Renal Dysfunction, Metabolic Syndrome and Cardiovascular Disease Mortality

Background. Renal disease is commonly described as a complication of metabolic syndrome (MetS) but some recent studies suggest that Chronic Kidney disease (CKD) may actually antecede MetS. Few studies have explored the predictive utility of co-clustering CKD with MetS for cardiovascular disease (CVD...

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Main Authors: David Martins, Chizobam Ani, Deyu Pan, Omolola Ogunyemi, Keith Norris
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Journal of Nutrition and Metabolism
Online Access:http://dx.doi.org/10.1155/2010/167162
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author David Martins
Chizobam Ani
Deyu Pan
Omolola Ogunyemi
Keith Norris
author_facet David Martins
Chizobam Ani
Deyu Pan
Omolola Ogunyemi
Keith Norris
author_sort David Martins
collection DOAJ
description Background. Renal disease is commonly described as a complication of metabolic syndrome (MetS) but some recent studies suggest that Chronic Kidney disease (CKD) may actually antecede MetS. Few studies have explored the predictive utility of co-clustering CKD with MetS for cardiovascular disease (CVD) mortality. Methods. Data from a nationally representative sample of United States adults (NHANES) was utilized. A sample of 13115 non-pregnant individuals aged ≥35 years, with available follow-up mortality assessment was selected. Multivariable Cox Proportional hazard regression analysis techniques explored the relationship between co-clustered CKD, MetS and CVD mortality. Bayesian analysis techniques tested the predictive accuracy for CVD Mortality of two models using co-clustered MetS and CKD and MetS alone. Results. Co-clustering early and late CKD respectively resulted in statistically significant higher hazard for CVD mortality (HR = 1.80, CI = 1.45–2.23, and HR = 3.23, CI = 2.56–3.70) when compared with individuals with no MetS and no CKD. A model with early CKD and MetS has a higher predictive accuracy (72.0% versus 67.6%), area under the ROC (0.74 versus 0.66), and Cohen's kappa (0.38 versus 0.21) than that with MetS alone. Conclusion. The study findings suggest that the co-clustering of early CKD with MetS increases the accuracy of risk prediction for CVD mortality.
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spelling doaj-art-9cb717777dfa4a379cf54e6b77e488e72025-02-03T01:25:02ZengWileyJournal of Nutrition and Metabolism2090-07242090-07322010-01-01201010.1155/2010/167162167162Renal Dysfunction, Metabolic Syndrome and Cardiovascular Disease MortalityDavid Martins0Chizobam Ani1Deyu Pan2Omolola Ogunyemi3Keith Norris4Department of Medicine, Charles Drew University of Medicine and Science, 1731 E 20th Street, Los Angeles, CA 90059, USADepartment of Medicine, Charles Drew University of Medicine and Science, 1731 E 20th Street, Los Angeles, CA 90059, USADepartment of Medicine, Charles Drew University of Medicine and Science, 1731 E 20th Street, Los Angeles, CA 90059, USADepartment of Medicine, Charles Drew University of Medicine and Science, 1731 E 20th Street, Los Angeles, CA 90059, USADepartment of Medicine, Charles Drew University of Medicine and Science, 1731 E 20th Street, Los Angeles, CA 90059, USABackground. Renal disease is commonly described as a complication of metabolic syndrome (MetS) but some recent studies suggest that Chronic Kidney disease (CKD) may actually antecede MetS. Few studies have explored the predictive utility of co-clustering CKD with MetS for cardiovascular disease (CVD) mortality. Methods. Data from a nationally representative sample of United States adults (NHANES) was utilized. A sample of 13115 non-pregnant individuals aged ≥35 years, with available follow-up mortality assessment was selected. Multivariable Cox Proportional hazard regression analysis techniques explored the relationship between co-clustered CKD, MetS and CVD mortality. Bayesian analysis techniques tested the predictive accuracy for CVD Mortality of two models using co-clustered MetS and CKD and MetS alone. Results. Co-clustering early and late CKD respectively resulted in statistically significant higher hazard for CVD mortality (HR = 1.80, CI = 1.45–2.23, and HR = 3.23, CI = 2.56–3.70) when compared with individuals with no MetS and no CKD. A model with early CKD and MetS has a higher predictive accuracy (72.0% versus 67.6%), area under the ROC (0.74 versus 0.66), and Cohen's kappa (0.38 versus 0.21) than that with MetS alone. Conclusion. The study findings suggest that the co-clustering of early CKD with MetS increases the accuracy of risk prediction for CVD mortality.http://dx.doi.org/10.1155/2010/167162
spellingShingle David Martins
Chizobam Ani
Deyu Pan
Omolola Ogunyemi
Keith Norris
Renal Dysfunction, Metabolic Syndrome and Cardiovascular Disease Mortality
Journal of Nutrition and Metabolism
title Renal Dysfunction, Metabolic Syndrome and Cardiovascular Disease Mortality
title_full Renal Dysfunction, Metabolic Syndrome and Cardiovascular Disease Mortality
title_fullStr Renal Dysfunction, Metabolic Syndrome and Cardiovascular Disease Mortality
title_full_unstemmed Renal Dysfunction, Metabolic Syndrome and Cardiovascular Disease Mortality
title_short Renal Dysfunction, Metabolic Syndrome and Cardiovascular Disease Mortality
title_sort renal dysfunction metabolic syndrome and cardiovascular disease mortality
url http://dx.doi.org/10.1155/2010/167162
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AT omololaogunyemi renaldysfunctionmetabolicsyndromeandcardiovasculardiseasemortality
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