Browsing by Author "Sciascia, Savino (26421432900)"
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Publication Circulating immune-complexes of IgG/IgM bound to B2-glycoprotein-I associated with complement consumption and thrombocytopenia in antiphospholipid syndrome(2022) ;Naranjo, Laura (57199155062) ;Stojanovich, Ljudmila (55917563000) ;Djokovic, Aleksandra (42661226500) ;Andreoli, Laura (23110534400) ;Tincani, Angela (7005623740) ;Maślińska, Maria (12782206900) ;Sciascia, Savino (26421432900) ;Infantino, Maria (36965614500) ;Garcinuño, Sara (57222357108) ;Kostyra-Grabczak, Kinga (57213618422) ;Manfredi, Mariangela (8927547000) ;Regola, Francesca (57199841161) ;Stanisavljevic, Natasa (36163559700) ;Milanovic, Milomir (7003857551) ;Saponjski, Jovica (56629875900) ;Roccatello, Dario (7005747589) ;Cecchi, Irene (57191501152) ;Radin, Massimo (57190688571) ;Benucci, Maurizio (6602125228) ;Pleguezuelo, Daniel (57192685701) ;Serrano, Manuel (57220615947) ;Shoenfeld, Yehuda (36879964800)Serrano, Antonio (56261738300)Background: Antiphospholipid syndrome (APS) is a multisystemic autoimmune disorder characterized by thrombotic events and/or gestational morbidity in patients with antiphospholipid antibodies (aPL). In a previous single center study, APS-related clinical manifestations that were not included in the classification criteria (livedo reticularis, thrombocytopenia, leukopenia) were associated with the presence of circulating immune-complexes (CIC) formed by beta-2-glycoprotein-I (B2GP1) and anti-B2GP1 antibodies (B2-CIC). We have performed a multicenter study on APS features associated with the presence of B2-CIC. Methods: A multicenter, cross-sectional and observational study was conducted on 303 patients recruited from six European hospitals who fulfilled APS classification criteria: 165 patients had primary APS and 138 APS associated with other systemic autoimmune diseases (mainly systemic lupus erythematosus, N=112). Prevalence of B2-CIC (IgG/IgM isotypes) and its association with clinical manifestations and biomarkers related to the disease activity were evaluated. Results: B2-CIC prevalence in APS patients was 39.3%. B2-CIC-positive patients with thrombotic APS presented a higher incidence of thrombocytopenia (OR: 2.32, p=0.007), heart valve thickening and dysfunction (OR: 9.06, p=0.015) and triple aPL positivity (OR: 1.83, p=0.027), as well as lower levels of C3, C4 and platelets (p-values: <0.001, <0.001 and 0.001) compared to B2-CIC-negative patients. B2-CIC of IgM isotype were significantly more prevalent in gestational than thrombotic APS. Conclusions: Patients with thrombotic events and positive for B2-CIC had lower platelet count and complement levels than those who were negative, suggesting a greater degree of platelet activation. Copyright © 2022 Naranjo, Stojanovich, Djokovic, Andreoli, Tincani, Maślińska, Sciascia, Infantino, Garcinuño, Kostyra-Grabczak, Manfredi, Regola, Stanisavljevic, Milanovic, Saponjski, Roccatello, Cecchi, Radin, Benucci, Pleguezuelo, Serrano, Shoenfeld and Serrano. - Some of the metrics are blocked by yourconsent settings
Publication Circulating immune-complexes of IgG/IgM bound to B2-glycoprotein-I associated with complement consumption and thrombocytopenia in antiphospholipid syndrome(2022) ;Naranjo, Laura (57199155062) ;Stojanovich, Ljudmila (55917563000) ;Djokovic, Aleksandra (42661226500) ;Andreoli, Laura (23110534400) ;Tincani, Angela (7005623740) ;Maślińska, Maria (12782206900) ;Sciascia, Savino (26421432900) ;Infantino, Maria (36965614500) ;Garcinuño, Sara (57222357108) ;Kostyra-Grabczak, Kinga (57213618422) ;Manfredi, Mariangela (8927547000) ;Regola, Francesca (57199841161) ;Stanisavljevic, Natasa (36163559700) ;Milanovic, Milomir (7003857551) ;Saponjski, Jovica (56629875900) ;Roccatello, Dario (7005747589) ;Cecchi, Irene (57191501152) ;Radin, Massimo (57190688571) ;Benucci, Maurizio (6602125228) ;Pleguezuelo, Daniel (57192685701) ;Serrano, Manuel (57220615947) ;Shoenfeld, Yehuda (36879964800)Serrano, Antonio (56261738300)Background: Antiphospholipid syndrome (APS) is a multisystemic autoimmune disorder characterized by thrombotic events and/or gestational morbidity in patients with antiphospholipid antibodies (aPL). In a previous single center study, APS-related clinical manifestations that were not included in the classification criteria (livedo reticularis, thrombocytopenia, leukopenia) were associated with the presence of circulating immune-complexes (CIC) formed by beta-2-glycoprotein-I (B2GP1) and anti-B2GP1 antibodies (B2-CIC). We have performed a multicenter study on APS features associated with the presence of B2-CIC. Methods: A multicenter, cross-sectional and observational study was conducted on 303 patients recruited from six European hospitals who fulfilled APS classification criteria: 165 patients had primary APS and 138 APS associated with other systemic autoimmune diseases (mainly systemic lupus erythematosus, N=112). Prevalence of B2-CIC (IgG/IgM isotypes) and its association with clinical manifestations and biomarkers related to the disease activity were evaluated. Results: B2-CIC prevalence in APS patients was 39.3%. B2-CIC-positive patients with thrombotic APS presented a higher incidence of thrombocytopenia (OR: 2.32, p=0.007), heart valve thickening and dysfunction (OR: 9.06, p=0.015) and triple aPL positivity (OR: 1.83, p=0.027), as well as lower levels of C3, C4 and platelets (p-values: <0.001, <0.001 and 0.001) compared to B2-CIC-negative patients. B2-CIC of IgM isotype were significantly more prevalent in gestational than thrombotic APS. Conclusions: Patients with thrombotic events and positive for B2-CIC had lower platelet count and complement levels than those who were negative, suggesting a greater degree of platelet activation. Copyright © 2022 Naranjo, Stojanovich, Djokovic, Andreoli, Tincani, Maślińska, Sciascia, Infantino, Garcinuño, Kostyra-Grabczak, Manfredi, Regola, Stanisavljevic, Milanovic, Saponjski, Roccatello, Cecchi, Radin, Benucci, Pleguezuelo, Serrano, Shoenfeld and Serrano.