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Lipoprotein(a) Serum Levels Predict Pulse Wave Velocity in Subjects in Primary Prevention for Cardiovascular Disease
Arrigo F G Cicero1,2, Federica Fogacci1,2, Giuseppe Derosa3
1Hypertension and Cardiovascular Risk Factors Research Center, Medical and Surgical Sciences Department, Sant'Orsola-Malpighi University Hospital, Via Albertoni 15, 40138 Bologna, Italy.
Insights
High lipoprotein(a) levels predict arterial stiffness in individuals with large apolipoprotein(a) isoforms, but not those with small isoforms. This finding highlights the importance of apolipoprotein(a) size in cardiovascular risk assessment.
Area of Science:
- Cardiovascular Science
- Lipid Metabolism
- Vascular Biology
Background:
- High lipoprotein(a) [Lp(a)] levels are linked to cardiovascular disease (CVD) risk.
- Apolipoprotein(a) [apo(a)] isoform size may influence this risk, with smaller isoforms often associated with higher risk.
- Early vascular aging, indicated by arterial stiffness, is a key CVD predictor.
Purpose of the Study:
- To investigate if Lp(a) levels predict early vascular aging (arterial stiffness) in individuals without CVD.
- To determine if apo(a) isoform size modifies the predictive value of Lp(a) for vascular aging.
Main Methods:
- Analysis of a subset of Brisighella Heart Study participants (n=978) free from CVD.
- Measurement of arterial stiffness using carotid-femoral pulse wave velocity (cfPWV).
- Step-wise linear regression to identify predictors of cfPWV, stratified by apo(a) isoform size (small vs. large).
Main Results:
- Overall, Lp(a) levels did not predict cfPWV in the study cohort.
- In individuals with large apo(a) isoforms, higher Lp(a) levels were significantly associated with increased arterial stiffness.
- In individuals with small apo(a) isoforms, Lp(a) did not predict arterial stiffness.
Conclusions:
- Apolipoprotein(a) isoform size is a critical factor in the relationship between Lp(a) and arterial stiffness.
- Lipoprotein(a) may serve as a specific predictor of vascular aging in individuals with large apo(a) isoforms.
- These findings suggest personalized risk assessment based on both Lp(a) levels and apo(a) size is warranted.
Abstract:
In the last decades, high serum levels of lipoprotein(a) (Lp(a)) have been associated with increased cardiovascular disease (CVD) risk, in particular among individuals with smaller apolipoprotein(a) (apo(a)) isoforms than those with larger sizes. The aim of our analysis was to evaluate whether Lp(a) levels could predict early vascular aging, and whether smaller apo(a) isoforms had a predictive value for vascular aging different than larger apo(a) isoforms in a cohort of subjects free from CVD. We considered the data of a subset of Brisighella Heart Study (BHS) participants free from CVD (462 men and 516 women) who were clinically evaluated during the 2012 BHS population survey. Predictors of arterial stiffness, measured as carotid-femoral pulse wave velocity (cfPWV) were estimated by the application of a step-wise linear regression model. In our cohort, there were 511 subjects with small apo(a) size and 467 subjects with large apo(a) isoforms. Subjects with larger apo(a) isoform sizes had significantly lower serum levels of Lp(a). In the BHS subpopulation sample, cfPWV was predicted by age, systolic blood pressure (SBP), serum levels of high-density lipoprotein cholesterol (HDL-C), triglycerides (TG) and sex, higher HDL-C serum levels and female sex associated with lower values of cfPWV. In subjects with smaller apo(a) isoform sizes, predictors of cfPWV were age, SBP, sex and serum levels of HDL-C, being higher HDL-C serum levels and female sex associated to lower values of cfPWV. In subjects with larger apo(a) isoform sizes, cfPWV was predicted by age, SBP, serum levels of Lp(a) and sex, with female sex associated with lower values of cfPWV. In our subpopulation sample, Lp(a) did not predict cfPWV. However, in subjects with large apo(a) isoform sizes, Lp(a) was a significant predictor of arterial stiffness.
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