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Updated: Sep 26, 2026

Assessing Whole-Body Lipid-Handling Capacity in Mice
Published on: November 24, 2020
Hepatic lipase and dyslipidemia: interactions among genetic variants, obesity, gender, and diet
Samir S Deeb1, Alberto Zambon, Molly C Carr
1Divisions of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA 98195, USA. sdeeb@u.washington.edu
Abstract:
Hepatic lipase (HL) plays a central role in LDL and HDL remodeling. High HL activity is associated with small, dense LDL particles and with reduced HDL2 cholesterol levels. HL activity is determined by an HL gene promoter polymorphism, by gender (lower in premenopausal women), and by visceral obesity with insulin resistance. The activity is affected by dietary fat intake and selected medications. There is evidence for an interaction of the HL promoter polymorphism with visceral obesity, dietary fat intake, and with lipid-lowering medications in determining the level of HL activity. The dyslipidemia with high HL activity is a potentially proatherogenic lipoprotein profile in the metabolic syndrome, in Type 2 diabetes, and in familial combined hyperlipidemia.
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