Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease

Ci Song1,2, Stephen Burgess3, John D Eicher4,2

  • 1Framingham Heart Study, Framingham, MA ci.song@nih.gov.

Insights

Elevated levels of plasminogen activator inhibitor type 1 (PAI-1) causally increase the risk of coronary heart disease (CHD). This link may be influenced by impaired glucose regulation, highlighting PAI-1 as a potential therapeutic target for cardiovascular disease prevention.

Area of Science:

  • Cardiovascular Science
  • Thrombosis Research
  • Metabolic Disease

Background:

  • Plasminogen activator inhibitor type 1 (PAI-1) is crucial in the fibrinolysis and thrombosis systems.
  • Population studies link blood PAI-1 levels to increased coronary heart disease (CHD) risk.
  • The causal role of PAI-1 in CHD development remains uncertain.

Purpose of the Study:

  • To investigate the observational and causal associations between PAI-1 levels and CHD risk.
  • To explore the impact of PAI-1 on cardiovascular risk factors, including metabolic and atherosclerosis measures.

Main Methods:

  • Systematic review and meta-analysis of observational studies on PAI-1 and CHD incidence.
  • Mendelian randomization analysis using genome-wide association study summary statistics.
  • Assessment of PAI-1's causal effect on cardiovascular risk factors.

Main Results:

  • Meta-analysis showed higher PAI-1 levels associated with increased CHD risk (OR=1.46; 95% CI: 1.13, 1.88) in multivariable models.
  • Mendelian randomization indicated a causal effect of elevated PAI-1 on CHD risk (OR=1.22 per unit increase of log-transformed PAI-1; 95% CI: 1.01, 1.47).
  • PAI-1 was found to causally influence blood glucose and high-density lipoprotein cholesterol levels.

Conclusions:

  • Elevated PAI-1 levels have a causal impact on coronary heart disease risk.
  • Glucose dysfunction may mediate the causal effect of PAI-1 on CHD.
  • These findings underscore PAI-1's role in cardiovascular pathophysiology.
Abstract

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