Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease Patients
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo de conferência |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.2215/CJN.03100608 http://repositorio.unifesp.br/handle/11600/31404 |
Resumo: | Background and objectives: Nephrolithiasis (LIT) is more prevalent in patients with autosomal dominant polycystic kidney disease (ADPKD) than in the general population. Renal ultrasonography may underdetect renal stones because of difficulties imposed by parenchymal and/or cyst wall calcifications.Design, setting, participants, & measurements: A total of 125 patients with ADPKD underwent ultrasonography and unenhanced computed tomography (CT) scan, routine blood chemistry, and spot and 24-h urine collections.Results: CT scan detected calculi in 32 patients, including 20 whose previous ultrasonography revealed no calculi. the percentage of hypocitraturia was high but not statistically different between patients with ADPKD+LIT or ADPKD. Hyperuricosuria and distal renal tubular acidosis were less prevalent but also did not differ between groups, whereas hyperoxaluria was significantly higher in the former. Hypercalciuria was not detected. Renal volume was significantly higher in patients with ADPKD+LIT versus ADPKD, and a stepwise multivariate logistic regression analysis showed that a renal volume >= 500 ml was a significant predictor of LIT in patients with ADPKD and normal renal function, after adjustments for age and hypertension.Conclusions: CT scan was better than ultrasonography to detect LIT in patients with ADPKD. Larger kidneys from patients with ADPKD were more prone to develop stones, irrespective of the presence of metabolic disturbances. |
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Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease PatientsBackground and objectives: Nephrolithiasis (LIT) is more prevalent in patients with autosomal dominant polycystic kidney disease (ADPKD) than in the general population. Renal ultrasonography may underdetect renal stones because of difficulties imposed by parenchymal and/or cyst wall calcifications.Design, setting, participants, & measurements: A total of 125 patients with ADPKD underwent ultrasonography and unenhanced computed tomography (CT) scan, routine blood chemistry, and spot and 24-h urine collections.Results: CT scan detected calculi in 32 patients, including 20 whose previous ultrasonography revealed no calculi. the percentage of hypocitraturia was high but not statistically different between patients with ADPKD+LIT or ADPKD. Hyperuricosuria and distal renal tubular acidosis were less prevalent but also did not differ between groups, whereas hyperoxaluria was significantly higher in the former. Hypercalciuria was not detected. Renal volume was significantly higher in patients with ADPKD+LIT versus ADPKD, and a stepwise multivariate logistic regression analysis showed that a renal volume >= 500 ml was a significant predictor of LIT in patients with ADPKD and normal renal function, after adjustments for age and hypertension.Conclusions: CT scan was better than ultrasonography to detect LIT in patients with ADPKD. Larger kidneys from patients with ADPKD were more prone to develop stones, irrespective of the presence of metabolic disturbances.Universidade Federal de São Paulo, Div Nephrol, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Radiol, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Div Nephrol, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Radiol, BR-04023900 São Paulo, BrazilWeb of ScienceAmer Soc NephrologyUniversidade Federal de São Paulo (UNIFESP)Nishiura, Jose Luiz [UNIFESP]Neves, Rodrigo F. C. A. [UNIFESP]Eloi, Samara Rodrigues Moreira [UNIFESP]Cintra, Susan M. L. F. [UNIFESP]Ajzen, Sergio Aron [UNIFESP]Heilberg, Ita Pfeferman [UNIFESP]2016-01-24T13:52:23Z2016-01-24T13:52:23Z2009-04-01info:eu-repo/semantics/conferenceObjectinfo:eu-repo/semantics/publishedVersion838-844http://dx.doi.org/10.2215/CJN.03100608Clinical Journal of the American Society of Nephrology. Washington: Amer Soc Nephrology, v. 4, n. 4, p. 838-844, 2009.10.2215/CJN.031006081555-9041http://repositorio.unifesp.br/handle/11600/31404WOS:000264937900026engClinical Journal of the American Society of Nephrologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2023-03-24T15:18:43Zoai:repositorio.unifesp.br/:11600/31404Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652023-03-24T15:18:43Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease Patients |
