<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(17)</volume><submitter>Sanmartin-Sanchez A</submitter><pubmed_abstract>&lt;b>Background/Objetives&lt;/b>: Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease with poor prognosis. Nutritional disorders, particularly cachexia, significantly impact morbidity and mortality in IPF but remain under-investigated. This study aimed to characterize cachexia phenotypes in IPF through morphofunctional assessment (MFA) and to evaluate their prognostic relevance, including the role of mitochondrial biomarkers. &lt;b>Methods&lt;/b>: In this prospective bicenter study, 85 IPF patients underwent MFA including bioelectrical impedance vector analysis (BIVA), nutritional ultrasound (NU), and T12-level computed tomography (T12-CT) for body composition. Functional and strength assessments included timed up and go test (TUG) and handgrip strength (HGS), respectively.</pubmed_abstract><journal>Nutrients</journal><pagination>2739</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12430740</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cachexia Phenotyping Through Morphofunctional Assessment and Mitocondrial Biomarkers (GDF-15 and PGC-1α) in Idiopathic Pulmonary Fibrosis.</pubmed_title><pmcid>PMC12430740</pmcid><pubmed_authors>Olivares-Alcolea J</pubmed_authors><pubmed_authors>Cornejo-Pareja I</pubmed_authors><pubmed_authors>Garrido-Sanchez L</pubmed_authors><pubmed_authors>Sanchez-Garcia A</pubmed_authors><pubmed_authors>Vegas-Aguilar I</pubmed_authors><pubmed_authors>Cabrera-Cesar E</pubmed_authors><pubmed_authors>Espildora-Hernandez F</pubmed_authors><pubmed_authors>Murri M</pubmed_authors><pubmed_authors>Tinahones FJ</pubmed_authors><pubmed_authors>Velasco-Garrido JL</pubmed_authors><pubmed_authors>Guirado-Pelaez P</pubmed_authors><pubmed_authors>Fernandez-Jimenez R</pubmed_authors><pubmed_authors>Amaya-Campos MDM</pubmed_authors><pubmed_authors>Villaplana-Garcia M</pubmed_authors><pubmed_authors>Garcia-Almeida JM</pubmed_authors><pubmed_authors>Simon-Frapolli VJ</pubmed_authors><pubmed_authors>Sanmartin-Sanchez A</pubmed_authors><pubmed_authors>Vidal-Suarez A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cachexia Phenotyping Through Morphofunctional Assessment and Mitocondrial Biomarkers (GDF-15 and PGC-1α) in Idiopathic Pulmonary Fibrosis.</name><description>&lt;b>Background/Objetives&lt;/b>: Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease with poor prognosis. Nutritional disorders, particularly cachexia, significantly impact morbidity and mortality in IPF but remain under-investigated. This study aimed to characterize cachexia phenotypes in IPF through morphofunctional assessment (MFA) and to evaluate their prognostic relevance, including the role of mitochondrial biomarkers. &lt;b>Methods&lt;/b>: In this prospective bicenter study, 85 IPF patients underwent MFA including bioelectrical impedance vector analysis (BIVA), nutritional ultrasound (NU), and T12-level computed tomography (T12-CT) for body composition. Functional and strength assessments included timed up and go test (TUG) and handgrip strength (HGS), respectively.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-04-23T03:23:03.877Z</modification><creation>2026-04-23T03:11:57.056Z</creation></dates><accession>S-EPMC12430740</accession><cross_references><pubmed>40944130</pubmed><doi>10.3390/nu17172739</doi></cross_references></HashMap>