Key result
Higher admission LDL-C linked to ~48% greater thrombus burden risk per mmol/L in STEMI.
Why the study?
High thrombus burden during primary PCI for STEMI is associated with adverse outcomes, but the direct role of LDL-C in acute thrombus formation remains unclear.
Does elevated admission LDL-C correlate with high angiographic thrombus burden in STEMI patients undergoing primary PCI?
Observational (n=236)
No
Does elevated admission LDL-C correlate with high angiographic thrombus burden in STEMI patients undergoing primary PCI?
Effect estimate: adjusted OR 1.48 (95% CI 1.03-2.13)
p-value: p=0.033
Elevated admission LDL-C is independently associated with a higher angiographic thrombus burden in STEMI patients undergoing primary PCI, suggesting a direct prothrombotic role during acute coronary syndromes.
Higher admission LDL-C identifies STEMI patients at elevated thrombus burden risk during primary PCI; extends observational links to this interventional setting.
Background High thrombus burden (HTB) during primary percutaneous coronary intervention (PCI) for ST‐segment elevation myocardial infarction (STEMI) is associated with adverse outcomes. Low‐density lipoprotein cholesterol (LDL‐C) is a key driver of atherosclerosis, but its direct role in acute thrombus formation remains unclear. Methods This single‐center observational study enrolled 236 consecutive STEMI patients undergoing primary PCI at our institution between November 2022 and July 2025. Thrombus burden was graded angiographically per TIMI criteria (Grades 1–3: low thrombus burden [LTB]; grades 4–5: HTB). Multivariable logistic regression evaluated associations between LDL‐C levels and thrombus burden. Restricted cubic spline (RCS) modeling explored potential nonlinear relationships. Stratified analyses assessed result robustness. Results HTB occurred in 78.4% (185/236) of STEMI patients receiving primary PCI. Patients with HTB demonstrated higher prior MI rates (13% vs. 2%, p = 0.024), elevated admission LDL‐C (1.8 ± 1.1 vs. 1.4 ± 0.9 mmol/L, p = 0.038), increased peak high‐sensitivity troponin T (1473.0 vs 718.0 ng/mL, p = 0.004), and longer hospitalization (6.0 ± 2.8 vs 4.9 ± 2.2 days, p = 0.007). After adjustment for age, sex, prior MI, systolic blood pressure, hemoglobin, HbA1c, and D‐dimer, each 1 mmol/L increment in admission LDL‐C was associated with a 48% increased HTB risk (adjusted OR 1.48; 95% CI 1.03–2.13, p = 0.033). Admission LDL‐C > 1.8 mmol/L predicted a 2.32‐fold higher likelihood of heavy thrombus burden (95% CI 1.04–5.18, p = 0.039). RCS analysis confirmed a linear dose–response association ( P for nonlinearity = 0.922). Sensitivity analyses using complete‐case data confirmed robustness, and subgroup analyses revealed consistent associations across age, sex, body mass index, smoking status, comorbidities, and lipoprotein(a) levels (all P for interaction > 0.05). Conclusion Elevated admission LDL‐C independently correlates with HTB in primary PCI‐treated STEMI patients, suggesting LDL‐C facilitates prothrombotic pathways during acute coronary syndrome. These findings reinforce LDL‐C reduction as a therapeutic approach to mitigate thrombotic complications.
No takes yet. Share an insight, caveat, or question.
Han et al. (2026) conducted an observational in ST-segment elevation myocardial infarction (STEMI) undergoing primary PCI (n=236). Admission LDL-C was evaluated on High thrombus burden (HTB) graded angiographically per TIMI criteria (grades 4-5) (adjusted OR 1.48, 95% CI 1.03-2.13, p=0.033). Each 1 mmol/L increment in admission LDL-C was associated with a 48% increased risk of high thrombus burden in STEMI patients undergoing primary PCI (adjusted OR 1.48; 95% CI 1.03-2.13; p=0.033).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: