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Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population

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Resumo:The isoenzyme UDP-glucuronosyltransferase 1A1 (UGT1A1) catalyzes bilirubin glucuronidation by converting bilirubin in water-soluble glucuronides that then undergo biliary or renal elimination. During the last years, molecular studies have suggested that the presence of two extra bases in the repetitive promoter TATA box region of the UGT1A1 gene, described as (TA)7 allele, is responsible for the reduced UGT1A1 activity leading to hyperbilirubinemia. Gilbert’s syndrome (GS) is a genetic recessive disorder characterized by a mild unconjugated hyperbilirubinemia occurring in the absence of haemolysis or other evidence of liver disease. Patients with GS are often homozygous for the TA duplication. Several studies establish that unconjugated hyperbilirubinemia exhibits a mode of inheritance where a “major” recessive gene (UGT1A1) accounts for only a part of the serum bilirubin concentration. Recently, it was described that increased red cell mass probably plays a role in the pathogenesis of GS. Objective: Our study aims to determine the influence of the TA polymorphism, the presence of some environmental factors and increased red cell mass in serum bilirubin levels variation in Portuguese population. Material and Methods: We include in this study we recruit 165 young adults with average age (19.5 ± 2.1 years). All volunteers give their written informed consent and standardized interviewer-administered questionnaire was performed that included questions about smoking habits, oral contraceptive therapy, caloric intake, fasting time and physical activity. Exclusion criteria included the presence of liver and/or hematological disorders. After an overnight fasting, venous blood samples were collected in order to determine total and direct-reacting bilirubin, blood cell count and surrogate markers and isolate genomic DNA to perform the molecular study of UGT1A1 promoter region. Results: For the UGT1A1 genotyping we identified 15 homozygous individuals for (TA7/TA7), 79 heterozygous (TA6/TA7) and 71 were homozygous for the normal allele (TA6/TA6). Estimated frequency of (TA) was 33%, close to the 38,7% described for caucasians. A trend to higher bilirubin levels, without statistical significance, was found in males than in females, in non-smoking subjects and in female subjects that were under oral contraceptive therapy. Statistically significant correlations were found between bilirubin serum levels and fasting time (p=0.001) and caloric intake (p=0.03). No significant association was found between serum bilirrubin levels and physical activity. Our results strongly suggest that genetic background plays a major role in serum bilirubin levels variation but caloric intake, fasting time and red blood cell mass also contribute to this inter-individual variation. Conclusions: Our results strongly suggest that genetic background plays a major role in serum bilirubin levels variation but red blood mass and fasting time contribute to this inter-individual variation.
Autores principais:Rodrigues, Carina
Outros Autores:Costa, Elísio; Santos, Rosário; Santos-Silva, Alice; Bronze-da-Rocha, Elsa
Assunto:Bilirubin Genetic and aquired factors
Ano:2010
País:Portugal
Tipo de documento:póster em conferência
Tipo de acesso:acesso aberto
Instituição associada:Instituto Politécnico de Bragança
Idioma:inglês
Origem:Biblioteca Digital do IPB
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author Rodrigues, Carina
author2 Costa, Elísio
Santos, Rosário
Santos-Silva, Alice
Bronze-da-Rocha, Elsa
author2_role author
author
author
author
author_facet Rodrigues, Carina
Costa, Elísio
Santos, Rosário
Santos-Silva, Alice
Bronze-da-Rocha, Elsa
author_role author
contributor_name_str_mv Biblioteca Digital do IPB
country_str PT
creators_json_txt [{\"Person.name\":\"Rodrigues, Carina\",\"Person.identifier.orcid\":\"0000-0001-9773-1413\"},{\"Person.name\":\"Costa, Elísio\"},{\"Person.name\":\"Santos, Rosário\"},{\"Person.name\":\"Santos-Silva, Alice\"},{\"Person.name\":\"Bronze-da-Rocha, Elsa\"}]
