受x连锁遗传性视网膜疾病影响的女性的生殖咨询和决策:来自携带者的观点

IF 1 4区 医学 Q4 GENETICS & HEREDITY
Ophthalmic Genetics Pub Date : 2025-06-01 Epub Date: 2025-02-14 DOI:10.1080/13816810.2025.2463679
Rebecca Clark, Haider Sarwar, Leland Wong, Elizabeth White, Lesley Everett, Molly Marra
{"title":"受x连锁遗传性视网膜疾病影响的女性的生殖咨询和决策:来自携带者的观点","authors":"Rebecca Clark, Haider Sarwar, Leland Wong, Elizabeth White, Lesley Everett, Molly Marra","doi":"10.1080/13816810.2025.2463679","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>X-linked inherited retinal diseases (XL-IRDs) are genetic disorders that typically present with higher disease burden in individuals assigned male at birth, often resulting in significant vision loss. Individuals assigned female at birth (AFAB) may also experience symptoms. Understanding the role of genetic counseling and testing in reproductive decision-making for AFAB individuals with XL-IRDs is crucial for improving reproductive empowerment.</p><p><strong>Methods: </strong>This study surveyed AFAB individuals with a confirmed or family history of XL-IRDs. Eligible participants completed an anonymous online survey between July 2023 and November 2023, which collected data on genetic testing, counseling experiences, and the impact of these on reproductive decision making.</p><p><strong>Results: </strong>Of the 118 survey respondents, 67% had confirmed genetics or a family history of <i>CHM</i>-related disease, 23% of <i>RPGR/RP2</i>, 5% of <i>RS1</i>, and 3% of <i>NYX/CACNA1F</i>. Fifty five percent of respondents would have preferred genetic testing earlier if it had been possible. Only 26 respondents (22.0%) received some sort of reproductive genetic counseling, the majority of which were counseled by a genetic counselor at a retinal dystrophy clinic. Most XX individuals with confirmed genetics or a family history of XL-IRDs had not received reproductive counseling about their diagnosis. However, their personal and familial experiences with an XL-IRD variably impacted their reproductive decision-making process.</p><p><strong>Conclusion: </strong>Recognition that retinal dystrophy clinics are the primary location for XL-IRD reproductive risk counseling informs the timing and content of counseling by ophthalmic genetics providers and genetic counselors.</p>","PeriodicalId":19594,"journal":{"name":"Ophthalmic Genetics","volume":" ","pages":"243-248"},"PeriodicalIF":1.0000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reproductive counseling and decision making in females affected by X-linked inherited retinal disease: perspectives from carriers.\",\"authors\":\"Rebecca Clark, Haider Sarwar, Leland Wong, Elizabeth White, Lesley Everett, Molly Marra\",\"doi\":\"10.1080/13816810.2025.2463679\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>X-linked inherited retinal diseases (XL-IRDs) are genetic disorders that typically present with higher disease burden in individuals assigned male at birth, often resulting in significant vision loss. Individuals assigned female at birth (AFAB) may also experience symptoms. Understanding the role of genetic counseling and testing in reproductive decision-making for AFAB individuals with XL-IRDs is crucial for improving reproductive empowerment.</p><p><strong>Methods: </strong>This study surveyed AFAB individuals with a confirmed or family history of XL-IRDs. Eligible participants completed an anonymous online survey between July 2023 and November 2023, which collected data on genetic testing, counseling experiences, and the impact of these on reproductive decision making.</p><p><strong>Results: </strong>Of the 118 survey respondents, 67% had confirmed genetics or a family history of <i>CHM</i>-related disease, 23% of <i>RPGR/RP2</i>, 5% of <i>RS1</i>, and 3% of <i>NYX/CACNA1F</i>. Fifty five percent of respondents would have preferred genetic testing earlier if it had been possible. Only 26 respondents (22.0%) received some sort of reproductive genetic counseling, the majority of which were counseled by a genetic counselor at a retinal dystrophy clinic. Most XX individuals with confirmed genetics or a family history of XL-IRDs had not received reproductive counseling about their diagnosis. However, their personal and familial experiences with an XL-IRD variably impacted their reproductive decision-making process.</p><p><strong>Conclusion: </strong>Recognition that retinal dystrophy clinics are the primary location for XL-IRD reproductive risk counseling informs the timing and content of counseling by ophthalmic genetics providers and genetic counselors.</p>\",\"PeriodicalId\":19594,\"journal\":{\"name\":\"Ophthalmic Genetics\",\"volume\":\" \",\"pages\":\"243-248\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ophthalmic Genetics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/13816810.2025.2463679\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ophthalmic Genetics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/13816810.2025.2463679","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/14 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

