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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.

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。

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Deep sequencing of 10,000 human genomes.一万个人类基因组的深度测序。
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