datacite.contributors.contributor.contributorName.fl_str_mv Biblioteca Digital do IPB
datacite.creators.creator.creatorName.fl_str_mv Rodrigues, Carina
Costa, Elísio
Santos, Rosário
Santos-Silva, Alice
Bronze-da-Rocha, Elsa
datacite.date.Accepted.fl_str_mv 2010-01-01T00:00:00Z
datacite.date.available.fl_str_mv 2012-06-28T15:38:50Z
datacite.date.embargoed.fl_str_mv 2012-06-28T15:38:50Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv Bilirubin
Genetic and aquired factors
datacite.titles.title.fl_str_mv Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population
dc.contributor.none.fl_str_mv Biblioteca Digital do IPB
dc.creator.none.fl_str_mv Rodrigues, Carina
Costa, Elísio
Santos, Rosário
Santos-Silva, Alice
Bronze-da-Rocha, Elsa
dc.date.Accepted.fl_str_mv 2010-01-01T00:00:00Z
dc.date.available.fl_str_mv 2012-06-28T15:38:50Z
dc.date.embargoed.fl_str_mv 2012-06-28T15:38:50Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv http://hdl.handle.net/10198/7087
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Universidade do Algarve
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.subject.none.fl_str_mv Bilirubin
Genetic and aquired factors
dc.title.fl_str_mv Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6670
description The isoenzyme UDP-glucuronosyltransferase 1A1 (UGT1A1) catalyzes bilirubin glucuronidation by converting bilirubin in water-soluble glucuronides that then undergo biliary or renal elimination. During the last years, molecular studies have suggested that the presence of two extra bases in the repetitive promoter TATA box region of the UGT1A1 gene, described as (TA)7 allele, is responsible for the reduced UGT1A1 activity leading to hyperbilirubinemia. Gilbert’s syndrome (GS) is a genetic recessive disorder characterized by a mild unconjugated hyperbilirubinemia occurring in the absence of haemolysis or other evidence of liver disease. Patients with GS are often homozygous for the TA duplication. Several studies establish that unconjugated hyperbilirubinemia exhibits a mode of inheritance where a “major” recessive gene (UGT1A1) accounts for only a part of the serum bilirubin concentration. Recently, it was described that increased red cell mass probably plays a role in the pathogenesis of GS. Objective: Our study aims to determine the influence of the TA polymorphism, the presence of some environmental factors and increased red cell mass in serum bilirubin levels variation in Portuguese population. Material and Methods: We include in this study we recruit 165 young adults with average age (19.5 ± 2.1 years). All volunteers give their written informed consent and standardized interviewer-administered questionnaire was performed that included questions about smoking habits, oral contraceptive therapy, caloric intake, fasting time and physical activity. Exclusion criteria included the presence of liver and/or hematological disorders. After an overnight fasting, venous blood samples were collected in order to determine total and direct-reacting bilirubin, blood cell count and surrogate markers and isolate genomic DNA to perform the molecular study of UGT1A1 promoter region. Results: For the UGT1A1 genotyping we identified 15 homozygous individuals for (TA7/TA7), 79 heterozygous (TA6/TA7) and 71 were homozygous for the normal allele (TA6/TA6). Estimated frequency of (TA) was 33%, close to the 38,7% described for caucasians. A trend to higher bilirubin levels, without statistical significance, was found in males than in females, in non-smoking subjects and in female subjects that were under oral contraceptive therapy. Statistically significant correlations were found between bilirubin serum levels and fasting time (p=0.001) and caloric intake (p=0.03). No significant association was found between serum bilirrubin levels and physical activity. Our results strongly suggest that genetic background plays a major role in serum bilirubin levels variation but caloric intake, fasting time and red blood cell mass also contribute to this inter-individual variation. Conclusions: Our results strongly suggest that genetic background plays a major role in serum bilirubin levels variation but red blood mass and fasting time contribute to this inter-individual variation.
