<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>43(2)</volume><submitter>Yu Y</submitter><funding>Ruggles Family Foundation, Moline, Illinois (US</funding><funding>Mr. and Ms. Rudy Ruggles</funding><pubmed_abstract>Key processes characterizing human aging are immunosenescence and inflammaging. The capacity of the immune system to adequately respond to external perturbations (e.g., pathogens, injuries, and biochemical irritants) and to repair somatic mutations that may cause cancers or cellular senescence declines. An important goal remains to identify genetic or biochemical, predictive biomarkers for healthy aging. We recruited two cohorts in the age range 70 to 82, one afflicted by chronic illnesses (non-healthy aging, NHA) and the other in good health (healthy aging, HA). NHA criteria included major cardiovascular, neurodegenerative, and chronic pulmonary diseases, diabetes, and cancers. Quantitative analysis of forty proinflammatory cytokines in blood plasma and more than 500 proteins in urine was</pubmed_abstract><journal>GeroScience</journal><pagination>593-606</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8110643</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Protein signatures from blood plasma and urine suggest changes in vascular function and IL-12 signaling in elderly with a history of chronic diseases compared with an age-matched healthy cohort.</pubmed_title><pmcid>PMC8110643</pmcid><pubmed_authors>Nelson KE</pubmed_authors><pubmed_authors>Singh H</pubmed_authors><pubmed_authors>Tsitrin T</pubmed_authors><pubmed_authors>Petrini J</pubmed_authors><pubmed_authors>Kwon K</pubmed_authors><pubmed_authors>Pieper R</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Protein signatures from blood plasma and urine suggest changes in vascular function and IL-12 signaling in elderly with a history of chronic diseases compared with an age-matched healthy cohort.</name><description>Key processes characterizing human aging are immunosenescence and inflammaging. The capacity of the immune system to adequately respond to external perturbations (e.g., pathogens, injuries, and biochemical irritants) and to repair somatic mutations that may cause cancers or cellular senescence declines. An important goal remains to identify genetic or biochemical, predictive biomarkers for healthy aging. We recruited two cohorts in the age range 70 to 82, one afflicted by chronic illnesses (non-healthy aging, NHA) and the other in good health (healthy aging, HA). NHA criteria included major cardiovascular, neurodegenerative, and chronic pulmonary diseases, diabetes, and cancers. Quantitative analysis of forty proinflammatory cytokines in blood plasma and more than 500 proteins in urine was</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2026-05-08T06:43:36.874Z</modification><creation>2024-12-04T09:31:15.763Z</creation></dates><accession>S-EPMC8110643</accession><cross_references><pubmed>32974878</pubmed><doi>10.1007/s11357-020-00269-y</doi></cross_references></HashMap>