Assessing awareness toward genetic testing among patients with inherited retinal dystrophy in Japan.

IF 2.7 3区 医学 Q2 OPHTHALMOLOGY
Go Mawatari, Taiji Sakamoto, Koji M Nishiguchi, Masato Akiyama, Akio Oishi, Kaoru Fujinami, Akiko Maeda, Michikazu Nakai, Yasuhiro Ikeda
{"title":"Assessing awareness toward genetic testing among patients with inherited retinal dystrophy in Japan.","authors":"Go Mawatari, Taiji Sakamoto, Koji M Nishiguchi, Masato Akiyama, Akio Oishi, Kaoru Fujinami, Akiko Maeda, Michikazu Nakai, Yasuhiro Ikeda","doi":"10.1007/s10384-026-01430-4","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To conduct a nationwide questionnaire survey among patients with inherited retinal dystrophy (IRD) with the aim of investigating the percentage of patients requesting or not requesting genetic testing and clarifying the reasons underlying these preferences.</p><p><strong>Study design: </strong>A questionnaire-based cross-sectional study.</p><p><strong>Methods: </strong>This study conducted a questionnaire survey targeting IRD patients aged 18 years or older. Participants were recruited from members of the Japanese Retinitis Pigmentosa Society, a patient advocacy organization for individuals with retinitis pigmentosa and other IRDs, and collaborating research institutions. The study announcement was also posted on the website of the Department of Ophthalmology, Faculty of Medicine, University of Miyazaki. Responses were collected in print, e-mail, and online formats between October 1, 2023 and March 31, 2025. The resulting data were statistically analyzed using simple tabulation and a logistic regression analysis.</p><p><strong>Results: </strong>A total of 153 valid responses were obtained. The survey revealed that 86.3% of IRD patients requested genetic testing and the main reasons were personal motivation, such as: To identify the cause of the disease (84.8%), followed by: To obtain information for my future treatment, and :To obtain information regarding my future prognosis (both 81.8%). Conversely, the most common reason for not requesting the test was Genetic testing is pointless because there is no treatment (52.4%). Genetic testing was more likely to be requested by participants with greater knowledge of related terms. Among the 49 participants who had previously participated in gene analysis research, the explanation for the most frequent reason for satisfaction with the result was: The implications for children, grandchildren, and family members were clarified (73.7%), while the most frequent reason for dissatisfaction was: The diagnosis was not finalized (60.0%).</p><p><strong>Conclusion: </strong>The present results indicate that the majority of patients possess a high level of interest and a positive attitude toward genetic testing. It is crucial to properly convey the significance of genetic testing and related information to patients, which will enable more patients to approach genetic testing positively and achieve a high level of satisfaction.</p>","PeriodicalId":14563,"journal":{"name":"Japanese Journal of Ophthalmology","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2026-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese Journal of Ophthalmology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10384-026-01430-4","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: To conduct a nationwide questionnaire survey among patients with inherited retinal dystrophy (IRD) with the aim of investigating the percentage of patients requesting or not requesting genetic testing and clarifying the reasons underlying these preferences.

Study design: A questionnaire-based cross-sectional study.

Methods: This study conducted a questionnaire survey targeting IRD patients aged 18 years or older. Participants were recruited from members of the Japanese Retinitis Pigmentosa Society, a patient advocacy organization for individuals with retinitis pigmentosa and other IRDs, and collaborating research institutions. The study announcement was also posted on the website of the Department of Ophthalmology, Faculty of Medicine, University of Miyazaki. Responses were collected in print, e-mail, and online formats between October 1, 2023 and March 31, 2025. The resulting data were statistically analyzed using simple tabulation and a logistic regression analysis.

Results: A total of 153 valid responses were obtained. The survey revealed that 86.3% of IRD patients requested genetic testing and the main reasons were personal motivation, such as: To identify the cause of the disease (84.8%), followed by: To obtain information for my future treatment, and :To obtain information regarding my future prognosis (both 81.8%). Conversely, the most common reason for not requesting the test was Genetic testing is pointless because there is no treatment (52.4%). Genetic testing was more likely to be requested by participants with greater knowledge of related terms. Among the 49 participants who had previously participated in gene analysis research, the explanation for the most frequent reason for satisfaction with the result was: The implications for children, grandchildren, and family members were clarified (73.7%), while the most frequent reason for dissatisfaction was: The diagnosis was not finalized (60.0%).

Conclusion: The present results indicate that the majority of patients possess a high level of interest and a positive attitude toward genetic testing. It is crucial to properly convey the significance of genetic testing and related information to patients, which will enable more patients to approach genetic testing positively and achieve a high level of satisfaction.

评估日本遗传性视网膜营养不良患者对基因检测的认识。
目的:在全国范围内对遗传性视网膜营养不良(IRD)患者进行问卷调查,目的是调查要求或不要求进行基因检测的患者的百分比,并阐明这些偏好的原因。研究设计:以问卷为基础的横断面研究。方法:本研究对年龄在18岁及以上的IRD患者进行问卷调查。参与者从日本视网膜色素变性协会(一个为视网膜色素变性患者和其他IRDs患者提供支持的组织)和合作研究机构的成员中招募。这项研究的公告也发布在宫崎大学医学院眼科的网站上。调查在2023年10月1日至2025年3月31日期间以印刷、电子邮件和在线形式收集。结果数据采用简单制表和逻辑回归分析进行统计分析。结果:共获得有效问卷153份。调查显示,86.3%的IRD患者要求进行基因检测,主要是出于个人动机,例如:确定疾病的原因(84.8%),其次是:获取我未来治疗的信息,以及:获取我未来预后的信息(均为81.8%)。相反,不要求检测的最常见原因是基因检测毫无意义,因为没有治疗方法(52.4%)。对相关术语了解较多的参与者更有可能要求进行基因检测。在49名曾参加过基因分析研究的参与者中,对结果满意的最常见原因是:对子女、孙辈和家庭成员的影响得到了澄清(73.7%),而不满意的最常见原因是:诊断未最终确定(60.0%)。结论:目前的结果表明,大多数患者对基因检测有很高的兴趣和积极的态度。正确地向患者传达基因检测的意义和相关信息是至关重要的,这将使更多的患者积极地接触基因检测,并获得高水平的满意度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
4.80
自引率
8.30%
发文量
65
审稿时长
6-12 weeks
期刊介绍: The Japanese Journal of Ophthalmology (JJO) was inaugurated in 1957 as a quarterly journal published in English by the Ophthalmology Department of the University of Tokyo, with the aim of disseminating the achievements of Japanese ophthalmologists worldwide. JJO remains the only Japanese ophthalmology journal published in English. In 1997, the Japanese Ophthalmological Society assumed the responsibility for publishing the Japanese Journal of Ophthalmology as its official English-language publication. Currently the journal is published bimonthly and accepts papers from authors worldwide. JJO has become an international interdisciplinary forum for the publication of basic science and clinical research papers.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书