dirty 0
eu_rights_str_mv openAccess
format conferencePoster
fulltext.url.fl_str_mv https://bibliotecadigital.ipb.pt/bitstreams/b42904d1-afc2-4760-973d-022e4e5791d1/download
id ipb_01c2dae8a58d43718a8f3457fa2b709b
identifier.url.fl_str_mv http://hdl.handle.net/10198/7087
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institution Instituto Politécnico de Bragança
instname_str Instituto Politécnico de Bragança
language eng
network_acronym_str ipb
network_name_str Biblioteca Digital do IPB
oai_identifier_str oai:bibliotecadigital.ipb.pt:10198/7087
organization_str_mv urn:organizationAcronym:ipb
person_str_mv Rodrigues, Carina
Rodrigues, Carina
https://www.ciencia-id.pt/C415-C677-0253
C415-C677-0253
http://orcid.org/0000-0001-9773-1413
0000-0001-9773-1413
Costa, Elísio
Santos, Rosário
Santos-Silva, Alice
Bronze-da-Rocha, Elsa
publishDate 2010
publisher.none.fl_str_mv Universidade do Algarve
reponame_str Biblioteca Digital do IPB
repository_id_str urn:repositoryAcronym:ipb
service_str_mv urn:repositoryAcronym:ipb
spelling engUniversidade do AlgarveporThe isoenzyme UDP-glucuronosyltransferase 1A1 (UGT1A1) catalyzes bilirubin glucuronidation by converting bilirubin in water-soluble glucuronides that then undergo biliary or renal elimination. During the last years, molecular studies have suggested that the presence of two extra bases in the repetitive promoter TATA box region of the UGT1A1 gene, described as (TA)7 allele, is responsible for the reduced UGT1A1 activity leading to hyperbilirubinemia. Gilbert’s syndrome (GS) is a genetic recessive disorder characterized by a mild unconjugated hyperbilirubinemia occurring in the absence of haemolysis or other evidence of liver disease. Patients with GS are often homozygous for the TA duplication. Several studies establish that unconjugated hyperbilirubinemia exhibits a mode of inheritance where a “major” recessive gene (UGT1A1) accounts for only a part of the serum bilirubin concentration. Recently, it was described that increased red cell mass probably plays a role in the pathogenesis of GS. Objective: Our study aims to determine the influence of the TA polymorphism, the presence of some environmental factors and increased red cell mass in serum bilirubin levels variation in Portuguese population. Material and Methods: We include in this study we recruit 165 young adults with average age (19.5 ± 2.1 years). All volunteers give their written informed consent and standardized interviewer-administered questionnaire was performed that included questions about smoking habits, oral contraceptive therapy, caloric intake, fasting time and physical activity. Exclusion criteria included the presence of liver and/or hematological disorders. After an overnight fasting, venous blood samples were collected in order to determine total and direct-reacting bilirubin, blood cell count and surrogate markers and isolate genomic DNA to perform the molecular study of UGT1A1 promoter region. Results: For the UGT1A1 genotyping we identified 15 homozygous individuals for (TA7/TA7), 79 heterozygous (TA6/TA7) and 71 were homozygous for the normal allele (TA6/TA6). Estimated frequency of (TA) was 33%, close to the 38,7% described for caucasians. A trend to higher bilirubin levels, without statistical significance, was found in males than in females, in non-smoking subjects and in female subjects that were under oral contraceptive therapy. Statistically significant correlations were found between bilirubin serum levels and fasting time (p=0.001) and caloric intake (p=0.03). No significant association was found between serum bilirrubin levels and physical activity. Our results strongly suggest that genetic background plays a major role in serum bilirubin levels variation but caloric intake, fasting time and red blood cell mass also contribute to this inter-individual variation. Conclusions: Our results strongly suggest that genetic background plays a major role in serum bilirubin levels variation but red blood mass and fasting time contribute to this inter-individual variation.application/pdfporInfluence of genetic and aquired factors that modify serum bilirubin levels in the portuguese populationPersonalRodrigues, CarinaDSpacehttp://dspace.org/items/ef666665-6593-48be-bc48-6a1bb58bedbdDSpacehttp://dspace.org/items/ef666665-6593-48be-bc48-6a1bb58bedbdRodriguesCarinaCiência IDhttps://www.ciencia-id.ptC415-C677-0253ORCIDhttp://orcid.org0000-0001-9773-1413Costa, ElísioSantos, RosárioSantos-Silva, AliceBronze-da-Rocha, ElsaHostingInstitutionOrganizationalBiblioteca Digital do IPBe-mailmailto:dspace@ipb.ptdspace@ipb.pt2012-06-28T15:38:50Z20102010-01-01T00:00:00ZHandlehttp://hdl.handle.net/10198/7087http://purl.org/coar/access_right/c_abf2open accessBilirubinGenetic and aquired factors4929959 bytesother research producthttp://purl.org/coar/resource_type/c_6670conference posterhttp://purl.org/coar/access_right/c_abf2application/pdffulltexthttps://bibliotecadigital.ipb.pt/bitstreams/b42904d1-afc2-4760-973d-022e4e5791d1/downloadIV SPB Clinical Biochemistry Workshop,Universidade do Algarve
spellingShingle Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population
Rodrigues, Carina
Bilirubin
Genetic and aquired factors
status SINGLETON
subject.fl_str_mv Bilirubin
Genetic and aquired factors
title Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population
title_full Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population
title_fullStr Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population
title_full_unstemmed Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population
title_short Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population
title_sort Influence of genetic and aquired factors that modify serum bilirubin levels in the portuguese population
topic Bilirubin
Genetic and aquired factors
topic_facet Bilirubin
Genetic and aquired factors
url http://hdl.handle.net/10198/7087
visible 1