Does Macrophage Migration Inhibitory Factor predict the prognosis of COVID-19 disease?
The aim of this study is to investigate whether macrophage migration inhibitory factor (MIF) predicts the prognosis of COVID-19 disease. This descriptive and cross-sectional study was conducted on 87 confirmed COVID-19 patients. The patients were separated into two groups according to the admission...
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Veröffentlicht in: | Journal of infection in developing countries 2021-03, Vol.15 (3), p.398-403 |
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creator | Dheir, Hamad Yaylaci, Selcuk Sipahi, Savas Genc, Ahmed Cihad Cekic, Deniz Tuncer, Fatma Betul Cokluk, Erdem Kocayigit, Havva Genc, Ahmed Bilal Salihi, Salih Varim, Ceyhun Karabay, Oguz |
description | The aim of this study is to investigate whether macrophage migration inhibitory factor (MIF) predicts the prognosis of COVID-19 disease.
This descriptive and cross-sectional study was conducted on 87 confirmed COVID-19 patients. The patients were separated into two groups according to the admission in the ICU or in the ward. MIF was determined batchwise in plasma obtained as soon as the patients were admitted. Both groups were compared with respect to demographic characteristics, biochemical parameters and prediction of requirement to ICU admission.
Forty seven patients in ICU, and 40 patients in ward were included. With respect to MIF levels and biochemical biomarkers, there was a statistically significant difference between the ICU and ward patients (p< 0.024). In terms of ICU requirement, the cut-off value of MIF was detected as 4.705 (AUC:0.633, 95%CI:0.561-0.79, p= 0.037), D-dimer was 789 (AUC:0.779, 95%CI: 0.681-0.877, p= 0.000), troponin was 8.15 (AUC: 0.820, 95%CI:0.729-0.911, p= 0.000), ferritin was 375 (AUC: 0.774, 95%CI:0.671-0.876, p= 0.000), and lactate dehydrogenase (LDH) was 359.5 (AUC:0.843, 95%CI: 0.753-0.933, p= 0.000). According to the logistic regression analysis; when MIF level > 4.705, the patient's requirement to ICU risk was increased to 8.33 (95%CI: 1.73-44.26, p= 0.009) fold. Similarly, elevation of troponin, ferritin and, LDH was shown to predict disease prognosis (p< 0.05).
Our study showed that MIF may play a role in inflammatory responses to COVID-19 through induction of pulmonary inflammatory cytokines, suggesting that pharmacotherapeutic approaches targeting MIF may hold promise for the treatment of COVID-19 pneumonia. |
doi_str_mv | 10.3855/jidc.14009 |
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This descriptive and cross-sectional study was conducted on 87 confirmed COVID-19 patients. The patients were separated into two groups according to the admission in the ICU or in the ward. MIF was determined batchwise in plasma obtained as soon as the patients were admitted. Both groups were compared with respect to demographic characteristics, biochemical parameters and prediction of requirement to ICU admission.
Forty seven patients in ICU, and 40 patients in ward were included. With respect to MIF levels and biochemical biomarkers, there was a statistically significant difference between the ICU and ward patients (p< 0.024). In terms of ICU requirement, the cut-off value of MIF was detected as 4.705 (AUC:0.633, 95%CI:0.561-0.79, p= 0.037), D-dimer was 789 (AUC:0.779, 95%CI: 0.681-0.877, p= 0.000), troponin was 8.15 (AUC: 0.820, 95%CI:0.729-0.911, p= 0.000), ferritin was 375 (AUC: 0.774, 95%CI:0.671-0.876, p= 0.000), and lactate dehydrogenase (LDH) was 359.5 (AUC:0.843, 95%CI: 0.753-0.933, p= 0.000). According to the logistic regression analysis; when MIF level > 4.705, the patient's requirement to ICU risk was increased to 8.33 (95%CI: 1.73-44.26, p= 0.009) fold. Similarly, elevation of troponin, ferritin and, LDH was shown to predict disease prognosis (p< 0.05).
