Evidence map›Paper›PMID 41765989›Full record

ArticleJournal of human genetics2026

Psychological distress and cancer worry in unaffected relatives undergoing cascade testing with multigene panel testing.

Kaori Kimura, Takeshi Kuwata, Yumie Hiraoka, Manami Matsukawa, Chikako Tomozawa, Miki Aitani, Yu Komura, Izumi Miki, Masashi Wakabayashi, Yosuke Furui and 16 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of human genetics, 2026. 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

26 authors.

Kaori KimuraDepartment of Genetic Medicine and Services, National Cancer Center Hospital East, Kashiwa, Japan.
Takeshi KuwataDepartment of Genetic Medicine and Services, National Cancer Center Hospital East, Kashiwa, Japan. tkuwata@east.ncc.go.jp.
Yumie HiraokaDepartment of Genetic Medicine and Services, National Cancer Center Hospital East, Kashiwa, Japan.
Manami MatsukawaDepartment of Genetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.
Chikako TomozawaDepartment of Genetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.
Miki AitaniDepartment of Genetic Medicine and Services, National Cancer Center Hospital East, Kashiwa, Japan.
Yu KomuraTranslational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.
Izumi MikiDepartment of Genetic Medicine and Services, National Cancer Center Hospital East, Kashiwa, Japan.
Masashi WakabayashiBiostatistics Division, Center for Research Administration and Support, National Cancer Center Hospital East, Kashiwa, Japan.
Yosuke FuruiFALCO Biosystems, Kyoto, Japan.
Hiroki KondoFALCO Biosystems, Kyoto, Japan.
Kazumasa SaigohDepartment of Clinical Genetics, Kinki University Hospital, Osaka, Japan.
Yasuko YamamotoDepartment of Hereditary Tumors, National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan.ORCID http://orcid.org/0009-0004-4440-2092
Kiwamu AkagiDepartment of Genetic Medicine and Services, National Cancer Center Hospital East, Kashiwa, Japan.
Hiroto NarimatsuDepartment of Genetic Medicine, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.
Megumu YokonoSchool of Social Sciences, Waseda University, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2818-7279
Shinsuke AmanoJapan Federation of Cancer Patient Organizations, Yokohama, Japan.
Kaori MutoDepartment of Public Policy, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Fuji NagamiTohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
Kazuto KatoDepartment of Biomedical Ethics and Public Policy, Graduate School of Medicine, The University of Osaka, Osaka, Japan.ORCID http://orcid.org/0000-0001-9006-9551
Riu YamashitaDivision of Translational Informatics, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa, Japan.
Issei ImotoAichi Cancer Center Research Institute, Nagoya, Japan.
Shinji KosugiDepartment of Genomic Medicine, Kyoto University School of Public Health, Kyoto, Japan.ORCID http://orcid.org/0000-0001-6036-6491
Makoto HirataDepartment of Genetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.ORCID http://orcid.org/0000-0002-9994-9958
Takayuki YoshinoDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Yoshiaki NakamuraTranslational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multigene panel testing (MGPT) is increasingly used for diagnosing hereditary cancers; however, its application in cascade testing remains limited, and the psychological impact on unaffected relatives is not well understood. This multicenter study in Japan recruited 123 first-degree relatives without a personal history of cancer to evaluate psychological responses before (T0) and two weeks after (T1) MGPT result disclosure. Participants completed the Japanese version of the Cancer Worry Scale (CWS-J) at both time points and the Impact of Event Scale-Revised (IES-R) at T1. Two weeks after disclosure, 6.5% of relatives met the threshold for clinically significant distress. Mean IES-R scores were higher among carriers of pathogenic variants (mean 8.2) than among those with negative results (mean 4.8) or variants of uncertain significance (mean 2.4). In contrast, multivariate analysis revealed no independent association between test result and post-disclosure distress. In contrast, higher baseline CWS-J scores were strongly associated with elevated IES-R scores after disclosure (p < 0.001). Children and relatives who frequently discussed cancer risk within their families exhibited higher distress levels than other subgroups. Overall, CWS-J scores showed no significant change from pre- to post-disclosure, with 41% of relatives maintaining persistently high worry. Across both time points, unaffected relatives consistently reported lower CWS-J scores than individuals with cancer (p < 0.0001). These findings suggest that MGPT has minimal psychological impact on unaffected relatives undergoing cascade testing, although those with higher preexisting cancer worry may require additional psychosocial support.

Indexed as

AnxietyFamilyGenetic Predisposition to DiseaseGenetic TestingNeoplasmsPsychological DistressStress, PsychologicalAdultAgedFemaleHumansJapanMaleMiddle Aged

Identifiers

PMID41765989
PMCPMC13303072

What OpenQuestion holds

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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 OpenQuestion graph.