Erythrocyte Indices and Hemoglobin Analysis for α-Thalassemia Screening in an Area with High Carrying Rate
Carriers of α-thalassemia exhibit hypochromic microcytosis with mean corpuscular volume (MCV) < 80 fL, mean corpuscular hemoglobin (MCH) < 27 pg, and reduced hemoglobin A 2 (HbA 2 ). We studied the distribution and diagnostic efficiencies of these indicators and their combinations in patients...
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Published in | Indian journal of hematology & blood transfusion Vol. 38; no. 2; pp. 352 - 358 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New Delhi
Springer India
01.04.2022
Springer Nature B.V |
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Abstract | Carriers of α-thalassemia exhibit hypochromic microcytosis with mean corpuscular volume (MCV) < 80 fL, mean corpuscular hemoglobin (MCH) < 27 pg, and reduced hemoglobin A
2
(HbA
2
). We studied the distribution and diagnostic efficiencies of these indicators and their combinations in patients with and without alpha-thalassemia. Based on genetic diagnosis, 10,883 participants were divided into alpha-thalassemia group (n = 1655) and negative-for-alpha-thalassemia group (n = 9228). Erythrocyte parameters and hemoglobin analysis of the groups were analyzed. Moreover, we compared the four screening schemes (MCV/MCH, MCV/MCH/HbA
2
, MCV + MCH, MCV + MCH + HbA
2
) to find the best for α-thalassemia screening. The genotypes of --
SEA
/αα, and -α
3.7
/αα are the most prevalent with 54.9% and 27.6% in Fujian Province, China. There were significant differences in the distribution of MCV, MCH, and HbA
2
in the two groups. Among the three, MCH exhibited the highest sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy. Although the four screening schemes have their advantages, there are significant differences in their sensitivity and specificity. MCV + MCH had the best diagnostic performance (72.6% sensitivity, 89.0% specificity) as well as the highest Youden index (61.59%). Our results showed that MCH could be used to screen α-thalassemia instead of MCV and HbA
2
. However, it is recommended that MCV/MCH/HbA
2
screening be used in areas with high α-thalassemia incidence to increased sensitivity. |
---|---|
AbstractList | Carriers of α-thalassemia exhibit hypochromic microcytosis with mean corpuscular volume (MCV) < 80 fL, mean corpuscular hemoglobin (MCH) < 27 pg, and reduced hemoglobin A
2
(HbA
2
). We studied the distribution and diagnostic efficiencies of these indicators and their combinations in patients with and without alpha-thalassemia. Based on genetic diagnosis, 10,883 participants were divided into alpha-thalassemia group (n = 1655) and negative-for-alpha-thalassemia group (n = 9228). Erythrocyte parameters and hemoglobin analysis of the groups were analyzed. Moreover, we compared the four screening schemes (MCV/MCH, MCV/MCH/HbA
2
, MCV + MCH, MCV + MCH + HbA
2
) to find the best for α-thalassemia screening. The genotypes of --
SEA
/αα, and -α
3.7
/αα are the most prevalent with 54.9% and 27.6% in Fujian Province, China. There were significant differences in the distribution of MCV, MCH, and HbA
2
in the two groups. Among the three, MCH exhibited the highest sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy. Although the four screening schemes have their advantages, there are significant differences in their sensitivity and specificity. MCV + MCH had the best diagnostic performance (72.6% sensitivity, 89.0% specificity) as well as the highest Youden index (61.59%). Our results showed that MCH could be used to screen α-thalassemia instead of MCV and HbA
2
. However, it is recommended that MCV/MCH/HbA
2
screening be used in areas with high α-thalassemia incidence to increased sensitivity. Carriers of α-thalassemia exhibit hypochromic microcytosis with mean corpuscular volume (MCV) < 80 fL, mean corpuscular hemoglobin (MCH) < 27 pg, and reduced hemoglobin A (HbA ). We studied the distribution and diagnostic efficiencies of these indicators and their combinations in patients with and without alpha-thalassemia. Based on genetic diagnosis, 10,883 participants were divided into alpha-thalassemia group (n = 1655) and negative-for-alpha-thalassemia group (n = 9228). Erythrocyte parameters and hemoglobin analysis of the groups were analyzed. Moreover, we compared the four screening schemes (MCV/MCH, MCV/MCH/HbA , MCV + MCH, MCV + MCH + HbA ) to find the best for α-thalassemia screening. The genotypes of -- /αα, and -α /αα are the most prevalent with 54.9% and 27.6% in Fujian Province, China. There were significant differences in the distribution of MCV, MCH, and HbA in the two groups. Among the three, MCH exhibited the highest sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy. Although