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巴基斯坦的β地中海贫血:木尔坦产前诊断试点项目

β-Thalassemia in Pakistan: a pilot program on prenatal diagnosis in Multan.

作者信息

Mahmood Baig Shahid, Sabih Dure, Rahim Muhammad Kashif, Azhar Aysha, Tariq Muhammad, Sajid Hussain Muhammad, Saqlan Naqvi Syed Muhammad, Raja Ghazala Kaukab, Khan Tahir Naeem, Jameel Muhammad, Iram Zahra, Noor Samia, Baig Usman Raza, Qureshi Javed Anver, Baig Shehla Anjum, Bakhtiar Syeda Marriam

机构信息

Human Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan.

出版信息

J Pediatr Hematol Oncol. 2012 Mar;34(2):90-2. doi: 10.1097/MPH.0b013e31823752f3.

DOI:10.1097/MPH.0b013e31823752f3
PMID:22258353
Abstract

Prenatal diagnosis (PND) of β-thalassemia has been underutilized in Pakistan because of a number of social and economic factors. National Institute for Biotechnology and Genetic Engineering Faisalabad in collaboration with Multan Institute of Nuclear Medicine and Radiotherapy Multan introduced free PND service for carrier couples of Multan district. Multan has a population of about 4 million. More than 170 couples registered for retrospective PND and in 2 years 105 PND were carried out through first trimester chorionic villus sampling. Almost 90% of these couples were unable to afford the cost of PND and would not have undergone the test as free service was not available. Monoplex and Multiplex Amplification Refractory Mutation System-polymerase chain reaction and genomic DNA sequencing were used for detection of IVS (intervening sequence)-I-5 (G-C), FSC (frameshift codon)-8/9 (+G), FSC-41/42 (-TTCT), IVS-I-1 (G-T), 619 bp deletion, and CD-15 (G-A) β-globin mutations. Eighty-one percent (85/105) couples analyzed were in a consanguineous marriage. Twenty-three fetuses were found homozygous mutant and all couples opted for discontinuation of affected pregnancies. More families are registering for PND after establishment of this free and accessible PND service.

摘要

由于一些社会和经济因素,巴基斯坦β地中海贫血的产前诊断(PND)未得到充分利用。费萨拉巴德国家生物技术和基因工程研究所与木尔坦核医学与放射治疗研究所合作,为木尔坦地区的携带夫妇推出了免费的PND服务。木尔坦人口约400万。超过170对夫妇登记进行回顾性PND,在两年内通过孕早期绒毛取样进行了105次PND。这些夫妇中近90%无力承担PND费用,若没有免费服务,他们不会接受检测。采用单重和多重扩增难治突变系统-聚合酶链反应以及基因组DNA测序来检测IVS(间隔序列)-I-5(G-C)、FSC(移码密码子)-8/9(+G)、FSC-41/42(-TTCT)、IVS-I-1(G-T)、619 bp缺失以及CD-15(G-A)β珠蛋白突变。接受分析的夫妇中有81%(85/105)是近亲结婚。发现23例胎儿为纯合突变体,所有夫妇都选择终止受影响的妊娠。在这项免费且可获得的PND服务建立后,有更多家庭登记进行PND。

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