The best linear unbiased prediction (BLUP) method as a tool to estimate the lifetime risk of pancreatic ductal adenocarcinoma in high-risk individuals with no known pathogenic germline variants.

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Familial Cancer Pub Date : 2024-08-01 Epub Date: 2024-05-23 DOI:10.1007/s10689-024-00397-w
Cristina-Marianini-Rios, María E Castillo Sanchez, Ana García García de Paredes, Mercedes Rodríguez, Emma Barreto, Jorge Villalón López, Raquel Fuentes, María Muñoz Beltrán, Alfonso Sanjuanbenito, Eduardo Lobo, Alejandra Caminoa, Ignacio Ruz-Caracuel, Sergio López Durán, José Ramón Foruny Olcina, Javier Blázquez, Enrique Vázquez Sequeros, Alfredo Carrato, Jose Carlos Martínez Ávila, Julie Earl
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引用次数: 0

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer-related death in the Western world. The number of diagnosed cases and the mortality rate are almost equal as the majority of patients present with advanced disease at diagnosis. Between 4 and 10% of pancreatic cancer cases have an apparent hereditary background, known as hereditary pancreatic cancer (HPC) and familial pancreatic cancer (FPC), when the genetic basis is unknown. Surveillance of high-risk individuals (HRI) from these families by imaging aims to detect PDAC at an early stage to improve prognosis. However, the genetic basis is unknown in the majority of HRIs, with only around 10-13% of families carrying known pathogenic germline mutations. The aim of this study was to assess an individual's genetic cancer risk based on sex and personal and family history of cancer. The Best Linear Unbiased Prediction (BLUP) methodology was used to estimate an individual's predicted risk of developing cancer during their lifetime. The model uses different demographic factors in order to estimate heritability. A reliable estimation of heritability for pancreatic cancer of 0.27 on the liability scale, and 0.07 at the observed data scale as obtained, which is different from zero, indicating a polygenic inheritance pattern of PDAC. BLUP was able to correctly discriminate PDAC cases from healthy individuals and those with other cancer types. Thus, providing an additional tool to assess PDAC risk HRI with an assumed genetic predisposition in the absence of known pathogenic germline mutations.

Abstract Image

将最佳线性无偏预测法(BLUP)作为一种工具,用于估算没有已知致病基因变异的高危人群终生胰腺导管腺癌的风险。
在西方国家,胰腺导管腺癌(PDAC)是导致癌症相关死亡的第四大原因。由于大多数患者在确诊时已是晚期,因此确诊病例数和死亡率几乎相当。4%-10%的胰腺癌病例有明显的遗传背景,在遗传基础未知的情况下被称为遗传性胰腺癌(HPC)和家族性胰腺癌(FPC)。通过成像对这些家族中的高危人群(HRI)进行监测,旨在早期发现 PDAC,从而改善预后。然而,大多数 HRI 的遗传基础不明,只有约 10-13% 的家族携带已知的致病性种系突变。本研究的目的是根据性别、个人和家族癌症病史评估个人的遗传性癌症风险。最佳线性无偏预测(BLUP)方法用于估算个人一生中罹患癌症的预测风险。该模型利用不同的人口统计学因素来估算遗传率。结果表明,胰腺癌的可靠遗传率估计值为 0.27(责任值)和 0.07(观察值),与零值不同,这表明胰腺癌存在多基因遗传模式。BLUP 能够正确区分 PDAC 病例与健康人及其他癌症类型。因此,在没有已知致病基因突变的情况下,BLUP 提供了一种额外的工具来评估假定具有遗传易感性的 PDAC 风险 HRI。
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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
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