Inflammation and cardiovascular events in individuals with and without chronic kidney disease.

Pubmed ID: 18401337

Pubmed Central ID: PMC4083694

Journal: Kidney international

Publication Date: June 1, 2008

Affiliation: Department of Medicine, Division of Nephrology, Tufts Medical Center, Boston, Massachusetts 02111, USA. dweiner@tuftsmedicalcenter.org

MeSH Terms: Humans, Male, Female, Cardiovascular Diseases, Risk Factors, Middle Aged, Chronic Disease, Kidney Diseases, Fibrinogen, Leukocyte Count, C-Reactive Protein, Inflammation, Serum Albumin, Biomarkers

Grants: K23 DK71636, R21 DK068310, T32 DK007777, K23 DK071636, K24 DK078204

Authors: Tighiouart H, Weiner DE, Salem DN, Levey AS, Sarnak MJ, Elsayed EF, Griffith JL

Cite As: Weiner DE, Tighiouart H, Elsayed EF, Griffith JL, Salem DN, Levey AS, Sarnak MJ. Inflammation and cardiovascular events in individuals with and without chronic kidney disease. Kidney Int 2008 Jun;73(12):1406-12. Epub 2008 Apr 9.

Studies:

Abstract

Inflammation and chronic kidney disease predict cardiovascular events. Here we evaluated markers of inflammation including fibrinogen, albumin and white blood cell count in individuals with and without stages 3-4 chronic kidney disease to assess inflammation as a risk factor for adverse events, the synergy between inflammation and chronic kidney disease, and the prognostic ability of these inflammatory markers relative to that of C-reactive protein. Using Atherosclerosis Risk in Communities and Cardiovascular Health Study data, inflammation was defined by worst quartile of at least 2 of these 3 markers. In Cox regression models, inflammation was assessed as a risk factor for a composite of cardiac events, stroke and mortality as well as components of this composite. Among 20 413 patients, inflammation was identified in 3594 and chronic kidney disease in 1649. In multivariable analyses, both inflammation and chronic kidney disease predicted all outcomes, but their interaction was non-significant. In 5597 patients with C-reactive protein levels, inflammation and elevated C-reactive protein had similar hazard ratios. When focusing only on individuals with the worst quartile of white cell count and albumin, results remained consistent.