Effects of long-term ketoconazole therapy on serum lipid levels
- PMID: 2934265
- DOI: 10.1007/BF00547430
Effects of long-term ketoconazole therapy on serum lipid levels
Abstract
Serum cholesterol and triglycerides were determined in 36 patients receiving an 8-month course of oral ketoconazole 200 mg/day in order to study its effect on lipid metabolism. The mean serum cholesterol concentration had decreased by 15% (p less than 0.001) after 1 month, but on continued medication it returned to the pretreatment state; after discontinuation of therapy it increased transiently by 13% (p less than 0.001). Triglycerides increased during ketoconazole administration and at the end of the trial the mean triglyceride concentration was 48% higher than the baseline value (p less than 0.02). Although most lipid values during therapy lay within the normal ranges, 6 patients developed transient hypertriglyceridaemia. There was no correlation between the changes in lipids and peak serum ketoconazole levels. In one subject studied in more detail the concentration of very low density lipoprotein triglycerides rose during therapy, whereas high density lipoprotein cholesterol decreased slightly. The lipoprotein lipase activity in muscle and, in particular, in adipose tissue was significantly suppressed during ketoconazole treatment. Serum lipids and, if possible, serum lipoproteins should be carefully monitored in patients receiving long-term oral ketoconazole therapy.
Similar articles
-
Gemfibrozil: effect on serum lipids, lipoproteins, postheparin plasma lipase activities and glucose tolerance in primary hypertriglyceridaemia.Proc R Soc Med. 1976;69 Suppl 2(Suppl 2):58-63. doi: 10.1177/00359157760690S215. Proc R Soc Med. 1976. PMID: 190608 Free PMC article.
-
Pharmacologic review: a review of the literature of ketoconazole therapy in the treatment of tinea pedis and onychomycosis.J Foot Surg. 1984 Sep-Oct;23(5):420-3. J Foot Surg. 1984. PMID: 6094646 Review.
-
Effect of sotalol withdrawal on serum lipids and lipoprotein lipase activity.Int J Clin Pharmacol Ther Toxicol. 1983 Feb;21(2):73-6. Int J Clin Pharmacol Ther Toxicol. 1983. PMID: 6840928
-
Changes in plasma lipids and lipoproteins during isotretinoin therapy for acne.N Engl J Med. 1985 Oct 17;313(16):981-5. doi: 10.1056/NEJM198510173131604. N Engl J Med. 1985. PMID: 2931603
-
Effect of amiodarone on serum lipids, lipoprotein lipase, and hepatic triglyceride lipase.Endocrinology. 1987 May;120(5):1991-5. doi: 10.1210/endo-120-5-1991. Endocrinology. 1987. PMID: 3569123
Cited by
-
Ketoconazole blocks bile acid synthesis in hepatocyte monolayer cultures and in vivo in rat by inhibiting cholesterol 7 alpha-hydroxylase.J Clin Invest. 1986 Oct;78(4):1064-71. doi: 10.1172/JCI112662. J Clin Invest. 1986. PMID: 3760182 Free PMC article.
-
Inhibition and induction of bile acid synthesis by ketoconazole. Effects on bile formation in the rat.Lipids. 1989 Sep;24(9):759-64. doi: 10.1007/BF02544580. Lipids. 1989. PMID: 2586232
-
Management of endocrine manifestations and the use of mitotane as a chemotherapeutic agent for adrenocortical carcinoma.J Clin Oncol. 2009 Sep 20;27(27):4619-29. doi: 10.1200/JCO.2008.17.2775. Epub 2009 Aug 10. J Clin Oncol. 2009. PMID: 19667279 Free PMC article. Review.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources