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Effects of glucose and blood pressure control on diabetic kidney disease in old patients with type 2 diabetes

AIMS: We determined the influence of age on the effects of glucose and blood pressure control on diabetic kidney disease in patients with type 2 diabetes. METHODS: A total of 721 patients with type 2 diabetes, aged 41–85 years and with an estimated glomerular filtration rate (eGFR) ≥30 mL/ [min · 1....

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Autores principales: Wu, Tzu-En, Chen, Yu-Hsin, Chen, Harn-Shen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124170/
https://www.ncbi.nlm.nih.gov/pubmed/25104976
http://dx.doi.org/10.1186/1758-5996-6-81
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author Wu, Tzu-En
Chen, Yu-Hsin
Chen, Harn-Shen
author_facet Wu, Tzu-En
Chen, Yu-Hsin
Chen, Harn-Shen
author_sort Wu, Tzu-En
collection PubMed
description AIMS: We determined the influence of age on the effects of glucose and blood pressure control on diabetic kidney disease in patients with type 2 diabetes. METHODS: A total of 721 patients with type 2 diabetes, aged 41–85 years and with an estimated glomerular filtration rate (eGFR) ≥30 mL/ [min · 1.73 m(2)], were enrolled in this study between August 2001 and December 2002. All participants were followed up at our clinics until December 31, 2010. Primary outcomes were the development of end-stage renal disease (ESRD) and all-cause mortality. Secondary outcomes were the development of clinical albuminuria and a severe decline in eGFR. RESULTS: During the follow-up period (median: 8.3 years), 27 (3.7%) patients developed ESRD, 130 (18.0%) patients died without developing ESRD, and 16 (2.2%) patients died after developing ESRD. Mortality rate increased with age, but the incidence rate of ESRD did not. Poor glucose and blood pressure control was associated with the development of clinical albuminuria and with a severe decline in eGFR in younger patients with diabetes, but not in older patients. The development of severe decline in eGFR and ESRD was significantly lower in the middle tertile of blood pressure (i.e., SBP of 128–141 mm Hg) in older patients. CONCLUSIONS: Adequate glucose and blood pressure control did not reduce the risk of ESRD; however, it may have delayed the onset of clinical albuminuria as well as eGFR decline in younger patients with type 2 diabetes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1758-5996-6-81) contains supplementary material, which is available to authorized users.
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spelling pubmed-41241702014-08-08 Effects of glucose and blood pressure control on diabetic kidney disease in old patients with type 2 diabetes Wu, Tzu-En Chen, Yu-Hsin Chen, Harn-Shen Diabetol Metab Syndr Research AIMS: We determined the influence of age on the effects of glucose and blood pressure control on diabetic kidney disease in patients with type 2 diabetes. METHODS: A total of 721 patients with type 2 diabetes, aged 41–85 years and with an estimated glomerular filtration rate (eGFR) ≥30 mL/ [min · 1.73 m(2)], were enrolled in this study between August 2001 and December 2002. All participants were followed up at our clinics until December 31, 2010. Primary outcomes were the development of end-stage renal disease (ESRD) and all-cause mortality. Secondary outcomes were the development of clinical albuminuria and a severe decline in eGFR. RESULTS: During the follow-up period (median: 8.3 years), 27 (3.7%) patients developed ESRD, 130 (18.0%) patients died without developing ESRD, and 16 (2.2%) patients died after developing ESRD. Mortality rate increased with age, but the incidence rate of ESRD did not. Poor glucose and blood pressure control was associated with the development of clinical albuminuria and with a severe decline in eGFR in younger patients with diabetes, but not in older patients. The development of severe decline in eGFR and ESRD was significantly lower in the middle tertile of blood pressure (i.e., SBP of 128–141 mm Hg) in older patients. CONCLUSIONS: Adequate glucose and blood pressure control did not reduce the risk of ESRD; however, it may have delayed the onset of clinical albuminuria as well as eGFR decline in younger patients with type 2 diabetes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1758-5996-6-81) contains supplementary material, which is available to authorized users. BioMed Central 2014-07-29 /pmc/articles/PMC4124170/ /pubmed/25104976 http://dx.doi.org/10.1186/1758-5996-6-81 Text en © Wu et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wu, Tzu-En
Chen, Yu-Hsin
Chen, Harn-Shen
Effects of glucose and blood pressure control on diabetic kidney disease in old patients with type 2 diabetes
title Effects of glucose and blood pressure control on diabetic kidney disease in old patients with type 2 diabetes
title_full Effects of glucose and blood pressure control on diabetic kidney disease in old patients with type 2 diabetes
title_fullStr Effects of glucose and blood pressure control on diabetic kidney disease in old patients with type 2 diabetes
title_full_unstemmed Effects of glucose and blood pressure control on diabetic kidney disease in old patients with type 2 diabetes
title_short Effects of glucose and blood pressure control on diabetic kidney disease in old patients with type 2 diabetes
title_sort effects of glucose and blood pressure control on diabetic kidney disease in old patients with type 2 diabetes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124170/
https://www.ncbi.nlm.nih.gov/pubmed/25104976
http://dx.doi.org/10.1186/1758-5996-6-81
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