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Prognostic value of osteoprotegerin in chronic heart failure: The GISSI-HF trial
Ragnhild Røysland1, Serge Masson, Torbjørn Omland
1Division of Medicine, Akershus University Hospital, Lørenskog, Norway.
Insights
Osteoprotegerin (OPG) predicts death in chronic heart failure (CHF) patients, independent of traditional risk factors. Higher OPG levels are linked to increased mortality and cardiovascular events in this population.
Area of Science:
- Cardiology
- Biomarkers
- Heart Failure Research
Background:
- Osteoprotegerin (OPG) is a tumor necrosis factor receptor superfamily member.
- Elevated OPG levels predict mortality and hospitalization in acute coronary syndrome patients.
- The prognostic value of OPG in chronic heart failure (CHF) remains unestablished.
Purpose of the Study:
- To investigate the association between plasma osteoprotegerin (OPG) levels and clinical outcomes in patients with chronic heart failure (CHF).
Main Methods:
- 1,229 CHF patients from the GISSI-HF trial had baseline plasma OPG measured via ELISA.
- Patients were randomized to n-3 polyunsaturated fatty acids, rosuvastatin, or placebo.
- Cox proportional hazards regression models assessed the relationship between OPG and outcomes.
Main Results:
- During a median 3.9-year follow-up, 332 deaths and 791 cardiovascular deaths/hospitalizations occurred.
- Baseline OPG strongly predicted death (HR 1.53 per SD increase, univariate).
- OPG remained a significant predictor of death (HR 1.20) and composite endpoint (HR 1.34) after risk factor adjustment.
Conclusions:
- Osteoprotegerin (OPG) is an independent predictor of mortality in patients with chronic heart failure (CHF).
- OPG provides prognostic information beyond conventional cardiovascular risk factors in CHF.
Background:
Circulating levels of osteoprotegerin (OPG), a member of the tumor necrosis factor receptor superfamily, is predictive of death and hospitalization for heart failure after acute coronary syndrome. The association between OPG and outcome in patients with chronic heart failure (CHF) is unknown.
Methods:
Plasma OPG levels at baseline were assessed in 1,229 patients with CHF recruited from 51 clinical centers and included in the Gruppo Italiano per lo Studio della Sopravvivenza nell'Infarto Miocardico-Heart Failure (GISSI-HF) trial. Patients were randomized to n-3 polyunsaturated fatty acids (1 g/d) or rosuvastatin (10 mg/d) versus placebo. Osteoprotegerin was analyzed by enzyme-linked immunosorbent assay. The association between OPG and outcome was assessed by Cox proportional hazards regression models.
Results:
During a median follow-up time of 3.9 years, 332 patients died; and 791 patients died or were hospitalized because of cardiovascular causes. By univariate analysis, baseline OPG levels were strongly associated with the incidence of death (hazard ratio {HR} [95% CI] 1.53 [1.40-1.67] per 1-SD increase in log OPG). After adjustment for conventional risk markers, OPG remained a significant predictor of death (HR [95% CI] 1.20 [1.06-1.35], P < .001). Similar findings were observed for the composite end point (HR [95% CI] 1.34 [1.07-1.69], P = .012).
Conclusion:
In patients with CHF, OPG is associated with the incidence of death independently of conventional cardiovascular risk factors.
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