简介:x连锁遗传性视网膜疾病(XL-IRDs)是一种遗传性疾病,通常在出生时被指定为男性的个体中存在较高的疾病负担,通常导致严重的视力丧失。出生时被指定为女性(AFAB)的个体也可能出现症状。了解遗传咨询和测试在患有XL-IRDs的AFAB个体的生殖决策中的作用对于提高生殖能力至关重要。方法:本研究调查了有确诊或家族史的AFAB患者。符合条件的参与者在2023年7月至2023年11月期间完成了一项匿名在线调查,该调查收集了有关基因检测、咨询经验及其对生殖决策的影响的数据。结果:在118名调查对象中,67%的人确认有chm相关疾病的遗传或家族史,23%的人有RPGR/RP2, 5%的人有RS1, 3%的人有NYX/CACNA1F。55%的受访者表示,如果可能的话,他们更希望尽早进行基因检测。只有26名受访者(22.0%)接受了某种形式的生殖遗传咨询,其中大多数是由视网膜营养不良诊所的遗传咨询师提供咨询的。大多数已确认遗传或有XL-IRDs家族史的XX个体未接受过有关其诊断的生殖咨询。然而,他们与xml - ird的个人和家庭经历不同程度地影响了他们的生殖决策过程。结论:认识到视网膜营养不良诊所是XL-IRD生殖风险咨询的主要地点,眼科遗传学提供者和遗传咨询师提供咨询的时间和内容。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reproductive counseling and decision making in females affected by X-linked inherited retinal disease: perspectives from carriers.

Introduction: X-linked inherited retinal diseases (XL-IRDs) are genetic disorders that typically present with higher disease burden in individuals assigned male at birth, often resulting in significant vision loss. Individuals assigned female at birth (AFAB) may also experience symptoms. Understanding the role of genetic counseling and testing in reproductive decision-making for AFAB individuals with XL-IRDs is crucial for improving reproductive empowerment.

Methods: This study surveyed AFAB individuals with a confirmed or family history of XL-IRDs. Eligible participants completed an anonymous online survey between July 2023 and November 2023, which collected data on genetic testing, counseling experiences, and the impact of these on reproductive decision making.

Results: Of the 118 survey respondents, 67% had confirmed genetics or a family history of CHM-related disease, 23% of RPGR/RP2, 5% of RS1, and 3% of NYX/CACNA1F. Fifty five percent of respondents would have preferred genetic testing earlier if it had been possible. Only 26 respondents (22.0%) received some sort of reproductive genetic counseling, the majority of which were counseled by a genetic counselor at a retinal dystrophy clinic. Most XX individuals with confirmed genetics or a family history of XL-IRDs had not received reproductive counseling about their diagnosis. However, their personal and familial experiences with an XL-IRD variably impacted their reproductive decision-making process.

Conclusion: Recognition that retinal dystrophy clinics are the primary location for XL-IRD reproductive risk counseling informs the timing and content of counseling by ophthalmic genetics providers and genetic counselors.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Ophthalmic Genetics
Ophthalmic Genetics 医学-眼科学
CiteScore
2.40
自引率
8.30%
发文量
126
审稿时长
>12 weeks
期刊介绍: Ophthalmic Genetics accepts original papers, review articles and short communications on the clinical and molecular genetic aspects of ocular diseases.
×
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