Evidence map›Paper›PMID 37673435›Full record

ArticleJournal of psychiatry & neuroscience : JPN

Transcript levels of 4 genes in umbilical cord blood are predictive of later autism development: a longitudinal follow-up study.

Qingzheng Jia, Huilin Li, Min Wang, Chongxia Wei, Lichao Xu, Lin Ye, Chunjun Wang, Shaofeng Ke, Ling Li, Paul Yao

Open access · diamondAbstract read
In one paragraph

Article in Journal of psychiatry & neuroscience : JPN. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  4. Review
  5. 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

10 authors.

Qingzheng Jia *From the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China.
Huilin Li *From the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China vasilis112@yahoo.com lcl115@163.com.
Min WangFrom the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China.
Chongxia WeiFrom the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China.
Lichao XuFrom the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China.
Lin YeFrom the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China.
Chunjun WangFrom the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China.
Shaofeng KeFrom the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China.
Ling LiFrom the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China.
Paul YaoFrom the Department of Pediatrics, Hainan Women and Children's Medical Center, Hainan, China vasilis112@yahoo.com lcl115@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOver recent decades, autism spectrum disorder (ASD) has been of increasing epidemiological importance, given the substantial increase in its prevalence; at present, clinical diagnosis is possible only after 2 years of age. In this study, we sought to develop a potential predictive model for ASD screening.

methodsWe conducted a longitudinal follow-up study of newborns over 3 years. We measured transcript levels of 4 genes (superoxide dismutase-2 [

resultsWe followed 2623 newborns; we identified 41 children with ASD, 63 with delayed development and 2519 typically developing children. We matched the 41 children with ASD to 41 typically developing children for UCBMC measurements. Our results showed that children with ASD had significantly higher levels of H3K9me3 histone modifications at the LIMITATIONS: Although the gene combinations produced a good pass/fail cut-off value for ASD evaluation, relatively few children in our study sample had ASD.

conclusionThe altered gene expression in UCBMC can predict later autism development, possibly providing a predictive model for ASD screening immediately after birth.

Indexed as

Autism Spectrum DisorderAutistic DisorderChildFetal BloodFollow-Up StudiesHumansInfant, Newborn

Identifiers

PMID37673435
PMCPMC10495168
OpenAlexW4386483007

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.