Hemoglobins of African origin in quilombola communities of Tocantins State, Brazil

Bibliographic Details
Main Author: Teles, Annyelle Figueredo
Publication Date: 2019
Other Authors: Silva, Luciana da Costa da, Silva, Amanda Cordeiro da, Souza, Lidiane Oliveira de, Santos, Márcio Galdino dos, Seibert, Carla Simone
Format: Article
Language: por
Source: Revista Pan-Amazônica de Saúde (RPAS)
Download full: https://ojs.iec.gov.br/rpas/article/view/414
Summary: OBJECTIVE: To verify the incidence of hemoglobins of African descent (HbS and HbC) in quilombola communities in Tocantins State, Brazil. MATERIALS AND METHODS: Blood samples were collected from 14 quilombola communities in the State; the screening was performed in cellulose acetate electrophoresis (pH 8.6), and those samples with altered standard were submitted to high performance liquid chromatography, recording gender and age of the quilombola people. RESULTS: The analysis of the results showed that of the 822 quilombolas investigated 95 presented abnormal hemoglobins, 0.5% with sickle cell disease (HbSS); 5.7% for hemoglobin S trait (HbAS); 4.9% for hemoglobin C trait (HbAC); 0.2% with increased fetal hemoglobin; 0.1% with increased hemoglobin A2; and 88.4% with normal hemoglobin (HbAA). HbSS was observed in infant and adolescent groups and HbAS and HbAC in all age groups. About sex, it was not possible to suggest the maternal effect for HbS due to the greater quantitative of males with this genetic information. CONCLUSION: In the current study the incidence of HbS and HbC observed in quilombola communities was within the expected range for the Northern Region of Brazil. However, the high prevalence of sickle cell disease and the high frequency of sickle cell trait were highlighted in some quilombola communities with special attention to the southern region of the State. Thus, the results presented in this study indicate an imminent risk for the increased incidence of that disease in Tocantins.
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spelling Hemoglobins of African origin in quilombola communities of Tocantins State, BrazilHemoglobinas de origen africana en comunidades quilombolas del Estado de Tocantins, BrasilHemoglobinas de origem africana em comunidades quilombolas do estado do Tocantins, BrasilSickle Cell AnemiaSickle Cell TraitHemoglobin CSickle HemoglobinAnemia FalciformeTraço FalciformeHemoglobina CHemoglobina FalciformeAnemia FalciformeTrazo FalciformeHemoglobina CHemoglobina Falciforme OBJECTIVE: To verify the incidence of hemoglobins of African descent (HbS and HbC) in quilombola communities in Tocantins State, Brazil. MATERIALS AND METHODS: Blood samples were collected from 14 quilombola communities in the State; the screening was performed in cellulose acetate electrophoresis (pH 8.6), and those samples with altered standard were submitted to high performance liquid chromatography, recording gender and age of the quilombola people. RESULTS: The analysis of the results showed that of the 822 quilombolas investigated 95 presented abnormal hemoglobins, 0.5% with sickle cell disease (HbSS); 5.7% for hemoglobin S trait (HbAS); 4.9% for hemoglobin C trait (HbAC); 0.2% with increased fetal hemoglobin; 0.1% with increased hemoglobin A2; and 88.4% with normal hemoglobin (HbAA). HbSS was observed in infant and adolescent groups and HbAS and HbAC in all age groups. About sex, it was not possible to suggest the maternal effect for HbS due to the greater quantitative of males with this genetic information. CONCLUSION: In the current study the incidence of HbS and HbC observed in quilombola communities was within the expected range for the Northern Region of Brazil. However, the high prevalence of sickle cell disease and the high frequency of sickle cell trait were highlighted in some quilombola communities with special attention to the southern region of the State. Thus, the results presented in this study indicate an imminent risk for the increased incidence of that disease in Tocantins. OBJETIVO: Verificar la incidencia de hemoglobinas de herencia africana en comunidades quilombolas del Estado de Tocantins, Brasil. MATERIALES Y MÉTODOS: Se recolectó sangre de quilombolas en 14 comunidades del Estado; la selección se hizo en electroforesis de acetato de celulosa (pH 8,6), y las de patrón alterado fueron sometidas a la cromatografía líquida de alta eficiencia (CLAE), registrándose