Zafar Uffan, Naseem Kamran, Baig Muhammad Usman, Khan Zain Ali, Zafar Fariha, Akram Saba
Radiology Department, Bahawal Victoria Hospital, Quaid-E-Azam Medical College, Bahawalpur, PAK.
Radiology Department, Bahawal Victoria Hospital, Quaid-E-Azam Medical College, Bahawalpur , PAK.
Cureus. 2018 Sep 7;10(9):e3265. doi: 10.7759/cureus.3265.
Introduction The prevalence of beta-thalassemia mutations is different in various castes, regions, and ethnic groups. By knowing this prevalence, we can conduct a targeted screening of only the high-risk population and only for the specific mutations that are prevalent in each group. Objective The purpose of this study was to determine the regional, caste-wise, and ethnic spectrum of beta-thalassemia mutations in couples referred for a prenatal diagnosis. Methods A cross-sectional analytical study was conducted at the thalassemia unit, Bahawal Victoria Hospital, Bahawalpur, from October 1, 2015, to May 15, 2018. After obtaining informed consent, chorionic villus sampling (CVS) was performed in 144 women having a gestational age of 12 to 16 weeks. We took blood samples of the couples. A chromosomal analysis for 13 mutations was done at Punjab Thalassaemia Prevention Programme (PTPP), Lahore. The researchers filled a questionnaire with all the details of couples like ethnicity, caste, and region. Results The most common mutation was Fr 8-9(+G), accounting for 29.8%, followed by IVS 1-5(G-C), which was 28.9%. We did not find three mutations in any chromosome. Fr 8-9 (+G) was the most common mutation among Punjabis and Pakhtoons. IVS 1-5 (G-C) was the most common mutation among Saraikis and Urdu-speaking people. In Rajputs, Arains, Jatts, and Pathans, Fr 8-9 (+G) was the most common mutation. IVS 1-5 (G-C) was the most common mutation among Sheikhs, Balochs, Syeds, and Miscellaneous. IVS 1-5 (G-C) was the most common mutation in the Bahawalpur division and Ghotki (Sindh) while Fr 8-9 (+G) was the most common mutation in the Multan division. The p-value of all the results was <0.001. Conclusion There is an ethnic, caste-wise, and regional distribution of mutations. We can conduct a targeted screening of the population and provide counseling about chorionic villus sampling by using this local data.
引言
β地中海贫血突变的患病率在不同种姓、地区和族群中有所不同。了解这种患病率后,我们可以仅对高危人群进行针对性筛查,且仅针对每组中普遍存在的特定突变进行筛查。
目的
本研究的目的是确定前来接受产前诊断的夫妇中β地中海贫血突变的地区、种姓和族群分布情况。
方法
2015年10月1日至2018年5月15日,在巴哈瓦尔布尔的巴哈瓦尔维多利亚医院地中海贫血科开展了一项横断面分析研究。在获得知情同意后,对144名孕周为12至16周的妇女进行了绒毛取样(CVS)。我们采集了夫妇双方的血液样本。在拉合尔的旁遮普地中海贫血预防项目(PTPP)对13种突变进行了染色体分析。研究人员填写了一份包含夫妇所有详细信息的问卷,如种族、种姓和地区。
结果
最常见的突变是Fr 8-9(+G),占29.8%,其次是IVS 1-5(G-C),占28.9%。我们在任何染色体上均未发现三种突变。Fr 8-9(+G)是旁遮普人和普什图人中最常见的突变。IVS 1-5(G-C)是萨拉基人和说乌尔都语人群中最常见的突变。在拉杰普特人、阿雷恩斯、贾特人和帕坦人中,Fr 8-9(+G)是最常见的突变。IVS 1-5(G-C)是谢赫、俾路支人、赛义德人和其他人群中最常见的突变。IVS 1-5(G-C)是巴哈瓦尔布尔分区和戈特基(信德省)最常见的突变,而Fr 8-9(+G)是木尔坦分区最常见的突变。所有结果的p值均<0.001。
结论
突变存在种族、种姓和地区分布。利用这些本地数据,我们可以对人群进行针对性筛查,并提供有关绒毛取样的咨询服务。