The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findings
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Publication Date: | 1998 |
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Format: | Article |
Language: | eng |
Source: | São Paulo medical journal (Online) |
Download full: | https://periodicosapm.emnuvens.com.br/spmj/article/view/2368 |
Summary: | INTRODUCTION: Renal osteodystrophy includes the complete range of mineral metabolism disorders that affect the skeleton in patients with chronic renal failure. PATIENTS AND METHODS: 200 patients with end-stage renal disease and on dialysis were investigated regarding the clinical, biochemical and histological findings of bone disease. RESULTS: The spectrum of renal osteodystrophy consisted mainly of high turnover bone lesions (74.5%), including osteitis fibrosa in 57.5%. Patients with mild bone disease were on dialysis for shorter periods of time and were mostly asymptomatic. Patients with aluminum-related bone disease (16.5%) had the greatest aluminum exposure, either orally or parenterally, and together with patients with high turnover mixed disease, were the most symptomatic. Although on a non-regular basis, the vast majority of the patients (82.5%) had been receiving vitamin D. The incidence of adynamic bone disease was high (n=8) among parathyroidectomized patients (n=12). Significantly higher serum levels of alkaline phosphatase were observed in osteitis fibrosa. CONCLUSIONS: The use of calcitriol and phosphate-binding agents on a non-regular basis seems to be the reason for the apparent reduced response to the treatment of secondary hyperparathyroidism. Alkaline phosphatase has been shown to be a fair marker for bone turnover in patients with osteitis fibrosa. The severity of the clinical manifestations of bone disease correlates with the histological features of bone lesion and to the time spent on dialysis. |
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The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findingsRenal osteodystrophyChronic renal failureHemodialysisAluminum intoxicationBone metabolismINTRODUCTION: Renal osteodystrophy includes the complete range of mineral metabolism disorders that affect the skeleton in patients with chronic renal failure. PATIENTS AND METHODS: 200 patients with end-stage renal disease and on dialysis were investigated regarding the clinical, biochemical and histological findings of bone disease. RESULTS: The spectrum of renal osteodystrophy consisted mainly of high turnover bone lesions (74.5%), including osteitis fibrosa in 57.5%. Patients with mild bone disease were on dialysis for shorter periods of time and were mostly asymptomatic. Patients with aluminum-related bone disease (16.5%) had the greatest aluminum exposure, either orally or parenterally, and together with patients with high turnover mixed disease, were the most symptomatic. Although on a non-regular basis, the vast majority of the patients (82.5%) had been receiving vitamin D. The incidence of adynamic bone disease was high (n=8) among parathyroidectomized patients (n=12). Significantly higher serum levels of alkaline phosphatase were observed in osteitis fibrosa. CONCLUSIONS: The use of calcitriol and phosphate-binding agents on a non-regular basis seems to be the reason for the apparent reduced response to the treatment of secondary hyperparathyroidism. Alkaline phosphatase has been shown to be a fair marker for bone turnover in patients with osteitis fibrosa. The severity of the clinical manifestations of bone disease correlates with the histological features of bone lesion and to the time spent on dialysis.INTRODUÇÃO: A osteodistrofia renal compreende todas as formas de alterações do metabolismo mineral que afetam o tecido ósseo de pacientes renais crônicos. PACIENTES E MÉTODOS: 200 pacientes submetidos a diálise regular foram investigados quanto aos aspectos clínicos, laboratoriais e histopatológicos relacionados com doença óssea. RESULTADOS: As lesões de alto turnover foram observadas em 74.5% dos pacientes, sendo que 57.5% eram portadores de osteíte fibrosa. Pacientes com lesão mínima estavam em diálise por menos tempo e em geral eram assintomáticos. Pacientes com osteopatia alumínica (16.5%) tiveram a maior exposição ao alumínio por via oral e/ou parenteral e, ao lado dos portadores de doença mista de alto turnover, eram os mais sintomáticos. A grande maioria dos pacientes (82.5%) fazia uso irregular de vitamina D. Foi alta a incidência de doença adinâmica (n=8) nos pacientes paratireoidectomizados (n=12). Na osteíte fibrosa foram observados os níveis mais elevados de fosfatase alcalina. CONCLUSÕES: A utilização de calcitriol e quelantes de fósforo de forma irregular e em doses insuficientes parece ter sido a principal causa para a resposta reduzida ao tratamento do hiperparatireoidismo secundário. A fosfatase alcalina pode ser considerada um bom marcador bioquímico do turnover ósseo. A intensidade das manifestações clínicas relacionadas com o sistema músculo esquelético correlacionam-se com o tipo histológico da lesão óssea e com o tempo em diálise.São Paulo Medical JournalSão Paulo Medical Journal1998-09-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://periodicosapm.emnuvens.com.br/spmj/article/view/2368São Paulo Medical Journal; Vol. 116 No. 5 (1998); 1790-1797São Paulo Medical Journal; v. 116 n. 5 (1998); 1790-17971806-9460reponame:São Paulo medical journal (Online)instname:Associação Paulista de Medicinainstacron:APMenghttps://periodicosapm.emnuvens.com.br/spmj/article/view/2368/2258https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessDuarte, Maria Eugênia LeitePeixoto, Ana Lúcia PassosPacheco, Andréa da SilvaPeixoto, Angela VieiraRodriguez, Rodrigo DezertoLugon, Jocemir RonaldoCruz, Elisa Albuquerque Sampaio da2023-10-02T14:17:30Zoai:ojs.diagnosticoetratamento.emnuvens.com.br:article/2368Revistahttp://www.scielo.br/spmjPUBhttps://old.scielo.br/oai/scielo-oai.phprevistas@apm.org.br1806-94601516-3180opendoar:2023-10-02T14:17:30São Paulo medical journal (Online) - Associação Paulista de Medicinafalse |
