Evidence map›Paper›PMID 30941018›Full record

ArticleFrontiers in cellular neuroscience2019

Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children.

Liming Shen, Chengyun Feng, Kaoyuan Zhang, Youjiao Chen, Yan Gao, Junyan Ke, Xinqian Chen, Jing Lin, Cuihua Li, Javed Iqbal and 2 more

Abstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

31 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  7. [Change of plasma level of valine and its relationship with developmental quotient in children with autism].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
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  19. Diet in treatment of autism spectrum disorders.Frontiers in neuroscience · 2022
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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

12 authors.

Liming ShenCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Chengyun FengMaternal and Child Health Hospital of Baoan, Shenzhen, China.
Kaoyuan ZhangCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Youjiao ChenCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Yan GaoMaternal and Child Health Hospital of Baoan, Shenzhen, China.
Junyan KeCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Xinqian ChenCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Jing LinCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Cuihua LiCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Javed IqbalCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Yuxi ZhaoCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Weibin WangSchool of Art, Shenzhen University, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism is one of the most common neurological developmental disorder associated with social isolation and restricted interests in children. The etiology of this disorder is still unknown. There is neither any confirmed laboratory test nor any effective therapeutic strategy to diagnose or cure it. To search for biomarkers for early detection and exploration of the disease mechanisms, here, we investigated the protein expression signatures of peripheral blood mononuclear cells (PBMCs) in autistic children compared with healthy controls by using isobaric tags for relative and absolute quantitation (iTRAQ) proteomics approach. The results showed a total of 41 proteins as differentially expressed in autistic group as compared to control. These proteins are found associated with metabolic pathways, endoplasmic reticulum (ER) stress and protein folding, endocytosis, immune and inflammatory response, plasma lipoprotein particle organization, and cell adhesion. Among these, 17 proteins (13 up-regulated and four down-regulated) are found to be linked with mitochondria. Eight proteins including three already reported proteins in our previous studies were selected to be verified. Five already reported autism associated pro-inflammatory cytokines [interferon-γ (IFN-γ), interleukin-1β (IL-1β), IL-6, IL-12, and tumor necrosis factor-α (TNF-α)] were detected in plasma by enzyme-linked immunosorbent assay (ELISA) analysis. The results were consistent with proteomic results and reports from previous literature. These results proposed that PBMCs from autistic children might be activated, and ER stress, unfolded protein response (UPR), acute-phase response (APR), inflammatory response, and endocytosis may be involved in autism occurrence. These reported proteins may serve as potential biomarkers for early diagnosis of autism. More specifically, simultaneous detection of three proteins [complement C3 (C3), calreticulin (CALR), and SERPINA1] in the plasma and PBMCs could increase the authenticity of detection.

Indexed as

autismbiomarkersiTRAQperipheral blood mononuclear cellsproteomics

Identifiers

PMID30941018
PMCPMC6433831

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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.