<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Andonian BJ</submitter><funding>NIDDK NIH HHS</funding><funding>NIA NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIAMS NIH HHS</funding><funding>NIH HHS</funding><funding>Marie Curie</funding><pagination>7450</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9076829</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>Rheumatoid arthritis (RA) T cells drive autoimmune features via metabolic reprogramming that reduces oxidative metabolism. Exercise training improves cardiorespiratory fitness (i.e., systemic oxidative metabolism) and thus may impact RA T cell oxidative metabolic function. In this pilot study of RA participants, we took advantage of heterogeneous responses to a high-intensity interval training (HIIT) exercise program to identify relationships between improvements in cardiorespiratory fitness with changes in peripheral T cell and skeletal muscle oxidative metabolism. In 12 previously sedentary persons with seropositive RA, maximal cardiopulmonary exercise tests, fasting blood, and vastus lateralis biopsies were obtained before and after 10 weeks of HIIT. Following HIIT, improvements in RA c</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Rheumatoid arthritis T cell and muscle oxidative metabolism associate with exercise-induced changes in cardiorespiratory fitness.</pubmed_title><pmcid>PMC9076829</pmcid><funding_grant_id>R03 AG067949</funding_grant_id><funding_grant_id>PIOF-GA-2013-629981</funding_grant_id><funding_grant_id>R21 AR076663</funding_grant_id><funding_grant_id>R01 DK089312</funding_grant_id><funding_grant_id>R03-AG067949</funding_grant_id><funding_grant_id>R21-AR076663</funding_grant_id><funding_grant_id>R01-DK089312</funding_grant_id><pubmed_authors>Hauser ER</pubmed_authors><pubmed_authors>Muoio DM</pubmed_authors><pubmed_authors>Koss A</pubmed_authors><pubmed_authors>Andonian BJ</pubmed_authors><pubmed_authors>Pober DM</pubmed_authors><pubmed_authors>Hubal MJ</pubmed_authors><pubmed_authors>MacIver NJ</pubmed_authors><pubmed_authors>Koves TR</pubmed_authors><pubmed_authors>Lord JM</pubmed_authors><pubmed_authors>Bartlett DB</pubmed_authors><pubmed_authors>St Clair EW</pubmed_authors><pubmed_authors>Kraus WE</pubmed_authors><pubmed_authors>Huffman KM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rheumatoid arthritis T cell and muscle oxidative metabolism associate with exercise-induced changes in cardiorespiratory fitness.</name><description>Rheumatoid arthritis (RA) T cells drive autoimmune features via metabolic reprogramming that reduces oxidative metabolism. Exercise training improves cardiorespiratory fitness (i.e., systemic oxidative metabolism) and thus may impact RA T cell oxidative metabolic function. In this pilot study of RA participants, we took advantage of heterogeneous responses to a high-intensity interval training (HIIT) exercise program to identify relationships between improvements in cardiorespiratory fitness with changes in peripheral T cell and skeletal muscle oxidative metabolism. In 12 previously sedentary persons with seropositive RA, maximal cardiopulmonary exercise tests, fasting blood, and vastus lateralis biopsies were obtained before and after 10 weeks of HIIT. Following HIIT, improvements in RA c</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-31T09:48:01.343Z</modification><creation>2025-04-05T15:22:54.483Z</creation></dates><accession>S-EPMC9076829</accession><cross_references><pubmed>35523821</pubmed><doi>10.1038/s41598-022-11458-4</doi></cross_references></HashMap>