Development and validation of cardiometabolic risk predictive models based on LDL oxidation and candidate geromarkers from the MARK-AGE data

Andrei Valeanu (Corresponding author), Denisa Margina, Daniela Weber, Wolfgang Stuetz, María Moreno-Villanueva, Martijn E.T. Dollé, Eugène HJM Jansen, Efstathios S. Gonos, Jürgen Bernhardt, Beatrix Grubeck-Loebenstein, Birgit Weinberger, Simone Fiegl, Ewa Sikora, Grazyna Mosieniak, Olivier Toussaint, Florence Debacq-Chainiaux, Miriam Capri, Paolo Garagnani, Chiara Pirazzini, Maria Giulia BacaliniAntti Hervonen, P. Eline Slagboom, Duncan Talbot, Nicolle Breusing, Jan Frank, Alexander Bürkle, Claudio Franceschi, Tilman Grune, Daniela Gradinaru

Publications: Contribution to journalArticlePeer Reviewed

Abstract

The predictive value of the susceptibility to oxidation of LDL particles (LDLox) in cardiometabolic risk assessment is incompletely understood. The main objective of the current study was to assess its relationship with other relevant biomarkers and cardiometabolic risk factors from MARK-AGE data. A cross-sectional observational study was carried out on 1089 subjects (528 men and 561 women), aged 40–75 years old, randomly recruited age- and sex-stratified individuals from the general population. A correlation analysis exploring the relationships between LDLox and relevant biomarkers was undertaken, as well as the development and validation of several machine learning algorithms, for estimating the risk of the combined status of high blood pressure and obesity for the MARK-AGE subjects. The machine learning models yielded Area Under the Receiver Operating Characteristic Curve Score ranging 0.783–0.839 for the internal validation, while the external validation resulted in an Under the Receiver Operating Characteristic Curve Score between 0.648 and 0.787, with the variables based on LDLox reaching significant importance within the obtained predictions. The current study offers novel insights regarding the combined effects of LDL oxidation and other ageing markers on cardiometabolic risk. Future studies might be extended on larger patient cohorts, in order to obtain reproducible clinical assessment models.

Original languageEnglish
Article number111987
JournalMechanisms of Ageing and Development
Volume222
DOIs
Publication statusPublished - Dec 2024

Austrian Fields of Science 2012

  • 301114 Cell biology
  • 302019 Geriatrics

Keywords

  • Cardiometabolic risk
  • LDL oxidation
  • Machine learning
  • MARK-AGE
  • Vascular ageing

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