Evidence map›Paper›PMID 31977880›Full record

Observational studyMedicine2020

Association of human serotonin receptor 4 promoter methylation with autism spectrum disorder.

Zhenyu Hu, Xiuru Ying, Ling Huang, Yuanzhi Zhao, Dongsheng Zhou, Jing Liu, Jie Zhong, Tianyi Huang, Wenwu Zhang, Fang Cheng and 1 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Autism and Cortical Thickness Deviation From Neurotypical Controls: Evidence for a Spatial Association With Serotonin Receptors.Autism research : official journal of the International Society for Autism Research · 2026
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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

11 authors at 2 institutions in 1 country.

Zhenyu HuNingbo Kangning Hospital, Ningbo Key Laboratory of Behavioral Neuroscience.
Xiuru YingMedical Genetics Center, School of Medicine, Ningbo University, Ningbo, Zhejiang, China.
Ling HuangNingbo Kangning Hospital, Ningbo Key Laboratory of Behavioral Neuroscience.
Yuanzhi ZhaoNingbo Kangning Hospital, Ningbo Key Laboratory of Behavioral Neuroscience.
Dongsheng ZhouNingbo Kangning Hospital, Ningbo Key Laboratory of Behavioral Neuroscience.
Jing LiuMedical Genetics Center, School of Medicine, Ningbo University, Ningbo, Zhejiang, China.
Jie ZhongMedical Genetics Center, School of Medicine, Ningbo University, Ningbo, Zhejiang, China.
Tianyi HuangMedical Genetics Center, School of Medicine, Ningbo University, Ningbo, Zhejiang, China.
Wenwu ZhangNingbo Kangning Hospital, Ningbo Key Laboratory of Behavioral Neuroscience.
Fang ChengNingbo Kangning Hospital, Ningbo Key Laboratory of Behavioral Neuroscience.
Shiwei DuanMedical Genetics Center, School of Medicine, Ningbo University, Ningbo, Zhejiang, China.
Ningbo Kangning Hospital · CNNingbo University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human serotonin receptor 4 (HTR4) encodes a 5-HT4 receptor involved in learning, memory, depression, anxiety, and feeding behavior. The aim of this study was to investigate the association between the deoxyribonucleic acid (DNA) methylation of HTR4 promoter and autism spectrum disorder (ASD), a disease characterized by communication disorder and repetitive or restrictive behavior.Peripheral blood DNA was obtained from 61 ASD children and 66 healthy children, and the DNA methylation of HTR4 promoter was assessed by quantitative methylation-specific polymerase chain reaction. We used percentage of methylated reference (PMR) to represent DNA methylation level.Due to significant age differences between ASD cases and controls (3 [2, 5] years and 6 [5, 6] years, P = 3.34E-10), we used binary logistic regression analysis for adjustment. Our results showed that the DNA methylation levels of HTR4 promoter were significantly lower in children with ASD than in healthy children (median PMR: 66.23% vs 94.31%,P = .028, age-adjusted P = .034). In addition, the DNA methylation of HTR4 promoter was inversely associated with age in male ASD cases (total cases: r = -0.283, P = .027; male cases: r = -0.431, P = .002; female cases: r = -0.108, P = .752). Dual-luciferase reporter gene assay showed that the reporter gene expression in the strain with recombinant pGL3-promoter-HTR4 plasmid was significantly higher than that in the strain with pGL3-promoter plasmid (fold change = 2.01, P = .0065), indicating that the HTR4 promoter fragment may contain transcription factors to upregulate promoter activity.Our study suggested that hypomethylation of the HTR4 promoter is a potential biomarker for predicting the risk of male ASD.

Indexed as

Autism Spectrum DisorderBiomarkersCase-Control StudiesChildChild, PreschoolChinaDNA MethylationFemaleHumansMaleReal-Time Polymerase Chain ReactionReceptors, Serotonin, 5-HT4Sex FactorsBiomarkersReceptors, Serotonin, 5-HT4

Identifiers

PMID31977880
PMCPMC7004686
OpenAlexW3001111704

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.