Skin advanced glycation end-products do not predict pulmonary function trajectories in adults from the ILERVAS cohort

Advanced glycation end-products (AGEs) activate specific receptors (RAGE) promoting inflammation and oxidative stress. The lungs, with high RAGE expression, may be particularly susceptible to AGE-related injury. This study assessed whether baseline skin AGE levels, measured by skin autofluorescence...

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Detalles Bibliográficos
Autores: Torres Cortada, Gerard, Gracia Lavedan, Esther, González, Jessica, Henríquez Beltrán, Mario, Targa, Adriano, Royo, Maria, Bermúdez López, Marcelino, Castro Boqué, Eva, Valdivielso Revilla, José Manuel, Pamplona Gras, Reinald, Mauricio Puente, Dídac, Lecube, Albert, Barbé Illa, Ferran, de Batlle, Jordi
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2026
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10459.1/469646
Acceso en línea:https://doi.org/10.1038/s41598-025-33414-8
https://hdl.handle.net/10459.1/469646
Access Level:acceso abierto
Palabra clave:Advanced glycation end-products (AGEs)
Cardiovascular risk
Lung function decline
Skin autofluorescence (SAF)
Descripción
Sumario:Advanced glycation end-products (AGEs) activate specific receptors (RAGE) promoting inflammation and oxidative stress. The lungs, with high RAGE expression, may be particularly susceptible to AGE-related injury. This study assessed whether baseline skin AGE levels, measured by skin autofluorescence (SAF), predict pulmonary function decline in middle-aged adults with cardiovascular risk factors. This ancillary analysis of the ILERVAS cohort included adults aged 45-70 years with cardiovascular risk factors but without diabetes or chronic kidney disease. Baseline data included demographics, lifestyle, and fasting blood tests. SAF was measured using AGE Reader™, and spirometry performed at baseline and after a median follow-up of 4 years. Associations between baseline SAF and annual declines in FEV, FVC, and FEV/FVC were analysed using adjusted models and generalized additive models, stratified by smoking status. Among 658 participants (median age 56 years, 48% female), median baseline SAF was 1.90 AU [1.60; 2.20]. Baseline lung function was preserved, with median FEV, FVC and FEV/FVC of 2795 mL [2270; 3,341], 3,525 mL [2870; 4300], and 78.6% [74.4; 82.8]. Annual declines were -  81.9 mL [- 120.6; - 43.3] for FEV, - 99.6 mL [- 159.3; - 37.9] for FVC, and - 0.04% [- 0.85; 0.70] for FEV/FVC. No significant associations were found between SAF and spirometry changes. Results were consistent across smoking subgroups. Baseline skin AGE levels did not predict pulmonary function decline over four years in middle-aged adults with cardiovascular risk factors. While SAF reflects cumulative AGE exposure, it has limited prognostic value for lung function in this population.