[Comparision of Mutational Spectrum between Elderly and Young Adults with Acute Myeloid Leukemia Based on Next Generation Sequencing]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Feb;28(1):12-17. doi: 10.19746/j.cnki.issn.1009-2137.2020.01.003.
[Article in Chinese]

Abstract

Objective: To compare the gene mutational spectrum between elderly and young adults with acute myeloid leukemia(AML) based on next generation sequencing(NGS).

Methods: The specimens of 250 AML patients in first affiliated hospital of Zhengzhou University from January 2018 to November 2018 were collected and analyzed retrospectively. The mutation of 22 related genes were detected by using AML NGS chips. Then, the differences between elderly (≥60 years old) and young adults (<60 years old) were compared.

Results: The most frequent mutations of 250 patients were as follows: NPM1(22.4%), FLT3-ITD(18.8%), NRAS(17.2%), DNMT3A(14.4%), TET2(11.6%), IDH2(9.6%), Biallelic CEBPA(8.8%), Moallelic CEBPA(8.4%), KIT(8.4%), RUNX1(7.6%), IDH1(7.6%), ASXL1(6.0%), U2AF1(5.2%), SRSF2 (3.2%), SF3B1(3.2%), TP53(2.4%), KRAS(2.0%). The NPM1, CEBPA, DNMT3A mutation significantly increased in intermediate prognosis group while KIT significantly increased in favourable prognosis group. The TET2 and IDH2 mutation rate in elderly patients were significantly higher than that in young patients (21.8% vs 8.7%) (χ2=7.180, P=0.007) and (20.0% vs 6.7%) ( χ2=8.788, P=0.003) respectively. Compared with young patients, the frequencies of DNA methylation and demethylation mutations (including DNMT3A, TET2, IDH1, IDH2) and RNA splicing enzyme mutations (inc-luding SRSF2, SF3B1, U2AF1, ZRSR2) in elderly patients significantly increased(67.3% vs 36.4%) (χ2=16.653, P=0.000) and (23.6% vs 8.7%)(χ2=9.041, P=0.003) respectively.

Conclusion: The gene mutational spectrum in elderly and young adult AML shows heterogeneity. Compared with young adults, the frequencies of DNA methylation and demethylation mutations and RNA splicing enzyme mutations in elderly patients significantly increase.

题目: 基于二代测序的老年和年轻成人急性髓系白血病患者突变基因谱比较.

目的: 比较基于二代测序(NGS)的老年和年轻急性髓系白血病(AML)患者突变基因谱,探讨老年AML的分子生物学特点.

方法: 回顾性分析2018年1月至2018年11月在郑州大学第一附属医院进行了基于22个基因突变谱的NGS检测初治AML(非急性早幼粒细胞白血病)患者的突变基因数据,并比较老年(≥60岁)和年轻(<60岁)AML患者之间的差异.

结果: 250例患者常见突变频率依次为NPM1(22.4%)、FLT3-ITD(18.8%)、NRAS(17.2%)、DNMT3A(14.4%)、TET2(11.6%)、IDH2(9.6%)、CEBPA双突变(8.8%)、CEBPA单突变(8.4%)、KIT(8.4%)、RUNX1(7.6%)、IDH1(7.6%)、ASXL1(6.0%)、U2AF1(5.2%)、SRSF2 (3.2%)、SF3B1(3.2%)、TP53(2.4%)、KRAS(2.0%)。NPM1、CEBPA 、DNMT3A突变常见于患者预后中等组,而KIT突变在患者预后良好组更常见。老年患者较年轻患者更多出现TET2突变(21.8% vs 8.7%)(χ2=7.180,P=0.007)和IDH2突变(20.0% vs 6.7%)(χ2=8.788,P=0.003)。将突变基因按照功能进行分组显示,老年患者更多发生DNA甲基化和去甲基化突变(包括DNMT3A、TET2、IDH1、IDH2)(67.3% vs 36.4%,χ2=16.653,P=0.000),以及RNA剪切酶突变(包括SRSF2、SF3B1 、U2AF1、ZRSR2)(23.6% vs 8.7%)(χ2=9.041,P=0.003).

结论: 基于NGS技术发现,不同年龄的AML患者常见突变种类存在显著差异,老年患者更多发生DNA甲基化和去甲基化突变以及RNA剪切酶突变.

MeSH terms

  • Aged
  • High-Throughput Nucleotide Sequencing*
  • Humans
  • Leukemia, Myeloid, Acute* / genetics
  • Middle Aged
  • Mutation
  • Nucleophosmin
  • Prognosis
  • Retrospective Studies
  • Young Adult