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Establishing cut-off values for apolipoprotein B and non-HDL-C according to LDL-C values in a South European
S Martinez-Hervas1, J T Real, M A Priego
1Service of Endocrinology and Nutrition, Hospital Clínico Universitario, Valencia, Spain CIBER de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Barcelona, Spain.sergio.martinez@uv.es
Insights
New cut-off values for apolipoprotein B (apoB) and non-HDL-C are proposed to better assess cardiovascular risk in populations with dyslipidaemia. These lipid markers offer improved risk classification beyond LDL-C alone, especially in Mediterranean populations.
Area of Science:
- Cardiovascular Disease Prevention
- Lipid Metabolism
- Clinical Biochemistry
Background:
- Low-density lipoprotein cholesterol (LDL-C) is the primary therapeutic target for dyslipidaemia and cardiovascular disease prevention.
- Current guidelines use specific LDL-C cut-off points for intervention.
- Dyslipidaemia with elevated triglycerides is common, potentially leading to misclassification of risk based solely on LDL-C.
Purpose of the Study:
- To establish cut-off point values for apolipoprotein B (apoB) and non-high-density lipoprotein cholesterol (non-HDL-C).
- To correlate these values with established LDL-C cut-off points for cardiovascular risk assessment.
- To evaluate their utility in a South European population.
Main Methods:
- Cross-sectional study of 1501 subjects (18-80 years).
- Fasting blood samples analyzed for cholesterol, HDL-C, triglycerides, and apoB.
- LDL-C calculated using the Friedewald formula; non-HDL-C calculated as total cholesterol minus HDL-C.
Main Results:
- Significant correlations found between apoB and LDL-C (r=0.86) and between apoB and non-HDL-C (r=0.91).
- Proposed apoB cut-off points for LDL-C goals (70, 100, 130, 160 mg/dL) are 70, 80, 100, 115 mg/dL.
- Proposed non-HDL-C cut-off values for LDL-C goals are 100, 120, 150, 190 mg/dL.
Conclusions:
- LDL-C cut-off values may inaccurately estimate cardiovascular risk in individuals with mild hypertriglyceridaemia, common in Mediterranean populations.
- Proposed apoB and non-HDL-C cut-off values can better account for atherogenic particles and patient risk classification.
- Further prospective trials are needed to validate these findings with cardiovascular outcomes.
Background:
Low-density lipoprotein cholesterol (LDL-C) remains the primary target of therapy in most strategies of dyslipidaemia management focused on cardiovascular disease prevention. Different guidelines have identified specific LDL-C cut-off points as targets for therapeutic intervention. Many clinical situations characterised by dyslipidaemia and elevated triglycerides are common in our environment and in overall industrialised countries. Thus, lipid goals based only on LDL-C could misclassify an important percentage of subjects. The objective of the present study was to establish cut-off point values for apoB and non-HDL-C in relation to the identified LDL-C cut-off points for cardiovascular risk in a South European population.
Methods:
We performed a cross-sectional study including 1501 subjects (770 women and 731 men) between 18 and 80 years of age. Samples were collected after 12-14 h of fasting. Cholesterol, HDL-C, triglycerides and apoB levels were measured using direct methods. LDL-C was calculated by the Friedewald formula. Non-HDL-C was calculated as total cholesterol minus HDL-C.
Results:
The Spearman's rank correlations between apoB and LDL-C (r 0.86, p < 0.0001), and between apoB and non-HDL-C (r 0.91, p < 0.0001) were both significant. The proposed cut-off points for apoB, according to LDL-C goals (70, 100, 130 and 160 mg/dl) in our population are 70, 80, 100 and 115 mg/dl respectively. The proposed cut-off values for non-HDL-C are 100, 120, 150 and 190 mg/dl respectively.
Conclusion:
The established LDL-C cut-off values could not be accurate to estimate cardiovascular risk in subjects with mild hypertriglyceridaemia, as frequently occurs in our Mediterranean population. To take into consideration the burden of atherogenic particles and better classify patients at risk we propose cut-off values for apoB or the equivalent for non-HDL-C. Prospective trials including cardiovascular variables are needed to validate our assumption.
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