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Updated: Aug 12, 2026

Cholesterol Efflux Assay
Published on: March 6, 2012
Atorvastatin, a New HMG-CoA Reductase Inhibitor, Does Not Affect Glucocorticoid Hormones in Patients With
Isaacsohn1, Bakker-Arkema, Fayyad
1Metabolic and Atherosclerosis Research Center, Cinicnnati, Ohio, USA
Insights
High-dose atorvastatin (Lipitor) and colestipol treatments effectively lower cholesterol without impacting adrenal function. This study confirms the safety of these lipid-lowering therapies for patients with severe hypercholesterolemia.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Pharmacology
Background:
- Atorvastatin calcium is a potent HMG-CoA reductase inhibitor used for hypercholesterolemia.
- Severe hypercholesterolemia necessitates evaluating the impact of aggressive lipid-lowering on adrenal function.
Purpose of the Study:
- To assess the effects of maximal atorvastatin and colestipol doses on adrenal function.
- To determine if pronounced cholesterol reduction influences cortisol levels under basal and stimulated conditions.
Main Methods:
- 40 patients with severe hypercholesterolemia underwent adrenal function tests (basal and ACTH-stimulated).
- Treatments included maximal doses of atorvastatin, colestipol, or combinations over 1 year.
- Lipid-lowering efficacy and serum cortisol levels were monitored.
Main Results:
- Significant reductions in LDL cholesterol were observed across treatment groups (up to 57%).
- No clinically significant changes in basal or ACTH-stimulated cortisol levels were noted.
- Adrenal function remained stable throughout the 1-year treatment period.
Conclusions:
- Maximal atorvastatin doses do not adversely affect adrenal function.
- Colestipol, alone or with statins, does not appear to impact adrenal function.
- These lipid-lowering therapies are safe concerning adrenal endocrine function.
Abstract:
BACKGROUND: Atorvastatin calcium (Lipitor) is a new 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor. The present study was conducted to examine the effect of pronounced cholesterol lowering on adrenal function in patients with severe hypercholesterolemia. METHODS AND RESULTS: Adrenal function was examined under basal conditions and following adrenal corticotropin hormone stimulation in 40 patients (36 with heterogeneous familial and 4 with polygenic hypercholesterolemia). The study was part of a larger study comparing the efficacy and safety of atorvastatin, colestipol, atorvastatin + colestipol, and simvastatin + colestipol treatment over a 1-year period. Maximum doses of all agents were studied: 80 mg atorvastatin once daily, 40 mg simvastatin once daily, and 20 g/day colestipol. At the end of the 1-year treatment period, reductions in low-density lipoprotein cholesterol were 57%, 54%, and 49% for the atorvastatin, colestipol + atorvastatin, and colestipol + simvastatin groups, respectively. No clinically significant changes in basal serum cortisol levels were seen in any treatment group during the 1-year treatment period. Mean serum cortisol concentrations and area under the curve for cortisol concentration versus time data following adrenal corticotropin hormone stimulation were not clinically different during treatment compared with values obtained at baseline for any of the treatment groups. CONCLUSIONS: Treatment with maximum doses of atorvastatin for 1-year did not have any adverse effects on adrenal function under basal conditions or during maximum stimulation. Similarly, colestipol therapy alone and in combination with either atorvastatin or simvastatin did not appear to affect adrenal function.
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