Shows that PCSK9 inhibition enhances macrophage-specific reverse cholesterol transport in heterozygous familial hypercholesterolemia models, indicating improved fecal cholesterol excretion.
PCSK9 inhibitors alter the distribution of macrophage-derived cholesterol within lipoproteins in plasma from heterozygous FH subjects during ex vivo cholesterol efflux, reducing LDL's capacity as a cholesterol acceptor while enhancing HDL's acceptor function.PCSK9 inhibition enhances the macrophage-specific reverse cholesterol transport pathway in human apoB100 transgenic mice, specifically under conditions of heterozygous LDL receptor deficiency.Anti-PCSK9 therapy facilitates the transfer of LDL-derived cholesterol to feces in heterozygous LDLR-deficient mice expressing human APOB100.
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Borràs et al. (2024) studied this question.
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