Our study showed that MIF may play a role in inflammatory responses to COVID-19 through induction of pulmonary inflammatory cytokines, suggesting that pharmacotherapeutic approaches targeting MIF may hold promise for the treatment of COVID-19 pneumonia.</description><identifier>ISSN: 1972-2680</identifier><identifier>ISSN: 2036-6590</identifier><identifier>EISSN: 1972-2680</identifier><identifier>DOI: 10.3855/jidc.14009</identifier><identifier>PMID: 33839715</identifier><language>eng</language><publisher>Italy: Journal of Infection in Developing Countries</publisher><subject>Adult ; Aged ; Biomarkers - blood ; Comorbidity ; Coronaviruses ; COVID-19 ; COVID-19 - diagnosis ; COVID-19 - immunology ; Cross-Sectional Studies ; Female ; Hospitalization - statistics & numerical data ; Humans ; Inflammation - blood ; Inflammation - virology ; Intensive Care Units - statistics & numerical data ; Intramolecular Oxidoreductases - blood ; Macrophage Migration-Inhibitory Factors - blood ; Male ; Medical prognosis ; Middle Aged ; Prognosis ; Qualitative Research ; ROC Curve</subject><ispartof>Journal of infection in developing countries, 2021-03, Vol.15 (3), p.398-403</ispartof><rights>Copyright (c) 2021 Hamad Dheir, Selcuk Yaylaci, Savas Sipahi, Ahmed Cihad Genc, Deniz Cekic, Fatma Betul Tuncer, Erdem Cokluk, Havva Kocayigit, Ahmed Bilal Genc, Salih Salihi, Ceyhun Varim, Oguz Karabay.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-59f0d3fe008775c0619b276fe19a46a2a3616ae5cc9e4b050f1c62085a3e5f603</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33839715$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dheir, Hamad</creatorcontrib><creatorcontrib>Yaylaci, Selcuk</creatorcontrib><creatorcontrib>Sipahi, Savas</creatorcontrib><creatorcontrib>Genc, Ahmed Cihad</creatorcontrib><creatorcontrib>Cekic, Deniz</creatorcontrib><creatorcontrib>Tuncer, Fatma Betul</creatorcontrib><creatorcontrib>Cokluk, Erdem</creatorcontrib><creatorcontrib>Kocayigit, Havva</creatorcontrib><creatorcontrib>Genc, Ahmed Bilal</creatorcontrib><creatorcontrib>Salihi, Salih</creatorcontrib><creatorcontrib>Varim, Ceyhun</creatorcontrib><creatorcontrib>Karabay, Oguz</creatorcontrib><title>Does Macrophage Migration Inhibitory Factor predict the prognosis of COVID-19 disease?</title><title>Journal of infection in developing countries</title><addtitle>J Infect Dev Ctries</addtitle><description>The aim of this study is to investigate whether macrophage migration inhibitory factor (MIF) predicts the prognosis of COVID-19 disease.
This descriptive and cross-sectional study was conducted on 87 confirmed COVID-19 patients. The patients were separated into two groups according to the admission in the ICU or in the ward. MIF was determined batchwise in plasma obtained as soon as the patients were admitted. Both groups were compared with respect to demographic characteristics, biochemical parameters and prediction of requirement to ICU admission.
Forty seven patients in ICU, and 40 patients in ward were included. With respect to MIF levels and biochemical biomarkers, there was a statistically significant difference between the ICU and ward patients (p< 0.024). In terms of ICU requirement, the cut-off value of MIF was detected as 4.705 (AUC:0.633, 95%CI:0.561-0.79, p= 0.037), D-dimer was 789 (AUC:0.779, 95%CI: 0.681-0.877, p= 0.000), troponin was 8.15 (AUC: 0.820, 95%CI:0.729-0.911, p= 0.000), ferritin was 375 (AUC: 0.774, 95%CI:0.671-0.876, p= 0.000), and lactate dehydrogenase (LDH) was 359.5 (AUC:0.843, 95%CI: 0.753-0.933, p= 0.000). According to the logistic regression analysis; when MIF level > 4.705, the patient's requirement to ICU risk was increased to 8.33 (95%CI: 1.73-44.26, p= 0.009) fold. Similarly, elevation of troponin, ferritin and, LDH was shown to predict disease prognosis (p< 0.05).
