Evidence map›Paper›PMID 31035713›Full record

ArticleBehavioral sciences (Basel, Switzerland)2019

Mohamed B Abou-Donia, Hagir B Suliman, Dario Siniscalco, Nicola Antonucci, Passent ElKafrawy

Open access · goldAbstract read
In one paragraph

Article in Behavioral sciences (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

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  9. Reply to: "Qualitative Evaluation of α-Synuclein: A Critical Step in Unravelling the Complexities of Autism Spectrum Disorder".Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2023
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  16. The Role of Lipidomics in Autism Spectrum Disorder.Molecular diagnosis & therapy · 2020
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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

5 authors at 3 institutions in 2 countries.

Mohamed B Abou-DoniaDepartment of Pharmacology and Cancer Biology, Department of Neurobiology, Duke University Medical Center, Durham 27710, NC, USA. donia@duke.edu.
Hagir B SulimanDepartment of Anesthesiology- Hyperbaric Division, Duke University Medical Center, Durham, NC 27710, NC, USA. hagir.suliman@duke.edu.
Dario SiniscalcoDepartment of Experimental Medicine, University of Campania, 80138 Naples, Italy. dariosin@uab.edu.
Nicola AntonucciBiomedical Center for Autism Research and Treatment, 70124 Bari, Italy. info@antonucci.eu.
Passent ElKafrawyFaculty of Science, Shebien El-KoomUniversity 32615 Shebien El-Koom, Egypt. basant.elkafrawi@science.menofia.edu.eg.
Duke University · USDuke Medical Center · USMenoufia University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism spectrum disorders (ASDs) are the most common neurodevelopmental disorders with unidentified etiology. The behavioral manifestations of ASD may be a consequence of genetic and/or environmental pathology in neurodevelopmental processes. In this limited study, we assayed autoantibodies to a panel of vital neuronal and glial proteins in the sera of 40 subjects (10 children with ASD and their mothers along with 10 healthy controls, age-matched children and their mothers). Serum samples were screened using Western Blot analysis to measure immunoglobulin (IgG) reactivity against a panel of 9 neuronal proteins commonly associated with neuronal degeneration: neurofilament triplet proteins (NFP), tubulin, microtubule-associated proteins (tau), microtubule-associated protein-2 (MAP-2), myelin basic protein (MBP), myelin-associated glycoprotein (MAG), α-synuclein (SNCA) and astrocytes proteins such as glial fibrillary acidic protein (GFAP) and S100B protein. Our data show that the levels of circulating IgG class autoantibodies against the nine proteins were significantly elevated in ASD children. Mothers of ASD children exhibited increased levels of autoantibodies against all panel of tested proteins except for S100B and tubulin compared to age-matched healthy control children and their mothers. Control children and their mothers showed low and insignificant levels of autoantibodies to neuronal and glial proteins. These results strongly support the importance of anti-neuronal and glial protein autoantibodies biomarker in screening for ASD children and further confirm the importance of the involvement of the maternal immune system as an index that should be considered in fetal

Indexed as

Autism Spectrum Disorderautoimmune disorderControl childrenmaternal autoantibodiesneuronal and astroglial biomarkersneuronal autoantibodies

Identifiers

PMID31035713
PMCPMC6563083
OpenAlexW2940528890

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.