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Published on: October 2, 2020
Galectin-3 Interacts with Vascular Cell Adhesion Molecule-1 to Increase Cardiovascular Mortality in Hemodialysis
Wen-Chin Ko1,2, Cheuk-Sing Choy3,4,5, Wei-Ning Lin6
1College of Medicine, Fu Jen Catholic University, New Taipei City 242, Taiwan. 086938@mail.fju.edu.tw.
Insights
In maintenance hemodialysis patients, high levels of galectin-3 and vascular cell adhesion molecule 1 (VCAM-1) significantly increase risks for all-cause and cardiovascular mortality. These biomarkers show a combined effect, highlighting their prognostic value.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Biomarker Research
Background:
- The combined impact of galectin-3 and vascular cell adhesion molecule 1 (VCAM-1) on mortality in maintenance hemodialysis (MHD) patients is not well understood.
- Understanding these interactions is crucial for improving prognostic assessments in this high-risk population.
Purpose of the Study:
- To investigate the independent and joint effects of serum galectin-3 and VCAM-1 on all-cause and cardiovascular (CV) mortality risks in MHD patients.
- To determine if galectin-3 and VCAM-1 can serve as dual biomarkers for predicting mortality.
Main Methods:
- Analysis of unadjusted and adjusted hazard ratios (aHRs) for mortality in patients categorized by higher and lower serum concentrations of galectin-3 and VCAM-1.
- Investigation of the modification effect between galectin-3 and VCAM-1 on mortality risk using an interaction product term.
Main Results:
- Both galectin-3 and VCAM-1 were independently associated with increased all-cause mortality risk.
- VCAM-1, but not galectin-3, showed a trend towards predicting cardiovascular mortality.
- Patients with combined high levels of galectin-3 and VCAM-1 exhibited the greatest risk for both all-cause and CV mortality, with statistically significant interactions observed (p < 0.01 for all-cause, p < 0.05 for CV).
Conclusions:
- Galectin-3 and VCAM-1 demonstrate significant joint effects on mortality risk in MHD patients.
- These biomarkers hold promise as a dual prognostic tool, potentially related to their roles in leukocyte trafficking and atherothrombosis.
Background:
Interactions and joint effects of galectin-3 and vascular cell adhesion molecule 1 (VCAM-1) on risks of all-cause and cardiovascular (CV) mortality remain unclear in patients with maintenance hemodialysis (MHD).
Methods:
Unadjusted and adjusted hazard ratios (aHRs) of mortality risks were analyzed between higher and lower concentration groups of serum galectin-3 and VCAM-1. The modification effect between serum galectin-3 and VCAM-1 on mortality risk was investigated using an interaction product term.
Results:
During follow-up, galectin-3 and VCAM-1 were associated with incremental risks of all-cause mortality (aHR: 1.038 (95% confidence interval (CI): 1.001⁻1.077) and 1.002 (95% CI: 1.001⁻1.003), respectively). Nonetheless, VCAM-1 but not galectin-3 predicted CV mortality (aHR: 1.043 (95% CI: 0.993⁻1.096) and 1.002 (95% CI: 1.001⁻1.003), respectively). In the interaction analysis, patients with combined higher galectin-3 (>29.5 ng/mL) and VCAM-1 (>1546.9 ng/mL) were at the greatest risk of all-cause and CV mortality (aHR: 4.6 (95% CI: 1.6⁻13.4), and 4.2 (95% CI: 1.3⁻14.4), respectively). The interactions between galectin-3 and VCAM-1 with respect to all-cause and CV mortality were statistically significant (p < 0.01 and < 0.05, respectively).
Conclusion:
Galectin-3 and VCAM-1 could serve as a promising dual biomarker for prognostic assessment, considering their joint effects on pathogenesis of leukocyte trafficking and atherothrombosis.
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