<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fiedler L</submitter><funding>Russian Science Foundation</funding><pagination>2889</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9687975</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(11)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>COVID-19 survivors reveal an increased long-term risk for cardiovascular disease. Biomarkers like troponins and sST-2 improve stratification of cardiovascular risk. Nevertheless, their prognostic value for identifying long-term cardiovascular risk after having survived COVID-19 has yet to be evaluated.&lt;h4>Methods&lt;/h4>In this single-center study, admission serum biomarkers of sST-2 and hs-TnI in a single cohort of 251 hospitalized COVID-19 survivors were evaluated. Concentrations were correlated with major cardiovascular events (MACE) defined as cardiovascular death and/or need for cardiovascular hospitalization during follow-up after hospital discharge [FU: 415 days (403; 422)].&lt;h4>Results&lt;/h4>MACE was a frequent finding during FU with an incidence of 8.4% (cardiovascular death: 2.8% and/or need for cardiovascular hospitalization: 7.2%). Both biomarkers were reliable indicators of MACE (hs-TnI: sensitivity = 66.7%&amp;specificity = 65.7%; sST-2: sensitivity = 33.3%&amp;specificity = 97.4%). This was confirmed in a multivariate proportional-hazards analysis: besides age (HR = 1.047, 95% CI = 1.012-1.084, &lt;i>p&lt;/i> = 0.009), hs-TnI (HR = 4.940, 95% CI = 1.904-12.816, &lt;i>p&lt;/i> = 0.001) and sST-2 (HR = 10.901, 95% CI =4.509-29.271, &lt;i>p&lt;/i> &amp;lt; 0.001) were strong predictors of MACE. The predictive value of the model was further improved by combining both biomarkers with the factor age (concordance index hs-TnI + sST2 + age = 0.812).&lt;h4>Conclusion&lt;/h4>During long-term FU, hospitalized COVID-19 survivors, hs-TnI and sST-2 at admission, were strong predictors of MACE, indicating both proteins to be involved in post-acute sequelae of COVID-19.</pubmed_abstract><journal>Biomedicines</journal><pubmed_title>Investigation of hs-TnI and sST-2 as Potential Predictors of Long-Term Cardiovascular Risk in Patients with Survived Hospitalization for COVID-19 Pneumonia.</pubmed_title><pmcid>PMC9687975</pmcid><funding_grant_id>22-25-00019</funding_grant_id><pubmed_authors>Jirak P</pubmed_authors><pubmed_authors>Kopp K</pubmed_authors><pubmed_authors>Lasinova G</pubmed_authors><pubmed_authors>Pistulli R</pubmed_authors><pubmed_authors>Dieplinger AM</pubmed_authors><pubmed_authors>Fiedler L</pubmed_authors><pubmed_authors>Hauptmann L</pubmed_authors><pubmed_authors>Hoppe UC</pubmed_authors><pubmed_authors>Tataurov A</pubmed_authors><pubmed_authors>Gareeva D</pubmed_authors><pubmed_authors>Lakman I</pubmed_authors><pubmed_authors>Pavlov V</pubmed_authors><pubmed_authors>Gumerov R</pubmed_authors><pubmed_authors>Zagidullin N</pubmed_authors><pubmed_authors>Davtyan P</pubmed_authors><pubmed_authors>Motloch LJ</pubmed_authors><pubmed_authors>Lichtenauer M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Investigation of hs-TnI and sST-2 as Potential Predictors of Long-Term Cardiovascular Risk in Patients with Survived Hospitalization for COVID-19 Pneumonia.</name><description>&lt;h4>Introduction&lt;/h4>COVID-19 survivors reveal an increased long-term risk for cardiovascular disease. Biomarkers like troponins and sST-2 improve stratification of cardiovascular risk. Nevertheless, their prognostic value for identifying long-term cardiovascular risk after having survived COVID-19 has yet to be evaluated.&lt;h4>Methods&lt;/h4>In this single-center study, admission serum biomarkers of sST-2 and hs-TnI in a single cohort of 251 hospitalized COVID-19 survivors were evaluated. Concentrations were correlated with major cardiovascular events (MACE) defined as cardiovascular death and/or need for cardiovascular hospitalization during follow-up after hospital discharge [FU: 415 days (403; 422)].&lt;h4>Results&lt;/h4>MACE was a frequent finding during FU with an incidence of 8.4% (cardiovascular death: 2.8% and/or need for cardiovascular hospitalization: 7.2%). Both biomarkers were reliable indicators of MACE (hs-TnI: sensitivity = 66.7%&amp;specificity = 65.7%; sST-2: sensitivity = 33.3%&amp;specificity = 97.4%). This was confirmed in a multivariate proportional-hazards analysis: besides age (HR = 1.047, 95% CI = 1.012-1.084, &lt;i>p&lt;/i> = 0.009), hs-TnI (HR = 4.940, 95% CI = 1.904-12.816, &lt;i>p&lt;/i> = 0.001) and sST-2 (HR = 10.901, 95% CI =4.509-29.271, &lt;i>p&lt;/i> &amp;lt; 0.001) were strong predictors of MACE. The predictive value of the model was further improved by combining both biomarkers with the factor age (concordance index hs-TnI + sST2 + age = 0.812).&lt;h4>Conclusion&lt;/h4>During long-term FU, hospitalized COVID-19 survivors, hs-TnI and sST-2 at admission, were strong predictors of MACE, indicating both proteins to be involved in post-acute sequelae of COVID-19.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-19T16:10:39.152Z</modification><creation>2025-04-19T16:10:39.152Z</creation></dates><accession>S-EPMC9687975</accession><cross_references><pubmed>36359409</pubmed><doi>10.3390/biomedicines10112889</doi></cross_references></HashMap>