartment of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, 130021, China.
Jikang ShiDepartment of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, 130021, China.
Yanbo GuoDepartment of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, 130021, China.
Zhijun LiDepartment of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, 130021, China.
Yi ChengInstitute of Translational Medicine, the First Hospital of Jilin University, Changchun, 130021, China. chengyi@jlu.edu.cn.
Yawen LiuDepartment of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, 130021, China. ywliu@jlu.edu.cn.
Jilin University · CN

Funding

China Postdoctoral Science Foundation 2013M530989Science and Technology Department of Jilin Province 20150101130JCthe Ministry of Science and Technology of the People's Republic of China grant 2015DFA31580
6 · The paper itself

Abstract

backgroundAutism spectrum disorder (ASD) is becoming increasingly prevalent of late. Methylenetetrahydrofolate reductase (MTHFR) has a significant role in folate metabolism. Owing to the inconsistencies and inconclusiveness on the association between MTHFR single nucleotide polymorphism (SNP) and ASD susceptibilities, a meta-analysis was conducted to settle the inconsistencies.

methodsFor this meta-analysis, a total of 15 manuscripts published up to January 26, 2020, were selected from PubMed, Google Scholar, Medline, WangFang, and CNKI databases using search terms "MTHFR" OR "methylenetetrahydrofolate reductase" AND "ASD" OR "Autism Spectrum Disorders" OR "Autism" AND "polymorphism" OR "susceptibility" OR "C677T" OR "A1298C".

resultsThe findings of the meta-analysis indicated that MTHFR C677T polymorphism is remarkably associated with ASD in the five genetic models, viz., allelic, dominant, recessive, heterozygote, and homozygote. However, the MTHFR A1298C polymorphism was not found to be significantly related to ASD in the five genetic models. Subgroup analyses revealed significant associations of ASD with the MTHFR (C677T and A1298C) polymorphism. Sensitivity analysis showed that this meta-analysis was stable and reliable. No publication bias was identified in the associations between MTHFRC677T polymorphisms and ASD in the five genetic models, except for the one with regard to the associations between MTHFRA1298C polymorphisms and ASD in the five genetic models.

conclusionThis meta-analysis showed that MTHFR C677T polymorphism is a susceptibility factor for ASD, and MTHFR A1298C polymorphism is not associated with ASD susceptibility.

Indexed as

Autism Spectrum DisorderMethylenetetrahydrofolate Reductase (NADPH2)AllelesGenetic Predisposition to DiseaseGenotypeHumansPolymorphism, Single NucleotideMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanAutism spectrum disorderGenetic modelsMeta-analysisMethylenetetrahydrofolate reductaseSingle nucleotide polymorphisms

Identifiers

PMID32972375
PMCPMC7517654
OpenAlexW3088305734

What OpenQuestion holds

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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.