散发性血友病内含子22倒置的显著突变:值得产前筛查吗?

IF 2.6 Q2 GENETICS & HEREDITY
W. Sasanakul, A. Chuansumrit, N. Sirachainan, P. Kadegasem
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引用次数: 1

摘要

背景对血友病患者进行充分的替换是昂贵的,尤其是在资源有限的国家。目的分析泰国A型血友病患者中最常见的因子VIII基因突变。将发现一名无血友病家族史且具有最常见因子VIII突变的女性的成本效益与治疗一名血友病患者的成本进行比较。方法对109例无关的A型血友病患者进行基因型分析,包括散发病例(n=58)和遗传病例(n=51)。结果34例散发性病例(58.6%)和27例遗传性病例(51.9%)出现内含子22倒置。在没有血友病家族史的女性中,有人建议在产前护理中筛查内含子22倒置。阳性结果的女性将在其男性后代中接受进一步的血友病产前诊断。相反,检测结果呈阴性的女性仍有可能因筛查中未包括的其他因子VIII基因突变而患上血友病,但风险没有内含子22倒置那么高。尽管在没有血友病家族史的女性中筛查因子VIII突变是不符合目前的做法的,但由于在资源有限的国家为血友病患者提供的治疗不足,这项工作已经开始。该研究计算出,在17064名没有血友病家族史的女性中,大约有一名内含子22倒置的女性。筛查费用(194870美元)远低于目前方案治疗一名从出生到40岁的血友病患者的费用(378000美元)。结论建议在没有血友病家族史的女性中进行内含子22倒置的产前筛查,特别是在经济欠发达、血友病患者治疗服务不足的国家。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prominent Mutation of Intron 22 Inversion in Sporadic Hemophilia: Is It Worth the Antenatal Screening?
Background Adequate replacement for patients with hemophilia is costly, especially in countries with limited resources. Objective Factor VIII gene mutations among Thai patients with hemophilia A were analyzed for the most common mutation. The cost-effectiveness of finding one female without family history of hemophilia possessing the most common factor VIII mutation was compared with the cost of treating one patient with hemophilia. Methods In all, 109 unrelated patients with hemophilia A, defined as sporadic cases (n=58) and hereditary cases (n=51), were enrolled for genotypic analysis. Results Intron 22 inversion was prominently found in 34 sporadic (58.6%) and 27 hereditary (51.9%) cases. The screening for intron 22 inversion among females without family history of hemophilia at antenatal care has been optionally suggested. A female with a positive result will undergo further prenatal diagnosis of hemophilia in her male offspring. On the contrary, a female with a negative test result remains at risk to have a hemophiliac son caused by other factor VIII gene mutations not included in the screening but the risk is not as high as intron 22 inversion. Although the screening of factor VIII mutation among females without family history of hemophilia is against the current practice, it has been initiated due to the inadequate treatment provided to patients with hemophilia in countries with limited resources. The study calculated approximately one female with intron 22 inversion would exist among 17,064 females without family history of hemophilia. The cost of screening (194,870 USD) was much less than that of treating one patient with hemophilia from birth to 40 years of age by the current regimen (378,000 USD). Conclusion Implementing antenatal screening of intron 22 inversion among females without family history of hemophilia is optionally suggested, especially in economically less-developed countries with inadequate treatment service for patients with hemophilia.
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来源期刊
Application of Clinical Genetics
Application of Clinical Genetics Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
5.40
自引率
0.00%
发文量
20
审稿时长
16 weeks
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