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Etiology of End-Stage Renal Disease and Arterial Stiffness among Hemodialysis Patients
Background. Prior studies have demonstrated that conventional and emerging CV risk factors are associated with worsening arterial stiffness among end-stage renal disease (ESRD) patients on hemodialysis. The present cross-sectional study evaluates the association between the etiology of ESRD and arte...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337343/ https://www.ncbi.nlm.nih.gov/pubmed/28299320 http://dx.doi.org/10.1155/2017/2543262 |
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author | El Ghoul, Balsam Daaboul, Yazan Korjian, Serge El Alam, Andrew Mansour, Anthony Hariri, Essa Samad, Salam Salameh, Pascale Dahdah, Georges Blacher, Jacques Safar, Michel E. Aoun Bahous, Sola |
author_facet | El Ghoul, Balsam Daaboul, Yazan Korjian, Serge El Alam, Andrew Mansour, Anthony Hariri, Essa Samad, Salam Salameh, Pascale Dahdah, Georges Blacher, Jacques Safar, Michel E. Aoun Bahous, Sola |
author_sort | El Ghoul, Balsam |
collection | PubMed |
description | Background. Prior studies have demonstrated that conventional and emerging CV risk factors are associated with worsening arterial stiffness among end-stage renal disease (ESRD) patients on hemodialysis. The present cross-sectional study evaluates the association between the etiology of ESRD and arterial stiffness among a cohort of hemodialysis patients. Methods. Etiology of ESRD was identified from patients' medical records and classified as either vascular renal disease, diabetic nephropathy, nondiabetic glomerulopathy, tubular interstitial nephropathy, hereditary nephropathy, or ESRD of unconfirmed etiology. Results. A total of 82 subjects were enrolled. cfPWV was independently associated with the composite of either diabetic nephropathy or vascular renal disease (p = 0.022), pulse pressure (p = 0.001), and a history of CV events (p = 0.025), but not history of hypertension or diabetes mellitus alone. The median cfPWVs in diabetic nephropathy and vascular renal disease were comparable and significantly higher than median cfPWVs in other etiologies of ESRD. Conclusion. The study suggests that the etiology of ESRD is independently associated with arterial stiffness among hemodialysis patients. Furthermore, arterial stiffness was higher among patients who developed renal sequelae of either diabetes mellitus or hypertension as compared with those who have a history of either diabetes mellitus or hypertension alone. |
format | Online Article Text |
id | pubmed-5337343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-53373432017-03-15 Etiology of End-Stage Renal Disease and Arterial Stiffness among Hemodialysis Patients El Ghoul, Balsam Daaboul, Yazan Korjian, Serge El Alam, Andrew Mansour, Anthony Hariri, Essa Samad, Salam Salameh, Pascale Dahdah, Georges Blacher, Jacques Safar, Michel E. Aoun Bahous, Sola Biomed Res Int Research Article Background. Prior studies have demonstrated that conventional and emerging CV risk factors are associated with worsening arterial stiffness among end-stage renal disease (ESRD) patients on hemodialysis. The present cross-sectional study evaluates the association between the etiology of ESRD and arterial stiffness among a cohort of hemodialysis patients. Methods. Etiology of ESRD was identified from patients' medical records and classified as either vascular renal disease, diabetic nephropathy, nondiabetic glomerulopathy, tubular interstitial nephropathy, hereditary nephropathy, or ESRD of unconfirmed etiology. Results. A total of 82 subjects were enrolled. cfPWV was independently associated with the composite of either diabetic nephropathy or vascular renal disease (p = 0.022), pulse pressure (p = 0.001), and a history of CV events (p = 0.025), but not history of hypertension or diabetes mellitus alone. The median cfPWVs in diabetic nephropathy and vascular renal disease were comparable and significantly higher than median cfPWVs in other etiologies of ESRD. Conclusion. The study suggests that the etiology of ESRD is independently associated with arterial stiffness among hemodialysis patients. Furthermore, arterial stiffness was higher among patients who developed renal sequelae of either diabetes mellitus or hypertension as compared with those who have a history of either diabetes mellitus or hypertension alone. Hindawi Publishing Corporation 2017 2017-02-19 /pmc/articles/PMC5337343/ /pubmed/28299320 http://dx.doi.org/10.1155/2017/2543262 Text en Copyright © 2017 Balsam El Ghoul et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article El Ghoul, Balsam Daaboul, Yazan Korjian, Serge El Alam, Andrew Mansour, Anthony Hariri, Essa Samad, Salam Salameh, Pascale Dahdah, Georges Blacher, Jacques Safar, Michel E. Aoun Bahous, Sola Etiology of End-Stage Renal Disease and Arterial Stiffness among Hemodialysis Patients |
title | Etiology of End-Stage Renal Disease and Arterial Stiffness among Hemodialysis Patients |
title_full | Etiology of End-Stage Renal Disease and Arterial Stiffness among Hemodialysis Patients |
title_fullStr | Etiology of End-Stage Renal Disease and Arterial Stiffness among Hemodialysis Patients |
title_full_unstemmed | Etiology of End-Stage Renal Disease and Arterial Stiffness among Hemodialysis Patients |
title_short | Etiology of End-Stage Renal Disease and Arterial Stiffness among Hemodialysis Patients |
title_sort | etiology of end-stage renal disease and arterial stiffness among hemodialysis patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337343/ https://www.ncbi.nlm.nih.gov/pubmed/28299320 http://dx.doi.org/10.1155/2017/2543262 |
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