全基因组芯片检测在MDS诊断及预后中的应用  

The study of SNP-Array in clinical application of MDS

作　　者：李叶琼 冶秀鹏[1] 宋丽君[1] 马燕萍[1] 张伟[1] 李蓉[1] 包慎[1] 白洁[1] 李芳[1] LI Yeqiong;YE Xiupeng;SONG Lijun;MA Yanping;ZHANG Wei;LI Rong;BAO Shen;BAI Jie;LI Fang(People's Hospital of Ningxia Hui Autonomous Region,First Affiliated Hospital of Northwest University for Nationalities,Ningxia Yinchuan 750002,China.)

机构地区：[1]宁夏回族自治区人民医院(西北民族大学附属第一医院),宁夏银川750002

出　　处：《现代肿瘤医学》2021年第13期2313-2317,共5页Journal of Modern Oncology

基　　金：宁夏自然科学基金项目(编号:2018AAC03174);宁夏人民医院振兴培育项目(编号:201920)。

摘　　要：目的:探讨全基因组芯片(SNP-A)检测在骨髓增生异常综合征(MDS)患者诊断方面的特异性、敏感性及预后中的应用价值。方法:对2019年09月到2020年04月期间我院诊治的20例初诊MDS患者,依据修订的国际预后积分系统(IPSS-R)对患者进行危险度分组,应用SNP-A对MDS患者进行全基因组范围DNA拷贝数的变异(CNV)和单亲二倍体(UPD)的检测,总结特点并与常规染色体核型分析(CCA)结果进行比较。结果:20例MDS患者染色体核型分析的异常检出率为40%,与SNP-A相结合染色体异常的检出率提高至65%,二者比较差异有统计学意义(P<0.05);低危组和高危组患者核型异常的检出率分别为15%和25%,与SNP-A相结合异常检出率分别提高至30%和35%(P<0.05);SNP-A检测出CNV和UPD高危组患者均明显高于低危组患者(P<0.01)。结论:SNP-A与CCA的联合使用,大大提高了MDS患者染色体变异的检出率,并且SNP-A能够对MDS患者提供更多更全面的遗传学信息,对于疾病的诊断和预后有重要价值。Objective:To explore the specificity,sensitivity and prognosis of single nucleotide polymorphasim array(SNP-A)detection in the newly diagnosis of myelodysplastic syndrome(MDS)patients.Methods:To study the 20 newly diagnosed MDS patients admitted to our hospital,group the patients according to the revised international prognostic score system(IPSS-R),and use SNP-A to perform genome-wide DNA copy number variation(CNV)and uniparental disomie(UPD),summarize the characteristics of CNV and UPD,then compare with the conventional cytogenetic analysis(CCA).Results:The abnormal detection rate of CCA of 20 MDS patients was 40%.It was increased to 65%combined with SNP-A.There was a statistical difference between them(P<0.05).The detection rates of CCA in low-risk and high-risk patients were 15%and 25%,respectively,and them were increased to 30%and 35%combined with SNP-A,respectively(P<0.05).The number of CNV and UPD in high-risk groups were significantly higher than those in low-risk groups(P<0.01).Conclusion:The combined use of SNP-A and CCA greatly improves the detection rate of chromosomal variation in MDS patients,and SNP-A can provide more comprehensive genetic information to MDS patients.It has important value for the diagnosis and prognosis of MDS.

关 键 词：骨髓增生异常综合征 染色体核型 基因组芯片 

分 类 号：R733.3[医药卫生—肿瘤]