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The genomic potential of the Aspirin in Reducing Events in the Elderly and Statins in Reducing Events in the Elderly studies.阿司匹林降低老年人事件风险和他汀类药物降低老年人事件风险研究的基因组潜力。
Intern Med J. 2017 Apr;47(4):461-463. doi: 10.1111/imj.13384.
2
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J Med Ethics. 2017 Oct;43(10):714-722. doi: 10.1136/medethics-2016-103967. Epub 2017 Mar 24.
3
Baseline Characteristics of Participants in the ASPREE (ASPirin in Reducing Events in the Elderly) Study.ASPREE(阿司匹林减少老年人事件)研究参与者的基线特征。
J Gerontol A Biol Sci Med Sci. 2017 Oct 12;72(11):1586-1593. doi: 10.1093/gerona/glw342.
4
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study.50726 例全外显子组序列中的功能变体的分布和临床影响:DiscovEHR 研究。
Science. 2016 Dec 23;354(6319). doi: 10.1126/science.aaf6814.
5
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.临床外显子组和基因组测序中次要发现报告的建议,2016年更新版(美国医学遗传学与基因组学学会次要发现v2.0):美国医学遗传学与基因组学学会政策声明
Genet Med. 2017 Feb;19(2):249-255. doi: 10.1038/gim.2016.190. Epub 2016 Nov 17.
6
Aggregate penetrance of genomic variants for actionable disorders in European and African Americans.欧洲裔和非裔美国人中可操作疾病的基因组变异的综合外显率。
Sci Transl Med. 2016 Nov 9;8(364):364ra151. doi: 10.1126/scitranslmed.aag2367.
7
Deep sequencing of 10,000 human genomes.一万个人类基因组的深度测序。
Proc Natl Acad Sci U S A. 2016 Oct 18;113(42):11901-11906. doi: 10.1073/pnas.1613365113. Epub 2016 Oct 4.
8
Analysis of protein-coding genetic variation in 60,706 humans.对60706名人类的蛋白质编码基因变异进行分析。
Nature. 2016 Aug 18;536(7616):285-91. doi: 10.1038/nature19057.
9
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases.分析 589306 个人的基因组,确定对严重孟德尔儿童疾病有抵抗力的个体。
Nat Biotechnol. 2016 May;34(5):531-8. doi: 10.1038/nbt.3514. Epub 2016 Apr 11.
10
Exploring the landscape of pathogenic genetic variation in the ExAC population database: insights of relevance to variant classification.在ExAC群体数据库中探索致病基因变异的情况:与变异分类相关的见解。
Genet Med. 2016 Aug;18(8):850-4. doi: 10.1038/gim.2015.180. Epub 2015 Dec 17.

外显率与健康老年人

Penetrance and the Healthy Elderly.

作者信息

Lacaze Paul, Winship Ingrid, McNeil John

机构信息

1 Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia .

2 Genetic Medicine and Family Cancer Clinic, Royal Melbourne Hospital , Melbourne, Australia .

出版信息

Genet Test Mol Biomarkers. 2017 Nov;21(11):637-640. doi: 10.1089/gtmb.2017.0126. Epub 2017 Sep 6.

DOI:10.1089/gtmb.2017.0126
PMID:28876137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5695739/
Abstract

The variable penetrance of pathogenic variants (PVs) represents a major challenge to the field of human genetics, often complicating clinical decision-making and risk management. Nonpenetrance, the detection of PVs in the absence of disease manifestation, is a common phenomenon, yet, we know very little about the underlying factors, which may protect some individuals and not others. Placing a new focus on the genomic study of the healthy elderly may be pivotal for advancing our understanding of penetrance. Studying those who remain unaffected late into life, despite harboring known genetic risk variants, could provide important insights into disease mechanisms and ultimately inform clinical care, yet, it has received relatively little attention as a research strategy. The ever increasing use of sequencing technology is further driving the requirement to understand the penetrance of ascertained variants. The ASPREE Biobank of Healthy Ageing provides a unique opportunity to address this area of need. DNA has been collected from a cohort of over 14,000 healthy elderly individuals aged 70 years or older enrolled in an aspirin clinical trial. The ASPREE cohort represents a healthy reference population ascertained without the typical biases of a genetic study. The cohort is depleted of expressed monogenetic disease, yet will contain hundreds of elderly individuals with known PVs in clinically actionable genes. Investigating this population along with other cohorts of the healthy elderly will provide critical new knowledge into the penetrance of actionable variants as a foundation for informing clinical care.

摘要

致病变异(PVs)的可变外显率是人类遗传学领域面临的一项重大挑战,常常使临床决策和风险管理变得复杂。非外显,即在没有疾病表现的情况下检测到PVs,是一种常见现象,然而,我们对其潜在因素知之甚少,这些因素可能保护了一些个体而未保护其他个体。将新的重点放在健康老年人的基因组研究上,可能对推进我们对外显率的理解至关重要。研究那些尽管携带已知遗传风险变异但到晚年仍未受影响的人,可能会为疾病机制提供重要见解,并最终为临床护理提供参考,然而,作为一种研究策略,它受到的关注相对较少。测序技术的日益广泛应用进一步推动了理解已确定变异外显率的需求。健康老龄化的ASPREE生物样本库为满足这一需求领域提供了独特的机会。已从参加阿司匹林临床试验的14000多名70岁及以上健康老年人队列中收集了DNA。ASPREE队列代表了一个健康的参考人群,其确定过程没有遗传研究中常见的偏差。该队列中没有明显的单基因疾病,但将包含数百名在临床可操作基因中携带已知PVs的老年人。对这一人群以及其他健康老年人队列进行研究,将为可操作变异的外显率提供关键的新知识,作为为临床护理提供参考的基础。