探索脉络膜血症对有疾病表型和/或基因型证据的妇女的影响:一项全球调查的启示。

IF 1.2 4区 医学 Q4 GENETICS & HEREDITY Ophthalmic Genetics Pub Date : 2024-10-01 Epub Date: 2024-06-07 DOI:10.1080/13816810.2024.2357705
Steven Bonneau, Merve Kulbay, Shigufa Kahn-Ali, Cynthia X Qian
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引用次数: 0

摘要

简介脉络膜血症(Choroideremia,CHM)是一种 X 连锁遗传性视网膜疾病,男性患者居多。然而,有 CHM 表型和/或基因型证据的女性可能会随着年龄的增长而出现退化性视力残疾。我们的目的是确定表型和/或基因型证据表明患有CHM的女性对视觉的影响及其相关的社会心理负担和对日常生活活动(ADLs)的影响:我们在 2022 年 4 月至 12 月期间进行了一项国际横断面调查,通过非营利性利益相关组织和社交媒体平台发放电子问卷:共有 55 名受访者(n = 55),大多数有 CHM 表型和/或基因型证据的女性(76%)报告其视力发生了变化。在评估其对日常活动能力的影响时,皮尔逊相关系数显示,驾驶能力(p = 0.046)和行动能力(0.046)与受访者的年龄呈负相关。半数以上的女性表示感到恐惧、焦虑和压力,其中 50 岁以下女性的苦恼和绝望程度(p = 0.003)、焦虑程度(p = 0.00007)、放松问题(p = 0.025)和个人消极想法(p = 0.042)明显更高:总之,这项调查概述了作为一名有 CHM 表型和/或基因型证据的女性所承受的生理和心理负担。鉴于针对受CHM影响的女性的临床研究有限,这份以患者为中心的调查对这些人来说是至关重要的宣传工具。
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Exploring the impact of Choroideremia on women with phenotypic and/or genotypic evidence of disease: insights from a global survey.

Introduction: Choroideremia (CHM) is an X-linked inherited retinal disease mostly affecting males. However, women with phenotypic and/or genotypic evidence of CHM may develop degenerative visual disability with advancing age. Our objective was to determine the visual impacts of phenotypic and/or genotypic evidence of CHM in women and its associated psychosocial burden and influence on activities of daily living (ADLs).

Methods: We conducted an international cross-sectional survey from April to December 2022 using an e-questionnaire distributed through not-for-profit stakeholder organizations and social media plat-forms.

Results: With a total of 55 respondents (n = 55), most women with phenotypic and/or genotypic evidence of CHM (76%) reported a change in their visual acuity. When assessing its impact on ADLs, Pearson's correlation coefficient showed a negative correlation between driving (p = 0.046) and mobility capabil-ities (0.046) with the respondent's age. More than half of women reported being afraid, anxious, and stressed, with women below the age of 50 years old reporting a significantly higher level of distress and hopelessness (p = 0.003), anxiety (p = 0.00007), issues with relaxing (p = 0.025), and negative personal thoughts (p = 0.042).

Conclusion: Overall, this survey outlines both physical and psychological burden of being a woman with phenotypic and/or genotypic evidence of CHM. Given the limited clinical research in females affected by CHM, this patient-centered survey is a crucial advocacy tool for these individuals.

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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.
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