Investigation of ADAMTS-13 levels in patients with COVID-19 infection

dc.authorid0000-0001-8024-8951
dc.authorid0000-0002-1730-1331
dc.contributor.authorKutlu, Huseyin H.
dc.contributor.authorSahin, Arzu
dc.contributor.authorMizrak, Soycan
dc.contributor.authorYilmaz, Abdurrahman
dc.contributor.authorDoganay, Songul
dc.contributor.authorGungor, Serdar
dc.contributor.authorYilmaz, Sema
dc.date.accessioned2025-05-20T18:53:38Z
dc.date.issued2024
dc.departmentBilecik Şeyh Edebali Üniversitesi
dc.description.abstractIntroduction: Coronavirus disease 2019 (COVID-19) patients are predisposed to thrombotic events. COVID-19 coagulopathy can be associated with ADAMTS-13 (a disintegrin-like and metalloprotease with thrombospondin type I repeats 13) levels. ADAMTS-13, the cleaving protease of highly thrombogenic ultra-large von Willebrand Factor (vWF) multimers, was rarely investigated in COVID-19 patients and inconsistent results were obtained. We measured ADAMTS-13 levels of patients admitted to emergency department. Methodology: A prospective study was carried out with 180 individuals at the Emergency Department of Usak Training and Research Hospital. The patients were divided into three groups: mild COVID-19 (group 2), severe COVID-19 with oxygen saturation below 94% (group 3), and control group (group 1). ADAMTS-13 levels were analyzed with an enzyme linked immunosorbent assay (ELISA) kit (SunRed, Shanghai, China). Demographic data, clinical findings, and routine laboratory test results (alanine aminotransferase (ALT), aspartate aminotransferase normalized ratio (INR), partial thromboplastin time, D-dimer, creatinine, urea) were evaluated. Results: ADAMTS-13 serum levels were slightly lower in groups 2 and 3 compared to the control group, with no significant difference between the ADAMTS-13 median values (p > 0.05). Groups 1 and 2 exhibited comparable outcomes. Group 3 demonstrated notably elevated levels of CRP, LDH, D-dimer, AST, ALT, creatinine; and decreased platelet counts and INR levels (p < 0.05). Conclusions: COVID-19-associated coagulopathy is still unclear. Based on our data, ADAMTS-13 levels cannot be used as a biomarker to help stratify patients' risks at the time of admission.
dc.identifier.doi10.3855/jidc.19439
dc.identifier.endpageS175
dc.identifier.issn1972-2680
dc.identifier.issue9
dc.identifier.pmid39499761
dc.identifier.scopus2-s2.0-85208603277
dc.identifier.scopusqualityQ2
dc.identifier.startpageS170
dc.identifier.urihttps://doi.org/10.3855/jidc.19439
dc.identifier.urihttps://hdl.handle.net/11552/6955
dc.identifier.volume18
dc.identifier.wosWOS:001407394900021
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWoS
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakWoS - Science Citation Index Expanded
dc.language.isoen
dc.publisherJ Infection Developing Countries
dc.relation.ispartofJournal of Infection in Developing Countries
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250518
dc.subjectCOVID-19
dc.subjectADAMTS-13
dc.subjectCOVID-19-associated coagulopathy
dc.titleInvestigation of ADAMTS-13 levels in patients with COVID-19 infection
dc.typeArticle

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