Investigation on the Distribution of Common Thalassemias in Various Cities and Counties under the Jurisdiction of Chongzuo City, Guangxi

Huang Zhao, Yan Chen, Jing Lan, Liu-Tao Huang, Tianyou Huang, Miaohong Li, Xing-hua Chen, Wanwei Yang, Fu Huang, Tongfeng Huang, Xiuge Li
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Abstract

Objective: To understand the distribution of thalassemia in all districts under the jurisdiction of Chongzuo City. Methods: Collect blood routine indicators from May 2014 to 31 December 2020 in the districts of this city to screen out suspected Mediterranean patients for genetic diagnosis; GGAP-PCR and PCR-reverse dot hybridization were used to analyze the thalassemia gene in the specimens of suspected patients; compare the prevalence of thalassemia in the counties and cities within the jurisdiction of this city, and provide corresponding medical advice to the health authorities. Results: 21,535 venous blood specimens from patients with suspected thalassemia were collected in the city. There were 14,215 positive cases of thalassemia, accounting for 66.01% of the total number of patients, among which 9455 cases (43.91%) were pure α gene positive. 3464 patients (16.09%) were positive for simple β gene. 1296 patients (6.02%) were positive for αβ double gene. The proportions of thalassemia gene testing for α-thalassaemia gene, β-thalassaemia gene, and α-β double gene in various counties and districts were different. According to the multiple rate or the chi-square test of the constituent ratio, the comparison of the distribution of the thalassaemia gene test results in each area, χ = 472.6917, P = 0.0000, the difference is statistically significant. Conclusion: Severe thalassemia is a tragedy for a family. It not only needs to spend a lot of money to prolong life, but it also cannot change the situation of losing life and financial emptiness in the end. It is suggested that timely screening, timely diagnosis and medical consultation should be carried out in married and unborn families and early pregnancy, so as to reduce the birth of children with severe thalassemia and avoid the occurrence of tragedies. *Co-First author. #Corresponding author. How to cite this paper: Zhao, H., Chen, Y., Lan, J., Huang, L.X., Huang, T.Y., Li, M.H., Chen, X.C., Yang, W.W., Huang, F., Huang, T.F. and Li, X.G. (2021) Investigation on the Distribution of Common Thalassemias in Various Cities and Counties under the Jurisdiction of Chongzuo City, Guangxi. Advances in Bioscience and Biotechnology, 12, 361-370. https://doi.org/10.4236/abb.2021.1211023 Received: September 29, 2021 Accepted: November 2, 2021 Published: November 5, 2021 Copyright © 2021 by author(s) and Scientific Research Publishing Inc. This work is licensed under the Creative Commons Attribution International License (CC BY 4.0). http://creativecommons.org/licenses/by/4.0/ Open Access
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广西崇左市辖区各市县常见地中海贫血分布调查
目的:了解崇左市下辖各区地中海贫血的分布情况。方法:收集2014年5月至2020年12月31日各区血常规指标,筛选出疑似地中海患者进行遗传诊断;采用GGAP-PCR和pcr -反向点杂交对疑似患者标本进行地中海贫血基因分析;比较本市辖区内各县市的地中海贫血患病率,并向卫生部门提供相应的医疗建议。结果:全市共采集疑似地中海贫血患者静脉血21535份。地中海贫血阳性14215例,占患者总数的66.01%,其中纯α基因阳性9455例,占43.91%。单纯β基因阳性3464例(16.09%)。αβ双基因阳性1296例(6.02%)。各区县对α-地中海贫血基因、β-地中海贫血基因和α-β双基因的地中海贫血基因检测比例不同。根据构成比的多重率或卡方检验,比较各地区地中海贫血基因检测结果的分布情况,χ = 472.6917, P = 0.0000,差异有统计学意义。结论:重度地中海贫血是一个家庭的悲剧。它不仅需要花费大量的钱来延长生命,而且最终也无法改变失去生命和财务空虚的局面。建议在已婚和未出生家庭及早期妊娠中进行及时筛查、及时诊断和医疗咨询,以减少重度地中海贫血患儿的出生,避免悲剧的发生。* Co-First作者。#通讯作者。本文引用方式:赵慧慧,陈艳,兰,杰,黄丽霞,黄廷玉,李明辉,陈晓春,杨文伟,黄凤芳,黄廷峰,李晓光(2021)广西崇左市辖区各市县常见地中海贫血分布调查。生物科学进展,12,361-370。https://doi.org/10.4236/abb.2021.1211023收稿日期:2021年9月29日收稿日期:2021年11月2日出版日期:2021年11月5日版权所有©作者与科研出版公司。本作品采用知识共享署名国际许可协议(CC BY 4.0)。http://creativecommons.org/licenses/by/4.0/开放获取
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