Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysis
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10316/109360 https://doi.org/10.1155/2014/175286 |
Resumo: | We evaluated the potential cardiovascular risk protection of bilirubin in hemodialysis (HD) patients. An enlarged set of studies were evaluated in 191 HD patients, including hematological study, lipid profile, iron metabolism, nutritional, inflammatory markers, and dialysis adequacy. The TA duplication screening in the UDP-glucuronosyltransferase 1 A1 (UGT1A1) promoter region was also performed. The UGT1A1 genotype frequencies in HD patients were 49.2%, 42.4%, and 8.4% for 6/6, 6/7, and 7/7 genotypes, respectively. Although no difference was found in UGT1A1 genotype distribution between the three tertiles of bilirubin, significant differences were found with increasing bilirubin levels, namely, a decrease in platelet, leukocyte, and lymphocyte counts, transferrin, oxidized low-density lipoprotein (ox-LDL), ox-LDL/low-density lipoprotein cholesterol ratio, apolipoprotein (Apo) A, Apo B, and interleukin-6 serum levels and a significant increased concentration of hemoglobin, hematocrit, erythrocyte count, iron, transferrin saturation, Apo A/Apo B ratio, adiponectin, and paraoxonase 1 serum levels. After adjustment for age these results remained significant. Our data suggest that higher bilirubin levels are associated with beneficial effects in HD patients, by improving lipid profile and reducing the inflammatory grade, which might contribute to increase in iron availability. These results suggest a potential cardiovascular risk protection of bilirubin in HD patients. |
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Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysisAgedBilirubinCardiovascular DiseasesDemographyFemaleGlucuronosyltransferaseHumansKidney Failure, ChronicMalePolymorphism, GeneticPromoter Regions, GeneticRisk FactorsRenal DialysisWe evaluated the potential cardiovascular risk protection of bilirubin in hemodialysis (HD) patients. An enlarged set of studies were evaluated in 191 HD patients, including hematological study, lipid profile, iron metabolism, nutritional, inflammatory markers, and dialysis adequacy. The TA duplication screening in the UDP-glucuronosyltransferase 1 A1 (UGT1A1) promoter region was also performed. The UGT1A1 genotype frequencies in HD patients were 49.2%, 42.4%, and 8.4% for 6/6, 6/7, and 7/7 genotypes, respectively. Although no difference was found in UGT1A1 genotype distribution between the three tertiles of bilirubin, significant differences were found with increasing bilirubin levels, namely, a decrease in platelet, leukocyte, and lymphocyte counts, transferrin, oxidized low-density lipoprotein (ox-LDL), ox-LDL/low-density lipoprotein cholesterol ratio, apolipoprotein (Apo) A, Apo B, and interleukin-6 serum levels and a significant increased concentration of hemoglobin, hematocrit, erythrocyte count, iron, transferrin saturation, Apo A/Apo B ratio, adiponectin, and paraoxonase 1 serum levels. After adjustment for age these results remained significant. Our data suggest that higher bilirubin levels are associated with beneficial effects in HD patients, by improving lipid profile and reducing the inflammatory grade, which might contribute to increase in iron availability. These results suggest a potential cardiovascular risk protection of bilirubin in HD patients.Hindawi2014info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/109360http://hdl.handle.net/10316/109360https://doi.org/10.1155/2014/175286eng2314-61332314-6141Faria, Maria do SameiroKohlova, MichaelaRibeiro, SandraRocha-Pereira, PetronilaTeixeira, LaetitiaNascimento, HenriqueReis, FlávioMiranda, VascoBronze-da-Rocha, ElsaQuintanilha, AlexandreBelo, LuísCosta, ElísioSantos-Silva, Aliceinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-10-19T10:47:40Zoai:estudogeral.uc.pt:10316/109360Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:25:33.688982Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysis |
title |
Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysis |
spellingShingle |
Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysis Faria, Maria do Sameiro Aged Bilirubin Cardiovascular Diseases Demography Female Glucuronosyltransferase Humans Kidney Failure, Chronic Male Polymorphism, Genetic Promoter Regions, Genetic Risk Factors Renal Dialysis |
title_short |
Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysis |
title_full |
Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysis |
title_fullStr |
Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysis |
title_full_unstemmed |
Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysis |
title_sort |
Potential cardiovascular risk protection of bilirubin in end-stage renal disease patients under hemodialysis |
author |
Faria, Maria do Sameiro |
author_facet |
Faria, Maria do Sameiro Kohlova, Michaela Ribeiro, Sandra Rocha-Pereira, Petronila Teixeira, Laetitia Nascimento, Henrique Reis, Flávio Miranda, Vasco Bronze-da-Rocha, Elsa Quintanilha, Alexandre Belo, Luís Costa, Elísio Santos-Silva, Alice |
author_role |
author |
author2 |
Kohlova, Michaela Ribeiro, Sandra Rocha-Pereira, Petronila Teixeira, Laetitia Nascimento, Henrique Reis, Flávio Miranda, Vasco Bronze-da-Rocha, Elsa Quintanilha, Alexandre Belo, Luís Costa, Elísio Santos-Silva, Alice |
author2_role |
author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Faria, Maria do Sameiro Kohlova, Michaela Ribeiro, Sandra Rocha-Pereira, Petronila Teixeira, Laetitia Nascimento, Henrique Reis, Flávio Miranda, Vasco Bronze-da-Rocha, Elsa Quintanilha, Alexandre Belo, Luís Costa, Elísio Santos-Silva, Alice |
dc.subject.por.fl_str_mv |
Aged Bilirubin Cardiovascular Diseases Demography Female Glucuronosyltransferase Humans Kidney Failure, Chronic Male Polymorphism, Genetic Promoter Regions, Genetic Risk Factors Renal Dialysis |
topic |
Aged Bilirubin Cardiovascular Diseases Demography Female Glucuronosyltransferase Humans Kidney Failure, Chronic Male Polymorphism, Genetic Promoter Regions, Genetic Risk Factors Renal Dialysis |
description |
We evaluated the potential cardiovascular risk protection of bilirubin in hemodialysis (HD) patients. An enlarged set of studies were evaluated in 191 HD patients, including hematological study, lipid profile, iron metabolism, nutritional, inflammatory markers, and dialysis adequacy. The TA duplication screening in the UDP-glucuronosyltransferase 1 A1 (UGT1A1) promoter region was also performed. The UGT1A1 genotype frequencies in HD patients were 49.2%, 42.4%, and 8.4% for 6/6, 6/7, and 7/7 genotypes, respectively. Although no difference was found in UGT1A1 genotype distribution between the three tertiles of bilirubin, significant differences were found with increasing bilirubin levels, namely, a decrease in platelet, leukocyte, and lymphocyte counts, transferrin, oxidized low-density lipoprotein (ox-LDL), ox-LDL/low-density lipoprotein cholesterol ratio, apolipoprotein (Apo) A, Apo B, and interleukin-6 serum levels and a significant increased concentration of hemoglobin, hematocrit, erythrocyte count, iron, transferrin saturation, Apo A/Apo B ratio, adiponectin, and paraoxonase 1 serum levels. After adjustment for age these results remained significant. Our data suggest that higher bilirubin levels are associated with beneficial effects in HD patients, by improving lipid profile and reducing the inflammatory grade, which might contribute to increase in iron availability. These results suggest a potential cardiovascular risk protection of bilirubin in HD patients. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014 |
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://hdl.handle.net/10316/109360 http://hdl.handle.net/10316/109360 https://doi.org/10.1155/2014/175286 |
url |
http://hdl.handle.net/10316/109360 https://doi.org/10.1155/2014/175286 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2314-6133 2314-6141 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Hindawi |
publisher.none.fl_str_mv |
Hindawi |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799134138112933888 |