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Updated: Sep 6, 2025

Author Spotlight: Assessing the Cardiovascular Profile of Patients with Metabolic Syndrome
Published on: September 27, 2024
Lipoprotein(a) Modulates Carotid Atherosclerosis in Metabolic Syndrome
Anna Laura Cremonini1,2, Andrea Pasta1, Federico Carbone1,2
1Department of Internal Medicine, University of Genoa, Genoa, Italy.
Insights
Elevated lipoprotein(a) [Lp(a)] is linked to severe carotid atherosclerosis (CA) in metabolic syndrome (MetS) patients. This finding highlights Lp(a) as a key indicator for cardiovascular risk in this population.
Area of Science:
- Cardiology
- Metabolic Disorders
- Vascular Biology
Background:
- High lipoprotein(a) [Lp(a)] is a known cardiovascular risk factor.
- The impact of mildly elevated Lp(a) on cardiovascular health remains unclear.
- Metabolic syndrome (MetS) is associated with increased cardiovascular risk.
Purpose of the Study:
- To investigate the association between Lp(a) levels and the severity of carotid atherosclerosis (CA).
- To examine this relationship specifically within the population of patients diagnosed with MetS.
Main Methods:
- Enrolled patients with diagnosed MetS and ultrasound-assessed CA.
- Categorized patients based on CA severity (moderate vs. severe).
- Collected data on Lp(a) levels, clinical, anthropometric, and biochemical parameters.
Main Results:
- Lp(a) levels were significantly higher in patients with severe CA compared to moderate CA.
- Lp(a) was the sole independent predictor of CA severity in MetS patients.
- A serum Lp(a) level of 10 mg/dl was identified as a potential cut-off for CA severity.
Conclusions:
- Lipoprotein(a) is independently associated with the severity of carotid atherosclerosis in patients with metabolic syndrome.
- Lp(a) may serve as a valuable biomarker for assessing cardiovascular risk in MetS patients.
- Further research with larger sample sizes is warranted to confirm these findings.
Abstract:
Background and Aim: High lipoprotein(a) [Lp(a)] is a well-established cardiovascular (CV) risk factor, but the effect of mildly elevated Lp(a) on CV health is largely unknown. Our aim was to evaluate if Lp(a) is associated with the severity of carotid atherosclerosis (CA) in the specific subset of metabolic syndrome (MetS). Patients and Methods: Subjects with diagnosed MetS and ultrasound-assessed CA were enrolled. Those patients were categorized according to the severity of CA (moderate vs. severe), and the circulating levels of Lp(a) alongside with clinical, anthropometric, and biochemical data were collected. Results: Sixty-five patients were finally included: twenty-five with moderate and forty with severe CA (all with asymptomatic disease). Intergroup comparison showed Lp(a) as the only significantly different variable [6 (2-12) mg/dl vs. 11.5 (6-29.5) mg/dl; p = 0.018]. Circulating levels of Lp(a) were also confirmed as the only variable independently associated with severity of CA at logistic regression analysis [OR 2.9 (95% CI 1.1-7.8); p = 0.040]. ROC curve analysis for Lp(a) confirmed a serum level of 10 mg/dl as the best cut-off value [AUC 0.675 (95% CI 0.548-0.786)]. Although sensitivity and specificity were suboptimal (69.0 and 70.4%, respectively)-likely due to the small sample size-this result is in line with those previously reported in the literature. Conclusion: Lp(a) is independently associated with severity of CA in the subgroup of MetS patients.
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