Is mild asymptomatic left ventricular systolic dysfunction always predictive of adverse events in high-risk

Mauro Gori1, Margaret M Redfield2, Alice Calabrese1

  • 1Cardiovascular Department, ASST Papa Giovanni XXIII Hospital, Bergamo, Italy.

Insights

Diastolic dysfunction (DD) refines risk for heart failure (HF) in patients with mild asymptomatic left ventricular systolic dysfunction (ALVSD). Combining echocardiogram findings of ALVSD and DD improves prediction of adverse cardiovascular events.

Area of Science:

  • Cardiology
  • Echocardiography
  • Heart Failure Research

Background:

  • Mild asymptomatic left ventricular systolic dysfunction (ALVSD) represents a gray zone in heart failure (HF) risk stratification.
  • Incremental risk refinement is needed for patients with ALVSD to better predict incident HF and mortality.

Purpose of the Study:

  • To investigate if diastolic dysfunction (DD) can refine the prediction of HF and death in patients with mild ALVSD.
  • To assess the combined prognostic value of ALVSD and DD in a high-risk population.

Main Methods:

  • Prospective enrollment of 623 asymptomatic outpatients at increased HF risk (age 55-80) in the DAVID-Berg study.
  • Classification based on left ventricular ejection fraction (LVEF) and DD: control, mild ALVSD without DD, and mild ALVSD with DD.
  • Cox proportional hazards model used to analyze HF/death events over a median follow-up of 5.7 years.

Main Results:

  • Mild ALVSD was associated with a higher risk of HF/death compared to controls (HR 1.80).
  • This increased risk was significant only in subjects with co-existing diastolic dysfunction (P=0.005), not in those without it (P=0.30).
  • Diastolic dysfunction significantly refined the risk prediction in the mild ALVSD group.

Conclusions:

  • Echocardiography is crucial for assessing systolic dysfunction, but diastolic dysfunction assessment is vital for risk stratification in mild ALVSD.
  • Mild ALVSD may predict adverse events primarily in individuals with concurrent diastolic dysfunction.
  • Further research is warranted to confirm these findings and their clinical implications.
Abstract

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