HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics

Detalhes bibliográficos
Autor(a) principal: Ondei, L. S. [UNESP]
Data de Publicação: 2007
Outros Autores: Zamaro, P. J A [UNESP], Mangonaro, P. H. [UNESP], Valêncio, C. R. [UNESP], Bonini-Domingos, C. R. [UNESP]
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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spelling 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
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