Epidemiological data suggest that vitamin D, a part from its well recognized role in bone and mineral metabolism could play a favorable role in cardiovascular health. It was previously observed an inverse association between vitamin D serum levels (25(OH)D) and markers of cardiovascular risk; in particular, low levels of 25(OH)D have been associated both with unfavorable lipid profile, and to a poorer response to atorvastatin. Aim of this study was to test the benefit of 25-OH cholecalciferol (calcifediol) supplementation on lipid profile. Postmenopausal osteopenic women at low risk of fracture and with 25(OH)D levels <30ng/ml were included if they were on atorvastatin therapy previously prescribed as appropriate. Recruited women (n=30, mean age 58.26±7.48 years) received oral calcifediol (125 μg) once a week. At baseline, a negative correlation was also found between 25(OH)D and total cholesterol (r=-0.46; p=0.009) and LDL-C (r=-0.5; p=0.003). In comparison to baseline, after 24 weeks a significant increase of mean serum 25(OH)D level (<0.0001) and an improvement of lipid profile were observed. A significant reduction of LDL-C (p=0.01) and an increase of HDL-C (p=0.02) were detected. Percent changes in 25(OH)D levels were found to correlate with the variations of LDL-C (r=-0.41; p=0.02). We found that calcifediol administration in osteopenic and dislipidemic postmenopausal women with low 25(OH)D improves lipid profile when added to an ongoing atorvastatin treatment. Our findings could have clinical implication.

Calcifediol improves lipid profile in atorvastatin treated postmenopausal women

CATALANO, ANTONINO;MORABITO, Nunziata;BELLONE, FEDERICA;FERRO, CHRISTIAN;BASILE, Giorgio;LASCO, Antonino
2015-01-01

Abstract

Epidemiological data suggest that vitamin D, a part from its well recognized role in bone and mineral metabolism could play a favorable role in cardiovascular health. It was previously observed an inverse association between vitamin D serum levels (25(OH)D) and markers of cardiovascular risk; in particular, low levels of 25(OH)D have been associated both with unfavorable lipid profile, and to a poorer response to atorvastatin. Aim of this study was to test the benefit of 25-OH cholecalciferol (calcifediol) supplementation on lipid profile. Postmenopausal osteopenic women at low risk of fracture and with 25(OH)D levels <30ng/ml were included if they were on atorvastatin therapy previously prescribed as appropriate. Recruited women (n=30, mean age 58.26±7.48 years) received oral calcifediol (125 μg) once a week. At baseline, a negative correlation was also found between 25(OH)D and total cholesterol (r=-0.46; p=0.009) and LDL-C (r=-0.5; p=0.003). In comparison to baseline, after 24 weeks a significant increase of mean serum 25(OH)D level (<0.0001) and an improvement of lipid profile were observed. A significant reduction of LDL-C (p=0.01) and an increase of HDL-C (p=0.02) were detected. Percent changes in 25(OH)D levels were found to correlate with the variations of LDL-C (r=-0.41; p=0.02). We found that calcifediol administration in osteopenic and dislipidemic postmenopausal women with low 25(OH)D improves lipid profile when added to an ongoing atorvastatin treatment. Our findings could have clinical implication.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3096997
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