Reticulocyte parameters in hemoglobinopathies and iron deficiency anemia
Flow cytometric reticulocyte analysis allows the evaluation of reticulocyte maturity. New reticulocyte parameters have been used in the diagnosis and management of anemias, in the bone marrow transplant setting and in the monitoring of iron replacement or erythropoiet in therapy. Reticulocyte number...
| Main Authors: | , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2003-01-01
|
| Series: | Revista Brasileira de Hematologia e Hemoterapia |
| Subjects: | |
| Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842003000200005 |
| _version_ | 1818555840079069184 |
|---|---|
| author | Cortellazzi Laura C. Teixeira Sara M. Borba Ronaldo Gervásio Sirlei Cintra Carmem S. Grotto Helena Z. W. |
| author_facet | Cortellazzi Laura C. Teixeira Sara M. Borba Ronaldo Gervásio Sirlei Cintra Carmem S. Grotto Helena Z. W. |
| author_sort | Cortellazzi Laura C. |
| collection | DOAJ |
| description | Flow cytometric reticulocyte analysis allows the evaluation of reticulocyte maturity. New reticulocyte parameters have been used in the diagnosis and management of anemias, in the bone marrow transplant setting and in the monitoring of iron replacement or erythropoiet in therapy. Reticulocyte numbers and maturation levels have been studied in different hemoglobinopathies and the results have been correlated with the degree of ineffective erythropoiesis. In order to verify differences in reticulocyte parameters in various types of anemias and to test the absolute number of immature reticulocytes as a possible discriminating factor among various types of anemias, reticulocyte counts were performed on 219 samples from patients with sickle cell anemia (SS) (n= 62), hemoglobin S trait (n=9), Sbeta thalassemia (n=7), hemoglobin SC disease (n=11), beta thalassemia trait (n=33) and iron deficiency anemia (n= 47), and non-anemic individuals (n= 50). Mean fluorescence index (MFI) was defined as representative of the degree of reticulocyte immaturity and it was evaluated as a percentage and in absolute values. Reticulocyte counts and MFI values were significantly higher in SS, Sbeta thalassemic and SC groups when compared to controls, but not different among the three anemia groups. Patients with hemoglobin S trait, iron deficiency anemia and beta thalassemia trait showed reticulocyte parameters similar to the non-anemic group. There was no difference between the b thalassemic trait and iron deficiency anemia in relation to any parameters. MFI in absolute numbers were significantly higher in anemias that develop with the hemolytic process, although this was not evident in MFI percentage values. Our results showed that the erythoid expansion in sickle cell diseases (SS, SC and Sb thalassemia) leads to an enhanced immature reticulocyte release from bone marrow and that the phenomena is more evident by the MFI counting in absolute figures than in percentages. We concluded that the assessment of reticulocyte maturity provides interesting data about the pathophysiology and erythopoietic response in different types of anemias. |
| first_indexed | 2024-12-12T09:58:53Z |
| format | Article |
| id | doaj.art-18c9c56b48674b8898c26cdd24b27517 |
| institution | Directory Open Access Journal |
| issn | 1516-8484 1806-0870 |
| language | English |
| last_indexed | 2024-12-12T09:58:53Z |
| publishDate | 2003-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Revista Brasileira de Hematologia e Hemoterapia |
| spelling | doaj.art-18c9c56b48674b8898c26cdd24b275172022-12-22T00:28:02ZengElsevierRevista Brasileira de Hematologia e Hemoterapia1516-84841806-08702003-01-0125297102Reticulocyte parameters in hemoglobinopathies and iron deficiency anemiaCortellazzi Laura C.Teixeira Sara M.Borba RonaldoGervásio SirleiCintra Carmem S.Grotto Helena Z. W.Flow cytometric reticulocyte analysis allows the evaluation of reticulocyte maturity. New reticulocyte parameters have been used in the diagnosis and management of anemias, in the bone marrow transplant setting and in the monitoring of iron replacement or erythropoiet in therapy. Reticulocyte numbers and maturation levels have been studied in different hemoglobinopathies and the results have been correlated with the degree of ineffective erythropoiesis. In order to verify differences in reticulocyte parameters in various types of anemias and to test the absolute number of immature reticulocytes as a possible discriminating factor among various types of anemias, reticulocyte counts were performed on 219 samples from patients with sickle cell anemia (SS) (n= 62), hemoglobin S trait (n=9), Sbeta thalassemia (n=7), hemoglobin SC disease (n=11), beta thalassemia trait (n=33) and iron deficiency anemia (n= 47), and non-anemic individuals (n= 50). Mean fluorescence index (MFI) was defined as representative of the degree of reticulocyte immaturity and it was evaluated as a percentage and in absolute values. Reticulocyte counts and MFI values were significantly higher in SS, Sbeta thalassemic and SC groups when compared to controls, but not different among the three anemia groups. Patients with hemoglobin S trait, iron deficiency anemia and beta thalassemia trait showed reticulocyte parameters similar to the non-anemic group. There was no difference between the b thalassemic trait and iron deficiency anemia in relation to any parameters. MFI in absolute numbers were significantly higher in anemias that develop with the hemolytic process, although this was not evident in MFI percentage values. Our results showed that the erythoid expansion in sickle cell diseases (SS, SC and Sb thalassemia) leads to an enhanced immature reticulocyte release from bone marrow and that the phenomena is more evident by the MFI counting in absolute figures than in percentages. We concluded that the assessment of reticulocyte maturity provides interesting data about the pathophysiology and erythopoietic response in different types of anemias.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842003000200005Reticulocytesickle cell diseaseanemia |
| spellingShingle | Cortellazzi Laura C. Teixeira Sara M. Borba Ronaldo Gervásio Sirlei Cintra Carmem S. Grotto Helena Z. W. Reticulocyte parameters in hemoglobinopathies and iron deficiency anemia Revista Brasileira de Hematologia e Hemoterapia Reticulocyte sickle cell disease anemia |
| title | Reticulocyte parameters in hemoglobinopathies and iron deficiency anemia |
| title_full | Reticulocyte parameters in hemoglobinopathies and iron deficiency anemia |
| title_fullStr | Reticulocyte parameters in hemoglobinopathies and iron deficiency anemia |
| title_full_unstemmed | Reticulocyte parameters in hemoglobinopathies and iron deficiency anemia |
| title_short | Reticulocyte parameters in hemoglobinopathies and iron deficiency anemia |
| title_sort | reticulocyte parameters in hemoglobinopathies and iron deficiency anemia |
| topic | Reticulocyte sickle cell disease anemia |
| url | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842003000200005 |
| work_keys_str_mv | AT cortellazzilaurac reticulocyteparametersinhemoglobinopathiesandirondeficiencyanemia AT teixeirasaram reticulocyteparametersinhemoglobinopathiesandirondeficiencyanemia AT borbaronaldo reticulocyteparametersinhemoglobinopathiesandirondeficiencyanemia AT gervasiosirlei reticulocyteparametersinhemoglobinopathiesandirondeficiencyanemia AT cintracarmems reticulocyteparametersinhemoglobinopathiesandirondeficiencyanemia AT grottohelenazw reticulocyteparametersinhemoglobinopathiesandirondeficiencyanemia |