Causes of Abnormal Hemoglobin Electrophoresis.
10.19746/j.cnki.issn.1009-2137.2023.03.031
- Author:
Xue-Li PANG
1
;
Hong-Fei DU
1
;
Yan YANG
1
;
Xiao-Ping ZHOU
1
;
Ning TANG
1
;
Jia-Wei LIU
1
;
Ying XU
2
Author Information
1. Department of Clinical Laboratory, The First Affiliated Hospital of Chengdu Medical College, 2Chengdu Medical College, Chengdu 610500, Sichuan Province, China.
2. Department of Clinical Laboratory, The First Affiliated Hospital of Chengdu Medical College, 2Chengdu Medical College, Chengdu 610500, Sichuan Province, China.E-mail: yingxu825@126.com.
- Publication Type:Journal Article
- Keywords:
iron deficiency anemia;
abnormal hemoglobin disease;
abnormal hemoglobin electrophoresis;
macrocytosis;
thalassemia;
thyroid dysfunction
- MeSH:
Humans;
Female;
Pregnancy;
beta-Thalassemia/genetics*;
Anemia, Iron-Deficiency;
Fetal Hemoglobin/analysis*;
alpha-Thalassemia;
Blood Protein Electrophoresis;
Hemoglobin A2/analysis*;
Hemoglobins, Abnormal/analysis*
- From:
Journal of Experimental Hematology
2023;31(3):830-836
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the possible causes of abnormal hemoglobin electrophoresis results.
METHODS:The hemoglobin electrophoresis results of 5 696 patients in the First Affiliated Hospital of Chengdu Medical College from September 2018 to July 2021 were collected, and the abnormal results and clinical significance were analyzed.
RESULTS:The results of 486 patients (accounting for 8.53%) were abnormal, of which 300 cases had increased HbA2, 135 cases had decreased HbA2, 44 cases had increased F alone, and 7 cases had abnormal hemoglobin bands. Among the 486 patients, 246 patients were thalassemia gene positive (the positive rate was 50.62%), including 29 cases of α thalassemia, 208 cases of β thalassemia and 9 cases of αβ thalassemia. Among the patients with elevated HbA2, 68.67% were detected β thalassemia, 3.00% αβ thalassemia, 9.33% were suspected to be caused by macrocytosis, 6.33% by thyroid dysfunction, and 12.67% by uncertainty of the method. Among the patients with reduced HbA2, 21.48% were detected α thalassemia, 60.00% iron deficiency anemia, 8.15% were suspected to be caused by thyroid dysfunction, and 10.37% by uncertainty of the method. Among the patients with elevated F alone, the results of thalassemia gene detection were negative, 40.91% of them were suspected to be caused by macrocytosis, 27.27% by hereditary persistence of fetal hemoglobin, 29.55% by special physiological condition of pregnant women, and 2.27% by hyperthyroidism. Abnormal hemoglobin bands were detected in 7 patients, including 4 cases of hemoglobin D, 2 cases of hemoglobin E, and 1 case of hemoglobin J.
CONCLUSION:Thalassemia, iron deficiency anemia, macrocytosis such as megaloblastic anemia and non-severe aplastic anemia, thyroid dysfunction, hereditary persistence of fetal hemoglobin, abnormal hemoglobin diseases, the uncertainty of the method are all important causes of abnormal hemoglobin electrophoresis results. In clinical work, the patient's indicators should be comprehensively analyzed to determine the possible cause.
