约旦人群中BRCA1/2潜在创始人变异:定制筛选小组的机会

IF 2 4区 医学 Q3 ONCOLOGY Hereditary Cancer in Clinical Practice Pub Date : 2023-07-03 DOI:10.1186/s13053-023-00256-2
Olfat Ahmad, Christian Sutter, Steffen Hirsch, Stefan M Pfister, Christian P Schaaf
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引用次数: 0

摘要

始祖变异是一种遗传变异,它从一个共同的祖先和周围的染色体段遗传而来,在一个特定的人群中观察到的频率很高。这种建立者效应是孤立种群长期近亲繁殖的结果。对于高风险的癌症易感基因,如BRCA1/2,在特定人群中识别始祖变异可以帮助设计定制的具有成本效益的癌症筛查小组。这一优势在为德系犹太人(AJ)人群设计一个定制的乳腺癌BRCA筛查小组中得到了最好的利用,该小组由三种BRCA创始变异组成,约占已确定BRCA变异的90%。事实上,AJ中致病性BRCA1/2变异的高患病率(约2%)也使得基于人群的筛查比基于家族史的筛查更具成本效益。在约旦,有多种人口特征支持创始人效应的提议。在上个世纪九十年代高达57%的高血缘率和最近30%的高血缘率是一个突出的因素,此外,该国不同亚种群经常实行近亲繁殖。本综述解释了奠基者效应的概念,然后将其应用于分析已发表的约旦BRCA变异,并得出结论:9个致病性(P)和可能致病性(LP) BRCA2变异以及1个致病性BRCA1变异是潜在的奠基者变异。在两个最大的研究队列——年轻患者和高风险患者中,它们分别占所有确定的BRCA1/2改变的43%和55%。这些变异是根据复发性、特定于种族群体或新出现的变异来确定的。此外,该报告强调了验证这些发现所需的测试方法,并提出了一个健康经济评估模型,以测试基于人群的约旦人群定制BRCA筛查小组的成本效益。本报告的目的是强调创始人变异在建立定制癌症易感性服务中的潜在应用,以鼓励在约旦和类似人群中进行更多基于人群的基因组研究。
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BRCA1/2 potential founder variants in the Jordanian population: an opportunity for a customized screening panel.

A founder variant is a genetic alteration, that is inherited from a common ancestor together with a surrounding chromosomal segment, and is observed at a high frequency in a defined population. This founder effect occurs as a consequence of long-standing inbreeding of isolated populations. For high-risk cancer predisposition genes, such as BRCA1/2, the identification of founder variants in a certain population could help designing customized cost-effective cancer screening panels. This advantage has been best utilized in designing a customized breast cancer BRCA screening panel for the Ashkenazi Jews (AJ) population, composed of the three BRCA founder variants which account for approximately 90% of identified BRCA alterations. Indeed, the high prevalence of pathogenic BRCA1/2 variants among AJ (~ 2%) has additionally contributed to make population-based screening cost-effective in comparison to family-history-based screening. In Jordan there are multiple demographic characteristics supporting the proposal of a founder effect. A high consanguinity rate of ~ 57% in the nineties of the last century and ~ 30% more recently is a prominent factor, in addition to inbreeding which is often practiced by different sub-populations of the country.This review explains the concept of founder effect, then applies it to analyze published Jordanian BRCA variants, and concludes that nine pathogenic (P) and likely pathogenic (LP) BRCA2 variants together with one pathogenic BRCA1 variant are potential founder variants. Together they make up 43% and 55% of all identified BRCA1/2 alterations in the two largest studied cohorts of young patients and high-risk patients respectively. These variants were identified based on being recurrent and either specific to ethnic groups or being novel. In addition, the report highlights the required testing methodologies to validate these findings, and proposes a health economic evaluation model to test cost-effectiveness of a population-based customized BRCA screening panel for the Jordanian population. The aim of this report is to highlight the potential utilization of founder variants in establishing customized cancer predisposition services, in order to encourage more population-based genomic studies in Jordan and similar populations.

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来源期刊
CiteScore
3.10
自引率
5.90%
发文量
38
审稿时长
>12 weeks
期刊介绍: Hereditary Cancer in Clinical Practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. Cancer genetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. With the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. Topics covered by the journal include but are not limited to: Original research articles on any aspect of inherited predispositions to cancer. Reviews of inherited cancer predispositions. Application of molecular and cytogenetic analysis to clinical decision making. Clinical aspects of the management of hereditary cancers. Genetic counselling issues associated with cancer genetics. The role of registries in improving health care of patients with an inherited predisposition to cancer.
期刊最新文献
BRCA2 germline mutation carrier with five malignancies: a case report. A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives. Breast cancer and ATM mutations: treatment implications. Meeting abstracts from the Annual Conference "Clinical Genetics of Cancer 2023". Validation of a guidelines-based digital tool to assess the need for germline cancer genetic testing.
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