[骨髓增生性肿瘤患者的 DTA 基因突变与血栓栓塞之间的关系]。

Min Wang, Hong-Yu Zhao, Da-Qi Li, Ping Chen
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引用次数: 0

摘要

目的分析骨髓增殖性肿瘤(MPN)患者的DTA(DNMT3A、TET2、ASXL1)突变情况,并初步探讨其与血栓栓塞的相关性:方法:回顾性分析山东第一医科大学附属中心医院2016年9月至2022年9月确诊的62例新发MPN患者的临床特征。采用新一代测序技术检测35个MPN相关基因,分析MPN患者的DTA突变及其与血栓栓塞事件的关系:结果:75.8%(47/62)的患者出现致病性非驱动基因突变,每位患者的平均致病性非驱动基因突变数为1.08。其中,最常见的非驱动基因突变是 TET2(38.7%,24/62)、DNMT3A(9.7%,6/62)和 ASXL1(6.5%,4/62)。在所有 MPN 患者中,DTA 基因突变的比例为 50%(31/62),且主要伴有驱动基因突变。年龄≥60 岁患者的 DTA 基因突变率明显高于 60 岁以上患者(P =0.039)。DTA基因突变患者血栓栓塞的发生率为58.1%(18/31),明显高于无DTA基因突变的患者(19.4%,6/31)(P =0.002)。血栓栓塞的MPN患者中TET2基因突变率为66.7%(16/24),明显高于无血栓栓塞的患者(21.1%,8/38)(P =0.00):结论:MPN患者的DTA突变发生率较高,且主要伴有驱动基因突变。有 DTA 突变的 MPN 患者血栓栓塞的发生率高于无 DTA 突变的患者。尤其是TET2突变的老年(≥60岁)原发性血小板增多症(ET)和真性多血细胞增多症(PV)患者应警惕血栓栓塞事件。
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[Relationship between DTA Mutations and Thromboembolism in Patients with Myeloproliferative Neoplasms].

Objective: To analyze the DTA (DNMT3A, TET2, ASXL1) mutations in patients with myeloproliferative neoplasms (MPN), and preliminarily explore their correlation with thromboembolism.

Methods: Clinical characteristics of 62 patients diagnosed de novo MPN at Central Hospital Affiliated to Shandong First Medical University from September 2016 to September 2022 were retrospectively analyzed. Next-generation sequencing was used to detect 35 MPN-related genes, and the DTA mutations in MPN patients and their relationship with thromboembolic events were analyzed.

Results: 75.8% (47/62) of the patients presented pathogenic non-driver mutations, and the mean number of pathogenic non-driver mutations per patient was 1.08. Among them, the most frequently mutated non-driver genes were TET2 (38.7%, 24/62), DNMT3A (9.7%, 6/62) and ASXL1 (6.5%, 4/62). The presence of DTA gene mutations was 50% (31/62) in the total MPN patients, and mainly accompanied by driver mutations. The mutation rate of DTA in patients aged ≥60 years was significantly higher than that in patients <60 years old (P =0.039). The incidence of thromboembolism in patients with DTA mutation was 58.1% (18/31), which was significantly higher than that in patients without DTA mutation (19.4%, 6/31) (P =0.002). The TET2 gene mutation rate in MPN patients with thromboembolism was 66.7% (16/24), which was significantly higher than that in patients without thromboembolism (21.1%, 8/38) (P =0.00).

Conclusion: Patients with MPN have a higher incidence of DTA mutations, which are mainly accompanied by driver gene mutations. The incidence of thromboembolism in MPN patients with DTA mutations is higher than that in patients without DTA mutations. Especially, the elderly (≥60 years) essential thrombocythemia(ET) and polycythemia vera(PV) patients with TET2 mutation should be vigilant for thromboembolic events.

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来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
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0.40
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7331
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