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多发性骨髓瘤患者一级和二级亲属中多发性骨髓瘤和其他恶性肿瘤的风险:一项基于人群的研究。

Risk of multiple myeloma and other malignancies among first- and second-degree relatives of patients with multiple myeloma: A population-based study.

机构信息

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

Department of Hematology, St. Olav's University Hospital, Trondheim, Norway.

出版信息

Eur J Haematol. 2022 Jun;108(6):486-492. doi: 10.1111/ejh.13757. Epub 2022 Mar 7.

Abstract

OBJECTIVES

We conducted a population-based study to assess the risk for multiple myeloma (MM) and other cancers in first- and second-degree relatives of MM patients, and to investigate whether evidence of anticipation is present in familial MM.

METHODS

We retrieved 24 845 first-degree relatives and 41 008 second-degree relatives of 7847 MM patients, and 86 984 first-degree relatives, and 138 660 second-degree relatives of 26 511 matched controls. A Cox model was used to assess the risk for MM and other cancers in relatives of MM patients. Anticipation was assessed by a Cox model, where all parents and offspring of MM patients were included in the risk set.

RESULTS

In second-degree relatives of MM patients, no overall significant association with an MM diagnosis was observed (HR 1.99; 95%CI:0.86-4.57). In parents and offspring of MM patients, we found no significant difference in the ages at onset of MM (HR 1.28;95% CI:0.50-3.28). In affected parent-offspring pairs, we observed no statistically significant difference in overall survival between the generations (HR 0.74; 95%CI:0.20-2.69).

CONCLUSIONS

Overall, second-degree relatives of MM patients were not associated with an increased risk for MM. Our study supports that genetic anticipation is not present in familial MM.

摘要

目的

我们进行了一项基于人群的研究,以评估多发性骨髓瘤(MM)患者的一级和二级亲属发生 MM 和其他癌症的风险,并探讨家族性 MM 中是否存在预期现象。

方法

我们检索了 7847 名 MM 患者的 24845 名一级亲属和 41008 名二级亲属,以及 26511 名匹配对照者的 86984 名一级亲属和 138660 名二级亲属。采用 Cox 模型评估 MM 患者亲属发生 MM 和其他癌症的风险。通过 Cox 模型评估预期,其中所有 MM 患者的父母和子女都包含在风险组中。

结果

在 MM 患者的二级亲属中,与 MM 诊断无显著总体相关性(HR 1.99;95%CI:0.86-4.57)。在 MM 患者的父母和子女中,我们未发现 MM 发病年龄存在显著差异(HR 1.28;95%CI:0.50-3.28)。在受影响的父母-子女对中,我们未观察到两代之间总生存期存在统计学显著差异(HR 0.74;95%CI:0.20-2.69)。

结论

总体而言,MM 患者的二级亲属与 MM 风险增加无关。我们的研究支持家族性 MM 中不存在遗传预期现象。

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本文引用的文献

1
Genetic predisposition for multiple myeloma.多发性骨髓瘤的遗传易感性。
Leukemia. 2020 Mar;34(3):697-708. doi: 10.1038/s41375-019-0703-6. Epub 2020 Jan 8.
4
A unified model for estimating and testing familial aggregation.
Stat Med. 2013 Dec 30;32(30):5353-65. doi: 10.1002/sim.6025. Epub 2013 Oct 21.
6
Familial multiple myeloma: report on two families and discussion of screening options.
Hered Cancer Clin Pract. 2007 Jun 15;5(2):72-8. doi: 10.1186/1897-4287-5-2-72.

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