Post-translational modification-derived products are associated with frailty status in elderly subjects

Background Identifying frail elderly subjects is of paramount importance in order to conduct a tailored care. The characterization of frailty status is currently based on the collection of clinical data and on the use of various tools such as Fried's criteria, which constitutes a difficult and...

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Veröffentlicht in:Clinical chemistry and laboratory medicine 2019-08, Vol.57 (8), p.1153-1161
Hauptverfasser: Mahmoudi, Rachid, Jaisson, Stéphane, Badr, Sarah, Jaidi, Yacine, Bertholon, Laurie-Anne, Novella, Jean-Luc, Gillery, Philippe
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Sprache:eng
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Zusammenfassung:Background Identifying frail elderly subjects is of paramount importance in order to conduct a tailored care. The characterization of frailty status is currently based on the collection of clinical data and on the use of various tools such as Fried's criteria, which constitutes a difficult and time-consuming process. Up to now, no biological markers have been described as reliable tools for frailty characterization. We tested the hypothesis that a link between frailty and protein molecular aging existed. This study aimed therefore at determining whether post-translational modification derived products (PTMDPs), recognized as biomarkers of protein aging, were associated with frailty status in elderly subjects. Methods Frailty status was determined according to Fried's criteria in 250 elderly patients (>65 years old) hospitalized in a short-term care unit. Serum concentrations of protein-bound PTMDPs, including carboxymethyllysine (CML), pentosidine, methylglyoxal-hydroimidazolone-1 and homocitrulline (HCit), were determined by liquid chromatography coupled with tandem mass spectrometry, and tissue content of advanced glycation end-products was assessed by skin autofluorescence (SAF) measurement. Associations between PTMDPs and frailty status were analyzed using logistic regression models. Results Frail patients had significantly (p
ISSN:1434-6621
1437-4331
DOI:10.1515/cclm-2018-1322