the four screening schemes have their advantages, there are significant differences in their sensitivity and specificity. MCV + MCH had the best diagnostic performance (72.6% sensitivity, 89.0% specificity) as well as the highest Youden index (61.59%). Our results showed that MCH could be used to screen α-thalassemia instead of MCV and HbA . However, it is recommended that MCV/MCH/HbA screening be used in areas with high α-thalassemia incidence to increased sensitivity. Carriers of α-thalassemia exhibit hypochromic microcytosis with mean corpuscular volume (MCV) < 80 fL, mean corpuscular hemoglobin (MCH) < 27 pg, and reduced hemoglobin A2 (HbA2). We studied the distribution and diagnostic efficiencies of these indicators and their combinations in patients with and without alpha-thalassemia. Based on genetic diagnosis, 10,883 participants were divided into alpha-thalassemia group (n = 1655) and negative-for-alpha-thalassemia group (n = 9228). Erythrocyte parameters and hemoglobin analysis of the groups were analyzed. Moreover, we compared the four screening schemes (MCV/MCH, MCV/MCH/HbA2, MCV + MCH, MCV + MCH + HbA2) to find the best for α-thalassemia screening. The genotypes of --SEA/αα, and -α3.7/αα are the most prevalent with 54.9% and 27.6% in Fujian Province, China. There were significant differences in the distribution of MCV, MCH, and HbA2 in the two groups. Among the three, MCH exhibited the highest sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy. Although the four screening schemes have their advantages, there are significant differences in their sensitivity and specificity. MCV + MCH had the best diagnostic performance (72.6% sensitivity, 89.0% specificity) as well as the highest Youden index (61.59%). Our results showed that MCH could be used to screen α-thalassemia instead of MCV and HbA2. However, it is recommended that MCV/MCH/HbA2 screening be used in areas with high α-thalassemia incidence to increased sensitivity. |
Author | Chen, Meihuan Shen, Qingmei Huang, Hailong Su, Linjuan Xu, Liangpu Wang, Meiying Zheng, Lin Wu, Xiaoqing |
Author_xml | – sequence: 1 givenname: Lin surname: Zheng fullname: Zheng, Lin organization: Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University – sequence: 2 givenname: Hailong surname: Huang fullname: Huang, Hailong organization: Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University – sequence: 3 givenname: Xiaoqing surname: Wu fullname: Wu, Xiaoqing organization: Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University – sequence: 4 givenname: Qingmei surname: Shen fullname: Shen, Qingmei organization: Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University – sequence: 5 givenname: Meihuan surname: Chen fullname: Chen, Meihuan organization: Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University – sequence: 6 givenname: Meiying surname: Wang fullname: Wang, Meiying organization: Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University – sequence: 7 givenname: Linjuan surname: Su fullname: Su, Linjuan organization: Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University – sequence: 8 givenname: Liangpu surname: Xu fullname: Xu, Liangpu email: xiliangpu@fjmu.edu.cn organization: Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University |
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Cites_doi | 10.1136/jcp.2003.014456 10.3109/03630261003677213 10.1016/j.hoc.2017.06.010 10.1038/s41598-017-00967-2 10.1016/j.gene.2018.02.058 10.1182/blood-2002-07-1975 10.1136/jcp.2008.056945 10.1016/j.hoc.2017.11.003 10.1373/clinchem.2005.054189 10.1016/j.bj.2015.10.001 10.3109/03630269.2015.1137933 10.3324/haematol.2013.099747 10.3109/03630269.2011.634698 10.1111/j.1751-553X.2011.01368.x 10.1182/blood-2010-08-300335 10.1016/j.bcmd.2014.01.003 10.1111/j.1365-2141.2009.08054.x 10.1093/clinchem/46.10.1692 10.1046/j.1365-2257.2002.00464.x 10.1182/blood-2006-02-002394 10.1186/1750-1172-5-11 10.1016/j.bpobgyn.2016.10.013 10.1002/ajh.22188 10.1182/blood.V91.7.2213 10.3324/haematol.2015.141200 10.1002/pbc.25882 10.1016/j.clinbiochem.2011.04.009 10.1016/j.hemonc.2017.02.002 10.3109/07853890.2015.1091942 10.1016/j.gene.2016.02.014 10.1186/1750-1172-5-13 10.1016/j.blre.2011.04.001 10.1097/AOG.0000000000001948 10.1111/ijlh.13035 |
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SubjectTerms | Blood diseases Blood Transfusion Medicine Diagnostic tests Erythrocytes Hematology Hemoglobin Human Genetics Medical screening Medicine Medicine & Public Health Oncology Original Original Article |
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Title | Erythrocyte Indices and Hemoglobin Analysis for α-Thalassemia Screening in an Area with High Carrying Rate |
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