Increased Incidence of Ischemic Cerebrovascular Events in Cardiovascular Patients With Elevated Apolipoprotein CIII

Oliviero Olivieri1, Manuel Cappellari2, Gianni Turcato3

  • 1From the Department of Medicine, Unit of Internal Medicine, University of Verona, Italy (O.O., D.G., F.P., S.F., A.C., N.M.).

Stroke
|December 5, 2019
PubMed

Insights

High levels of apolipoprotein CIII (Apo CIII) are linked to an increased risk of ischemic stroke and transient ischemic attacks (TIA) in cardiovascular patients. This finding highlights Apo CIII as a potential predictor for cerebrovascular events.

Area of Science:

  • Cardiovascular Medicine
  • Metabolic Disorders
  • Neurology

Background:

  • Apolipoprotein CIII (Apo CIII) regulates lipoprotein metabolism and is implicated in coagulation.
  • Elevated Apo CIII is associated with increased thromboembolic risk in arterial and venous systems.

Purpose of the Study:

  • To investigate the association between Apo CIII plasma concentration and the risk of acute ischemic cerebrovascular events.
  • To determine if Apo CIII predicts ischemic stroke/TIA in cardiovascular patients.

Main Methods:

  • Systematic review of medical records and quantification of ischemic events in 950 cardiovascular patients (with/without coronary artery disease).
  • Prospective follow-up for a median of 130 months, with assessment of plasma lipid and apolipoprotein profiles at enrollment.
  • Statistical analysis including hazard ratios and propensity score matching to adjust for confounders.

Main Results:

  • 95 subjects (10%) experienced ischemic stroke/TIA events during follow-up.
  • Higher Apo CIII plasma concentration was observed in subjects with stroke/TIA compared to those without.
  • Apo CIII levels above the median (10.6 mg/dL) were associated with an approximately 2-fold increased risk of stroke/TIA, even after adjusting for multiple confounders.

Conclusions:

  • High plasma Apo CIII concentration is a potential predictor of ischemic stroke/TIA risk in cardiovascular patients.
  • This association was consistent across patient subgroups and validated using propensity score matching.

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