Circulating Galectin-3 Is Associated With Cardiometabolic Disease in the Community

Matthew Nayor1, Na Wang2, Martin G Larson3

  • 1National Heart, Lung, and Blood Institute's and Boston University's Framingham Heart Study, Framingham, MA (M.N., M.G.L., R.S.V., D.L., J.E.H.) Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (M.N.).

Insights

Higher Galectin-3 (Gal-3) levels correlate with obesity and hypertension but do not predict future cardiometabolic diseases. Further research is needed to understand Gal-3

Area of Science:

  • Cardiovascular Medicine
  • Endocrinology
  • Metabolic Research

Background:

  • Circulating Galectin-3 (Gal-3) is linked to heart failure, atrial fibrillation, chronic kidney disease, and mortality.
  • Emerging evidence suggests Gal-3 influences cardiometabolic factors like adiposity, insulin resistance, and hyperglycemia.

Purpose of the Study:

  • To investigate the association between blood Gal-3 concentrations and cardiometabolic disease traits.
  • To determine if Gal-3 predicts incident cardiometabolic diseases in a community-based cohort.

Main Methods:

  • Cross-sectional and prospective analyses were conducted on 2946 participants from the Framingham Heart Study.
  • Associations between Gal-3 levels and various cardiometabolic risk factors and disease incidence were examined.

Main Results:

  • Higher Gal-3 concentrations were significantly associated with increased body mass index, waist circumference, triglycerides, obesity, and hypertension.
  • Gal-3 showed associations with incident metabolic syndrome and diabetes in age- and sex-adjusted models, but these did not persist after multivariable adjustment.

Conclusions:

  • Circulating Gal-3 is associated with abdominal adiposity, dyslipidemia, and hypertension cross-sectionally.
  • Gal-3 did not predict incident cardiometabolic disease in multivariable-adjusted analyses.
  • Further research should explore the mechanisms linking Gal-3 to cardiometabolic disease and its potential as a therapeutic target.
Abstract

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