Evidence map›Paper›PMID 32739868›Full record

ArticleEBioMedicine2020

VLDL-specific increases of fatty acids in autism spectrum disorder correlate with social interaction.

Noriyoshi Usui, Keiko Iwata, Taishi Miyachi, Shu Takagai, Keisuke Wakusawa, Takahiro Nara, Kenji J Tsuchiya, Kaori Matsumoto, Daisuke Kurita, Yosuke Kameno and 16 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Environmental pollutants and autism spectrum disorder: Effects of plasticizers on core phenotypes and molecular targets.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  5. Very low-density lipoprotein and the human health.World journal of experimental medicine · 2026
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  18. Metabolomic changes in children with autism.World journal of clinical pediatrics · 2024
    Article
  19. Article
  20. 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

26 authors at 8 institutions in 1 country.

Noriyoshi UsuiResearch Center for Child Mental Development, University of Fukui, 23-3, Matsuokashimoaizuki, Eiheiji-cho, Yoshida-gun, Fukui 910-1193, Japan; Department of Child Development, United Graduate School of Child Development, Osaka University, Osaka 565-0871, Japan; Life Science Innovation Center, University of Fukui, Fukui 910-1193, Japan; Center for Medical Research and Education, and Department of Neuroscience and Cell Biology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan; Department of Neuroscience and Cell Biology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan; Global Center for Medical Engineering and Informatics, Osaka University, Osaka 565-0871, Japan; Addiction Research Unit, Osaka Psychiatric Research Center, Osaka Psychiatric Medical Center, Osaka 541-8567, Japan.
Keiko IwataResearch Center for Child Mental Development, University of Fukui, 23-3, Matsuokashimoaizuki, Eiheiji-cho, Yoshida-gun, Fukui 910-1193, Japan; Department of Child Development, United Graduate School of Child Development, Osaka University, Osaka 565-0871, Japan; Life Science Innovation Center, University of Fukui, Fukui 910-1193, Japan.
Taishi MiyachiDepartment of Pediatrics, Nagoya City University Medical School, Aichi 467-8601, Japan.
Shu TakagaiDepartment of Child and Adolescent Psychiatry, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.
Keisuke WakusawaDepartment of Rehabilitation, Miyagi Children's Hospital, Miyagi 989-3126, Japan.
Takahiro NaraDepartment of Rehabilitation, Miyagi Children's Hospital, Miyagi 989-3126, Japan.
Kenji J TsuchiyaResearch Center for Child Mental Development, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.
Kaori MatsumotoGraduate School of Psychology, Kanazawa Institute of Technology, Ishikawa 921-8054, Japan.
Daisuke KuritaDepartment of Psychiatry, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.
Yosuke KamenoDepartment of Psychiatry, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.
Tomoyasu WakudaDepartment of Psychiatry, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.
Kiyokazu TakebayashiDepartment of Psychiatry, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.
Yasuhide IwataDepartment of Psychiatry and Neurology, Fukude Nishi Hospital, Shizuoka 437-1216, Japan.
Toru FujiokaResearch Center for Child Mental Development, University of Fukui, 23-3, Matsuokashimoaizuki, Eiheiji-cho, Yoshida-gun, Fukui 910-1193, Japan; Department of Child Development, United Graduate School of Child Development, Osaka University, Osaka 565-0871, Japan.
Takaharu HiraiDepartment of Child Development, United Graduate School of Child Development, Osaka University, Osaka 565-0871, Japan; Department of Community Health Nursing, School of Medical Sciences, University of Fukui, Fukui 910-1193, Japan.
Manabu ToyoshimaLaboratory for Molecular Psychiatry, RIKEN Center for Brain Science, Saitama 351-0198, Japan.
Tetsuo OhnishiLaboratory for Molecular Psychiatry, RIKEN Center for Brain Science, Saitama 351-0198, Japan.
Tomoko ToyotaLaboratory for Molecular Psychiatry, RIKEN Center for Brain Science, Saitama 351-0198, Japan.
Motoko MaekawaLaboratory for Molecular Psychiatry, RIKEN Center for Brain Science, Saitama 351-0198, Japan.
Takeo YoshikawaLaboratory for Molecular Psychiatry, RIKEN Center for Brain Science, Saitama 351-0198, Japan.
Masato MaekawaDepartment of Laboratory Medicine, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.
Kazuhiko NakamuraDepartment of Psychiatry, Hirosaki University School of Medicine, Aomori 036-8562, Japan.
Masatsugu TsujiiSchool of Contemporary Sociology, Chukyo University, Aichi 470-0393, Japan.
Toshiro SugiyamaResearch Center for Child Mental Development, University of Fukui, 23-3, Matsuokashimoaizuki, Eiheiji-cho, Yoshida-gun, Fukui 910-1193, Japan.
Norio MoriDepartment of Psychiatry and Neurology, Fukude Nishi Hospital, Shizuoka 437-1216, Japan.
Hideo MatsuzakiResearch Center for Child Mental Development, University of Fukui, 23-3, Matsuokashimoaizuki, Eiheiji-cho, Yoshida-gun, Fukui 910-1193, Japan; Department of Child Development, United Graduate School of Child Development, Osaka University, Osaka 565-0871, Japan; Life Science Innovation Center, University of Fukui, Fukui 910-1193, Japan. Electronic address: matsuzah@u-fukui.ac.jp.
Hamamatsu University School of Medicine · JPRIKEN Center for Brain Science · JPUniversity of Fukui · JPMiyagi Children's Hospital · JPChukyo University · JPHirosaki University · JPKanazawa Institute of Technology · JPNagoya City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAbnormalities of lipid metabolism contributing to the autism spectrum disorder (ASD) pathogenesis have been suggested, but the mechanisms are not fully understood. We aimed to characterize the lipid metabolism in ASD and to explore a biomarker for clinical evaluation.

