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作 者:郭志萍[1] 陈剑芳[1] 秦秀玉[1] 张耀方[1] 杨林花[1]
机构地区:[1]山西医科大学第二医院血液科,太原030001
出 处:《中华血液学杂志》2013年第11期918-921,共4页Chinese Journal of Hematology
基 金:国家自然科学基金(81270587);卫生公益性行业科研专项(201202017);山西省卫生厅科技攻关计划(20100111):山西省回国留学人员重点科研项目(2009重点7)
摘 要:目的检测重型血友病A(HA)患者凝血因子Ⅷ(FⅧ)基因内含子22倒位(INV22)的发生频率,探讨部分重型HA患者的发病机制,并对患者家系女性成员进行携带者诊断。方法126例重型HA患者均为男性,中位年龄14岁(4个月~63岁)。应用一期法检测凝血因子Ⅷ活性(FⅧ:C);采用长距离PCR(LD—PCR)结合脉冲场凝胶电泳(PFGE)进行FⅧ基因1NV22检测,并对其中3例1NV22阳性患者进行家系调查。结果126例重型HA患者中检mINV22阳性患者52例(41.3%)。3个INV22阳性家系中疑为携带者的11例女性成员中检m携带者4例,其中3例为患者母亲,1例为患者胞姐。其中1个家系无家族史,该家系8名女性成员中除患者的姨表妹未检测外,其余7名成员检测结果显示患者母亲为INV22携带者,其外祖母及2个姨母、2个同胞姐妹及1个姨表姐均为非携带者。结论LD—PCR结合PFGE检测FⅧ基因INV22可用于部分重型HA患者和携带者基因诊断。Objective To investigate the incidence of intron 22 inversion (INV22) of factor Ⅷ (F Ⅷ ) gene in severe hemophilia A (HA) patients, clarify its pathological mechanism, and identify INV22 carrier in the female family members. Methods One-stage method was used to assay the F Ⅷ activity (FVnI : C) in 126 severe HA patients with a median age of 14 years old (range: 4 months-63 years). INV22 was analyzed by long-distance polymerase chain reaction (LD-PCR) and pulsed field gel electrophoresis (PFGE), and pedigree were conducted in 3 involved HA families. Results Of all the 126 severe HA, 52 (41.3%) cases had the INV22. Four females including 3 mothers and 1 sister of probands were diagnosed as INV22 carriers among 11 suspected carrier mosaicisms from 3 INV22 positive HA families. In 8 females from one family without HA history, the patient' s mother was a INV22 carrier, but her maternal grandmother, 2 maternal aunts, 2 female siblings and 1 elder female cousin were negative. Conclusion LD-PCR and PFGE could be used to diagnose severe HA patients with 1NV22 and identify the carriers.
关 键 词:血友病A 内含子 聚合酶链反应 电泳 凝胶 脉冲场
分 类 号:R554.1[医药卫生—血液循环系统疾病]
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