dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | Alijotas-Reig, Jaume |
dc.contributor.author | Anunciación-Llunell, Ariadna |
dc.contributor.author | Morales-Pérez, Stephanie |
dc.contributor.author | Trape, Jaume |
dc.contributor.author | Esteve-Valverde, Enrique |
dc.contributor.author | Miro-Mur, Francesc A. |
dc.date.accessioned | 2023-09-01T12:43:46Z |
dc.date.available | 2023-09-01T12:43:46Z |
dc.date.issued | 2023-08-18 |
dc.identifier.citation | Alijotas-Reig J, Anunciación-Llunell A, Morales-Pérez S, Trapé J, Esteve-Valverde E, Miro-Mur F. Thrombosis and Hyperinflammation in COVID-19 Acute Phase Are Related to Anti-Phosphatidylserine and Anti-Phosphatidylinositol Antibody Positivity. Biomedicines. 2023 Aug 18;11(8):2301. |
dc.identifier.issn | 2227-9059 |
dc.identifier.uri | https://hdl.handle.net/11351/10213 |
dc.description | COVID-19; Antiphospholipid antibodies; Thrombosis |
dc.description.abstract | Antiphospholipid antibodies (APLA) are strongly associated with thrombosis seen in patients with antiphospholipid syndrome. In COVID-19, thrombosis has been observed as one of the main comorbidities. In patients hospitalised for COVID-19, we want to check whether APLA positivity is associated with COVID-19-related thrombosis, inflammation, severity of disease, or long COVID-19. We enrolled 92 hospitalised patients with COVID-19 between March and April 2020 who were tested for 18 different APLAs (IgG and IgM) with a single line-immunoassay test. A total of 30 healthy blood donors were used to set the cut-off for each APLA positivity. Of the 92 COVID-19 inpatients, 30 (32.61%; 95% CI [23.41–43.29]) tested positive for APLA, of whom 10 (33.3%; 95% CI [17.94–52.86]) had more than one APLA positivity. Anti-phosphatidylserine IgM positivity was described in 5.4% of inpatients (n = 5) and was associated with the occurrence of COVID-19-related thrombosis (p = 0.046). Anti-cardiolipin IgM positivity was the most prevalent among the inpatients (n = 12, 13.0%) and was associated with a recorded thrombosis in their clinical history (p = 0.044); however, its positivity was not associated with the occurrence of thrombosis during their hospitalisation for COVID-19. Anti-phosphatidylinositol IgM positivity, with a prevalence of 5.4% (n = 5), was associated with higher levels of interleukin (IL)-6 (p = 0.007) and ferritin (p = 0.034). Neither of these APLA positivities was a risk factor for COVID-19 severity or a predictive marker for long COVID-19. In conclusion, almost a third of COVID-19 inpatients tested positive for at least one APLA. Anti-phosphatidylserine positivity in IgM class was associated with thrombosis, and anti-phosphatidylinositol positivity in IgM class was associated with inflammation, as noticed by elevated levels of IL-6. Thus, testing for non-criteria APLA to assess the risk of clinical complications in hospitalised COVID-19 patients might be beneficial. However, they were not related to disease severity or long COVID-19. |
dc.language.iso | eng |
dc.publisher | MDPI |
dc.relation.ispartofseries | Biomedicines;11(8) |
dc.rights | Attribution 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
dc.source | Scientia |
dc.subject | COVID-19 (Malaltia) |
dc.subject | Trombosi |
dc.subject | Autoanticossos |
dc.subject.mesh | Coronavirus Infections |
dc.subject.mesh | Antibodies, Antiphospholipid |
dc.subject.mesh | Thrombosis |
dc.title | Thrombosis and Hyperinflammation in COVID-19 Acute Phase Are Related to Anti-Phosphatidylserine and Anti-Phosphatidylinositol Antibody Positivity |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.3390/biomedicines11082301 |
dc.subject.decs | infecciones por Coronavirus |
dc.subject.decs | anticuerpos antifosfolípidos |
dc.subject.decs | trombosis |
dc.relation.publishversion | https://doi.org/10.3390/biomedicines11082301 |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.organismes | Institut Català de la Salut |
dc.contributor.authoraffiliation | [Alijotas-Reig J] Unitat de Recerca de Malalties Autoimmunes Sistèmiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Unitat de Recerca de Malalties Autoimmunes Sistèmiques, Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament de Medicina, Facultat de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Anunciación-Llunell A, Miro-Mur F] Unitat de Recerca de Malalties Autoimmunes Sistèmiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Morales-Pérez S, Trapé J] Systemic Autoimmune Disease Unit, Internal Medicine Department, Althaia Healthcare University Network of Manresa, Manresa, Catalonia, Spain. [Esteve-Valverde E] Systemic Autoimmune Diseases Unit, Department of Internal Medicine, Hospital Universitari Parc Taulí, Sabadell, Catalonia, Spain |
dc.identifier.pmid | 37626797 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |