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10.1002/acr2.11245

http://scihub22266oqcxt.onion/10.1002/acr2.11245
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33738987!8063141!33738987
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suck abstract from ncbi


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pmid33738987      ACR+Open+Rheumatol 2021 ; 3 (4): 267-276
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  • Beta-2-Glycoprotein-I Deficiency Could Precipitate an Antiphospholipid Syndrome-like Prothrombotic Situation in Patients With Coronavirus Disease 2019 #MMPMID33738987
  • Serrano M; Espinosa G; Lalueza A; Bravo-Gallego LY; Diaz-Simon R; Garcinuno S; Gil-Etayo J; Moises J; Naranjo L; Prieto-Gonzalez S; Ruiz-Ortiz E; Sanchez B; Moreno-Castano AB; Diaz-Pedroche C; Vinas-Gomis O; Cervera R; Serrano A
  • ACR Open Rheumatol 2021[Apr]; 3 (4): 267-276 PMID33738987show ga
  • OBJECTIVE: Patients with coronavirus disease 2019 (COVID-19) present coagulation abnormalities and thromboembolic events that resemble antiphospholipid syndrome (APS). This work has aimed to study the prevalence of APS-related antigens, antibodies, and immune complexes in patients with COVID-19 and their association with clinical events. METHODS: A prospective study was conducted on 474 adults with severe acute respiratory syndrome coronavirus 2 infection hospitalized in two Spanish university hospitals. Patients were evaluated for classic and extra-criteria antiphospholipid antibodies (aPLs), immunoglobulin G (IgG)/immunoglobulin M (IgM) anticardiolipin, IgG/IgM/immunoglobulin A (IgA) anti-beta2-glicoprotein-I (abeta2GPI), IgG/IgM antiphosphatidylserine/prothrombin (aPS/PT), the immune complex of IgA abeta2GPI (IgA-abeta2GPI), bounded to beta2-glicoprotein-1 (beta2GPI) and beta2GPI levels soon after COVID-19 diagnosis and were followed-up until medical discharge or death. RESULTS: Prevalence of aPLs in patients with COVID-19 was as follows: classic aPLs, 5.8%; aPS/PT, 4.6%; IgA-abeta2GPI, 15%; and any aPL, 21%. When patients were compared with individuals of a control group of a similar age, the only significant difference found was the higher prevalence of IgA-abeta2GPI (odds ratio: 2.31; 95% confidence interval: 1.16-4.09). No significant differences were observed in survival, thrombosis, or ventilatory failure in aPL-positive versus aPL-negative patients. beta2GPI median levels were much lower in patients with COVID-19 (15.9 mg/l) than in blood donors (168.8 mg/l; P < 0.001). Only 3.5% of patients with COVID-19 had normal levels of beta2GPI (>85 mg/l). Low levels of beta2GPI were significantly associated with ventilatory failure (P = 0.026). CONCLUSION: beta2GPI levels were much lower in patients with COVID-19 than in healthy people. Low beta2GPI-levels were associated with ventilatory failure. No differences were observed in the COVID-19 evolution between aPL-positive and aPL-negative patients. Functional beta2GPI deficiency could trigger a clinical process similar to that seen in APS but in the absence of aPLs.
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