Evidence map›Paper›PMID 38868412›Full record

ArticlePCN reports : psychiatry and clinical neurosciences2023

Relationship between high trait anxiety in 22q11.2 deletion syndrome and the difficulties in medical, welfare, and educational services.

Naomi Nakajima, Miho Tanaka, Akiko Kanehara, Ryo Morishima, Yousuke Kumakura, Noriko Ohkouchi, Junko Hamada, Tomoko Ogawa, Hidetaka Tamune, Mutsumi Nakahara and 10 more

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In one paragraph

Article in PCN reports : psychiatry and clinical neurosciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

20 authors.

Naomi NakajimaDepartment of Neuropsychiatry The University of Tokyo Hospital Tokyo Japan.ORCID 0000-0002-5215-5878
Miho TanakaDepartment of Neuropsychiatry The University of Tokyo Hospital Tokyo Japan.
Akiko KaneharaDepartment of Neuropsychiatry The University of Tokyo Hospital Tokyo Japan.
Ryo MorishimaThe Health Care Science Institute Tokyo Japan.
Yousuke KumakuraDepartment of Neuropsychiatry The University of Tokyo Hospital Tokyo Japan.
Noriko OhkouchiDepartment of Neuropsychiatry The University of Tokyo Hospital Tokyo Japan.
Junko HamadaDepartment of Neuropsychiatry The University of Tokyo Hospital Tokyo Japan.
Tomoko OgawaDepartment of Child Psychiatry The University of Tokyo Hospital Tokyo Japan.
Hidetaka TamuneDepartment of Cellular Neurobiology, Graduate School of Medicine The University of Tokyo Tokyo Japan.
Mutsumi NakaharaGraduate School of Clinical Psychology Kagoshima University Kagoshima Japan.
Shunsuke MoriDepartment of Neuropsychiatry, Graduate School of Medicine The University of Tokyo Tokyo Japan.
Kayo IchihashiDepartment of Neuropsychiatry The University of Tokyo Hospital Tokyo Japan.
Seiichiro JindeDepartment of Neuropsychiatry The University of Tokyo Hospital Tokyo Japan.
Yukiko KanoDepartment of Child Psychiatry The University of Tokyo Hospital Tokyo Japan.ORCID 0000-0002-2341-5095
Ichiro SakamotoDepartment of Cardiovascular Medicine Kyushu University Graduate School of Medical Sciences Fukuoka Japan.
Kyoko TanakaDepartment of Psychosocial Medicine National Center for Child Health and Development Tokyo Japan.
Yoichiro HirataDepartment of Pediatrics Kitasato University School of Medicine Kanagawa Japan.
Hirofumi OhashiDivision of Medical Genetics Saitama Children's Medical Center Saitama Japan.
Tokuko ShinoharaDepartment of Pediatric Cardiology and Adult Congenital Cardiology Tokyo Women's Medical University Tokyo Japan.
Kiyoto KasaiDepartment of Neuropsychiatry The University of Tokyo Hospital Tokyo Japan.ORCID 0000-0002-4443-4535

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: The 22q11.2 deletion syndrome (22q11DS) is associated with a high prevalence of mental health comorbidities. However, not enough attention has been paid to the elevated prevalence of high trait anxiety that begins early in life and may be enduring. We sought to identify specific medical, welfare, or educational difficulties associated with high trait anxiety in 22q11DS. Methods: A questionnaire-based survey was conducted for the parents of 22q11DS individuals ( Results: The multiple regression analysis confirmed that the high trait anxiety was significantly associated with parental psychological distress ( Conclusion: To our knowledge, this is the first study to clarify quantitatively how the characteristic of high anxiety level in 22q11DS individuals is related to the caregivers' perceived difficulties in medical, welfare, and educational services. These results suggest the necessity of designing service structures informed of the fact that high trait anxiety is an important clinical feature of the syndrome.

Indexed as

22q11.2 deletion syndromeanxietycaregivereducationalmedicalwelfare

Identifiers

PMID38868412
PMCPMC11114383

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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.