Galectin-3 and Risk of Heart Failure and Death in Blacks and Whites

John W McEvoy1, Yuan Chen2, Marc K Halushka3

  • 1Department of Epidemiology and the Welch Center for Prevention, Epidemiology and Clinical Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD Ciccarone Center for the Prevention of Heart Disease, Johns Hopkins University School of Medicine, Baltimore, MD.

Insights

Galectin-3 is a strong predictor of heart failure (HF) or death in white adults, but not in black adults. This study highlights potential racial differences in the prognostic utility of galectin-3 for cardiovascular outcomes.

Area of Science:

  • Cardiovascular Medicine
  • Biomarkers
  • Racial Disparities in Health

Background:

  • The association between galectin-3 and heart failure (HF) or death is established in white populations.
  • This association has not been well-defined in black adults.

Purpose of the Study:

  • To investigate the prognostic utility of galectin-3 for heart failure (HF) or death in a diverse cohort.
  • To determine if race modifies the association between galectin-3 and cardiovascular outcomes.

Main Methods:

  • Analysis of galectin-3 levels in 1809 participants (1375 white, 434 black) from the Atherosclerosis Risk in Communities (ARIC) study.
  • Use of Cox proportional hazard models to assess the association between galectin-3 and HF or death, stratified by race.
  • Evaluation of galectin-3's ability to improve risk discrimination for composite outcomes.

Main Results:

  • Galectin-3 was not independently associated with HF or death overall.
  • In race-stratified analyses, galectin-3 was significantly associated with HF or death in white participants (HR 2.2, Q4 vs Q1), but not in black participants (HR 0.8, Q4 vs Q1).
  • Galectin-3 improved risk discrimination for HF or death in whites, but not in blacks, with a significant interaction by race (P=0.03).

Conclusions:

  • Galectin-3 may have limited prognostic value for predicting heart failure (HF) or death in black adults compared to white adults.
  • Racial differences in galectin-3's role in disease mediation may exist.
  • Further research is needed to validate these findings and explore underlying mechanisms.
Abstract

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