HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://www.geneticsmr.com//year2007/vol6-2/pdf/gmr0312.pdf http://www.geneticsmr.com/articles/371 http://hdl.handle.net/11449/69878 |
Resumo: | The purpose of the present study was to establish reference values for hemoglobins (Hb) using HPLC, in samples containing normal Hb (AA), sickle cell trait without alpha-thalassemia (AS), sickle cell trait with alpha-thalassemia (ASH), sickle cell anemia (SS), and Hb SC disease (SC). The blood samples were analyzed by electrophoresis, HPLC and molecular procedures. The Hb A2 mean was 4.30 ± 0.44% in AS, 4.18 ± 0.42% in ASH, 3.90 ± 1.14% in SS, and 4.39 ± 0.35% in SC. They were similar, but above the normal range. Between the AS and ASH groups, only the amount of Hb S was higher in the AS group. The Hb S mean in the AS group was 38.54 ± 3.01% and in the ASH it was 36.54 ± 3.76%. In the qualitative analysis, using FastMap, distinct groups were seen: AA and SS located at opposite extremes, AS and ASH with overlapping values and intermediate distribution, SC between heterozygotes and the SS group. Hb S was confirmed by allele-specific polymerase chain reaction. The Hb values established will be available for use as a reference for the Brazilian population, drawing attention to the increased levels of Hb A2, which should be considered with caution to prevent incorrect diagnoses. ©FUNPEC-RP. |
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HPLC determination of hemoglobins to establish reference values with the aid of statistics and informaticsHemoglobinsHigh-performance liquid chromatographyReference valueshemoglobinhemoglobin Ahemoglobin A2hemoglobin Chemoglobin Fhemoglobin Salpha thalassemiablood samplingcontrolled studyelectrophoresishemoglobin determinationhigh performance liquid chromatographyhumanphenotypereference valuesickle cell anemiasickle cell traitalpha-ThalassemiaBrazilChromatography, High Pressure LiquidComputational BiologyElectrophoresisGenetic TechniquesHeterozygoteHumansModels, StatisticalMutationPhenotypeReference ValuesSickle Cell TraitThe purpose of the present study was to establish reference values for hemoglobins (Hb) using HPLC, in samples containing normal Hb (AA), sickle cell trait without alpha-thalassemia (AS), sickle cell trait with alpha-thalassemia (ASH), sickle cell anemia (SS), and Hb SC disease (SC). The blood samples were analyzed by electrophoresis, HPLC and molecular procedures. The Hb A2 mean was 4.30 ± 0.44% in AS, 4.18 ± 0.42% in ASH, 3.90 ± 1.14% in SS, and 4.39 ± 0.35% in SC. They were similar, but above the normal range. Between the AS and ASH groups, only the amount of Hb S was higher in the AS group. The Hb S mean in the AS group was 38.54 ± 3.01% and in the ASH it was 36.54 ± 3.76%. In the qualitative analysis, using FastMap, distinct groups were seen: AA and SS located at opposite extremes, AS and ASH with overlapping values and intermediate distribution, SC between heterozygotes and the SS group. Hb S was confirmed by allele-specific polymerase chain reaction. The Hb values established will be available for use as a reference for the Brazilian population, drawing attention to the increased levels of Hb A2, which should be considered with caution to prevent incorrect diagnoses. ©FUNPEC-RP.Laboratório de Hemoglobinas e Genética Das Doenças Hematológicas Departamento de Biologia IBILCE/UNESP, S. José do Rio Preto, SPGrupo de Banco de Dados Departamento de Ciências da Computação e Estatística IBILCE/UNESP, S. José do Rio Preto, SPLaboratório de Hemoglobinas e Genética Das Doenças Hematológicas Departamento de Biologia IBILCE/UNESP, S. José do Rio Preto, SPGrupo de Banco de Dados Departamento de Ciências da Computação e Estatística IBILCE/UNESP, S. José do Rio Preto, SPUniversidade Estadual Paulista (Unesp)Ondei, L. S. [UNESP]Zamaro, P. J A [UNESP]Mangonaro, P. H. [UNESP]Valêncio, C. R. [UNESP]Bonini-Domingos, C. R. [UNESP]2014-05-27T11:22:35Z2014-05-27T11:22:35Z2007-09-03info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article453-460application/pdfhttp://www.geneticsmr.com//year2007/vol6-2/pdf/gmr0312.pdfhttp://www.geneticsmr.com/articles/371Genetics and Molecular Research, v. 6, n. 2, p. 453-460, 2007.1676-5680http://hdl.handle.net/11449/69878WOS:0002516964000232-s2.0-345482938602-s2.0-34548293860.pdf32794280661767190000-0002-4603-9467Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengGenetics and Molecular Research0,439info:eu-repo/semantics/openAccess2023-12-08T06:17:50Zoai:repositorio.unesp.br:11449/69878Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:45:26.460380Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics |
title |
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics |
spellingShingle |
