Evidence map›Paper›PMID 37743992›Full record

ArticleFrontiers in psychiatry2023

Association of adverse childhood experiences and cortical neurite density alterations with posttraumatic stress disorder symptoms in autism spectrum disorder.

Soichiro Kitamura, Kiwamu Matsuoka, Masato Takahashi, Hiroaki Yoshikawa, Akihiro Minami, Hiroki Ohnishi, Rio Ishida, Toshiteru Miyasaka, Yumi Tai, Tomoko Ochi and 2 more

Abstract read
In one paragraph

Article in Frontiers in psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

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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.

Soichiro KitamuraDepartment of Psychiatry, Nara Medical University School of Medicine, Kashihara, Japan.
Kiwamu MatsuokaDepartment of Psychiatry, Nara Medical University School of Medicine, Kashihara, Japan.
Masato TakahashiDepartment of Psychiatry, Nara Medical University School of Medicine, Kashihara, Japan.
Hiroaki YoshikawaDepartment of Psychiatry, Nara Medical University School of Medicine, Kashihara, Japan.
Akihiro MinamiDepartment of Psychiatry, Nara Medical University School of Medicine, Kashihara, Japan.
Hiroki OhnishiDepartment of Psychiatry, Nara Medical University School of Medicine, Kashihara, Japan.
Rio IshidaDepartment of Psychiatry, Nara Medical University School of Medicine, Kashihara, Japan.
Toshiteru MiyasakaDepartment of Radiology and Nuclear Medicine, Nara Medical University, Kashihara, Japan.
Yumi TaiDepartment of Radiology and Nuclear Medicine, Nara Medical University, Kashihara, Japan.
Tomoko OchiDepartment of Radiology and Nuclear Medicine, Nara Medical University, Kashihara, Japan.
Toshihiro TanakaDepartment of Radiology and Nuclear Medicine, Nara Medical University, Kashihara, Japan.
Manabu MakinodanDepartment of Psychiatry, Nara Medical University School of Medicine, Kashihara, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Posttraumatic stress disorder (PTSD) can be a source of significant social and daily distress in autism spectrum disorder (ASD). Compared to typically developed (TD) individuals, people with ASD are at an increased risk of adverse childhood experiences (ACEs), which can result in abnormal neuronal development. However, whether or how ACEs influence abnormal neural development and PTSD symptoms in ASD has not been fully elucidated. Methods: Thirty-nine TD individuals and 41 individuals with ASD underwent T1-weighted magnetic resonance imaging and neurite orientation dispersion and density imaging (NODDI), with axonal and dendritic densities assessed in terms of the orientation dispersion index and neurite density index (NDI), respectively. Voxel-based analyses were performed to explore the brain regions associated with PTSD symptoms, and the relationships between the severity of ACEs and PTSD symptoms and NODDI parameters in the extracted brain regions were examined. Results: There was a significant positive association between PTSD symptom severity and NDI in the bilateral supplementary motor area; right superior frontal, left supramarginal, and right superior temporal gyrus; and right precuneus in the ASD group, but not in the TD group. ACE severity was significantly associated with NDI in the right superior frontal and left supramarginal gyrus and right precuneus in the ASD group. Moreover, NDI in the right precuneus mainly predicted the severity of PTSD symptoms in the ASD group, but not the TD group. Conclusion: These results suggest that ACE-associated higher neurite density is of clinical importance in the pathophysiology of PTSD symptoms in ASD.

Indexed as

adverse childhood experienceautism spectrum disorderneurite densityNODDIposttraumatic stress disorder

Identifiers

PMID37743992
PMCPMC10515392

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