Our study showed that MIF may play a role in inflammatory responses to COVID-19 through induction of pulmonary inflammatory cytokines, suggesting that pharmacotherapeutic approaches targeting MIF may hold promise for the treatment of COVID-19 pneumonia.</description><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers - blood</subject><subject>Comorbidity</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>COVID-19 - diagnosis</subject><subject>COVID-19 - immunology</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Hospitalization - statistics & numerical data</subject><subject>Humans</subject><subject>Inflammation - blood</subject><subject>Inflammation - virology</subject><subject>Intensive Care Units - statistics & numerical data</subject><subject>Intramolecular Oxidoreductases - blood</subject><subject>Macrophage Migration-Inhibitory Factors - blood</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Qualitative Research</subject><subject>ROC Curve</subject><issn>1972-2680</issn><issn>2036-6590</issn><issn>1972-2680</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkMFPwjAchRujEUQv_gGmiRdjMm3XtVtPxoAoCYSLcl1K9yuUwIrtduC_twga4-m9w5eXlw-ha0oeWMH548pW-oFmhMgT1KUyT5NUFOT0T--gixBWhHDJOD1HHcYKJnPKu2g2cBDwRGnvtku1ADyxC68a62o8qpd2bhvnd3iodEy89VBZ3eBmCbG7Re2CDdgZ3J_ORoOESlzZACrA0yU6M2od4OqYPfQxfHnvvyXj6euo_zxONKO8Sbg0pGIGCCnynGsiqJynuTBApcqEShUTVCjgWkvI5oQTQ7VIScEVA24EYT10d9iNdz5bCE25sUHDeq1qcG0oU05pIXkhaURv_6Er1_o6vouUiPJERrJI3R-oKCQED6bcertRfldSUu5tl3vb5bftCN8cJ9v5Bqpf9Ecv-wLnBHia</recordid><startdate>20210331</startdate><enddate>20210331</enddate><creator>Dheir, Hamad</creator><creator>Yaylaci, Selcuk</creator><creator>Sipahi, Savas</creator><creator>Genc, Ahmed Cihad</creator><creator>Cekic, Deniz</creator><creator>Tuncer, Fatma Betul</creator><creator>Cokluk, Erdem</creator><creator>Kocayigit, Havva</creator><creator>Genc, Ahmed Bilal</creator><creator>Salihi, Salih</creator><creator>Varim, Ceyhun</creator><creator>Karabay, Oguz</creator><general>Journal of Infection in Developing Countries</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8C1</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20210331</creationdate><title>Does Macrophage Migration Inhibitory Factor predict the prognosis of COVID-19 disease?</title><author>Dheir, Hamad ; 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This descriptive and cross-sectional study was conducted on 87 confirmed COVID-19 patients. The patients were separated into two groups according to the admission in the ICU or in the ward. MIF was determined batchwise in plasma obtained as soon as the patients were admitted. Both groups were compared with respect to demographic characteristics, biochemical parameters and prediction of requirement to ICU admission.
Forty seven patients in ICU, and 40 patients in ward were included. With respect to MIF levels and biochemical biomarkers, there was a statistically significant difference between the ICU and ward patients (p< 0.024). In terms of ICU requirement, the cut-off value of MIF was detected as 4.705 (AUC:0.633, 95%CI:0.561-0.79, p= 0.037), D-dimer was 789 (AUC:0.779, 95%CI: 0.681-0.877, p= 0.000), troponin was 8.15 (AUC: 0.820, 95%CI:0.729-0.911, p= 0.000), ferritin was 375 (AUC: 0.774, 95%CI:0.671-0.876, p= 0.000), and lactate dehydrogenase (LDH) was 359.5 (AUC:0.843, 95%CI: 0.753-0.933, p= 0.000). According to the logistic regression analysis; when MIF level > 4.705, the patient's requirement to ICU risk was increased to 8.33 (95%CI: 1.73-44.26, p= 0.009) fold. Similarly, elevation of troponin, ferritin and, LDH was shown to predict disease prognosis (p< 0.05).
Our study showed that MIF may play a role in inflammatory responses to COVID-19 through induction of pulmonary inflammatory cytokines, suggesting that pharmacotherapeutic approaches targeting MIF may hold promise for the treatment of COVID-19 pneumonia.</abstract><cop>Italy</cop><pub>Journal of Infection in Developing Countries</pub><pmid>33839715</pmid><doi>10.3855/jidc.14009</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Biomarkers - blood Comorbidity Coronaviruses COVID-19 COVID-19 - diagnosis COVID-19 - immunology Cross-Sectional Studies Female Hospitalization - statistics & numerical data Humans Inflammation - blood Inflammation - virology Intensive Care Units - statistics & numerical data Intramolecular Oxidoreductases - blood Macrophage Migration-Inhibitory Factors - blood Male Medical prognosis Middle Aged Prognosis Qualitative Research ROC Curve |
title | Does Macrophage Migration Inhibitory Factor predict the prognosis of COVID-19 disease? |
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