Alterações renais em pacientes com doença falciforme

Bibliographic Details
Main Author: Silva Júnior, Geraldo Bezerra da
Publication Date: 2013
Format: Doctoral thesis
Language: por
Source: Repositório Institucional da Universidade Federal do Ceará (UFC)
dARK ID: ark:/83112/001300001d19q
Download full: http://www.repositorio.ufc.br/handle/riufc/6919
Summary: Background - Kidney abnormalities are one of the main chronic complications of sickle cell disease (SCD). The aim of this study is to investigate the occurrence of renal abnormalities among patients with SCD. Methods - This is a cohort study with 26 SCD patients followed in a medical center in Fortaleza, Ceará, Brazil. Urinary acidification and concentration tests were performed using calcium chloride (CaCl2), and after a 12h period of water and food deprivation. Fractional excretion of sodium (FENa), transtubular potassium gradient (TTKG) and solute free water reabsorption (TcH2O) were calculated. The SCD group was compared to a group of 15 healthy volunteers (control group). Aquaporin-2 (AQP2) and renal outer medullary K+ channels (ROMK) were quantified through exosomes search in urine. Results - Patient`s average age and gender were similar to controls. Urinary acidification deficit was found in 5 SCD patients (19.2%), who presented urinary pH > 5.5 after CaCl2 test. Urinary osmolality was significantly lower in SCD patients (355±60 vs. 818±202mOsm/kg, p=0.0001, after 12h period water deprivation). Urinary concentration deficit was found in all SCD patients (100%). FENa was higher among SCD patients (0.75±0.3 vs. 0.55±0.2%, p=0.02). The TTKG was higher in SCD patients (5.5±2.5 vs. 3.0±1.5, p=0.001), and TcH2O was lower (0.22±0.3 vs. 1.1±0.3L/day, p=0.0001). The search for AQP2 did not show significant difference between SCD patients and control group (102±6.0 vs. 100±7.2%, p=0.874), as well as for ROMK (172±38 vs. 100±25%, p=0.207). Conclusions - SCD is associated with important kidney dysfunction. The main abnormalities found were urinary concentrating and incomplete distal acidification defect. There was also an increase in the potassium transport and decrease in water transport, evidencing the occurrence of distal tubular dysfunction.
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spelling Alterações renais em pacientes com doença falciformeRenal abnormalities in patients with sickle cell diseaseDoença da Hemoglobina SCTaxa de Filtração GlomerularFalência Renal CrônicaBackground - Kidney abnormalities are one of the main chronic complications of sickle cell disease (SCD). The aim of this study is to investigate the occurrence of renal abnormalities among patients with SCD. Methods - This is a cohort study with 26 SCD patients followed in a medical center in Fortaleza, Ceará, Brazil. Urinary acidification and concentration tests were performed using calcium chloride (CaCl2), and after a 12h period of water and food deprivation. Fractional excretion of sodium (FENa), transtubular potassium gradient (TTKG) and solute free water reabsorption (TcH2O) were calculated. The SCD group was compared to a group of 15 healthy volunteers (control group). Aquaporin-2 (AQP2) and renal outer medullary K+ channels (ROMK) were quantified through exosomes search in urine. Results - Patient`s average age and gender were similar to controls. Urinary acidification deficit was found in 5 SCD patients (19.2%), who presented urinary pH > 5.5 after CaCl2 test. Urinary osmolality was significantly lower in SCD patients (355±60 vs. 818±202mOsm/kg, p=0.0001, after 12h period water deprivation). Urinary concentration deficit was found in all SCD patients (100%). FENa was higher among SCD patients (0.75±0.3 vs. 0.55±0.2%, p=0.02). The TTKG was higher in SCD patients (5.5±2.5 vs. 3.0±1.5, p=0.001), and TcH2O was lower (0.22±0.3 vs. 1.1±0.3L/day, p=0.0001). The search for AQP2 did not show significant difference between SCD patients and control group (102±6.0 vs. 100±7.2%, p=0.874), as well as for ROMK (172±38 vs. 100±25%, p=0.207). Conclusions - SCD is associated with important kidney dysfunction. The main abnormalities found were urinary concentrating and incomplete distal acidification defect. There was also an increase in the potassium transport and decrease in water transport, evidencing the occurrence of distal tubular dysfunction.Introdução - Alterações renais representam uma das complicações crônicas principais da doença falciforme (DF). O objetivo deste estudo é investigar a ocorrência de alterações renais em pacientes com DF. Métodos - Foi realizado estudo de coorte com 26 pacientes com DF acompanhados em um ambulatório de Fortaleza, Ceará, Brasil. Testes de acidificação e concentração urinárias foram realizados usando cloreto de cálcio (CaCl2) e após período de 12h de jejum e privação hídrica. Foram calculados fração de excreção de sódio (FENa), transporte transtubular de potássio (TTKG) e transporte de água livre de solutos (TcH2O). O grupo de pacientes com DF foi comparado com um grupo de 15 voluntários sadios (grupo controle). Os transportadores aquaporina-2 (AQP2) e canal de K+ apical (ROMK) foram quantificados pela pesquisa de exossomas na urina. Resultados - A média de idade e a distribuição de gênero foi similar entre os dois grupos. Déficit de acidificação urinária foi encontrada em 5 pacientes com DF (19,2%), que apresentaram pH urinário > 5,5 após o teste com CaCl2. A osmolaridade urinária foi significativamente menor entre os pacientes com DF (355±60 vs. 818±202mOsm/kg, p=0,0001, após