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Published on: November 10, 2017
Is it LDL particle size or number that correlates with risk for cardiovascular disease?
H Robert Superko1, Radhika R Gadesam
1Center for Genomics and Human Health, Saint Joseph's Translational Research Institute, 5673 Peachtree Dunwoody Road NE, Suite 675, Atlanta, GA 30342, USA. rsuperko@sjha.org
Insights
Low-density lipoprotein cholesterol (LDL-C) levels are known to impact cardiovascular disease (CVD) risk. However, LDL particle number (LDL-Num) may be a more accurate predictor of CVD risk than LDL-C alone.
Area of Science:
- Cardiovascular Medicine
- Lipidology
- Biochemistry
Background:
- Low-density lipoprotein cholesterol (LDL-C) is a well-established factor in cardiovascular disease (CVD) pathogenesis.
- Despite successful LDL-C lowering therapies, many high-risk patients still experience clinical events.
- Current measures of LDL characteristics may not fully identify all individuals at risk or those who would benefit from specific treatments.
Purpose of the Study:
- To evaluate whether LDL particle size and number (LDL-Num) are superior predictors of CVD risk compared to LDL-C.
- To determine if LDL-Num, measured via apoprotein B, offers a more comprehensive assessment of atherogenicity.
Main Methods:
- Assessment of LDL particle size and number (LDL-Num) as measures of atherogenicity.
- Determination of plasma apoprotein B as a proxy for LDL-Num, as each LDL particle contains one apoprotein B-100 molecule.
- Comparison of the predictive value of LDL-C, LDL particle size, and LDL-Num for CVD risk.
Main Results:
- LDL particle size and number provide independent measures of atherogenicity.
- LDL-Num, assessed by apoprotein B, is suggested as a more reliable indicator of atherogenicity than LDL-C alone.
- Interindividual variation in cholesterol content per LDL particle means LDL-C and LDL-Num provide non-equivalent information regarding absolute CVD risk.
Conclusions:
- LDL particle number and size are strong, independent predictors of cardiovascular disease.
- Measuring LDL particle number (via apoprotein B) may offer a more accurate assessment of an individual's absolute CVD risk than LDL-C alone.
- Further investigation into LDL characteristics beyond LDL-C is warranted for comprehensive CVD risk stratification and targeted therapy.
Abstract:
The role of low-density lipoprotein cholesterol (LDL-C) in the pathogenesis of cardiovascular disease (CVD) and the clinical benefit of lowering LDL-C in high-risk patients is well established. What remains controversial is whether we are using the best measure(s) of LDL characteristics to identify all individuals who are at CVD risk or if they would benefit from specific therapies. Despite the successful LDL-C reduction trials, substantial numbers of patients continue to have clinical events in the treatment groups. The size of LDL particles and assessment of the number of LDL particles (LDL-Num) have been suggested as a more reliable method of atherogenicity. Each LDL particle has one apoprotein B-100 measure attached; therefore, determination of whole plasma apoprotein B can be considered the best measure of LDL-Num. Because the cholesterol content per LDL particle exhibits large interindividual variation, the information provided by LDL-C and LDL-Num is not equivalent. Individuals with the same level of LDL-C may have higher or lower numbers of LDL particles and, as a result, may differ in terms of absolute CVD risk. LDL particle size and number provide independent measures of atherogenicity and are strong predictors of CVD.
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