<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Gabernet G</submitter><funding>NCATS NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NIAID NIH HHS</funding><pubmed_abstract>Following SARS-CoV-2 infection, ~10-35% of COVID-19 patients experience long COVID (LC), in which often debilitating symptoms persist for at least three months. Elucidating the biologic underpinnings of LC could identify therapeutic opportunities. We utilized machine learning methods on biologic analytes and patient reported outcome surveys provided over 12 months after hospital discharge from >500 hospitalized COVID-19 patients in the IMPACC cohort to identify a multi-omics "recovery factor". IMPACC participants who experienced LC had lower recovery factor scores compared to participants without LC. Biologic characterization revealed increased levels of plasma proteins associated with inflammation, elevated transcriptional signatures of heme metabolism, and decreased androgenic steroids i</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2025.02.12.637926</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11844572</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification of a multi-omics factor predictive of long COVID in the IMPACC study.</pubmed_title><pmcid>PMC11844572</pmcid><funding_grant_id>R01 AI135803</funding_grant_id><funding_grant_id>R01 AI104870</funding_grant_id><funding_grant_id>UM1 TR004528</funding_grant_id><funding_grant_id>U19 AI062629</funding_grant_id><funding_grant_id>T32 DA018926</funding_grant_id><funding_grant_id>U19 AI090023</funding_grant_id><funding_grant_id>U01 AI167892</funding_grant_id><funding_grant_id>U54 AI142766</funding_grant_id><funding_grant_id>U19 AI118610</funding_grant_id><funding_grant_id>U19 AI077439</funding_grant_id><funding_grant_id>R01 AI145835</funding_grant_id><funding_grant_id>U19 AI118608</funding_grant_id><funding_grant_id>U19 AI125357</funding_grant_id><funding_grant_id>U19 AI057229</funding_grant_id><funding_grant_id>U19 AI128910</funding_grant_id><funding_grant_id>R01 AI122220</funding_grant_id><funding_grant_id>U19 AI089992</funding_grant_id><funding_grant_id>U19 AI128913</funding_grant_id><pubmed_authors>Peters B</pubmed_authors><pubmed_authors>Simon V</pubmed_authors><pubmed_authors>Kheradmand F</pubmed_authors><pubmed_authors>Moore JF</pubmed_authors><pubmed_authors>Schaenman J</pubmed_authors><pubmed_authors>Rouphael N</pubmed_authors><pubmed_authors>Maecker HT</pubmed_authors><pubmed_authors>Corry DB</pubmed_authors><pubmed_authors>Sekaly RP</pubmed_authors><pubmed_authors>McComsey GA</pubmed_authors><pubmed_authors>Davis MM</pubmed_authors><pubmed_authors>Reed EF</pubmed_authors><pubmed_authors>Metcalf JP</pubmed_authors><pubmed_authors>Ehrlich LIR</pubmed_authors><pubmed_authors>Haddad EK</pubmed_authors><pubmed_authors>Diray-Arce J</pubmed_authors><pubmed_authors>Ozonoff A</pubmed_authors><pubmed_authors>Chu T</pubmed_authors><pubmed_authors>Melamed E</pubmed_authors><pubmed_authors>Cairns CB</pubmed_authors><pubmed_authors>Baden LR</pubmed_authors><pubmed_authors>Kim-Schulze S</pubmed_authors><pubmed_authors>Pulendran B</pubmed_authors><pubmed_authors>Syphurs C</pubmed_authors><pubmed_authors>Hough CL</pubmed_authors><pubmed_authors>Smolen KK</pubmed_authors><pubmed_authors>Nadeau KC</pubmed_authors><pubmed_authors>Montgomery RR</pubmed_authors><pubmed_authors>Kraft M</pubmed_authors><pubmed_authors>Bime C</pubmed_authors><pubmed_authors>Levy O</pubmed_authors><pubmed_authors>IMPACC Network</pubmed_authors><pubmed_authors>Brackenridge SC</pubmed_authors><pubmed_authors>Gygi JP</pubmed_authors><pubmed_authors>Steen H</pubmed_authors><pubmed_authors>Eckalbar W</pubmed_authors><pubmed_authors>Hoch A</pubmed_authors><pubmed_authors>Hafler DA</pubmed_authors><pubmed_authors>Agudelo Higuita NI</pubmed_authors><pubmed_authors>Calfee CS</pubmed_authors><pubmed_authors>Krammer F</pubmed_authors><pubmed_authors>Gabernet G</pubmed_authors><pubmed_authors>Maciuch J</pubmed_authors><pubmed_authors>Erle DJ</pubmed_authors><pubmed_authors>Kleinstein SH</pubmed_authors><pubmed_authors>Shaw AC</pubmed_authors><pubmed_authors>Altman MC</pubmed_authors><pubmed_authors>Messer WB</pubmed_authors><pubmed_authors>Guan L</pubmed_authors><pubmed_authors>Fourati S</pubmed_authors><pubmed_authors>Jayavelu ND</pubmed_authors><pubmed_authors>Bosinger SE</pubmed_authors><pubmed_authors>Westendorf K</pubmed_authors><pubmed_authors>Atkinson MA</pubmed_authors><pubmed_authors>Fernandez-Sesma A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of a multi-omics factor predictive of long COVID in the IMPACC study.</name><description>Following SARS-CoV-2 infection, ~10-35% of COVID-19 patients experience long COVID (LC), in which often debilitating symptoms persist for at least three months. Elucidating the biologic underpinnings of LC could identify therapeutic opportunities. We utilized machine learning methods on biologic analytes and patient reported outcome surveys provided over 12 months after hospital discharge from >500 hospitalized COVID-19 patients in the IMPACC cohort to identify a multi-omics "recovery factor". IMPACC participants who experienced LC had lower recovery factor scores compared to participants without LC. Biologic characterization revealed increased levels of plasma proteins associated with inflammation, elevated transcriptional signatures of heme metabolism, and decreased androgenic steroids i</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-05-22T03:18:48.938Z</modification><creation>2025-04-04T13:46:37.934Z</creation></dates><accession>S-EPMC11844572</accession><cross_references><pubmed>39990442</pubmed><doi>10.1101/2025.02.12.637926</doi></cross_references></HashMap>