el género y la edad de las personas del muestreo. RESULTADOS: El análisis de los resultados demostró que, de los 822 quilombolas investigados, 95 presentaron hemoglobinas anormales, siendo 0,5% con enfermedad falciforme (HbSS); 5,7% trazo para hemoglobina S (HbAS); 4,9% trazo para hemoglobina C (HbAC); 0,2% con hemoglobina fetal aumentada; 0,1% con hemoglobina A2 aumentada; y 88,4% con hemoglobina normal (HbAA). La enfermedad falciforme se observó en la franja etaria infantil y adolescente y el trazo para HbS y HbC en todas las franjas etarias. En relación al sexo, no fue posible sugerir el efecto materno para HbS debido al mayor número de personas del sexo masculino con esa información genética. CONCLUSIÓN: En este estudio, la incidencia de las HbS y HbC, observada en las comunidades quilombolas, estuvo dentro de lo esperado para la Región Norte de Brasil. Sin embargo, se destaca la elevada prevalencia de la enfermedad falciforme y la elevada frecuencia de trazos falciformes en algunas de las comunidades estudiadas, con especial atención para la región sur del Estado. De ese modo, los resultados aquí presentados señalan riesgo inminente para el aumento de la incidencia de la enfermedad en Tocantins. OBJETIVO: Verificar a incidência de hemoglobinas de descendência africana (HbS e HbC) em comunidades quilombolas do estado do Tocantins, Brasil. MATERIAIS E MÉTODOS: Foi coletado o sangue de quilombolas em 14 comunidades do Estado; a triagem foi realizada em eletroforese de acetato de celulose (pH 8,6), e aquelas com padrão alterado foram submetidas à cromatografia líquida de alta eficiência, sendo registrados o gênero e a idade das pessoas amostradas. RESULTADOS: A análise dos resultados demonstrou que, dos 822 quilombolas investigados, 95 apresentaram hemoglobinas anormais, sendo 0,5% com doença falciforme (HbSS); 5,7% traço para hemoglobina S (HbAS); 4,9% traço para hemoglobina C (HbAC); 0,2% com hemoglobina fetal aumentada; 0,1% com hemoglobina A2 aumentada; e 88,4% com hemoglobina normal (HbAA). HbSS foi observada na faixa etária infantil e adolescente e HbAS e HbAC em todas as faixas etárias. Em relação ao sexo, não foi possível sugerir o efeito materno para HbS, devido ao maior quantitativo de pessoas do sexo masculino com essa informação genética. CONCLUSÃO: Neste estudo, a incidência das HbS e HbC, observada nas comunidades quilombolas, esteve dentro do esperado para a Região Norte do Brasil. No entanto, destacam-se a elevada prevalência da doença falciforme e a grande frequência de traço falciforme em algumas das comunidades estudadas, com atenção especial para a região sul do Estado. Desse modo, os resultados aqui apresentados sinalizam risco iminente para o aumento da incidência da doença no Tocantins. Instituto Evandro Chagas/SCTIE/MS2019-06-25info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/xmlapplication/pdfhttps://ojs.iec.gov.br/rpas/article/view/41410.5123/S2176-62232017000100006Revista Pan-Amazônica de Saúde; v. 8 n. 1 (2017); 8Pan-Amazonian Journal of Health; Vol. 8 No. 1 (2017); 8Revista Pan-Amazônica de Saúde; Vol. 8 Núm. 1 (2017); 82176-62232176-6215reponame:Revista Pan-Amazônica de Saúde (RPAS)instname:Instituto Evandro Chagas (IEC)instacron:IECporhttps://ojs.iec.gov.br/rpas/article/view/414/339https://ojs.iec.gov.br/rpas/article/view/414/340Teles, Annyelle FigueredoSilva, Luciana da Costa daSilva, Amanda Cordeiro daSouza, Lidiane Oliveira deSantos, Márcio Galdino dosSeibert, Carla Simoneinfo:eu-repo/semantics/openAccess2021-01-01T17:57:52Zoai:revista.iec.gov.br:article/414Revistahttp://revista.iec.gov.br/PRIhttps://ojs.iec.gov.br/index.php/rpas/oairevista@iec.gov.br2176-62152176-6223opendoar:2021-01-01T17:57:52Revista Pan-Amazônica de Saúde (RPAS) - Instituto Evandro Chagas (IEC)false
dc.title.none.fl_str_mv Hemoglobins of African origin in quilombola communities of Tocantins State, Brazil
Hemoglobinas de origen africana en comunidades quilombolas del Estado de Tocantins, Brasil
Hemoglobinas de origem africana em comunidades quilombolas do estado do Tocantins, Brasil
title Hemoglobins of African origin in quilombola communities of Tocantins State, Brazil
spellingShingle Hemoglobins of African origin in quilombola communities of Tocantins State, Brazil
Teles, Annyelle Figueredo
Sickle Cell Anemia
Sickle Cell Trait
Hemoglobin C
Sickle Hemoglobin
Anemia Falciforme
Traço Falciforme
Hemoglobina C
