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山东大学学报 (医学版) ›› 2019, Vol. 57 ›› Issue (12): 57-61.doi: 10.6040/j.issn.1671-7554.0.2019.803

• 临床医学 • 上一篇    

山东省55例血友病A患者基因检测及分析

张文慧1,陈昀1,常亚丽1,周亚伟1,房云海2,张心声2,郭农建1   

  1. 1. 山东大学附属济南市中心医院血液科, 山东 济南 250013;2. 山东省血液中心山东省血友病诊疗中心, 山东 济南 250013
  • 发布日期:2022-09-27
  • 通讯作者: 郭农建. E-mail:gnjian2002@aliyun.com

Gene detection and analysis of 55 patients with hemophilia A in Shandong Province

ZHANG Wenhui1, CHEN Yun1, CHANG Yali1, ZHOU Yawei1, FANG Yunhai2, ZHANG Xinsheng2, GUO Nongjian1   

  1. 1. Department of Hematology, Jinan Central Hospital Affiliated to Shandong University, Jinan 250013, Shandong, China;
    2. Hemophilia Treatment Center of Shandong Province, Blood Center of Shandong Province, Jinan 250013, Shandong, China
  • Published:2022-09-27

摘要: 目的 分析山东省55例血友病A(HA)患者基因突变类型,探讨HA发病机制。 方法 采用LD-PCR法检测山东省55例HA患者凝血因子Ⅷ(FⅧ)基因的内含子22倒位突变,阴性者采用高通量测序法检测FⅧ基因的26个外显子,并与人类基因突变数据库比对。 结果 55例HA患者中内含子22倒位突变20例,其他35例共检测到28种突变类型,其中3例同时检测出2种突变,有6例未检测到基因突变。共发现c.2034_2062del、c.6052_6058del、c.6046_6047del、c.1009+1G>T、c.2997dupA、c.4001delT、c.1334T>A、c.1493G>A、c.557A>T等9种未被报道过的新突变。 结论 FⅧ基因突变是导致HA的根本原因。重型血友病患者中最常见的突变类型为内含子22倒位突变。编码区突变最常见的突变类型为错义突变。新发现的9种新突变丰富了基因突变谱,为探讨HA发病机制提供了基础。

关键词: 血友病A, 凝血因子Ⅷ, 基因突变, 内含子22倒位, 基因测序

Abstract: Objective To analyze the genetic mutation types of 55 patients with hemophilia A(HA)in Shandong Province, and explore its molecular mechanism. Methods The intron 22 inversion mutation of factor Ⅷ(FⅧ)in all patients was detected with LD-PCR. The 26 exons of FⅧ negative patients were detected with next-generation sequencing and matched in the humangene mutation database. Results Of all 55 patients, 20 had intron 22 inversion mutation, and the other 35 had 28 different types of mutations, of whom 3 had 2 simultaneous mutations, while 6 had no mutation. Altogether 9 new mutation types unreported before were discovered, including c.2034_2062del, c.6052_6058del, c.6046_6047del, c.1009+1G>T, c.2997dupA, c.4001delT, c.1334T>A, c.1493G>A and c.557A>T. Conclusion FⅧ mutation is the direct cause of HA. The most common mutation in severe HA is intron 22 inversion mutation. The most common mutation in coding region mutation is the missense. The 9 new mutations discovered in the study enrich the gene mutation profile and provide reference for the study of HA pathogenesis.

Key words: Hemophilia A, Coagulation factor Ⅷ, Gene mutation, Intron 22 inversion, Gene sequencing

中图分类号: 

  • R574
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