title |
Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease Patients |
spellingShingle |
Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease Patients Nishiura, Jose Luiz [UNIFESP] |
title_short |
Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease Patients |
title_full |
Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease Patients |
title_fullStr |
Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease Patients |
title_full_unstemmed |
Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease Patients |
title_sort |
Evaluation of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease Patients |
author |
Nishiura, Jose Luiz [UNIFESP] |
author_facet |
Nishiura, Jose Luiz [UNIFESP] Neves, Rodrigo F. C. A. [UNIFESP] Eloi, Samara Rodrigues Moreira [UNIFESP] Cintra, Susan M. L. F. [UNIFESP] Ajzen, Sergio Aron [UNIFESP] Heilberg, Ita Pfeferman [UNIFESP] |
author_role |
author |
author2 |
Neves, Rodrigo F. C. A. [UNIFESP] Eloi, Samara Rodrigues Moreira [UNIFESP] Cintra, Susan M. L. F. [UNIFESP] Ajzen, Sergio Aron [UNIFESP] Heilberg, Ita Pfeferman [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Nishiura, Jose Luiz [UNIFESP] Neves, Rodrigo F. C. A. [UNIFESP] Eloi, Samara Rodrigues Moreira [UNIFESP] Cintra, Susan M. L. F. [UNIFESP] Ajzen, Sergio Aron [UNIFESP] Heilberg, Ita Pfeferman [UNIFESP] |
description |
Background and objectives: Nephrolithiasis (LIT) is more prevalent in patients with autosomal dominant polycystic kidney disease (ADPKD) than in the general population. Renal ultrasonography may underdetect renal stones because of difficulties imposed by parenchymal and/or cyst wall calcifications.Design, setting, participants, & measurements: A total of 125 patients with ADPKD underwent ultrasonography and unenhanced computed tomography (CT) scan, routine blood chemistry, and spot and 24-h urine collections.Results: CT scan detected calculi in 32 patients, including 20 whose previous ultrasonography revealed no calculi. the percentage of hypocitraturia was high but not statistically different between patients with ADPKD+LIT or ADPKD. Hyperuricosuria and distal renal tubular acidosis were less prevalent but also did not differ between groups, whereas hyperoxaluria was significantly higher in the former. Hypercalciuria was not detected. Renal volume was significantly higher in patients with ADPKD+LIT versus ADPKD, and a stepwise multivariate logistic regression analysis showed that a renal volume >= 500 ml was a significant predictor of LIT in patients with ADPKD and normal renal function, after adjustments for age and hypertension.Conclusions: CT scan was better than ultrasonography to detect LIT in patients with ADPKD. Larger kidneys from patients with ADPKD were more prone to develop stones, irrespective of the presence of metabolic disturbances. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-04-01 2016-01-24T13:52:23Z 2016-01-24T13:52:23Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/conferenceObject |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
conferenceObject |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.2215/CJN.03100608 Clinical Journal of the American Society of Nephrology. Washington: Amer Soc Nephrology, v. 4, n. 4, p. 838-844, 2009. 10.2215/CJN.03100608 1555-9041 http://repositorio.unifesp.br/handle/11600/31404 WOS:000264937900026 |
url |
http://dx.doi.org/10.2215/CJN.03100608 http://repositorio.unifesp.br/handle/11600/31404 |
identifier_str_mv |
Clinical Journal of the American Society of Nephrology. Washington: Amer Soc Nephrology, v. 4, n. 4, p. 838-844, 2009. 10.2215/CJN.03100608 1555-9041 WOS:000264937900026 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Clinical Journal of the American Society of Nephrology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
838-844 |
dc.publisher.none.fl_str_mv |
Amer Soc Nephrology |
publisher.none.fl_str_mv |
Amer Soc Nephrology |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
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Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268300931104768 |