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.

Gerontology
|January 21, 2021
PubMed

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.
Abstract

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