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Higher sRAGE Levels Predict Mortality in Frail Older Adults with Cardiovascular Disease
Lee Butcher1, Jose Antonio Carnicero2, Karine Pérès3
1The Cellular Senescence and Pathophysiology Group, Cardiff Metropolitan University, Cardiff, United Kingdom.
Insights
Soluble receptor for advanced glycation end products (sRAGE) predicts mortality in cardiovascular disease (CVD) patients, especially when combined with frailty. High sRAGE levels significantly increase mortality risk in frail CVD individuals.
Area of Science:
- Gerontology
- Cardiology
- Biomarkers
Background:
- The predictive value of soluble receptor for advanced glycation end products (sRAGE) for mortality in cardiovascular diseases (CVD) remains unclear.
- Frailty is a significant factor in older adults and may influence disease prognosis.
Purpose of the Study:
- To investigate the association between serum sRAGE levels and mortality in individuals with and without CVD.
- To determine if frailty status modifies the relationship between sRAGE and mortality in CVD patients.
Main Methods:
- Analysis of data from 1,016 participants across 3 European cohorts (FRAILOMIC project).
- Stratification by CVD history and frailty status, with mortality recorded over 8 years.
- Adjusted Cox regression, Kaplan-Meier, and ROC curve analyses were employed.
Main Results:
- Serum sRAGE was associated with increased mortality risk in CVD patients (HR 1.64), but not in non-CVD individuals.
- The association was significantly stronger in frail CVD patients (CVD-F, HR 1.97) compared to non-frail CVD patients (CVD-NF, HR 1.50).
- High sRAGE levels were linked to a 2.9-year shorter survival in frail CVD patients, and sRAGE improved mortality prediction models for this subgroup.
Conclusions:
- Frailty status significantly influences the prognostic value of sRAGE for mortality in older adults with CVD.
- sRAGE emerges as a potential prognostic biomarker for mortality risk, particularly in frail individuals with cardiovascular disease.
Introduction:
The evidence that blood levels of the soluble receptor for advanced glycation end products (sRAGE) predict mortality in people with cardiovascular diseases (CVD) is inconsistent. To clarify this matter, we investigated if frailty status influences this association.
Methods:
We analysed data of 1,016 individuals (median age, 75 years) from 3 population-based European cohorts, enrolled in the FRAILOMIC project. Participants were stratified by history of CVD and frailty status. Mortality was recorded during 8 years of follow-up.
Results:
In adjusted Cox regression models, baseline serum sRAGE was positively associated with an increased risk of mortality in participants with CVD (HR 1.64, 95% CI 1.09-2.49, p = 0.019) but not in non-CVD. Within the CVD group, the risk of death was markedly enhanced in the frail subgroup (CVD-F, HR 1.97, 95% CI 1.18-3.29, p = 0.009), compared to the non-frail subgroup (CVD-NF, HR 1.50, 95% CI 0.71-3.15, p = 0.287). Kaplan-Meier analysis showed that the median survival time of CVD-F with high sRAGE (>1,554 pg/mL) was 2.9 years shorter than that of CVD-F with low sRAGE, whereas no survival difference was seen for CVD-NF. Area under the ROC curve analysis demonstrated that for CVD-F, addition of sRAGE to the prediction model increased its prognostic value.
Conclusions:
Frailty status influences the relationship between sRAGE and mortality in older adults with CVD. sRAGE could be used as a prognostic marker of mortality for these individuals, particularly if they are also frail.
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