Model-based meta-analysis of changes in circulatory system physiology in patients with chronic heart failure

CPT Pharmacometrics Syst Pharmacol. 2021 Sep;10(9):1081-1091. doi: 10.1002/psp4.12676. Epub 2021 Jul 16.

Abstract

To characterize and compare various medicines for chronic heart failure (CHF), changes in circulatory physiological parameter during pharmacotherapy were investigated by a model-based meta-analysis (MBMA) of circulatory physiology. The clinical data from 61 studies mostly in patients with heart failure with reduced ejection fraction (HFrEF), reporting changes in heart rate, blood pressure, or ventricular volumes after treatment with carvedilol, metoprolol, bisoprolol, bucindolol, enalapril, aliskiren, or felodipine, were analyzed. Seven cardiac and vasculature function indices were estimated without invasive measurements using models based on appropriate assumptions, and their correlations with the mortality were assessed. Estimated myocardial oxygen consumption, a cardiac load index, correlated excellently with the mortality at 3, 6, and 12 months after treatment initiation, and it explained differences in mortality across the different medications. The analysis based on the present models were reasonably consistent with the hypothesis that the treatment of HFrEF with various medications is due to effectively reducing the cardiac load. Assessment of circulatory physiological parameters by using MBMA would be insightful for quantitative understanding of CHF treatment.

Publication types

  • Comparative Study
  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Pressure / drug effects
  • Cardiovascular Agents / administration & dosage*
  • Cardiovascular Agents / pharmacology
  • Chronic Disease
  • Heart Failure / drug therapy*
  • Heart Failure / mortality
  • Heart Failure / physiopathology
  • Heart Rate / drug effects
  • Humans
  • Models, Biological*
  • Randomized Controlled Trials as Topic
  • Stroke Volume / drug effects
  • Time Factors

Substances

  • Cardiovascular Agents