Authors
- Dijana Bešić — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0001-9701-0253
- Petra Bistrović — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0002-3650-3297
- Tomislav Čikara — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0001-8012-4481
- Klara Pospiš — Special Hospital for Medical Rehabilitation Krapinske Toplice, Krapinske Toplice, Croatia — ORCID: 0000-0002-4090-5512
- Sara Varga — ”Dr. Ivo Pedišić” General Hospital, Sisak, Croatia — ORCID: 0009-0005-1125-8108
- Dominik Buljan — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0001-9603-2610
- Fran Rode — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0002-8787-2455
- Fran Šaler — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0002-1428-3940
- Marko Galić — ”Dr. J. Benčević” General Hospital, Slavonski Brod, Croatia — ORCID: 0009-0003-0437-6750
- Merljinda Ljušaj — Čakovec County Hospital, Čakovec, Croatia — ORCID: 0009-0007-8228-1457
- Marija Radić — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0003-2317-6300
- Marin Viđak — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0003-0341-9598
- Martina God — Varaždin General Hospital, Varaždin, Croatia — ORCID: 0009-0009-8838-0549
- Šime Manola — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0001-6444-2674
- Ivana Jurin — Dubrava University Hospital, Zagreb, Croatia — ORCID: 0000-0002-2637-9691
Keywords
lipoprotein(a), low-density lipoprotein cholesterol, acute coronary syndrome, chronic coronary syndrome
DOI
https://doi.org/10.15836/ccar2024.519Full Text
**Background:** Independent of low-density lipoprotein cholesterol (LDL-C) levels, lipoprotein (a), or Lp(a), is a widely acknowledged biomarker for atherosclerosis and coronary artery disease. Studies have demonstrated the role of Lp(a) in the development of acute coronary syndrome (ACS), however it is unclear if Lp(a) could have a significant role in identifying those individuals who are at risk of developing chronic coronary syndrome (CCS). (1, 2) This study sought to investigate the association of Lp(a) and LDL-C levels with occurrence of acute and chronic coronary syndrome. **Patients and Methods**: We analyzed patients included in CaRD registry (NCT06090591) who underwent coronary angiography in Dubrava University Hospital between June 2024 and September 2024. Logistic regression analysis was conducted to investigate the association of higher Lp(a) and LDL-C levels with occurrence of ACS and CCS. A p value of 0.05 was regarded as statistically significant. **Results:** This registry-based study included 141 patients with a median age of 63 years (IQR 54-71). Male patients were more prevalent than female patients (77% vs 23%, respectively). Notably, women were more likely to display higher Lp(a) levels (p=.004). No statistically significant correlation of Lp(a) with age was observed, though older patients tend to have higher LDL-C value (p=.011). Patients with higher LDL-C levels were more likely to experience acute coronary syndrome (p=.005), while patients with higher Lp(a) levels more frequently presented with chronic coronary syndrome (p=.024). **Conclusion:** Based on results of our study, joined Lp(a) and LDL-C analysis might be invaluable tool in primary prevention setting, with the objective of distinguishing high-risk individuals who are more likely to present with CCS from those who are more likely to present with ACS. Additional research and larger sample sizes with longer follow-up are required to investigate the role of Lp(a) and LDL-C as markers of chronic and acute coronary syndrome, respectively.
Literature
- Farzam K, Zubair M, Senthilkumaran S, Lipoprotein A. 2024 Feb 27. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. https://pubmed.ncbi.nlm.nih.gov/34033383/
- Liu HH, Li S, Zhang Y, Guo YL, Zhu CG, Wu NQ, et al. Joint Association of Lipoprotein(a) and a Family History of Coronary Artery Disease with the Cardiovascular Outcomes in Patients with Chronic Coronary Syndrome. J Atheroscler Thromb. 2024 September 1;31(9):1319–32. https://doi.org/10.5551/jat.64693