<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Torres G</submitter><funding>Generalitat de Catalunya</funding><funding>Instituto de Salud Carlos III</funding><funding>Ministerio de Ciencia, Innovación y Universidades</funding><funding>Diputació de Lleida</funding><funding>ICREA Academia programme</funding><funding>irblleida “Grants for Research Staff in Training” (11th Edition, Modality E) of the IREP Program “amb la col·laboració de: Diputació de Lleida”</funding><pagination>3428</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12835136</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>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 i</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Skin advanced glycation end-products do not predict pulmonary function trajectories in adults from the ILERVAS cohort.</pubmed_title><pmcid>PMC12835136</pmcid><funding_grant_id>IJC2018-037792-I; PID2023-152233OB-I00</funding_grant_id><funding_grant_id>CP23/00095 (Miguel Servet 2023)</funding_grant_id><funding_grant_id>FI23/00253</funding_grant_id><funding_grant_id>AGAUR - 2021SGR00990</funding_grant_id><funding_grant_id>PI23/00237</funding_grant_id><pubmed_authors>Castelblanco E</pubmed_authors><pubmed_authors>Franch-Nadal J</pubmed_authors><pubmed_authors>Torres G</pubmed_authors><pubmed_authors>Henriquez-Beltran M</pubmed_authors><pubmed_authors>de Batlle J</pubmed_authors><pubmed_authors>Barbe F</pubmed_authors><pubmed_authors>Pamplona R</pubmed_authors><pubmed_authors>Ortega M</pubmed_authors><pubmed_authors>Portero-Otin M</pubmed_authors><pubmed_authors>Godoy P</pubmed_authors><pubmed_authors>Lecube A</pubmed_authors><pubmed_authors>Simo R</pubmed_authors><pubmed_authors>Jove M</pubmed_authors><pubmed_authors>Hernandez C</pubmed_authors><pubmed_authors>Castro-Boque E</pubmed_authors><pubmed_authors>Royo M</pubmed_authors><pubmed_authors>Hernandez M</pubmed_authors><pubmed_authors>Fernandez E</pubmed_authors><pubmed_authors>Bermudez-Lopez M</pubmed_authors><pubmed_authors>Miquel E</pubmed_authors><pubmed_authors>Rius F</pubmed_authors><pubmed_authors>Martinez-Alonso M</pubmed_authors><pubmed_authors>Mauricio D</pubmed_authors><pubmed_authors>Gonzalez J</pubmed_authors><pubmed_authors>Targa ADS</pubmed_authors><pubmed_authors>Valdivielso JM</pubmed_authors><pubmed_authors>Gracia-Lavedan E</pubmed_authors><pubmed_authors>ILERVAS team</pubmed_authors></additional><is_claimable>false</is_claimable><name>Skin advanced glycation end-products do not predict pulmonary function trajectories in adults from the ILERVAS cohort.</name><description>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 i</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-16T03:08:43.857Z</modification><creation>2026-06-16T03:06:45.158Z</creation></dates><accession>S-EPMC12835136</accession><cross_references><pubmed>41535697</pubmed><doi>10.1038/s41598-025-33414-8</doi></cross_references></HashMap>