科研之友
微信
新浪微博
Facebook
分享链接
摘要
background: the aim of this study is to analyze the global prevalence of carriers of heterozygous hemoglobinopathies among pregnant women settled in lanzarote. patients and methods: a epidemiologic cross-sectional observational investigation was undertaken to study the prevalence of hemoglobinopathies in 2,436 pregnant women in lanzarote. the techniques of primary screening were hemoglobin electrophoresis on cellulose acetate at alkaline ph for the detection of hemoglobin variants, and the quantification of hba2 and hbf for the diagnosis of ˋ thalassemia trait. the study to confirm the diagnosis of structural hemoglobinopathies was based on hemoglobin electrophoresis on citrate agar at acid ph, isolectric focusing and high-performance liquid chromatography (hplc). the molecular characterization of ˋ thalassemia trait (hba2 %26gt;3.5%) was carried out by techniques using a real time pcr procedure with specific fluorescently labelled hybridization probes and allele-specific amplification (pcr-arms). results: the global prevalence of hemoglobinopathies was 11.90㏑ corresponding to 9.44㏑ for structural hemoglobinopathies and 2.46㏑ for heterozygous ˋ thalassemias. a variant hemoglobin was detected on 23 women and the distribution was as follows: thirteen carriers of hemoglobin s, seven hbc trait, two hbd trait and one %26quot;unstable%26quot; hemoglobin. 82.6% of the variant hemoglobins found were from migrant population from africa and america. conclusions: the high prevalence of carriers of structural hemoglobinopathies in lanzarote justifies the initation of programs for screening for hemoglobinopathies to prevent the emergence of severe states causing disease.
