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High GRP78 levels in Covid-19 infection: A case-control study

INTRODUCTION: Covid-19 infection was declared a global pandemic by WHO on March 11, 2020. GRP78 protein is known to be involved in the intrusion of numerous viruses. Our current study tries to provide some insight into the variation of GRP78 protein levels in patients with Covid-19 (−) pneumonia, Co...

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Autores principales: Sabirli, Ramazan, Koseler, Aylin, Goren, Tarik, Turkcuer, Ibrahim, Kurt, Ozgur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674149/
https://www.ncbi.nlm.nih.gov/pubmed/33220289
http://dx.doi.org/10.1016/j.lfs.2020.118781
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author Sabirli, Ramazan
Koseler, Aylin
Goren, Tarik
Turkcuer, Ibrahim
Kurt, Ozgur
author_facet Sabirli, Ramazan
Koseler, Aylin
Goren, Tarik
Turkcuer, Ibrahim
Kurt, Ozgur
author_sort Sabirli, Ramazan
collection PubMed
description INTRODUCTION: Covid-19 infection was declared a global pandemic by WHO on March 11, 2020. GRP78 protein is known to be involved in the intrusion of numerous viruses. Our current study tries to provide some insight into the variation of GRP78 protein levels in patients with Covid-19 (−) pneumonia, Covid-19 (+) pneumonia, and CT negative Covid-19 infection in comparison to the normal population through a larger number of cases. MATERIALS AND METHODS: 42 patients who have Covid-19 (−) pneumonia; 72 patients who have Covid-19 infection (30 pneumonia,42 CT negative patients) and 30 patient who have no known diseases (control group) have included in the study after the clinical and radiological evaluation. Serum GRP78 levels of the subjects were measured through a commercially available enzyme-linked immunosorbent assay (ELISA) kit. RESULTS: The GRP78 level was found to be significantly higher in the Covid-19 infection group than both Covid-19 (−) pneumonia and control group (p = 0.031 and p = 0.0001, respectively).No significant difference was evident between Covid-19 (−) pneumonia, Covid-19 (+) pneumonia and CT negative Covid 19 infection groups with respect to GRP78 levels (p = 0.09). In addition, the GRP78 levels were significantly higher in the Covid-19 (−) pneumonia group than the control group (p = 0.0001). CONCLUSION: This prospective case-control study reveals that the serum GRP78 levels significantly increased during Covid-19 infection in comparison to both the Covid-19 (−) pneumonia and the control group. As the association between SARS-CoV-2 virus and GRP78 protein is revealed more clearly, this association may come to the fore as a therapeutic target.
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spelling pubmed-76741492020-11-19 High GRP78 levels in Covid-19 infection: A case-control study Sabirli, Ramazan Koseler, Aylin Goren, Tarik Turkcuer, Ibrahim Kurt, Ozgur Life Sci Article INTRODUCTION: Covid-19 infection was declared a global pandemic by WHO on March 11, 2020. GRP78 protein is known to be involved in the intrusion of numerous viruses. Our current study tries to provide some insight into the variation of GRP78 protein levels in patients with Covid-19 (−) pneumonia, Covid-19 (+) pneumonia, and CT negative Covid-19 infection in comparison to the normal population through a larger number of cases. MATERIALS AND METHODS: 42 patients who have Covid-19 (−) pneumonia; 72 patients who have Covid-19 infection (30 pneumonia,42 CT negative patients) and 30 patient who have no known diseases (control group) have included in the study after the clinical and radiological evaluation. Serum GRP78 levels of the subjects were measured through a commercially available enzyme-linked immunosorbent assay (ELISA) kit. RESULTS: The GRP78 level was found to be significantly higher in the Covid-19 infection group than both Covid-19 (−) pneumonia and control group (p = 0.031 and p = 0.0001, respectively).No significant difference was evident between Covid-19 (−) pneumonia, Covid-19 (+) pneumonia and CT negative Covid 19 infection groups with respect to GRP78 levels (p = 0.09). In addition, the GRP78 levels were significantly higher in the Covid-19 (−) pneumonia group than the control group (p = 0.0001). CONCLUSION: This prospective case-control study reveals that the serum GRP78 levels significantly increased during Covid-19 infection in comparison to both the Covid-19 (−) pneumonia and the control group. As the association between SARS-CoV-2 virus and GRP78 protein is revealed more clearly, this association may come to the fore as a therapeutic target. Elsevier Inc. 2021-01-15 2020-11-19 /pmc/articles/PMC7674149/ /pubmed/33220289 http://dx.doi.org/10.1016/j.lfs.2020.118781 Text en © 2020 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Sabirli, Ramazan
Koseler, Aylin
Goren, Tarik
Turkcuer, Ibrahim
Kurt, Ozgur
High GRP78 levels in Covid-19 infection: A case-control study
title High GRP78 levels in Covid-19 infection: A case-control study
title_full High GRP78 levels in Covid-19 infection: A case-control study
title_fullStr High GRP78 levels in Covid-19 infection: A case-control study
title_full_unstemmed High GRP78 levels in Covid-19 infection: A case-control study
title_short High GRP78 levels in Covid-19 infection: A case-control study
title_sort high grp78 levels in covid-19 infection: a case-control study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674149/
https://www.ncbi.nlm.nih.gov/pubmed/33220289
http://dx.doi.org/10.1016/j.lfs.2020.118781
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