TY - JOUR
T1 - Effect of atorvastatin and bezafibrate on plasma levels of C-reactive protein in combined (mixed) hyperlipidemia
AU - Gómez-Gerique, Juan A.
AU - Ros, Emilio
AU - Oliván, Josefina
AU - Mostaza, Jose M.
AU - Vilardell, Miquel
AU - Pintó, Xavier
AU - Civeira, Fernando
AU - Hernández, Antonio
AU - Da Silva, Pedro Marqués
AU - Rodriguez-Botaro, Antonio
AU - Zambón, Daniel
AU - Lima, Joan
AU - Díaz, Cristina
AU - Aristegui, Rosa
AU - Sol, Josep M.
AU - Chaves, Jose
AU - Hernández, Gonzalo
PY - 2002
Y1 - 2002
N2 - C-reactive protein (CRP) is a non-specific but sensitive marker of underlying systemic inflammation. High CRP plasma levels correlate with risk for future cardiovascular events. The present study evaluated the effects of atorvastatin (10-40 mg) and bezafibrate (400 mg) on CRP concentrations after 6 and 12 months of treatment in 103 patients with combined (mixed) hyperlipidemia. The number of cardiovascular risk factors present in a given patient was associated with baseline CRP levels. After 6 months and 1 year, atorvastatin treatment was associated with significant (P<0.001) decreases from baseline of CRP concentrations by 29 and 43%, respectively, while bezafibrate-treated patients showed non-significant reductions of 2.3 and 14.6%, respectively (P=0.056 and 0.005 for the respective differences between the two treatment arms at 6 months and 1 year). The magnitude of change in CRP after 1 year was directly related to baseline CRP levels. Covariance analysis showed that CRP decreases in the atorvastatin group were unrelated to total cholesterol and LDL cholesterol reductions; however, they were directly related to triglyceride changes (r=0.28, P=0.047) and inversely related to HDL cholesterol changes (r=-0.28, P=0.045). A model including baseline CRP values and treatment effect showed that atorvastatin use was a significant predictor of change in CRP levels over time (β=0.82, P=0.023). These results suggest a potential anti-atherosclerotic additional benefit of atorvastatin in patients at a risk of cardiovascular disease.
AB - C-reactive protein (CRP) is a non-specific but sensitive marker of underlying systemic inflammation. High CRP plasma levels correlate with risk for future cardiovascular events. The present study evaluated the effects of atorvastatin (10-40 mg) and bezafibrate (400 mg) on CRP concentrations after 6 and 12 months of treatment in 103 patients with combined (mixed) hyperlipidemia. The number of cardiovascular risk factors present in a given patient was associated with baseline CRP levels. After 6 months and 1 year, atorvastatin treatment was associated with significant (P<0.001) decreases from baseline of CRP concentrations by 29 and 43%, respectively, while bezafibrate-treated patients showed non-significant reductions of 2.3 and 14.6%, respectively (P=0.056 and 0.005 for the respective differences between the two treatment arms at 6 months and 1 year). The magnitude of change in CRP after 1 year was directly related to baseline CRP levels. Covariance analysis showed that CRP decreases in the atorvastatin group were unrelated to total cholesterol and LDL cholesterol reductions; however, they were directly related to triglyceride changes (r=0.28, P=0.047) and inversely related to HDL cholesterol changes (r=-0.28, P=0.045). A model including baseline CRP values and treatment effect showed that atorvastatin use was a significant predictor of change in CRP levels over time (β=0.82, P=0.023). These results suggest a potential anti-atherosclerotic additional benefit of atorvastatin in patients at a risk of cardiovascular disease.
KW - Atorvastatin
KW - Bezafibrate
KW - C-reactive protein (CRP)
KW - Combined hyperlipidemia
KW - Inflammation markers
KW - Lipid lowering drugs
UR - https://www.scopus.com/pages/publications/0036242297
U2 - 10.1016/S0021-9150(01)00708-0
DO - 10.1016/S0021-9150(01)00708-0
M3 - Article
C2 - 11996943
AN - SCOPUS:0036242297
SN - 0021-9150
VL - 162
SP - 245
EP - 251
JO - Atherosclerosis
JF - Atherosclerosis
IS - 2
ER -