Evidence map›Paper›PMID 37638188›Full record

ArticleFrontiers in neurology2023

Reduced neurite density index in the prefrontal cortex of adults with autism assessed using neurite orientation dispersion and density imaging.

Takashi Arai, Koji Kamagata, Wataru Uchida, Christina Andica, Kaito Takabayashi, Yuya Saito, Rukeye Tuerxun, Zaimire Mahemuti, Yuichi Morita, Ryusuke Irie and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 14 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

12 authors at 1 institution in 1 country.

Takashi AraiDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Koji KamagataFaculty of Health Data Science, Juntendo University, Chiba, Japan.
Wataru UchidaDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Christina AndicaDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Kaito TakabayashiDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yuya SaitoDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Rukeye TuerxunDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Zaimire MahemutiDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yuichi MoritaDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Ryusuke IrieDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Eiji KirinoDepartment of Psychiatry, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Shigeki AokiDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Juntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Core symptoms of autism-spectrum disorder (ASD) have been associated with prefrontal cortex abnormalities. However, the mechanisms behind the observation remain incomplete, partially due to the challenges of modeling complex gray matter (GM) structures. This study aimed to identify GM microstructural alterations in adults with ASD using neurite orientation dispersion and density imaging (NODDI) and voxel-wise GM-based spatial statistics (GBSS) to reduce the partial volume effects from the white matter and cerebrospinal fluid. Materials and methods: A total of 48 right-handed participants were included, of which 22 had ASD (17 men; mean age, 34.42 ± 8.27 years) and 26 were typically developing (TD) individuals (14 men; mean age, 32.57 ± 9.62 years). The metrics of NODDI (neurite density index [NDI], orientation dispersion index [ODI], and isotropic volume fraction [ISOVF]) were compared between groups using GBSS. Diffusion tensor imaging (DTI) metrics and surface-based cortical thickness were also compared. The associations between magnetic resonance imaging-based measures and ASD-related scores, including ASD-spectrum quotient, empathizing quotient, and systemizing quotient were also assessed in the region of interest (ROI) analysis. Results: After controlling for age, sex, and intracranial volume, GBSS demonstrated significantly lower NDI in the ASD group than in the TD group in the left prefrontal cortex (caudal middle frontal, lateral orbitofrontal, pars orbitalis, pars triangularis, rostral middle frontal, and superior frontal region). In the ROI analysis of individuals with ASD, a significantly positive correlation was observed between the NDI in the left rostral middle frontal, superior frontal, and left frontal pole and empathizing quotient score. No significant between-group differences were observed in all DTI metrics, other NODDI (i.e., ODI and ISOVF) metrics, and cortical thickness. Conclusion: GBSS analysis was used to demonstrate the ability of NODDI metrics to detect GM microstructural alterations in adults with ASD, while no changes were detected using DTI and cortical thickness evaluation. Specifically, we observed a reduced neurite density index in the left prefrontal cortices associated with reduced empathic abilities.

Indexed as

autismdiffusion tensor imagingdiffusion-weighted imaginggray matterneurite orientation dispersion and density imagingneuronal losssurface-based cortical thickness measurement

Identifiers

PMID37638188
PMCPMC10450631
OpenAlexW4385761720

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.