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研究概况:青光眼遗传学研究。

Study profile: the Genetics of Glaucoma Study.

机构信息

Statistical Genetics Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia

Faculty of Medicine, School of Biomedical Sciences, The University of Queensland, Brisbane, Queensland, Australia.

出版信息

BMJ Open. 2023 Aug 3;13(8):e068811. doi: 10.1136/bmjopen-2022-068811.

Abstract

PURPOSE

Glaucoma, a major cause of irreversible blindness, is a highly heritable human disease. Currently, the majority of the risk genes for glaucoma are unknown. We established the Genetics of Glaucoma Study (GOGS) to identify disease genes and improve genetic prediction of glaucoma risk and response to treatment.

PARTICIPANTS

More than 5700 participants with glaucoma or a family history of glaucoma were recruited through a media campaign and the Australian Government healthcare service provider, Services Australia, making GOGS one of the largest genetic studies of glaucoma globally. The mean age of the participants was 65.30±9.36 years, and 62% were female. Participants completed a questionnaire obtaining information about their glaucoma-related medical history such as family history, glaucoma status and subtypes, surgical procedures, and prescriptions. The questionnaire also obtained information about other eye and systemic diseases. Approximately 80% of the participants provided a DNA sample and ~70% consented to data linkage to their Australian Government Medicare and Pharmaceutical Benefits Scheme schedules.

FINDINGS TO DATE

4336 GOGS participants reported that an optometrist or ophthalmologist has diagnosed them with glaucoma and 3639 participants reported having a family history of glaucoma. The vast majority of the participants (N=4393) had used at least one glaucoma-related medication; latanoprost was the most commonly prescribed drug (54% of the participants who had a glaucoma prescription). A subset of the participants reported a surgical treatment for glaucoma including a laser surgery in 2008 participants and a non-laser operation in 803 participants. Several comorbid eye and systemic diseases were also observed; the most common reports were ocular hypertension (53% of the participants), cataract (48%), hypertension (40%), nearsightedness (31%), astigmatism (22%), farsightedness (16%), diabetes (12%), sleep apnoea (11%) and migraines (10%).

FUTURE PLANS

GOGS will contribute to the global gene-mapping efforts as one of the largest genetic studies for glaucoma. We will also use GOGS to develop or validate genetic risk prediction models to stratify glaucoma risk, particularly in individuals with a family history of glaucoma, and to predict clinical outcomes (eg, which medication works better for an individual and whether glaucoma surgery is required). GOGS will also help us answer various research questions about genetic overlap and causal relationships between glaucoma and its comorbidities.

摘要

目的

青光眼是一种不可逆转的失明的主要原因,是一种具有高度遗传性的人类疾病。目前,大多数青光眼的风险基因尚不清楚。我们建立了青光眼遗传学研究(GOGS),以确定疾病基因,并提高对青光眼风险和治疗反应的遗传预测。

参与者

通过媒体宣传和澳大利亚政府医疗服务提供商 Services Australia 招募了 5700 多名患有青光眼或青光眼家族史的参与者,使 GOGS 成为全球最大的青光眼遗传学研究之一。参与者的平均年龄为 65.30±9.36 岁,其中 62%为女性。参与者完成了一份问卷,获取了有关他们与青光眼相关的医疗史的信息,例如家族史、青光眼状况和亚型、手术程序和处方。问卷还获取了有关其他眼部和系统性疾病的信息。大约 80%的参与者提供了 DNA 样本,约 70%的参与者同意将其数据与澳大利亚政府医疗保险和药品福利计划安排进行链接。

迄今为止的发现

4336 名 GOGS 参与者报告称,验光师或眼科医生已诊断出他们患有青光眼,3639 名参与者报告称有青光眼家族史。绝大多数参与者(N=4393)至少使用了一种与青光眼相关的药物;拉坦前列素是最常用的药物(54%有青光眼处方的参与者)。一部分参与者报告了治疗青光眼的手术,包括 2008 年的激光手术和 803 名参与者的非激光手术。还观察到几种合并的眼部和系统性疾病;最常见的报告是眼压升高(53%的参与者)、白内障(48%)、高血压(40%)、近视(31%)、散光(22%)、远视(16%)、糖尿病(12%)、睡眠呼吸暂停(11%)和偏头痛(10%)。

未来计划

GOGS 将作为最大的青光眼遗传学研究之一,为全球基因图谱绘制工作做出贡献。我们还将使用 GOGS 开发或验证遗传风险预测模型,以分层青光眼风险,特别是在有青光眼家族史的个体中,并预测临床结果(例如,哪种药物对个体更有效,是否需要进行青光眼手术)。GOGS 还将帮助我们回答有关青光眼及其合并症之间遗传重叠和因果关系的各种研究问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644b/10401214/4b439ded4639/bmjopen-2022-068811f01.jpg

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