Evidence map›Paper›PMID 30180836›Full record

ArticleBMC psychiatry2018

FADS1-FADS2 and ELOVL2 gene polymorphisms in susceptibility to autism spectrum disorders in Chinese children.

Caihong Sun, Mingyang Zou, Xuelai Wang, Wei Xia, Yongjuan Ma, Shuang Liang, Yanqiu Hao, Lijie Wu, Songbin Fu

Open access · goldAbstract read
In one paragraph

Article in BMC psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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  4. MGenes and environment : the official journal of the Japanese Environmental Mutagen Society · 2023
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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

9 authors at 1 institution in 1 country.

Caihong SunDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, 150081, China.
Mingyang ZouDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, 150081, China.
Xuelai WangDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, 150081, China.
Wei XiaDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, 150081, China.
Yongjuan MaDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, 150081, China.
Shuang LiangDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, 150081, China.
Yanqiu HaoDepartment of Pediatric, The Second Affiliated Hospital, Harbin Medical University, Harbin, 150081, China.
Lijie WuDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, 150081, China. wulijiehyd@126.com.
Songbin FuLaboratory of Medical Genetics, Harbin Medical University, Harbin, 150081, China. fusb@ems.hrbmu.edu.cn.
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroudAutism spectrum disorders (ASD) are a complex group of neurodevelopmental disorders with a genetic basis. The role of long-chain polyunsaturated fatty acids (LC-PUFAs) and the occurrence of autism has been the focus of many recent studies. The present study investigates whether genetic variants of the fatty acid desaturase (FADS) 1/2 and elongation of very long-chain fatty acids protein (ELOVL) 2 genes, which are involved in LC-PUFA metabolism, are associated with ASD risk.

methodsA cohort of 243 ASD patients and 243 unrelated healthy controls were enrolled in this case control study. Sixteen tag single nucleotide polymorphisms from the FADS1-2 and ELOVL2 genes were genotyped using the Sequenom Mass Array.

resultsThere were significant differences in allelic distribution of FADS2 rs526126 (OR = 0.55, 95% CI = 0.42-0.72, p

conclusionsThese findings provide evidence of an association between FADS2 and ELOVL2 polymorphisms and ASD susceptibility in Chinese children.

Indexed as

AcetyltransferasesAsian PeopleAutism Spectrum DisorderCase-Control StudiesChildChild, PreschoolChinaCohort StudiesDelta-5 Fatty Acid DesaturaseFatty Acid DesaturasesFatty Acid ElongasesFemaleGenetic Predisposition to DiseaseHumansMalePolymorphism, Single NucleotideAcetyltransferasesDelta-5 Fatty Acid DesaturaseELOVL2 protein, humanFADS1 protein, humanFADS2 protein, humanFatty Acid DesaturasesFatty Acid ElongasesAutism spectrum disordersFADS1–2; ELOVL2Long-chain polyunsaturated fatty acidsSingle nucleotide polymorphisms

Identifiers

PMID30180836
PMCPMC6122697
OpenAlexW2890166307

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.