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Lipoprotein(a) and Adverse Outcomes After Successful Percutaneous Coronary Intervention for Chronic Total Occlusion:
Jing Wang1, Qiheng Wan2, Zehan Huang2
1Department of Cardiology, Shenzhen Luohu Hospital Group Luohu People's Hospital, The Third Affiliated Hospital of Shenzhen University, Shenzhen 518000, China.
Insights
Elevated Lipoprotein(a) [Lp(a)] significantly increases cardiovascular death risk after successful chronic total occlusion (CTO) percutaneous coronary intervention (PCI). This finding highlights Lp(a) as a key prognostic marker for risk stratification in high-risk patients.
Area of Science:
- Cardiology
- Biochemistry
Background:
- Lipoprotein(a) [Lp(a)] is a known atherogenic and prothrombotic lipoprotein.
- The prognostic significance of Lp(a) in patients undergoing successful chronic total occlusion (CTO) percutaneous coronary intervention (PCI) is not well-defined.
Purpose of the Study:
- To investigate the association between Lp(a) levels and cardiovascular outcomes in patients with successful CTO PCI.
- To determine if Lp(a) can serve as a prognostic marker for risk stratification in this patient population.
Main Methods:
- A single-center retrospective cohort study of 1509 patients who underwent successful CTO PCI.
- Primary outcome: cardiovascular death. Secondary outcome: major adverse cardiovascular events (MACEs).
- Multivariable Cox regression and restricted cubic splines (RCS) were used to analyze Lp(a) and outcomes.
Main Results:
- Elevated Lp(a) was independently associated with increased risk of cardiovascular death and MACEs.
- Each 1-SD increase in log-transformed Lp(a) correlated with a 51% higher risk of cardiovascular death and 44% higher risk of MACEs.
- A linear dose-response relationship was observed between Lp(a) levels and adverse cardiovascular events.
Conclusions:
- In patients with successful CTO PCI, elevated Lp(a) is an independent predictor of cardiovascular death and MACEs.
- Lp(a) may enhance risk stratification in this high-risk group.
- Further prospective studies are needed to validate these findings for clinical application.
Abstract:
Background: Lipoprotein(a) [Lp(a)] is a genetically determined, atherogenic, and prothrombotic lipoprotein. However, its prognostic value in patients who undergo successful chronic total occlusion (CTO) percutaneous coronary intervention (PCI) remains undefined. Methods: This single-center retrospective cohort study included 1509 patients who underwent successful CTO PCI. The primary outcome was cardiovascular death; secondary outcome was major adverse cardiovascular events (MACEs, cardiovascular death or nonfatal myocardial infarction). Multivariable Cox regression and restricted cubic splines (RCS) assessed the association between Lp(a) and outcomes. Results: Over median follow-up of 810 days, 53 (3.5%) cardiovascular deaths and 62 (4.1%) MACEs occurred. Each 1-SD increase in log-transformed Lp(a) was associated with a 51% higher risk of cardiovascular death (aHR 1.51, 95% CI 1.11-2.05, p = 0.008) and a 44% higher risk of MACEs (aHR 1.44, 95% CI 1.09-1.91, p = 0.011). Compared with Lp(a) < 30 mg/dL, Lp(a) ≥ 50 mg/dL conferred a 2.07-fold higher risk of cardiovascular death (95% CI 1.07-4.00, p = 0.029) and a 1.94-fold higher risk of MACEs (95% CI 1.07-3.53, p = 0.030). RCS analysis demonstrated a linear dose-response relationship between log-transformed Lp(a) and both cardiovascular death (p for nonlinearity = 0.653) and MACEs (p for nonlinearity = 0.562). The association was modified by age, hypertension, and left ventricular ejection fraction and remained robust in sensitivity analyses. Conclusions: In patients undergoing successful CTO PCI, elevated Lp(a) was independently and linearly associated with higher risks of cardiovascular death and MACEs. These findings suggest that Lp(a) may serve as a useful prognostic marker to enhance risk stratification in this high-risk population. Large-scale prospective cohorts are needed to validate these findings before clinical translation can be considered.
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