Atenção!


O atendimento às questões referentes ao Repositório Institucional será interrompido entre os dias 20 de dezembro de 2025 a 4 de janeiro de 2026.

Pedimos a sua compreensão e aproveitamos para desejar boas festas!

Logo do repositório

Predictors of autosomal dominant polycystic kidney disease progression: a Brazilian single-center cohort

dc.contributor.authorHitoshi Nishimoto, Igor [UNESP]
dc.contributor.authorGonçalves Santos, Andrey [UNESP]
dc.contributor.authorMandelbaun Bianchini, Júlia [UNESP]
dc.contributor.authorBrenneisen Santos, Luiz Gustavo [UNESP]
dc.contributor.authorRodrigues Martini, Maria Carolina [UNESP]
dc.contributor.authordos Santos Silva, Vanessa [UNESP]
dc.contributor.authorCuadrado Martin, Luis [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T20:07:36Z
dc.date.issued2024-01-01
dc.description.abstractIntroduction: Identifying risk factors for autosomal dominant polycystic kidney disease (ADPKD) progression is important. However, studies that have evaluated this subject using a Brazilian sample is sparce. Therefore, the aim of this study was to identify risk factors for renal outcomes and death in a Brazilian cohort of ADPKD patients. Methods: Patients had the first medical appointment between January 2002 and December 2014, and were followed up until December 2019. Associations between clinical and laboratory variables with the primary outcome (sustained decrease of at least 57% in the eGFR from baseline, need for dialysis or renal transplantation) and the secondary outcome (death from any cause) were analyzed using a multiple Cox regression model. Among 80 ADPKD patients, those under 18 years, with glomerular filtration rate <30 mL/min/1.73 m2, and/or those with missing data were excluded. There were 70 patients followed. Results: The factors independently associated with the renal outcomes were total kidney length – adjusted Hazard Ratio (HR) with a 95% confidence interval (95% CI): 1.137 (1.057–1.224), glomerular filtration rate – HR (95% CI): 0.970 (0.949–0.992), and serum uric acid level – HR (95% CI): 1.643 (1.118–2.415). Diabetes mellitus - HR (95% CI): 8.115 (1.985–33.180) and glomerular filtration rate - HR (95% CI): 0.957 (0.919–0.997) were associated with the secondary outcome. Conclusions: These findings corroborate the hypothesis that total kidney length, glomerular filtration rate and serum uric acid level may be important prognostic predictors of ADPKD in a Brazilian cohort, which could help to select patients who require closer follow up.en
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho Escola de Medicina, SP
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho Escola de Medicina Departamento de Medicina Interna, SP
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho Escola de Medicina, SP
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho Escola de Medicina Departamento de Medicina Interna, SP
dc.identifierhttp://dx.doi.org/10.1590/2175-8239-JBN-2023-0040en
dc.identifier.citationBrazilian Journal of Nephrology, v. 46, n. 3, 2024.
dc.identifier.doi10.1590/2175-8239-JBN-2023-0040en
dc.identifier.issn2175-8239
dc.identifier.issn0101-2800
dc.identifier.scopus2-s2.0-85197638554
dc.identifier.urihttps://hdl.handle.net/11449/306908
dc.language.isoeng
dc.relation.ispartofBrazilian Journal of Nephrology
dc.sourceScopus
dc.subjectMortality
dc.subjectPolycystic Kidney, Autosomal Dominant
dc.subjectRate
dc.subjectRenal Insufficiency
dc.subjectRisk Factors
dc.titlePredictors of autosomal dominant polycystic kidney disease progression: a Brazilian single-center cohorten
dc.titlePreditores de progressão da doença renal policística autossômica dominante: uma coorte brasileira de centro únicopt
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0009-0007-8338-9822[1]
unesp.author.orcid0000-0002-6900-8030[2]
unesp.author.orcid0000-0003-4225-7616[3]
unesp.author.orcid0000-0001-9828-853X[4]
unesp.author.orcid0000-0001-9323-0718[5]
unesp.author.orcid0000-0001-7903-0939[6]
unesp.author.orcid0000-0003-1435-7994[7]

Arquivos

Coleções