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Haematological and electrophoretic characterisation of -thalassaemia in Yunnan province of Southwestern China

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机构: [1]First Peoples Hosp Yunnan Prov, Genet Diag Ctr, Yunnan Prov Key Lab Birth Defects & Genet Dis, Kunming, Peoples R China [2]Kunming Univ Sci & Technol, Dept Genet, Kunming, Peoples R China [3]First Peoples Hosp Yunnan Prov, Dept Clin Lab, Kunming, Peoples R China
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关键词: thalassemia capillary electrophoresis hematological and biochemical parameter values mutation cut-off value

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Objectives -Thalassaemia is widely found in Southwestern China. Characterisation of -thalassaemia can improve screening and prenatal diagnosis for at-risk populations. Design A retrospective study. Methods In this study, the levels of haemoglobin alpha 2 (HbA(2)) and haemoglobin alpha (HbA) were analysed by gender for a total of 15067 subjects screened by capillary electrophoresis. The cut-off value with the highest accuracy was established to identify -thalassaemia in 723 patients suspected to have this disease. Haematological and electrophoretic characterisation of eight common types of -thalassaemia were analysed in 486 -thalassaemia subjects. Results HbA levels were significantly higher in men than in women, but there was no significant difference on HbA(2) levels. A new cut-off value for the diagnosis of -thalassaemia (HbA(2)4.0%) with the highest accuracy was proposed for the studied populations. Haemoglobin (Hb) was significantly higher in men compared with women (p<0.05), whereas no statistically significant differences were found for mean cell volume (MCV), mean cell haemoglobin (MCH), HbA and HbA(2). The haemoglobin E (HbE) group showed comparatively higher values for haematological indices (Hb, MCV and MCH) than the other genotypes in heterozygous -thalassaemia groups (p<0.05), and -28 (A>G) (HBB (-globin):c.-78A>C) had significantly higher HbA(2) values compared with other -thalassaemia. Conclusions Ethnic groups have diversified -globin gene mutations and considerable haematological variations. Our study will lay the foundation for screening programmes and clinical management of thalassaemia in Southwestern China.

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出版当年[2017]版:
大类 | 3 区 医学
小类 | 3 区 医学:内科
最新[2023]版:
大类 | 3 区 医学
小类 | 3 区 医学:内科
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出版当年[2016]版:
Q1 MEDICINE, GENERAL & INTERNAL
最新[2023]版:
Q1 MEDICINE, GENERAL & INTERNAL

影响因子: 最新[2023版] 最新五年平均 出版当年[2016版] 出版当年五年平均 出版前一年[2015版] 出版后一年[2017版]

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第一作者机构: [1]First Peoples Hosp Yunnan Prov, Genet Diag Ctr, Yunnan Prov Key Lab Birth Defects & Genet Dis, Kunming, Peoples R China [2]Kunming Univ Sci & Technol, Dept Genet, Kunming, Peoples R China
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通讯机构: [1]First Peoples Hosp Yunnan Prov, Genet Diag Ctr, Yunnan Prov Key Lab Birth Defects & Genet Dis, Kunming, Peoples R China [2]Kunming Univ Sci & Technol, Dept Genet, Kunming, Peoples R China
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