SaaG e-Posters: Atherogenic lipoproteins: on prognostics and mechanisms

137 - Atherogenic Lipoproteins and Carotid Intimal Medial Thickness Progression over 5 years (ID 93)

Session Name
SaaG e-Posters: Atherogenic lipoproteins: on prognostics and mechanisms
Presentation Topic
3.1 Epidemiology of cardiovascular diseases and risk factors

Abstract

Background and Aims

Carotid intimal medical thickness (cIMT) is associated with cardiovascular disease (CVD). The association between atherogenic lipoproteins including small dense low-density lipoprotein cholesterol (sdLDL-C) and carotid intimal medial thickness progression has not been fully evaluated in a prospective cohort study. We assessed the hypothesis that sdLDL-C is the most atherogenic lipoproteins with regard to cIMT progression.

Methods

Plasma total cholesterol, low-density lipoprotein cholesterol (LDL-C), sdLDL-C, LDL-triglycerides (LDL-TG), high density lipoprotein cholesterol (HDL-C), HDL2-C, HDL3-C, triglycerides, lipoprotein(a) [Lp(a)], and adiponectin were measured in 2,030 men and women (median age 59 years, free of CVD and off cholesterol lowering medication). At both baseline and after 5 years of follow-up, cIMT was assessed. Univariate, multivariate regression, and least square analyses were performed to examine the relationships between direct LDL-C, sdLDL-C, Lp(a), and other lipoproteins with cIMT progression.

Results

Median cIMT at baseline was 0.63 mm and median 5 year progression was 0.18 mm. After adjustment for standard CVD risk factor including age, gender, systolic blood pressure, total cholesterol, HDL-C, smoking, diabetes, and hypertension treatment, only LDL-C, sdLDL-C, and the sdLDL-C/LDL-C ratio were associated with cIMT progression. Even in subjects with direct LDL-C < 100 mg/dL, considered to be at low CVD risk, elevated sdLDL-C were associated with cIMT progression (P for trend = 0.009) in a model with established CVD risk factors, although the sdLDL-C/LDL-C ratio did not.

Conclusions

Both sdLDL-C and direct LDL-C are significantly associated with cIMT progression; therefore, measurement of sdLDL-C may allow for the formulation of optimal therapy to cIMT progression.

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