período de 12h de jejum e privação hídrica). Déficit de concentração urinária foi encontrado em todos os casos de DF (100%). A FENa foi maior entre os pacientes com DF (0,75±0,3 vs. 0,55±0,2%, p=0,02). O TTKG também foi maior nos pacientes com DF (5,5±2,5 vs. 3,0±1,5, p=0,001), e o TcH2O foi menor (0,22±0,3 vs. 1,1±0,3L/dia, p=0,0001). A pesquisa de AQP2 não mostrou diferença significativa em relação ao grupo controle (102±6,0 vs. 100±7,2%, p=0,874), bem como a do canal ROMK (172±38 vs. 100±25%, p=0,207). Conclusão - A DF é associada a importantes alterações renais. As principais alterações encontradas foram déficit de concentração e acidificação urinária. Foi ainda observado aumento no transporteDaher, Elizabeth de FrancescoSilva Júnior, Geraldo Bezerra da2013-12-09T12:23:23Z2013-12-09T12:23:23Z2013info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfSILVA JUNIOR, Geraldo Bezerra da. Alterações renais em pacientes com doença falciforme. 2013. 136 f. Tese (Doutorado em Ciências Médicas) - Universidade Federal do Ceará. Faculdade de Medicina, Fortaleza, 2013.http://www.repositorio.ufc.br/handle/riufc/6919ark:/83112/001300001d19qporreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2022-03-04T18:02:11Zoai:repositorio.ufc.br:riufc/6919Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2022-03-04T18:02:11Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.none.fl_str_mv Alterações renais em pacientes com doença falciforme
Renal abnormalities in patients with sickle cell disease
title Alterações renais em pacientes com doença falciforme
spellingShingle Alterações renais em pacientes com doença falciforme
Silva Júnior, Geraldo Bezerra da
Doença da Hemoglobina SC
Taxa de Filtração Glomerular
Falência Renal Crônica
title_short Alterações renais em pacientes com doença falciforme
title_full Alterações renais em pacientes com doença falciforme
title_fullStr Alterações renais em pacientes com doença falciforme
title_full_unstemmed Alterações renais em pacientes com doença falciforme
title_sort Alterações renais em pacientes com doença falciforme
author Silva Júnior, Geraldo Bezerra da
author_facet Silva Júnior, Geraldo Bezerra da
author_role author
dc.contributor.none.fl_str_mv Daher, Elizabeth de Francesco
dc.contributor.author.fl_str_mv Silva Júnior, Geraldo Bezerra da
dc.subject.por.fl_str_mv Doença da Hemoglobina SC
Taxa de Filtração Glomerular
Falência Renal Crônica
topic Doença da Hemoglobina SC
Taxa de Filtração Glomerular
Falência Renal Crônica
description Background - Kidney abnormalities are one of the main chronic complications of sickle cell disease (SCD). The aim of this study is to investigate the occurrence of renal abnormalities among patients with SCD. Methods - This is a cohort study with 26 SCD patients followed in a medical center in Fortaleza, Ceará, Brazil. Urinary acidification and concentration tests were performed using calcium chloride (CaCl2), and after a 12h period of water and food deprivation. Fractional excretion of sodium (FENa), transtubular potassium gradient (TTKG) and solute free water reabsorption (TcH2O) were calculated. The SCD group was compared to a group of 15 healthy volunteers (control group). Aquaporin-2 (AQP2) and renal outer medullary K+ channels (ROMK) were quantified through exosomes search in urine. Results - Patient`s average age and gender were similar to controls. Urinary acidification deficit was found in 5 SCD patients (19.2%), who presented urinary pH > 5.5 after CaCl2 test. Urinary osmolality was significantly lower in SCD patients (355±60 vs. 818±202mOsm/kg, p=0.0001, after 12h period water deprivation). Urinary concentration deficit was found in all SCD patients (100%). FENa was higher among SCD patients (0.75±0.3 vs. 0.55±0.2%, p=0.02). The TTKG was higher in SCD patients (5.5±2.5 vs. 3.0±1.5, p=0.001), and TcH2O was lower (0.22±0.3 vs. 1.1±0.3L/day, p=0.0001). The search for AQP2 did not show significant difference between SCD patients and control group (102±6.0 vs. 100±7.2%, p=0.874), as well as for ROMK (172±38 vs. 100±25%, p=0.207). Conclusions - SCD is associated with important kidney dysfunction. The main abnormalities found were urinary concentrating and incomplete distal acidification defect. There was also an increase in the potassium transport and decrease in water transport, evidencing the occurrence of distal tubular dysfunction.
publishDate 2013
dc.date.none.fl_str_mv 2013-12-09T12:23:23Z
2013-12-09T12:23:23Z
2013
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv SILVA JUNIOR, Geraldo Bezerra da. Alterações renais em pacientes com doença falciforme. 2013. 136 f. Tese (Doutorado em Ciências Médicas) - Universidade Federal do Ceará. Faculdade de Medicina, Fortaleza, 2013.
http://www.repositorio.ufc.br/handle/riufc/6919
dc.identifier.dark.fl_str_mv ark:/83112/001300001d19q
identifier_str_mv SILVA JUNIOR, Geraldo Bezerra da. Alterações renais em pacientes com doença falciforme. 2013. 136 f. Tese (Doutorado em Ciências Médicas) - Universidade Federal do Ceará. Faculdade de Medicina, Fortaleza, 2013.
ark:/83112/001300001d19q
url http://www.repositorio.ufc.br/handle/riufc/6919
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Ceará (UFC)
instname:Universidade Federal do Ceará (UFC)
instacron:UFC
instname_str Universidade Federal do Ceará (UFC)
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institution UFC
reponame_str Repositório Institucional da Universidade Federal do Ceará (UFC)
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