Authors |
Anne
Hiukka, Jukka Westerbacka, Eeva S. Leinonen, Hiroshi Watanabe, Olov Wiklund,
Lillemor Mattson Hulten, Jukka T. Salonen, Tomi-Pekka Tuomainen, Hannele
Yki-Järvinen, Anthony C. Keech, and Marja-Riitta Taskinen
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Abstract
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Objectives:
The aim of this substudy was to ascertain whether long-term treatment
with fenofibrate reduces surrogate measures of atherosclerosis, biomarkers
of inflammation, and endothelial activation in patients with type 2 diabetes.
Background: Some fibrates may decrease cardiovascular events, improve
endothelial function, and reduce levels of acute-phase proteins. In the
FIELD (Fenofibrate Intervention and Event Lowering in Diabetes) study,
fenofibrate failed to decrease the primary end point of coronary events
in patients with type 2 diabetes.
Methods: A total of 170 patients with type 2 diabetes of the FIELD Helsinki
cohort were randomly assigned to micronized fenofibrate 200 mg/day or
placebo in a double-blind design. Carotid intima-media thickness (IMT)
and the augmentation index (a measure of large artery stiffness) were
measured at baseline and at second- and fifth-year visits. Plasma levels
of interleukin (IL)-6, C-reactive protein (CRP), serum amyloid A (SAA),
secretory phospholipase A2 IIA (SPLA2), E-selectin, vascular cellular
adhesion molecule (VCAM)-1, and intercellular adhesion molecule (CAM)-1
were determined by commercial enzyme-linked immunosorbent assay kits at
the same visits.
Results: IMT and the augmentation index increased similarly in both treatment
groups during the study. Plasma levels of CRP, IL-6, SPLA2, SAA, VCAM-1,
ICAM-1, and E-selectin remained unchanged in both groups.
Conclusions: Fenofibrate treatment was not associated with beneficial
changes in IMT, augmentation index, or biomarkers of inflammation and
endothelial function. (Fenofibrate Intervention and Event Lowering in
Diabetes; NCT00132886)
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