the rate of cholesterol synthesis in the liver shows diurnal periodicity, with production peaking at nighttime
statins act by inhibiting the enzyme HMG CoA reductase, which controls synthesis of cholesterol in the liver. Most manufacturers of statins recommend that they are taken at night, on the basis of physiological studies which show that most cholesterol is synthesised when dietary intake is at its lowest (1)
Timing of dosing of simvastatin - nighttime or morning?
a small study by Lund et al (2) found significant differences in total cholesterol and LDL when comparing simvastatin use in the morning and at nighttime
Lund et al have shown that simvastatin, which has a short elimination half-life, taken in the evening instead of the morning decreases the total cholesterol and LDL cholesterol levels more significantly and that alternating times of simvastatin ingestion does not change HDL cholesterol or triglyceride levels
found a 7.3% higher total cholesterol and a 13.4% increase in LDL when the ingestion time was in the morning compared to the patient previously taking medication at nighttime
a systematic review has also concluded that the evidence base supports evening administation of simvastatin (3)
Timing of dosing of other statins
a systematic review revealed a statistically nonsignificant trend in the LDL-C percentage reduction favouring evening statin administration with lovastatin, pravastatin, and rosuvastatin (3)
atorvastatin (a longer elimination half-life than simvastatin) demonstrated similar LDL-C reduction regardless of administration time
the study authors concluded that there are sufficient data to support evening administration of simvastatin to achieve optimal lowering of LDL-C levels
there is however insufficient evidence to support nightime or evening administration of the other statins included in the review
a fluvastatin study revealed that the efficacy and safety profiles of fluvastatin XL are equivalent for morning and evening administration
Notes:
the elimination half-lives of atorvastatin, pravastatin and rosuvastatin are significantly longer than that of simvastatin and this is probably significant in the ability to take these other statins in the morning with non-significant changes in lipid lowering compared to evening administration:
half-lives
simvastatin < 5 hours
atorvastatin 14 hours
rosuvastatin 19 hours
and pravastatin 22 hours
atorvastatin also has active metabolites with half-lives ranging from 20 to 30 hours
this data therefore supports the night-time dosing of simvastatin but there is insufficient evidence to recommend only night-time dosing of statins other than simvastatin
Reference:
1. Jones PJH, Schoeller DA. Evidence ofor diurnal periodicity in human cholesterol synthesis. J Lipid Res 1990;31:667-673
2. Lund TM et al. .Effect of morning versus evening intake of simvastatin on the serum cholesterol level in patients with coronary artery disease. The American Journal of Cardiology 2002;90 (7): 784-786.
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