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. 2017 May:260:27-33.
doi: 10.1016/j.atherosclerosis.2017.03.015. Epub 2017 Mar 10.

Effect of ezetimibe on low- and high-density lipoprotein subclasses in sitosterolemia

Affiliations

Effect of ezetimibe on low- and high-density lipoprotein subclasses in sitosterolemia

Rgia A Othman et al. Atherosclerosis. 2017 May.

Abstract

Background and aims: Sitosterolemia displays high plasma total sterols [high plant sterols (PS) + normal to high total cholesterol (TC)] with normal to moderately elevated low-density lipoprotein (LDL) levels. High LDL, intermediate-density lipoprotein (IDL) and very low-density lipoprotein (VLDL) particles, low high-density lipoprotein (HDL), and increased non-HDL and the ratios of TC and triglycerides (TG) to HDL can increase the risk for atherosclerosis. Ezetimibe (EZE) can reduce plasma PS and TC levels in sitosterolemia, but its effect on lipoprotein subclasses has not been previously reported.

Methods: Sitosterolemia patients (n = 8) were taken off EZE for 14 weeks (OFF EZE) and placed on EZE (10 mg/d) for 14 weeks (ON EZE). Serum lipids were measured enzymatically and lipoprotein subclasses were assessed by polyacrylamide gel electrophoresis.

Results: EZE reduced (p < 0.05) total sterols (-12.5 ± 4.1%) and LDL-sterol (-22.7 ± 5.7%) and its sterol mass of large VLDL (-24.4 ± 4.5%), VLDL remnants (-21.1 ± 7.9%) and large IDL (-22.4 ± 7.2%) compared to OFF EZE. EZE did not affect large LDL subclasses or mean LDL particle size (273.8 ± 0.6 vs. 274.6 ± 0.3 Å). EZE increased HDL-sterol (25.5 ± 8.0%, p = 0.008) including intermediate (34 ± 14%, p = 0.02) and large (33 ± 16%, p = 0.06) HDL. EZE reduced non-HDL-sterol (-21.8± 5.0%), total sterols/HDL (-28.2 ± 5.5%) and TG/HDL (-27.4 ± 6.5%, all p < 0.01).

Conclusions: EZE improves VLDL and HDL subfraction distribution, thereby reducing the atherogenic lipid profile, thus providing potential clinical benefit in sitosterolemia beyond TC and PS reduction.

Keywords: Ezetimibe; HDL subclasses; LDL cholesterol; LDL subclasses; Mean LDL particle size; Non-HDL cholesterol; Sitosterolemia; Sterols.

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Conflict of interest statement

Conflict of interest

The authors declared they do not have anything to disclose regarding conflict of interest with respect to this manuscript.

Figures

Fig. 1
Fig. 1
Concentrations of LDL sterol and LDL subfractions at 14 weeks off and 14 weeks on ezetimibe in sitosterolemia patients. (A) VLDL and Midband IDL concentrations, and (B) LDL levels and LDL subfractions; LDL3 was detectable only in two patients from samples of 14 weeks OFF EZE and in one patient from samples of 14 weeks ON EZE. Values are means ± SEM (n = 8). ND, not detectable. *p<0.05, ** p<0.01.
Fig. 2
Fig. 2
Concentrations of HDL sterol and HDL subfractions at 14 weeks off and 14 weeks on ezetimibe in sitosterolemia patients. (A) HDL sterol and the three HDL subclasses, and (B) the lipoprotein subfractions in the three HDL subclasses. Values are means ± SEM (n = 8). * p<0.05, ** p<0.01.

Comment in

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