Hemoglobina Falciforme
Anemia Falciforme
Trazo Falciforme
Hemoglobina C
Hemoglobina Falciforme
title_short Hemoglobins of African origin in quilombola communities of Tocantins State, Brazil
title_full Hemoglobins of African origin in quilombola communities of Tocantins State, Brazil
title_fullStr Hemoglobins of African origin in quilombola communities of Tocantins State, Brazil
title_full_unstemmed Hemoglobins of African origin in quilombola communities of Tocantins State, Brazil
title_sort Hemoglobins of African origin in quilombola communities of Tocantins State, Brazil
author Teles, Annyelle Figueredo
author_facet Teles, Annyelle Figueredo
Silva, Luciana da Costa da
Silva, Amanda Cordeiro da
Souza, Lidiane Oliveira de
Santos, Márcio Galdino dos
Seibert, Carla Simone
author_role author
author2 Silva, Luciana da Costa da
Silva, Amanda Cordeiro da
Souza, Lidiane Oliveira de
Santos, Márcio Galdino dos
Seibert, Carla Simone
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Teles, Annyelle Figueredo
Silva, Luciana da Costa da
Silva, Amanda Cordeiro da
Souza, Lidiane Oliveira de
Santos, Márcio Galdino dos
Seibert, Carla Simone
dc.subject.por.fl_str_mv Sickle Cell Anemia
Sickle Cell Trait
Hemoglobin C
Sickle Hemoglobin
Anemia Falciforme
Traço Falciforme
Hemoglobina C
Hemoglobina Falciforme
Anemia Falciforme
Trazo Falciforme
Hemoglobina C
Hemoglobina Falciforme
topic Sickle Cell Anemia
Sickle Cell Trait
Hemoglobin C
Sickle Hemoglobin
Anemia Falciforme
Traço Falciforme
Hemoglobina C
Hemoglobina Falciforme
Anemia Falciforme
Trazo Falciforme
Hemoglobina C
Hemoglobina Falciforme
description OBJECTIVE: To verify the incidence of hemoglobins of African descent (HbS and HbC) in quilombola communities in Tocantins State, Brazil. MATERIALS AND METHODS: Blood samples were collected from 14 quilombola communities in the State; the screening was performed in cellulose acetate electrophoresis (pH 8.6), and those samples with altered standard were submitted to high performance liquid chromatography, recording gender and age of the quilombola people. RESULTS: The analysis of the results showed that of the 822 quilombolas investigated 95 presented abnormal hemoglobins, 0.5% with sickle cell disease (HbSS); 5.7% for hemoglobin S trait (HbAS); 4.9% for hemoglobin C trait (HbAC); 0.2% with increased fetal hemoglobin; 0.1% with increased hemoglobin A2; and 88.4% with normal hemoglobin (HbAA). HbSS was observed in infant and adolescent groups and HbAS and HbAC in all age groups. About sex, it was not possible to suggest the maternal effect for HbS due to the greater quantitative of males with this genetic information. CONCLUSION: In the current study the incidence of HbS and HbC observed in quilombola communities was within the expected range for the Northern Region of Brazil. However, the high prevalence of sickle cell disease and the high frequency of sickle cell trait were highlighted in some quilombola communities with special attention to the southern region of the State. Thus, the results presented in this study indicate an imminent risk for the increased incidence of that disease in Tocantins.
publishDate 2019
dc.date.none.fl_str_mv 2019-06-25
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://ojs.iec.gov.br/rpas/article/view/414
10.5123/S2176-62232017000100006
url https://ojs.iec.gov.br/rpas/article/view/414
identifier_str_mv 10.5123/S2176-62232017000100006
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://ojs.iec.gov.br/rpas/article/view/414/339
https://ojs.iec.gov.br/rpas/article/view/414/340
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/xml
application/pdf
dc.publisher.none.fl_str_mv Instituto Evandro Chagas/SCTIE/MS
publisher.none.fl_str_mv Instituto Evandro Chagas/SCTIE/MS
dc.source.none.fl_str_mv Revista Pan-Amazônica de Saúde; v. 8 n. 1 (2017); 8
Pan-Amazonian Journal of Health; Vol. 8 No. 1 (2017); 8
Revista Pan-Amazônica de Saúde; Vol. 8 Núm. 1 (2017); 8
2176-6223
2176-6215
reponame:Revista Pan-Amazônica de Saúde (RPAS)
instname:Instituto Evandro Chagas (IEC)
instacron:IEC
instname_str Instituto Evandro Chagas (IEC)
instacron_str IEC
institution IEC
reponame_str Revista Pan-Amazônica de Saúde (RPAS)
collection Revista Pan-Amazônica de Saúde (RPAS)
repository.name.fl_str_mv Revista Pan-Amazônica de Saúde (RPAS) - Instituto Evandro Chagas (IEC)
repository.mail.fl_str_mv revista@iec.gov.br
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