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Cystatin C, Albuminuria, and Mortality Among Older Adults With Diabetes

OBJECTIVE: Albuminuria and impaired glomerular filtration rate (GFR) are each associated with poor health outcomes among individuals with diabetes. Joint associations of albuminuria and impaired GFR with mortality have not been comprehensively evaluated in this population. RESEARCH DESIGN AND METHOD...

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Autores principales: de Boer, Ian H., Katz, Ronit, Cao, Jie J., Fried, Linda F., Kestenbaum, Bryan, Mukamal, Ken, Rifkin, Dena E., Sarnak, Mark J., Shlipak, Michael G., Siscovick, David S.
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752913/
https://www.ncbi.nlm.nih.gov/pubmed/19587367
http://dx.doi.org/10.2337/dc09-0191
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author de Boer, Ian H.
Katz, Ronit
Cao, Jie J.
Fried, Linda F.
Kestenbaum, Bryan
Mukamal, Ken
Rifkin, Dena E.
Sarnak, Mark J.
Shlipak, Michael G.
Siscovick, David S.
author_facet de Boer, Ian H.
Katz, Ronit
Cao, Jie J.
Fried, Linda F.
Kestenbaum, Bryan
Mukamal, Ken
Rifkin, Dena E.
Sarnak, Mark J.
Shlipak, Michael G.
Siscovick, David S.
author_sort de Boer, Ian H.
collection PubMed
description OBJECTIVE: Albuminuria and impaired glomerular filtration rate (GFR) are each associated with poor health outcomes among individuals with diabetes. Joint associations of albuminuria and impaired GFR with mortality have not been comprehensively evaluated in this population. RESEARCH DESIGN AND METHODS: This is a cohort study among Cardiovascular Health Study participants with diabetes, mean age 78 years. GFR was estimated using serum cystatin C and serum creatinine. Albumin-to-creatinine ratio (ACR) was measured in single-voided urine samples. RESULTS: Of 691 participants, 378 died over 10 years of follow-up. Cystatin C–estimated GFR <60 ml/min per 1.73 m(2), creatinine-based estimated GFR <60 ml/min per 1.73 m(2), and urine ACR ≥30 mg/g were each associated with increased mortality risk with hazard ratios of 1.73 (95% CI 1.37–2.18), 1.54 (1.21–1.97), and 1.73 (1.39–2.17), respectively, adjusting for age, sex, race, diabetes duration, hypoglycemic medications, hypertension, BMI, smoking, cholesterol, lipid-lowering medications, prevalent cardiovascular disease (CVD), and prevalent heart failure. Cystatin C–estimated GFR and urine ACR were additive in terms of mortality risk. Cystatin C–estimated GFR predicted mortality more strongly than creatinine-based estimated GFR. CONCLUSIONS: Albuminuria and impaired GFR were independent, additive risk factors for mortality among older adults with diabetes. These findings support current recommendations to regularly assess both albuminuria and GFR in the clinical care of patients with diabetes; a focus on interventions to prevent or treat CVD in the presence of albuminuria, impaired GFR, or both; and further consideration of cystatin C use in clinical care.
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spelling pubmed-27529132010-10-01 Cystatin C, Albuminuria, and Mortality Among Older Adults With Diabetes de Boer, Ian H. Katz, Ronit Cao, Jie J. Fried, Linda F. Kestenbaum, Bryan Mukamal, Ken Rifkin, Dena E. Sarnak, Mark J. Shlipak, Michael G. Siscovick, David S. Diabetes Care Original Research OBJECTIVE: Albuminuria and impaired glomerular filtration rate (GFR) are each associated with poor health outcomes among individuals with diabetes. Joint associations of albuminuria and impaired GFR with mortality have not been comprehensively evaluated in this population. RESEARCH DESIGN AND METHODS: This is a cohort study among Cardiovascular Health Study participants with diabetes, mean age 78 years. GFR was estimated using serum cystatin C and serum creatinine. Albumin-to-creatinine ratio (ACR) was measured in single-voided urine samples. RESULTS: Of 691 participants, 378 died over 10 years of follow-up. Cystatin C–estimated GFR <60 ml/min per 1.73 m(2), creatinine-based estimated GFR <60 ml/min per 1.73 m(2), and urine ACR ≥30 mg/g were each associated with increased mortality risk with hazard ratios of 1.73 (95% CI 1.37–2.18), 1.54 (1.21–1.97), and 1.73 (1.39–2.17), respectively, adjusting for age, sex, race, diabetes duration, hypoglycemic medications, hypertension, BMI, smoking, cholesterol, lipid-lowering medications, prevalent cardiovascular disease (CVD), and prevalent heart failure. Cystatin C–estimated GFR and urine ACR were additive in terms of mortality risk. Cystatin C–estimated GFR predicted mortality more strongly than creatinine-based estimated GFR. CONCLUSIONS: Albuminuria and impaired GFR were independent, additive risk factors for mortality among older adults with diabetes. These findings support current recommendations to regularly assess both albuminuria and GFR in the clinical care of patients with diabetes; a focus on interventions to prevent or treat CVD in the presence of albuminuria, impaired GFR, or both; and further consideration of cystatin C use in clinical care. American Diabetes Association 2009-10 2009-07-08 /pmc/articles/PMC2752913/ /pubmed/19587367 http://dx.doi.org/10.2337/dc09-0191 Text en © 2009 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
de Boer, Ian H.
Katz, Ronit
Cao, Jie J.
Fried, Linda F.
Kestenbaum, Bryan
Mukamal, Ken
Rifkin, Dena E.
Sarnak, Mark J.
Shlipak, Michael G.
Siscovick, David S.
Cystatin C, Albuminuria, and Mortality Among Older Adults With Diabetes
title Cystatin C, Albuminuria, and Mortality Among Older Adults With Diabetes
title_full Cystatin C, Albuminuria, and Mortality Among Older Adults With Diabetes
title_fullStr Cystatin C, Albuminuria, and Mortality Among Older Adults With Diabetes
title_full_unstemmed Cystatin C, Albuminuria, and Mortality Among Older Adults With Diabetes
title_short Cystatin C, Albuminuria, and Mortality Among Older Adults With Diabetes
title_sort cystatin c, albuminuria, and mortality among older adults with diabetes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752913/
https://www.ncbi.nlm.nih.gov/pubmed/19587367
http://dx.doi.org/10.2337/dc09-0191
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