Extra-criteria manifestations of antiphospholipid syndrome: Risk assessment and management
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | RADIN, Massimo | |
dc.contributor.author | UGOLINI-LOPES, Michelle Remiao | |
dc.contributor.author | SCIASCIA, Savino | |
dc.contributor.author | ANDRADE, Danieli | |
dc.date.accessioned | 2018-09-13T15:27:44Z | |
dc.date.available | 2018-09-13T15:27:44Z | |
dc.date.issued | 2018 | |
dc.description.abstract | Objectives: Extra-criteria manifestations of antiphospholipid syndrome (APS) might impact on prognosis and morbidity of the disease. In this study, we aimed to evaluate a population of patients with primary APS (PAPS) whether the extra-criteria manifestations were more frequently found in subjects with higher adjusted Global APS Score (aGAPSS) values when compared to patients with thrombotic and/or obstetric APS (""criteria"" manifestations) only. Methods: Clinical records were analyzed to retrieve extra-criteria manifestation of APS, cardiovascular risk factors and antiphospholipid antibodies profile. The aGAPSS was calculated by adding the points, as follows: 3 for hyperlipidaemia, 1 for arterial hypertension, 5 for anticardiolipin antibodies IgG/IgM, 4 for anti-beta 2 glycoprotein I IgG/IgM, and 4 for lupus anticoagulant. Results: This retrospective multicenter study included 89 consecutive PAPS [mean age 43.1 (S.D. +/- 12.9), female 67%, 52% arterial and 65% venous]. Twenty-seven patients (30.3%) had a history of livedo, 19 (21.3%) had a history of confirmed thrombocytopenia, 3 (3.4%) had biopsy-proven antiphospholipid antibodies (aPL)-related nephropathy and 3 (3.4%) had a history of valvulopathy. Patients with extra criteria manifestations presented a mean aGAPSS significantly higher [mean 10.30 (S.D. +/- 3.57, range: 4-17) vs mean 8.16 (S.D. +/- 3.52;range: 4-16, p = 0.005). When comparing patients with and without extra-criteria manifestations, the first group had significantly higher incidence of anti-beta 2GPI antibodies positivity (59% and 33%, respectively, p = 0.015), double aPL positivities (53% and 31%, respectively, p = 0.034), cerebrovascular events history (52% and 24%, respectively, p = 0.007) and arterial hypertension (52% and 24%, respectively, p = 0.007). Conclusions: Our results suggest that patients with higher aGAPSS, might be at higher risk for developing extra-criteria manifestations of APS and should therefore undergo a thorough laboratory and instrumental evaluation. | |
dc.description.index | MEDLINE | |
dc.identifier.citation | SEMINARS IN ARTHRITIS AND RHEUMATISM, v.48, n.1, p.117-120, 2018 | |
dc.identifier.doi | 10.1016/j.semarthrit.2017.12.006 | |
dc.identifier.eissn | 1532-866X | |
dc.identifier.issn | 0049-0172 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/28380 | |
dc.language.iso | eng | |
dc.publisher | W B SAUNDERS CO-ELSEVIER INC | |
dc.relation.ispartof | Seminars in Arthritis and Rheumatism | |
dc.rights | restrictedAccess | |
dc.rights.holder | Copyright W B SAUNDERS CO-ELSEVIER INC | |
dc.subject | Antiphosphospholipid syndrome | |
dc.subject | APS | |
dc.subject | Livedo | |
dc.subject | Thrombocytopenia | |
dc.subject | GAPSS | |
dc.subject | aGAPSS | |
dc.subject | Risk score | |
dc.subject | Thrombosis | |
dc.subject.other | syndrome score | |
dc.subject.other | syndrome aps | |
dc.subject.other | cohort | |
dc.subject.other | update | |
dc.subject.other | validation | |
dc.subject.other | thrombosis | |
dc.subject.other | gapss | |
dc.subject.wos | Rheumatology | |
dc.title | Extra-criteria manifestations of antiphospholipid syndrome: Risk assessment and management | |
dc.type | article | |
dc.type.category | review | |
dc.type.version | publishedVersion | |
dspace.entity.type | Publication | |
hcfmusp.affiliation.country | Itália | |
hcfmusp.affiliation.countryiso | it | |
hcfmusp.author.external | RADIN, Massimo:Univ Turin, Dept Clin & Biol Sci, Ctr Res Immunopathol & Rare Dis, Coordinating Ctr Piemonte & Valle Aosta Network R, Turin, Italy; Univ Turin, SCDU Nephrol & Dialysis, Turin, Italy; S Giovanni Bosco Hosp, Turin, Italy | |
hcfmusp.author.external | SCIASCIA, Savino:Univ Turin, Dept Clin & Biol Sci, Ctr Res Immunopathol & Rare Dis, Coordinating Ctr Piemonte & Valle Aosta Network R, Turin, Italy; Univ Turin, SCDU Nephrol & Dialysis, Turin, Italy; S Giovanni Bosco Hosp, Turin, Italy | |
hcfmusp.citation.scopus | 37 | |
hcfmusp.contributor.author-fmusphc | MICHELLE REMIAO UGOLINI LOPES | |
hcfmusp.contributor.author-fmusphc | DANIELI CASTRO OLIVEIRA DE ANDRADE | |
hcfmusp.description.beginpage | 117 | |
hcfmusp.description.endpage | 120 | |
hcfmusp.description.issue | 1 | |
hcfmusp.description.volume | 48 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 29395258 | |
hcfmusp.origem.scopus | 2-s2.0-85041002491 | |
hcfmusp.origem.wos | WOS:000441703600016 | |
hcfmusp.publisher.city | PHILADELPHIA | |
hcfmusp.publisher.country | USA | |
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hcfmusp.scopus.lastupdate | 2024-05-10 | |
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relation.isAuthorOfPublication.latestForDiscovery | ae8b2495-d8b0-455e-9cc3-acc8f6763f8f |
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