<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(12)</volume><submitter>Galassi A</submitter><pubmed_abstract>A cytokine storm drives the pathogenesis of severe COVID-19 infection and several biomarkers have been linked to mortality. Chronic kidney disease (CKD) emerged as a risk factor for severe COVID-19. We investigated the association between selected biomarkers and mortality in 77 patients hospitalized for COVID-19, and whether they differ in patients with eGFR higher and lower than 45 mL/min. The association between patients' characteristics, plasma biomarkers and mortality was conducted by univariate logistic regression models and independent predictors of mortality were then used to create a multivariate prediction model through Cox regression. Patients with lower eGFR had a significant increase of GDF-15, CD-25 and RAGE, with higher plasma levels in non-survivors and in patients who needed ventilation. At univariate analysis, low and mid-low GDF-15 quartiles (&amp;lt;4.45 ng/mL) were associated with lower mortality risk, while mid-high and high quartiles (&amp;gt;4.45 ng/mL) were associated with higher mortality risk. Independent association between GDF-15 quartiles and mortality risk was confirmed in the Cox model and adjusted for eGFR, age, fever and dyspnea (HR 2.28, CI 1.53-3.39, p &amp;lt; 0.0001). The strength of the association between GDF-15 quartiles and mortality risk increased in patients with lower compared to higher eGFR (HR 2.53, CI 1.34-4.79 versus HR 1.99, CI 1.17-3.39). Our findings may suggest a further investigation of the effect of GDF-15 signaling pathway inhibition in CKD.</pubmed_abstract><journal>Biomedicines</journal><pagination>3251</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9775159</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Growth Differentiation Factor 15 (GDF-15) Levels Associate with Lower Survival in Chronic Kidney Disease Patients with COVID-19.</pubmed_title><pmcid>PMC9775159</pmcid><pubmed_authors>D'Arminio Monforte A</pubmed_authors><pubmed_authors>Galassi A</pubmed_authors><pubmed_authors>Artioli L</pubmed_authors><pubmed_authors>Yellenki V</pubmed_authors><pubmed_authors>Bono V</pubmed_authors><pubmed_authors>Marchetti G</pubmed_authors><pubmed_authors>Rovito R</pubmed_authors><pubmed_authors>Tincati C</pubmed_authors><pubmed_authors>Hadla M</pubmed_authors><pubmed_authors>Cozzolino M</pubmed_authors><pubmed_authors>Sala M</pubmed_authors><pubmed_authors>Magagnoli L</pubmed_authors><pubmed_authors>Ciceri P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Growth Differentiation Factor 15 (GDF-15) Levels Associate with Lower Survival in Chronic Kidney Disease Patients with COVID-19.</name><description>A cytokine storm drives the pathogenesis of severe COVID-19 infection and several biomarkers have been linked to mortality. Chronic kidney disease (CKD) emerged as a risk factor for severe COVID-19. We investigated the association between selected biomarkers and mortality in 77 patients hospitalized for COVID-19, and whether they differ in patients with eGFR higher and lower than 45 mL/min. The association between patients' characteristics, plasma biomarkers and mortality was conducted by univariate logistic regression models and independent predictors of mortality were then used to create a multivariate prediction model through Cox regression. Patients with lower eGFR had a significant increase of GDF-15, CD-25 and RAGE, with higher plasma levels in non-survivors and in patients who needed ventilation. At univariate analysis, low and mid-low GDF-15 quartiles (&amp;lt;4.45 ng/mL) were associated with lower mortality risk, while mid-high and high quartiles (&amp;gt;4.45 ng/mL) were associated with higher mortality risk. Independent association between GDF-15 quartiles and mortality risk was confirmed in the Cox model and adjusted for eGFR, age, fever and dyspnea (HR 2.28, CI 1.53-3.39, p &amp;lt; 0.0001). The strength of the association between GDF-15 quartiles and mortality risk increased in patients with lower compared to higher eGFR (HR 2.53, CI 1.34-4.79 versus HR 1.99, CI 1.17-3.39). Our findings may suggest a further investigation of the effect of GDF-15 signaling pathway inhibition in CKD.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-21T23:15:43.608Z</modification><creation>2025-04-05T19:06:13.501Z</creation></dates><accession>S-EPMC9775159</accession><cross_references><pubmed>36552007</pubmed><doi>10.3390/biomedicines10123251</doi></cross_references></HashMap>