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Prognostic value of changes in galectin-3 levels over time in patients with heart failure: data from CORONA and COACH
A Rogier van der Velde1, Lars Gullestad, Thor Ueland
1Department of Cardiology, Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Insights
Monitoring changes in galectin-3 levels over time significantly improves risk prediction for heart failure (HF) patients. Rising galectin-3 indicates a higher risk of HF hospitalization and mortality.
Area of Science:
- Cardiology
- Biomarkers
- Heart Failure Research
Background:
- Baseline galectin-3 levels are linked to adverse outcomes in heart failure (HF).
- The prognostic utility of serial galectin-3 measurements in HF remains unestablished.
Purpose of the Study:
- To investigate the clinical significance of repeated galectin-3 measurements in predicting HF morbidity and mortality.
Main Methods:
- Galectin-3 was measured at baseline and follow-up (3 or 6 months) in 1329 (CORONA) and 324 (COACH) HF patients.
- Patients were categorized by galectin-3 level changes (threshold: 17.8 ng/mL or 15% change).
- Outcomes assessed included HF hospitalization and mortality, adjusted for clinical factors.
Main Results:
- Increasing galectin-3 levels were associated with significantly higher rates of HF hospitalization and mortality in both cohorts.
- A >15% increase in galectin-3 from baseline elevated the relative hazard of adverse events by 50% (HR 1.50, P=0.001).
- Prognostic value was independent of established HF risk factors and biomarkers.
Conclusions:
- Serial galectin-3 measurements provide significant prognostic value in patients with chronic and acute decompensated HF.
- Changes in galectin-3 levels effectively identify patients at elevated risk for future HF events.
- This approach enhances risk stratification beyond baseline assessments.
Background:
In several cross-sectional analyses, circulating baseline levels of galectin-3, a protein involved in myocardial fibrosis and remodeling, have been associated with increased risk for morbidity and mortality in patients with heart failure (HF). The importance and clinical use of repeated measurements of galectin-3 have not yet been reported.
Methods And Results:
Plasma galectin-3 was measured at baseline and at 3 months in patients enrolled in the Controlled Rosuvastatin Multinational Trial in Heart Failure (CORONA) trial (n=1329), and at baseline and at 6 months in patients enrolled in the Coordinating Study Evaluating Outcomes of Advising and Counseling Failure (COACH) trial (n=324). Patient results were analyzed by categorical and percentage changes in galectin-3 level. A threshold value of 17.8 ng/mL or 15% change from baseline was used to categorize patients. Increasing galectin-3 levels over time, from a low to high galectin-3 category, were associated with significantly more HF hospitalization and mortality compared with stable or decreasing galectin-3 levels (hazard ratio in CORONA, 1.60; 95% confidence interval, 1.13-2.25; P=0.007; hazard ratio in COACH, 2.38; 95% confidence interval, 1.02-5.55; P=0.046). In addition, patients whose galectin-3 increased by >15% between measurements had a 50% higher relative hazard of adverse event than those whose galectin-3 stayed within ±15% of the baseline value, independent of age, sex, diabetes mellitus, left ventricular ejection fraction, renal function, medication (β-blocker, angiotensin converting enzyme inhibitor, and angiotensin receptor blocker), and N-terminal probrain natriuretic peptide (hazard ratio in CORONA, 1.50; 95% confidence interval, 1.17-1.92; P=0.001). The impact of changing galectin-3 levels on other secondary end points was comparable.
Conclusions:
In 2 large cohorts of patients with chronic and acute decompensated HF, repeated measurements of galectin-3 level provided important and significant prognostic value in identifying patients with HF at elevated risk for subsequent HF morbidity and mortality.
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