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Mineral and bone disorders, morbidity and mortality in end-stage renal failure patients on chronic dialysis

BACKGROUND AND AIM: In spite of numerous interventions, the control of mineral disturbances remains poor in end-stage renal failure (ESRF) patients. Chronic kidney disease - mineral and bone disorders (CKD-MBD) represent an important cause of mortality and morbidity. The aim of this study is to anal...

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Autores principales: MOLDOVAN, DIANA, RUSU, CRINA, KACSO, INA MARIA, POTRA, ALINA, PATIU, IOAN MIHAI, GHERMAN-CAPRIOARA, MIRELA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iuliu Hatieganu University of Medicine and Pharmacy 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777475/
https://www.ncbi.nlm.nih.gov/pubmed/27004031
http://dx.doi.org/10.15386/cjmed-515
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author MOLDOVAN, DIANA
RUSU, CRINA
KACSO, INA MARIA
POTRA, ALINA
PATIU, IOAN MIHAI
GHERMAN-CAPRIOARA, MIRELA
author_facet MOLDOVAN, DIANA
RUSU, CRINA
KACSO, INA MARIA
POTRA, ALINA
PATIU, IOAN MIHAI
GHERMAN-CAPRIOARA, MIRELA
author_sort MOLDOVAN, DIANA
collection PubMed
description BACKGROUND AND AIM: In spite of numerous interventions, the control of mineral disturbances remains poor in end-stage renal failure (ESRF) patients. Chronic kidney disease - mineral and bone disorders (CKD-MBD) represent an important cause of mortality and morbidity. The aim of this study is to analyze the relationship between mineral and bone disorders (MBD) and their components impact on all-cause mortality and cardiovascular (CDV) mortality and morbidity in chronic dialysis patients. METHODS: This prospective study was carried out in a cohort of 92 randomly selected patients with ESRF treated with hemodialysis (HD) and peritoneal dialysis (PD). The data regarding demographic and clinical characteristics were recorded, including vascular disease (coronary, cerebral, peripheral). The follow-up lasted 40 months and the final evaluation included the number and causes of deaths, CDV events and disease. Serum Ca, P, ALP, iPTH, albumin, cholesterol, urea and creatinine levels were measured. The plain radiographic films of hands and pelvis evaluated all bone abnormalities suggestive of renal osteodystrophy (ROD) and peripheral vascular calcification (VC). RESULTS: All-cause annual mortality represented 9.25% in HD and 9.09% in PD patients. The CDV mortality represented almost 44% in HD patients and 66% in PD patients from all deaths. There was a high prevalence of CDV diseases and events. High and low serum P levels were associated with a worse survival rate. Hypercalcaemia was associated with high risk for CDV events in HD patients. In PD patients, the relationship between increased ALP levels and all-cause mortality was significant. Other mineral markers were not predictive of the outcome in the studied patients. In the HD patients the severity of VC was associated with all-cause and CDV mortality, and with CDV events. Male gender, hypercholesterolemia, decreased URR, albumin and creatinine were identified as risk factors for all-cause mortality. The diabetics had higher death rates. Low dialysis efficacy represented a risk factor for mortality and CDV diseases and events. In PD patients, low albumin induced a higher death rate. In PD patients the death rate was similar to HD patients. CONCLUSION: All-cause mortality was higher than in general population, but lower than the chronic dialysis patients’ mortality reported in other studies. The death rates in HD and PD patients were similar. VC and serum P levels influenced the outcome in the HD patients – increased the risk for all-cause and CDV mortality, but also for CDV events. ALP levels influenced outcome in PD patients. There were no significant differences between HD and PD patients regarding outcome.
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spelling pubmed-47774752016-03-21 Mineral and bone disorders, morbidity and mortality in end-stage renal failure patients on chronic dialysis MOLDOVAN, DIANA RUSU, CRINA KACSO, INA MARIA POTRA, ALINA PATIU, IOAN MIHAI GHERMAN-CAPRIOARA, MIRELA Clujul Med Original Research BACKGROUND AND AIM: In spite of numerous interventions, the control of mineral disturbances remains poor in end-stage renal failure (ESRF) patients. Chronic kidney disease - mineral and bone disorders (CKD-MBD) represent an important cause of mortality and morbidity. The aim of this study is to analyze the relationship between mineral and bone disorders (MBD) and their components impact on all-cause mortality and cardiovascular (CDV) mortality and morbidity in chronic dialysis patients. METHODS: This prospective study was carried out in a cohort of 92 randomly selected patients with ESRF treated with hemodialysis (HD) and peritoneal dialysis (PD). The data regarding demographic and clinical characteristics were recorded, including vascular disease (coronary, cerebral, peripheral). The follow-up lasted 40 months and the final evaluation included the number and causes of deaths, CDV events and disease. Serum Ca, P, ALP, iPTH, albumin, cholesterol, urea and creatinine levels were measured. The plain radiographic films of hands and pelvis evaluated all bone abnormalities suggestive of renal osteodystrophy (ROD) and peripheral vascular calcification (VC). RESULTS: All-cause annual mortality represented 9.25% in HD and 9.09% in PD patients. The CDV mortality represented almost 44% in HD patients and 66% in PD patients from all deaths. There was a high prevalence of CDV diseases and events. High and low serum P levels were associated with a worse survival rate. Hypercalcaemia was associated with high risk for CDV events in HD patients. In PD patients, the relationship between increased ALP levels and all-cause mortality was significant. Other mineral markers were not predictive of the outcome in the studied patients. In the HD patients the severity of VC was associated with all-cause and CDV mortality, and with CDV events. Male gender, hypercholesterolemia, decreased URR, albumin and creatinine were identified as risk factors for all-cause mortality. The diabetics had higher death rates. Low dialysis efficacy represented a risk factor for mortality and CDV diseases and events. In PD patients, low albumin induced a higher death rate. In PD patients the death rate was similar to HD patients. CONCLUSION: All-cause mortality was higher than in general population, but lower than the chronic dialysis patients’ mortality reported in other studies. The death rates in HD and PD patients were similar. VC and serum P levels influenced the outcome in the HD patients – increased the risk for all-cause and CDV mortality, but also for CDV events. ALP levels influenced outcome in PD patients. There were no significant differences between HD and PD patients regarding outcome. Iuliu Hatieganu University of Medicine and Pharmacy 2016 2016-01-15 /pmc/articles/PMC4777475/ /pubmed/27004031 http://dx.doi.org/10.15386/cjmed-515 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
spellingShingle Original Research
MOLDOVAN, DIANA
RUSU, CRINA
KACSO, INA MARIA
POTRA, ALINA
PATIU, IOAN MIHAI
GHERMAN-CAPRIOARA, MIRELA
Mineral and bone disorders, morbidity and mortality in end-stage renal failure patients on chronic dialysis
title Mineral and bone disorders, morbidity and mortality in end-stage renal failure patients on chronic dialysis
title_full Mineral and bone disorders, morbidity and mortality in end-stage renal failure patients on chronic dialysis
title_fullStr Mineral and bone disorders, morbidity and mortality in end-stage renal failure patients on chronic dialysis
title_full_unstemmed Mineral and bone disorders, morbidity and mortality in end-stage renal failure patients on chronic dialysis
title_short Mineral and bone disorders, morbidity and mortality in end-stage renal failure patients on chronic dialysis
title_sort mineral and bone disorders, morbidity and mortality in end-stage renal failure patients on chronic dialysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777475/
https://www.ncbi.nlm.nih.gov/pubmed/27004031
http://dx.doi.org/10.15386/cjmed-515
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