Mitotane-Induced Hyperlipidemia: A Retrospective Cohort Study
Author(s) -
Hassan Shawa,
Ferhat Denız,
Hadil Bazerbashi,
Mike Hernández,
Rena VassilopoulouSellin,
Camilo Jiménez,
Mouhammed Amir Habra
Publication year - 2013
Publication title -
international journal of endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.875
H-Index - 60
eISSN - 1687-8345
pISSN - 1687-8337
DOI - 10.1155/2013/624962
Subject(s) - mitotane , medicine , triglyceride , endocrinology , hyperlipidemia , cholesterol , body mass index , adrenocortical carcinoma , diabetes mellitus
Limited data are available about mitotane-nduced hyperlipidemia. We retrospectively analyzed lipid data in 38 patients with adrenocortical carcinoma (ACC) who received mitotane therapy with emphasis on HDL cholesterol (HDL-c) and clinical predictors of lipid changes. At baseline, the mean levels of HDL-c, LDL-c, and triglycerides were 53.3 mg/dL, 114.4 mg/dL, and 149 mg/dL, respectively. HDL-c, LDL-c, and triglyceride concentrations significantly increased with mitotane therapy to a mean HDL peak (HDL-P) of 86.3 mg/dL ( P < 0.001), a mean LDL peak of 160.1 mg/dL ( P < 0.001), and a mean triglyceride peak (Tg-P) of 216.7 mg/dL ( P = 0.042). HDL-P positively correlated with mitotane concentration (r = 0.52, P < 0.001), while LDL-P levels and Tg-P did not. Gender, body mass index, cortisol overproduction, baseline levels of HDL-c, and triglyceride did not predict change in HDL-c. Similar changes were noticed in subgroup analysis after excluding patients who were using lipid-lowering agents. In conclusion, in ACC patients, mitotane caused significant increases in HDL-c that may counteract the deleterious atherosclerotic effects of LDL-c and Tg rise. Understanding the mechanism of HDL change may lead to the discovery of novel HDL-c-elevating drugs.
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