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作 者:李坦[1] 戴菁[2] 吴竞生 丁秋兰[2] 丁凯阳[1] 郑昌成[1] 孙萍[1] 王学锋[2]
机构地区:[1]安徽医科大学附属省立医院血液科,合肥230001 [2]上海交通大学医学院附属瑞金医院
出 处:《中华血液学杂志》2009年第3期150-153,共4页Chinese Journal of Hematology
基 金:诺和诺德血友病基金“中国血友病防治”项目
摘 要:目的 对血友病A(HA)患者及其家系携带者进行凝血因子Ⅷ(FⅧ)基因内含子1及22倒位分析,并探讨其与FⅧ抗体产生的相关性。方法对157例HA患者进行FⅧ活性(FⅧ:C)及FVH抗体检测;同时采用双管多重PCR及长距离PCR(LD—PCR)技术对其中81例HA患者进行FⅧ内含子1及内含子22倒位分析;并对其中6例患者进行家系调查。结果81例HA患者中3例为内含子1倒位,均为重型,占重型HA的4.6%(65例中3例);内含子1倒位患者中1例为FⅧ抗体阳性。用该基因信息对1个内含子1倒位患者家系的2名女性进行了检测,1例为携带者,1例为非携带者。81例HA患者中25例为内含子22倒位,均为重型,占重型HA的38.5%(65例中25例),内含子22倒位患者中发现1例为FVI抗体阳性。用该基因信息对5个内含子22倒位患者家系的9名女性进行了检测,7例为携带者,2例为非携带者。结论内含子1倒位是继内含子22倒位外导致重型HA的另一重要分子发病机制。FⅧ内含子倒位检测不仅可用于血友病直接基因诊断、进行家系调查;同时还可纠正表型分型的偏差。FVH内含子1和内含子22倒位可能是抗体产生的高危因素之一。Objective To analyze intron 1 and 22 inversions in factor Ⅷ (FⅧ) gene in hemophilia A(HA) patients and and their families and to investigate the correlation between intron inversion and FⅧ antibody. Methods All patients were detected FⅧ: C and FVⅧ antibody. In addition, 81 unrelated HA patients were directly detected by multiplex PCR and long-distance PCR for intron 1 and 22 inversions in FⅧ gene. Pedigree investingation for some patients were conducted. Results In 81 unrelated HA patients, 3 severe cases were found intron 1 inversion which accounted for 4.6% of total 65 severe cases. Of the 3 cases, one was FⅧ antibody positive. Two female family members of a intron 1 inversion patient were identified as one carrier and one non-carrier. Twenty five of 65(38.5%) severe cases were found intron 22 inversion. Of the 25 cases 1 was Fvm antibody positive. Nine female members in 5 HA families which had patients with intron 22 inversion were identified as 7 carries and 2 non-carriers. Conclusion Besides intron 22 inversion, intron 1 inversion was another important molecular defect in resulting in severe HA. Intron inversion analysis can also be used for deviation rectification of experiment grouping in HA patients. Intron 1 and 22 inversions may be one of the higher risk factors for resulting in FⅧ antibodies.
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