Evidence map›Paper›PMID 29524106›Full record

ArticleNeurotoxicity research2018

Association Study Between Metallothionein-3 Protein Polymorphisms and Autism.

MingXia Yu, Tao Cao, Dan Yu, Fusheng Huang

Abstract read
PubMed Publisher
In one paragraph

Article in Neurotoxicity research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 52% 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, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. 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

4 authors at 2 institutions in 1 country.

MingXia YuCenter for Gene Diagnosis, Zhongnan Hospital of Wuhan University, No. 169, East Lake Road, Wuchang District, Wuhan, 430071, Hubei, People's Republic of China.
Tao CaoDepartment of Laboratory, Hubei Cancer Hospital, No. 116, Zhuo Dao Springs South Road, Hongshan District, Wuhan, 430000, Hubei, People's Republic of China.
Dan YuCenter for Gene Diagnosis, Zhongnan Hospital of Wuhan University, No. 169, East Lake Road, Wuchang District, Wuhan, 430071, Hubei, People's Republic of China.
Fusheng HuangCenter for Gene Diagnosis, Zhongnan Hospital of Wuhan University, No. 169, East Lake Road, Wuchang District, Wuhan, 430071, Hubei, People's Republic of China. Huangfsuse@sina.com.
Wuhan University · CNHubei Cancer Hospital · CN

Funding

the National Natural Science Foundation of China Grant No: 81171669
6 · The paper itself

Abstract

Genetic susceptibility to high mercury body burden has been suggested as an autism risk factor in children. Metallothionein III (MT3) is the brain-specific form of the metallothionein family, which plays a key role in metal metabolism. We therefore looked for genetic variations in the MT3 gene that might increase the predisposition to autism. DNA was extracted from 132 autistic children and 132 age and gender-matched unrelated controls. All the samples were analyzed for nine single nucleotide polymorphisms (SNPs) with minor allele frequency > 10% in the MT3 gene. The mRNA levels of MT3 in white blood cells were evaluated by real-time PCR. We did not detect any association between these MT3 polymorphisms and the mRNA levels of MT3. We did not detect any association between MT3 polymorphisms and autism risk. However, we detected four novel MT3 SNPs that are not in the human SNP database. The clinical importance of these SNPs needs further investigation. Our data suggest that MT3 gene polymorphisms are not associated with autism.

Indexed as

Autistic DisorderChildChild, PreschoolFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansLinkage DisequilibriumMaleMetallothionein 3Nerve Tissue ProteinsPolymorphism, Single NucleotideRNA, MessengerMetallothionein 3Nerve Tissue ProteinsRNA, MessengerAssociation studyAutismMercuryMetallothionein III (MT3)SNP

Identifiers

PMID29524106
OpenAlexW2790040998

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.