dc.title.none.fl_str_mv |
The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findings |
title |
The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findings |
spellingShingle |
The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findings Duarte, Maria Eugênia Leite Renal osteodystrophy Chronic renal failure Hemodialysis Aluminum intoxication Bone metabolism |
title_short |
The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findings |
title_full |
The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findings |
title_fullStr |
The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findings |
title_full_unstemmed |
The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findings |
title_sort |
The spectrum of bone disease in 200 chronic hemodialysis patients: a correlation between clinical, biochemical and histological findings |
author |
Duarte, Maria Eugênia Leite |
author_facet |
Duarte, Maria Eugênia Leite Peixoto, Ana Lúcia Passos Pacheco, Andréa da Silva Peixoto, Angela Vieira Rodriguez, Rodrigo Dezerto Lugon, Jocemir Ronaldo Cruz, Elisa Albuquerque Sampaio da |
author_role |
author |
author2 |
Peixoto, Ana Lúcia Passos Pacheco, Andréa da Silva Peixoto, Angela Vieira Rodriguez, Rodrigo Dezerto Lugon, Jocemir Ronaldo Cruz, Elisa Albuquerque Sampaio da |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Duarte, Maria Eugênia Leite Peixoto, Ana Lúcia Passos Pacheco, Andréa da Silva Peixoto, Angela Vieira Rodriguez, Rodrigo Dezerto Lugon, Jocemir Ronaldo Cruz, Elisa Albuquerque Sampaio da |
dc.subject.por.fl_str_mv |
Renal osteodystrophy Chronic renal failure Hemodialysis Aluminum intoxication Bone metabolism |
topic |
Renal osteodystrophy Chronic renal failure Hemodialysis Aluminum intoxication Bone metabolism |
description |
INTRODUCTION: Renal osteodystrophy includes the complete range of mineral metabolism disorders that affect the skeleton in patients with chronic renal failure. PATIENTS AND METHODS: 200 patients with end-stage renal disease and on dialysis were investigated regarding the clinical, biochemical and histological findings of bone disease. RESULTS: The spectrum of renal osteodystrophy consisted mainly of high turnover bone lesions (74.5%), including osteitis fibrosa in 57.5%. Patients with mild bone disease were on dialysis for shorter periods of time and were mostly asymptomatic. Patients with aluminum-related bone disease (16.5%) had the greatest aluminum exposure, either orally or parenterally, and together with patients with high turnover mixed disease, were the most symptomatic. Although on a non-regular basis, the vast majority of the patients (82.5%) had been receiving vitamin D. The incidence of adynamic bone disease was high (n=8) among parathyroidectomized patients (n=12). Significantly higher serum levels of alkaline phosphatase were observed in osteitis fibrosa. CONCLUSIONS: The use of calcitriol and phosphate-binding agents on a non-regular basis seems to be the reason for the apparent reduced response to the treatment of secondary hyperparathyroidism. Alkaline phosphatase has been shown to be a fair marker for bone turnover in patients with osteitis fibrosa. The severity of the clinical manifestations of bone disease correlates with the histological features of bone lesion and to the time spent on dialysis. |
publishDate |
1998 |
dc.date.none.fl_str_mv |
1998-09-09 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://periodicosapm.emnuvens.com.br/spmj/article/view/2368 |
url |
https://periodicosapm.emnuvens.com.br/spmj/article/view/2368 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://periodicosapm.emnuvens.com.br/spmj/article/view/2368/2258 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
São Paulo Medical Journal São Paulo Medical Journal |
publisher.none.fl_str_mv |
São Paulo Medical Journal São Paulo Medical Journal |
dc.source.none.fl_str_mv |
São Paulo Medical Journal; Vol. 116 No. 5 (1998); 1790-1797 São Paulo Medical Journal; v. 116 n. 5 (1998); 1790-1797 1806-9460 reponame:São Paulo medical journal (Online) instname:Associação Paulista de Medicina instacron:APM |
instname_str |
Associação Paulista de Medicina |
instacron_str |
APM |
institution |
APM |
reponame_str |
São Paulo medical journal (Online) |
collection |
São Paulo medical journal (Online) |
repository.name.fl_str_mv |
São Paulo medical journal (Online) - Associação Paulista de Medicina |
repository.mail.fl_str_mv |
revistas@apm.org.br |
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1825135074662678528 |