Optimal low-density lipoprotein cholesterol lowering—morning versus evening statin administration

R Plakogiannis, H Cohen - Annals of Pharmacotherapy, 2007 - journals.sagepub.com
R Plakogiannis, H Cohen
Annals of Pharmacotherapy, 2007journals.sagepub.com
Objective: To determine the best time to administer statins for optimal lowering of low-density
lipoprotein cholesterol (LDL-C) by reviewing the clinical evidence evaluating the
chronobiologic effects of morning versus evening statin administration. Data Sources: Using
the MeSH terms HMG-CoA reductase inhibitors, statins, morning and evening dosing, and
clinical trials, a literature review was conducted to identify articles in MEDLINE (1966–
December 2006), International Pharmaceutical Abstracts (1970–Deccmber 2006), and …
Objective
To determine the best time to administer statins for optimal lowering of low-density lipoprotein cholesterol (LDL-C) by reviewing the clinical evidence evaluating the chronobiologic effects of morning versus evening statin administration.
Data Sources
Using the MeSH terms HMG-CoA reductase inhibitors, statins, morning and evening dosing, and clinical trials, a literature review was conducted to identify articles in MEDLINE (1966–December 2006), International Pharmaceutical Abstracts (1970–Deccmber 2006), and IOWA Drug Information Systems (1985–December 2006).
Data Synthesis
Seven English-language studies evaluating morning and evening statin administration were identified and evaluated. Based on the available data, simvastatin demonstrated a pronounced LDL-C percentage reduction with evening closing. Although not statistically significant, a trend in the LDL-C percentage reduction favoring evening statin administration was noted with lovastatin, pravastatin, and rosuvastatin. Atorvastatin demonstrated similar LDL-C reduction regardless of administration time. With the exception of simvastatin, the trials comparing morning versus evening effects of statins on LDL-C have several significant methodologic shortcomings, including small sample size, lack of statistical power, and inappropriate exclusion criteria that did not include or did not mention drug-induced effects on lipids.
Conclusions
There are sufficient data to support evening administration of simvastatin to achieve optimal lowering of LDL-C levels. Rigorous and robust trials are necessary to determine the best administration time to achieve optimal LDL-C lowering for lovastatin, pravastatin, rosuvastatin, atorvastatin, and fluvastatin.
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