Evidence map›Paper›PMID 35136021›Full record

ArticleTranslational psychiatry2022

The amplitude of fNIRS hemodynamic response in the visual cortex unmasks autistic traits in typically developing children.

Raffaele Mazziotti, Elena Scaffei, Eugenia Conti, Viviana Marchi, Riccardo Rizzi, Giovanni Cioni, Roberta Battini, Laura Baroncelli

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

NCT06292884 unknown statusnot on this mapstarted 2023, after this paper: background citation

Establishing Novel Functional Biomarkers for Creatine Deficiency Syndromes

TypeobservationalSponsorIRCCS Fondazione Stella MarisRan2023 to 2025Enrolled30ConditionsCreatine Deficiency, X-linked, Creatine Deficiency Syndrome Due to Gamt Deficiency
NCT06293027 unknown statusnot on this mapstarted 2023, after this paper: background citation

Establishing Novel Functional Biomarkers for Fragile X Syndrome

TypeobservationalSponsorIRCCS Fondazione Stella MarisRan2023 to 2025Enrolled40ConditionsFragile X Syndrome
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Raffaele Mazziotti *Department of Developmental Neuroscience, IRCCS Stella Maris Foundation, I-56128, Pisa, Italy.
Elena Scaffei *Department of Developmental Neuroscience, IRCCS Stella Maris Foundation, I-56128, Pisa, Italy.
Eugenia ContiDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, I-56128, Pisa, Italy.
Viviana MarchiDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, I-56128, Pisa, Italy.
Riccardo RizziDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, I-56128, Pisa, Italy.ORCID http://orcid.org/0000-0001-7446-6688
Giovanni CioniDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, I-56128, Pisa, Italy.
Roberta BattiniDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, I-56128, Pisa, Italy.
Laura BaroncelliDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, I-56128, Pisa, Italy. baroncelli@in.cnr.it.ORCID http://orcid.org/0000-0001-6739-2860
Fondazione Stella Maris · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autistic traits represent a continuum dimension across the population, with autism spectrum disorder (ASD) being the extreme end of the distribution. Accumulating evidence shows that neuroanatomical and neurofunctional profiles described in relatives of ASD individuals reflect an intermediate neurobiological pattern between the clinical population and healthy controls. This suggests that quantitative measures detecting autistic traits in the general population represent potential candidates for the development of biomarkers identifying early pathophysiological processes associated with ASD. Functional near-infrared spectroscopy (fNIRS) has been extensively employed to investigate neural development and function. In contrast, the potential of fNIRS to define reliable biomarkers of brain activity has been barely explored. Features of non-invasiveness, portability, ease of administration, and low-operating costs make fNIRS a suitable instrument to assess brain function for differential diagnosis, follow-up, analysis of treatment outcomes, and personalized medicine in several neurological conditions. Here, we introduce a novel standardized procedure with high entertaining value to measure hemodynamic responses (HDR) in the occipital cortex of adult subjects and children. We found that the variability of evoked HDR correlates with the autistic traits of children, assessed by the Autism-Spectrum Quotient. Interestingly, HDR amplitude was especially linked to social and communication features, representing the core symptoms of ASD. These findings establish a quick and easy strategy for measuring visually-evoked cortical activity with fNIRS that optimize the compliance of young subjects, setting the background for testing the diagnostic value of fNIRS visual measurements in the ASD clinical population.

Indexed as

Autism Spectrum DisorderAutistic DisorderVisual CortexAdultChildCommunicationHemodynamicsHumans

Identifiers

PMID35136021
PMCPMC8826368
OpenAlexW4225479897

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.