methodsAn age-matched case-control study was designed. Lipidomics was conducted using the plasma samples from 30 children with ASD compared to 30 typical developmental control (TD) children. Large-scale lipoprotein analyses were also conducted using the serum samples from 152 children with ASD compared to 122 TD children. Data comparing ASD to TD subjects were evaluated using univariate (Mann-Whitney test) and multivariate analyses (conditional logistic regression analysis) for main analyses using cofounders (diagnosis, sex, age, height, weight, and BMI), Spearman rank correlation coefficient, and discriminant analyses.

findingsForty-eight significant metabolites involved in lipid biosynthesis and metabolism, oxidative stress, and synaptic function were identified in the plasma of ASD children by lipidomics. Among these, increased fatty acids (FAs), such as omega-3 (n-3) and omega-6 (n-6), showed correlations with clinical social interaction score and ASD diagnosis. Specific reductions of very-low-density lipoprotein (VLDL) and apoprotein B (APOB) in serum of ASD children also were found by large-scale lipoprotein analysis. VLDL-specific reduction in ASD was correlated with APOB, indicating VLDL-specific dyslipidaemia associated with APOB in ASD children.

interpretationOur results demonstrated that the increases in FAs correlated positively with social interaction are due to VLDL-specific degradation, providing novel insights into the lipid metabolism underlying ASD pathophysiology.

fundingThis study was supported mainly by MEXT, Japan.

Indexed as

AdolescentApolipoprotein B-100Autism Spectrum DisorderCase-Control StudiesChildChild, PreschoolDyslipidemiasFatty AcidsFemaleHumansJapanLipidomicsLipoproteins, VLDLLogistic ModelsMaleMetabolomicsAPOB protein, humanApolipoprotein B-100Fatty AcidsLipoproteins, VLDLAutism spectrum disorderLipid metabolismOxidative stressPolyunsaturated fatty acidSocial communicationVLDL

Identifiers

PMID32739868
PMCPMC7393524
OpenAlexW3045500998

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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.