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ABSTRACT: Background
Fibrosis is a key pathological process in many chronic inflammatory disease states.Aims
We hypothesized that tissue inhibitor metalloproteinase-1 and matrix metalloproteinase-9 (TIMP-1 and MMP-9), biomarkers of fibrosis, would predict all-cause mortality and we assessed the incremental value of these biomarkers when adjusting for clinical and other biomarkers.Methods
The cohort included 5511 community-dwelling participants in the AGES-Reykjavik Study. The baseline Cox proportional hazards regression model was based on the Framingham Risk Score variables; we added TIMP-1, MMP-9, serum high-sensitivity C-reactive protein (hsCRP), and estimated glomerular filtration rate (eGFR). The primary outcome was all-cause 10-year mortality. Cause of death was categori
SUBMITTER: LaRocca G
PROVIDER: S-EPMC5837193 | biostudies-literature | 2017 Dec
REPOSITORIES: biostudies-literature