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics Ondei, L. S. [UNESP] Hemoglobins High-performance liquid chromatography Reference values hemoglobin hemoglobin A hemoglobin A2 hemoglobin C hemoglobin F hemoglobin S alpha thalassemia blood sampling controlled study electrophoresis hemoglobin determination high performance liquid chromatography human phenotype reference value sickle cell anemia sickle cell trait alpha-Thalassemia Brazil Chromatography, High Pressure Liquid Computational Biology Electrophoresis Genetic Techniques Heterozygote Humans Models, Statistical Mutation Phenotype Reference Values Sickle Cell Trait |
title_short |
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics |
title_full |
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics |
title_fullStr |
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics |
title_full_unstemmed |
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics |
title_sort |
HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics |
author |
Ondei, L. S. [UNESP] |
author_facet |
Ondei, L. S. [UNESP] Zamaro, P. J A [UNESP] Mangonaro, P. H. [UNESP] Valêncio, C. R. [UNESP] Bonini-Domingos, C. R. [UNESP] |
author_role |
author |
author2 |
Zamaro, P. J A [UNESP] Mangonaro, P. H. [UNESP] Valêncio, C. R. [UNESP] Bonini-Domingos, C. R. [UNESP] |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Ondei, L. S. [UNESP] Zamaro, P. J A [UNESP] Mangonaro, P. H. [UNESP] Valêncio, C. R. [UNESP] Bonini-Domingos, C. R. [UNESP] |
dc.subject.por.fl_str_mv |
Hemoglobins High-performance liquid chromatography Reference values hemoglobin hemoglobin A hemoglobin A2 hemoglobin C hemoglobin F hemoglobin S alpha thalassemia blood sampling controlled study electrophoresis hemoglobin determination high performance liquid chromatography human phenotype reference value sickle cell anemia sickle cell trait alpha-Thalassemia Brazil Chromatography, High Pressure Liquid Computational Biology Electrophoresis Genetic Techniques Heterozygote Humans Models, Statistical Mutation Phenotype Reference Values Sickle Cell Trait |
topic |
Hemoglobins High-performance liquid chromatography Reference values hemoglobin hemoglobin A hemoglobin A2 hemoglobin C hemoglobin F hemoglobin S alpha thalassemia blood sampling controlled study electrophoresis hemoglobin determination high performance liquid chromatography human phenotype reference value sickle cell anemia sickle cell trait alpha-Thalassemia Brazil Chromatography, High Pressure Liquid Computational Biology Electrophoresis Genetic Techniques Heterozygote Humans Models, Statistical Mutation Phenotype Reference Values Sickle Cell Trait |
description |
The purpose of the present study was to establish reference values for hemoglobins (Hb) using HPLC, in samples containing normal Hb (AA), sickle cell trait without alpha-thalassemia (AS), sickle cell trait with alpha-thalassemia (ASH), sickle cell anemia (SS), and Hb SC disease (SC). The blood samples were analyzed by electrophoresis, HPLC and molecular procedures. The Hb A2 mean was 4.30 ± 0.44% in AS, 4.18 ± 0.42% in ASH, 3.90 ± 1.14% in SS, and 4.39 ± 0.35% in SC. They were similar, but above the normal range. Between the AS and ASH groups, only the amount of Hb S was higher in the AS group. The Hb S mean in the AS group was 38.54 ± 3.01% and in the ASH it was 36.54 ± 3.76%. In the qualitative analysis, using FastMap, distinct groups were seen: AA and SS located at opposite extremes, AS and ASH with overlapping values and intermediate distribution, SC between heterozygotes and the SS group. Hb S was confirmed by allele-specific polymerase chain reaction. The Hb values established will be available for use as a reference for the Brazilian population, drawing attention to the increased levels of Hb A2, which should be considered with caution to prevent incorrect diagnoses. ©FUNPEC-RP. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-09-03 2014-05-27T11:22:35Z 2014-05-27T11:22:35Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://www.geneticsmr.com//year2007/vol6-2/pdf/gmr0312.pdf http://www.geneticsmr.com/articles/371 Genetics and Molecular Research, v. 6, n. 2, p. 453-460, 2007. 1676-5680 http://hdl.handle.net/11449/69878 WOS:000251696400023 2-s2.0-34548293860 2-s2.0-34548293860.pdf 3279428066176719 0000-0002-4603-9467 |
url |
http://www.geneticsmr.com//year2007/vol6-2/pdf/gmr0312.pdf http://www.geneticsmr.com/articles/371 http://hdl.handle.net/11449/69878 |
identifier_str_mv |
Genetics and Molecular Research, v. 6, n. 2, p. 453-460, 2007. 1676-5680 WOS:000251696400023 2-s2.0-34548293860 2-s2.0-34548293860.pdf 3279428066176719 0000-0002-4603-9467 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Genetics and Molecular Research 0,439 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
453-460 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129113619169280 |