Evidence map›Paper›PMID 32661284›Full record

ArticleJournal of human genetics2020

Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan.

Mio Tsuchiya, Takahiro Yamada, Rina Akaishi, Haruka Hamanoue, Akira Hirasawa, Maki Hyodo, Issei Imoto, Tomoki Kosho, Kenji Kurosawa, Hiromi Murakami and 11 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of human genetics, 2020. 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

21 authors.

Mio TsuchiyaDepartment of Medical Ethics and Medical Genetics, Kyoto University School of Public Health, Kyoto, Japan.
Takahiro YamadaDepartment of Medical Ethics and Medical Genetics, Kyoto University School of Public Health, Kyoto, Japan. taka0197@kuhp.kyoto-u.ac.jp.ORCID http://orcid.org/0000-0002-5370-7873
Rina AkaishiThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Haruka HamanoueThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Akira HirasawaThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Maki HyodoThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Issei ImotoThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Tomoki KoshoThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.ORCID http://orcid.org/0000-0002-8344-7507
Kenji KurosawaThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.ORCID http://orcid.org/0000-0002-6817-7748
Hiromi MurakamiDepartment of Medical Ethics and Medical Genetics, Kyoto University School of Public Health, Kyoto, Japan.
Kaname NakataniThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Fumio NomuraThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Aiko SasakiThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Kenji ShimizuThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.ORCID http://orcid.org/0000-0002-2732-8722
Mariko TamaiThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Hiroshi UmemuraThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Atsushi WatanabeThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Akiko YoshidaThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Hiroshi YoshihashiThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Junko YotsumotoThe Social, Ethical and Legal Issues Committee, Japanese Society for Genetic Counseling, Tokyo, Japan.
Shinji KosugiDepartment of Medical Ethics and Medical Genetics, Kyoto University School of Public Health, Kyoto, Japan.

Funding

Japan Agency for Medical Research and Development (AMED) 17kk0305006h0001
6 · The paper itself

Abstract

The management of secondary findings (SFs), which are beyond the intended purpose of the analysis, from clinical comprehensive genomic analysis using next generation sequencing (NGS) presents challenges. Policy statements regarding their clinical management have been announced in Japan and other countries. In Japan, however, the current status of and attitudes of clinical genetics professionals toward reporting them are unclear. We conducted a questionnaire survey of clinical genetics professionals at two time points (2013 and 2019) to determine the enforcement of the SF management policy in cases of comprehensive genetic analysis of intractable diseases and clinical cancer genome profiling testing. According to the survey findings, 40% and 70% of the respondents stated in the 2013 and 2019 surveys, respectively, that they had an SF policy in the field of intractable diseases, indicating that SF policy awareness in Japan has changed significantly in recent years. Furthermore, a total of 80% of respondents stated that their facility had established a policy for clinical cancer genome profiling testing in the 2019 survey. In both surveys, the policies included the selection criteria for genes to be disclosed and the procedure to return SFs, followed by recommendations and proposals regarding SFs in Japan and other countries. To create a better list of the genes to be disclosed, further examination is needed considering the characteristics of each analysis.

Indexed as

DisclosureExomeGenetic TestingGenome, HumanGenomicsHigh-Throughput Nucleotide SequencingHumansJapanNeoplasmsSurveys and Questionnaires

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.