Key result
Elevated lipoprotein(a) (>=30 mg/dL) was not significantly associated with mid-term MACE (HR 1.32, 95% CI 0.67-2.60, P=0.43) in Japanese ACS patients surviving primary PCI to discharge.
Why the study?
Previous studies on lipoprotein(a) as a prognostic factor in ACS have yielded conflicting results, with limited data in Japanese populations and inconsistent inclusion of early in-hospital deaths.
Does elevated lipoprotein(a) (>= 30 mg/dL) predict mid-term major adverse cardiac events in Japanese acute coronary syndrome patients surviving primary PCI to hospital discharge?
Cohort (n=347)
No
Does elevated lipoprotein(a) (>= 30 mg/dL) predict mid-term major adverse cardiac events in Japanese acute coronary syndrome patients surviving primary PCI to hospital discharge?
Answers are grounded in this paper and cite their sources.
In Japanese ACS patients surviving primary PCI on contemporary high-rate statin therapy, elevated Lp(a) did not independently predict mid-term MACE, whereas traditional risk factors (age >= 70, male sex, and CKD) remained the primary drivers of prognosis.
Previous studies investigating lipoprotein(a) [Lp(a)] as a prognostic factor in acute coronary syndrome (ACS) have yielded conflicting results, with limited data in Japanese populations. Inconsistent inclusion of early in-hospital deaths further limits clinical applicability for secondary prevention strategies.To evaluate the prognostic value of Lp(a) levels in ACS patients who underwent successful primary percutaneous coronary intervention (PCI) and survived to hospital discharge.This single-center retrospective study enrolled 347 consecutive Japanese ACS patients who underwent primary PCI between December 2016 and March 2021 and were discharged alive. Patients were stratified by Lp(a) levels: < 30 mg/dL (n = 275) and ≥ 30 mg/dL (n = 72). The primary endpoint was major adverse cardiac events (MACE), defined as all-cause death, nonfatal myocardial infarction, nonfatal stroke, and heart failure requiring hospitalization. Kaplan-Meier survival analysis and multivariable Cox regression models were performed.During a median follow-up of 37 months, 59 MACE events (17.0%) occurred. The median Lp(a) level was 14 mg/dL. Kaplan-Meier analysis showed no significant difference in MACE-free survival between groups (log-rank P = 0.46). In all multivariable analyses, Lp(a) ≥ 30 mg/dL was not associated with mid-term MACE. Significant predictors were age ≥ 70 years, male sex, and chronic kidney disease.Elevated Lp(a) levels did not significantly predict mid-term MACE in Japanese ACS patients surviving primary PCI. Traditional risk factors, including age, male sex, and chronic kidney disease, were the primary determinants of mid-term prognosis in this population.
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Okubo et al. (2026) conducted a cohort in Acute coronary syndrome (ACS) surviving primary percutaneous coronary intervention (PCI) to hospital discharge (n=347). Elevated lipoprotein(a) [Lp(a) >= 30 mg/dL] vs. Lp(a) < 30 mg/dL was evaluated on Major adverse cardiac events (MACE: composite of all-cause death, nonfatal myocardial infarction, nonfatal stroke, and congestive heart failure requiring hospitalization) (HR 1.32, 95% CI 0.67-2.60, p=0.43). Elevated lipoprotein(a) (>=30 mg/dL) was not significantly associated with mid-term MACE (HR 1.32, 95% CI 0.67-2.60, P=0.43) in Japanese ACS patients surviving primary PCI to discharge.
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