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遗传性种系致病性变异携带者弥漫性胃癌风险的初步估计。

First estimates of diffuse gastric cancer risks for carriers of germline pathogenic variants.

机构信息

Département de Génétique, Institut Curie, Paris, France.

CNRS UMR 5558 LBBE, Université de Lyon, Villeurbanne, France.

出版信息

J Med Genet. 2022 Dec;59(12):1189-1195. doi: 10.1136/jmg-2022-108740. Epub 2022 Aug 29.

Abstract

BACKGROUND

Pathogenic variants (PV) of are found in families fulfilling criteria for hereditary diffuse gastric cancer (HDGC) but no risk estimates were available until now. The aim of this study is to evaluate diffuse gastric cancer (DGC) risks for carriers of germline PV.

METHODS

Data from published CTNNA1 families were updated and new families were identified through international collaborations. The cumulative risk of DGC by age for PV carriers was estimated with the genotype restricted likelihood (GRL) method, taking into account non-genotyped individuals and conditioning on all observed phenotypes and genotypes of the index case to obtain unbiased estimates. A non-parametric (NP) and the Weibull functions were used to model the shape of penetrance function with the GRL. Kaplan-Meier incidence curve and standardised incidence ratios were also computed. A 'leave-one-out' strategy was used to evaluate estimate uncertainty.

RESULTS

Thirteen families with 46 carriers of PV were included. The cumulative risks of DGC at 80 years for carriers of PV are 49% and 57%, respectively with the Weibull GRL and NP GRL methods. Risk ratios to population incidence reach particularly high values at early ages and decrease with age. At 40 years, they are equal to 65 and 833, respectively with the Weibull GRL and NP GRL.

CONCLUSION

This is the largest series of families that provides the first risk estimates of GC. These data will help to improve management and surveillance for these patients and support inclusion of in germline testing panels.

摘要

背景

在满足遗传性弥漫性胃癌 (HDGC) 标准的家族中发现了 的致病变异 (PV),但直到现在才得到风险估计。本研究旨在评估携带胚系 PV 的个体患弥漫性胃癌 (DGC) 的风险。

方法

更新了已发表的 CTNNA1 家族的数据,并通过国际合作确定了新的家族。使用基因型受限似然 (GRL) 方法估计 PV 携带者的 DGC 累积风险,同时考虑未进行基因分型的个体,并对指数病例的所有观察到的表型和基因型进行条件化,以获得无偏估计。使用非参数 (NP) 和威布尔函数结合 GRL 来对穿透函数的形状进行建模。还计算了 Kaplan-Meier 发病曲线和标准化发病比。采用“逐一排除”策略来评估估计的不确定性。

结果

纳入了 13 个家族的 46 名 PV 携带者。PV 携带者 80 岁时 DGC 的累积风险分别为 49%和 57%,采用威布尔 GRL 和 NP GRL 方法。风险比与人群发病率在早期达到特别高的值,然后随着年龄的增长而降低。在 40 岁时,它们分别为 65 和 833,采用威布尔 GRL 和 NP GRL 方法。

结论

这是最大的一组 家族系列,提供了 GC 的首个风险估计。这些数据将有助于改善对这些患者的管理和监测,并支持将 纳入胚系检测面板。

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