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Galectin-3 in Cardiorenal Syndrome: A Systematic Review and Meta-analysis
Yujia Zhou1, Yaobin Liang1, Zonglin Shen1
1Department of Cardiovascular, Guangzhou University of Traditional Chinese Medicine Dongguan Hospital, Dongguan 523000, Guangdong, China.
Insights
Galectin-3 (Gal-3) predicts cardiorenal syndrome (CRS) incidence and mortality in heart failure (HF) and chronic kidney disease (CKD) patients. Elevated Gal-3 levels are linked to increased risks for CRS, HF, and CKD mortality.
Area of Science:
- Biomedical research
- Cardiology
- Nephrology
Background:
- Galectin-3 (Gal-3) is implicated in cellular processes including adhesion, apoptosis, inflammation, and immune responses.
- Conflicting findings exist regarding the role of Gal-3 in cardiorenal syndrome (CRS).
Purpose of the Study:
- To systematically evaluate Galectin-3 (Gal-3) as a predictor for cardiorenal syndrome (CRS) subtypes and mortality.
- To clarify the association between serum Gal-3 levels and outcomes in patients with heart failure (HF) and chronic kidney disease (CKD).
Main Methods:
- A comprehensive literature search was conducted across multiple databases (PubMed, EMBASE, Cochrane Library, Web of Science, CNKI) up to March 1, 2026.
- Included studies were observational and investigated serum Gal-3 levels in relation to CRS incidence, HF mortality, CKD mortality, and all-cause mortality in CRS patients.
Main Results:
- High Gal-3 levels significantly predicted incident heart failure (HF) in chronic kidney disease (CKD) patients (HR: 1.19) and all-cause mortality in CKD patients (HR: 2.45).
- Elevated Gal-3 levels in HF patients were associated with a higher risk of CRS occurrence (OR: 1.12) and predicted all-cause mortality (HR: 1.55).
- Two studies indicated a significant association between Gal-3 and all-cause mortality in CRS patients.
Conclusions:
- Galectin-3 (Gal-3) may serve as a significant predictor for the incidence of Type 2 and Type 4 cardiorenal syndrome (CRS).
- Gal-3 is a potential prognostic biomarker for mortality risk in heart failure (HF) and chronic kidney disease (CKD) patients.
- Gal-3 is associated with all-cause mortality in cardiorenal syndrome (CRS) patients.
Background:
Galectin-3 (Gal-3) regulates cell adhesion, apoptosis, inflammation, and immune activation. Recent studies on Gal-3 and renocardiac or cardiorenal syndrome (CRS) show conflicting results. This meta-analysis systematically evaluated Gal-3 in predicting CRS subtypes and mortality.
Methods:
We searched PubMed, EMBASE, The Cochrane Library, Web of Science, and the China National Knowledge Infrastructure (CNKI) for papers investigating the relationship between serum Gal-3 levels and CRS, from database inception to July 10, 2025, with an updated search conducted on March 1, 2026. Observational studies evaluating Gal-3 in relation to CRS incidence and mortality, heart failure (HF) mortality, and chronic kidney disease (CKD) mortality were included.
Results:
A total of 281 articles were retrieved, and 22 were ultimately included after screening. High Gal-3 levels significantly predicted incident HF in CKD patients (hazard ratios [HR]: 1.19; 95% confidence interval [CI]: 1.10-1.28; P<0.0001) and predicted all-cause mortality in CKD patients (HR: 2.45; 95% CI: 1.37-4.37; P=0.002). In HF patients, Elevated Gal-3 levels were associated with a higher risk of the occurrence of CRS (odds ratios [OR]: 1.12; 95% CI: 1.03-1.22; P=0.01) and also predicted all-cause mortality (HR: 1.55; 95% CI: 1.33-1.82; P<0.00001). Finally, the 2 included studies indicated that Gal-3 was significantly associated with all-cause mortality in CRS patients.
Conclusions:
Gal-3 may serve as a significant predictor for the incidence of Type 2 and Type 4 CRS, the risk of mortality in HF and CKD patients, and all-cause mortality in CRS patients.
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