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首页> 外文期刊>Pathology and Laboratory Medicine International >Abnormal hemoglobin variants, ABO, and Rhesus blood group distribution among students in the Niger Delta of Nigeria
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Abnormal hemoglobin variants, ABO, and Rhesus blood group distribution among students in the Niger Delta of Nigeria

机译:尼日利亚尼日尔三角洲学生中血红蛋白变异,ABO和恒河猴血型分布异常

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Background: Communities in Africa constitute a major part of the population that is vulnerable to many erythrocytic hereditary and hematological disorders such as hemoglobinopathies. The frequencies of abnormal hemoglobin variants, ABO, and Rhesus blood groups vary from one population to another.Methods: The aim of this study was to find the prevalence/spectrum of hemoglobin variants, ABO, and Rhesus blood group distribution among 204 undergraduate students of African descent in Port Harcourt in the heart of the Niger Delta geopolitical zone of Nigeria. Standard alkaline cellulose acetate electrophoretic technique using the Shandon electrophoretic tank with tris-ethylene diamine tetracetic acid (EDTA) borate buffer and hemagglutination techniques were employed for the determination of abnormal hemoglobin variants, ABO and Rhesus blood groups, respectively. Results: Two hundred and four apparently healthy students of African descent comprising 124 males (60.8%) and 80 (39.2%) females with a mean age 24.5 ± 6.5 years took part in the study. Subjects were screened for abnormal hemoglobin variants, ABO, and Rhesus groups. Normal hemoglobin accounted for 69.1%, followed by abnormal sickle cell trait in 29.4%, and the sickle cell disease in 1.5% of the study population. The distribution of the various blood groups indicated that 46% were blood group O, 26.6% were group A, 23.6% were group B while 3.8% were group AB. Rhesus (RhD) positivity rate was 93% while RhD negativity accounted for 7%.Conclusion: This research indicates a high prevalence of hemoglobin variants in the study population. Carrier screening and mutation identification can become the cornerstones of any prevention program for hemoglobin disorders. It can also help in the formulation of genetic counseling policies to help prospective couples make informed decisions in a bid to reduce the sickling gene pool in the Niger Delta of Nigeria.
机译:背景:非洲社区构成了人口的主要部分,易患许多红细胞遗传性和血液学疾病,例如血红蛋白病。方法:本研究的目的是找出204名高校在校大学生的血红蛋白变异,ABO和恒河猴血型分布的患病率/频谱。非洲裔在尼日利亚尼日尔三角洲地缘政治区中心的哈科特港。使用Shandon电泳槽和三乙二胺四乙酸(EDTA)硼酸盐缓冲液的标准碱性醋酸纤维素电泳技术以及血凝技术分别用于测定异常的血红蛋白变体,ABO和恒河猴血型。结果:包括124名男性(60.8%)和80名女性(39.2%)的非洲人后裔的240名表面健康的学生参加了研究,平均年龄为24.5±6.5岁。筛选受试者的异常血红蛋白变体,ABO和恒河猴组。正常血红蛋白占69.1%,其次是镰状细胞性状异常(占29.4%),镰状细胞疾病占1.5%。各种血型的分布表明,O型血为46%,A型血为26.6%,B型血为23.6%,AB型血为3.8%。恒河猴(RhD)阳性率为93%,而RhD阴性则为7%。结论:这项研究表明在研究人群中血红蛋白变异率很高。携带者筛查和突变鉴定可以成为任何预防血红蛋白疾病计划的基础。它还可以帮助制定遗传咨询政策,帮助准夫妻做出知情的决定,以减少尼日利亚尼日尔三角洲的镰状基因库。

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