Do all antiphospholipid antibodies confer the same risk for major organ involvement in systemic lupus erythematosus patients?


Por: Riancho-Zarrabeitia, L, Martinez-Taboada, V, Rua-Figueroa, I, Alonso, F, Galindo-Izquierdo, M, Ovalles, J, Olive-Marques, A, Vazquez, NM, Calvo-Alen, J, Menor-Almagro, R, Tomero-Muriel, E, Uriarte-Isacelaya, E, Botenau, A, Andres, M, Freire-Gonzalez, M, Soler, GS, Ruiz-Lucea, E, Ibanez-Barcelo, M, Castellvi, I, Galisteo, C, Vila, VQ, Raya, E, Narvaez, J, Exposito, L, Hernandez-Beriain, JA, Horcada, L, Aurrecoechea, E, Pego-Reigosa, JM

Publicada: 1 may 2021
Resumen:
Objective We aimed to investigate the association between the different antiphospholipid antibodies (aPL) and both systemic lupus erythematosus (SLE) and antiphospholipid syndrome (APS) manifestations. Methods Patients from the RELESSER registry, a Spanish retrospective, cross-sectional, forty-five hospital registry of adult SLE patients, were included. Results Out of a total of 3,658 SLE patients, 1372 were aPL positive (555 of them fulfilled criteria for APS). All aPL types showed a negative association with cutaneous SLE manifestations. Lupus anticoagulant (LA) and anticardiolipin antibodies (aCL) were both associated with haematological, ophthalmological and neuropsychiatric manifestations. IgG isotypes were associated with a higher risk of lupus manifestations compared with IgM. We found that the risk of neuropsychiatric and ophthalmological manifestations significantly increased with a higher number of positive aPL whereas the risk of cutaneous symptoms showed a negative correlation. All types of aPL, and more strongly LA, were associated with non-criteria antiphospholipid syndrome (APS) manifestations such as thrombocytopenia and haemolytic anaemia. Moreover, LA and aCL (particularly IgG isotype) were also associated with Libman-Sacks endocarditis and cognitive impairment. This association was stronger with more than one positive aPL. All types of aPL were also associated with classic APS manifestations, although LA, IgG isotypes, and patients with more than one aPL displayed a higher risk. Conclusion There is a hierarchy for aPL and the risk of APS and SLE manifestations. aCL, and especially LA, confer a higher risk for major organ involvement in SLE. IgG isotypes seem to have a more important role. The load of aPL confer a higher risk for APS and certain SLE manifestations.

Filiaciones:
Riancho-Zarrabeitia, L:
 Hosp Sierrallana, IDIVAL, Dept Rheumatol, Torrelavega, Spain

Martinez-Taboada, V:
 Hosp Sierrallana, IDIVAL, Dept Rheumatol, Torrelavega, Spain

 Univ Cantabria, Hosp Univ Doctor Negrin, IDIVAL, Cantabria, Spain

Rua-Figueroa, I:
 Hosp Univ Doctor Negrin, Los Palmas, Spain

Alonso, F:
 Soc Espanola Reumatol, Unidad Invest, Madrid, Spain

Galindo-Izquierdo, M:
 Hosp Univ Doce Octubre, Madrid, Spain

Ovalles, J:
 Hosp Gen Univ Gregorio Maranon, Barcelona, Spain

Olive-Marques, A:
 Hosp Badalona Germans Trias & Pujol, Barcelona, Spain

Vazquez, NM:
 Hosp Reg Univ Malaga, Malaga, Spain

Calvo-Alen, J:
 Hosp Univ Araba, Alava, Spain

Menor-Almagro, R:
 Hosp Jerez, Cadiz, Spain

Tomero-Muriel, E:
 Hosp Univ Princesa, Madrid, Spain

Uriarte-Isacelaya, E:
 Hosp Univ Donostia, San Sebastian, Spain

Botenau, A:
 Hosp Univ Ramon & Cajal, Madrid, Spain

Andres, M:
 Hosp Gen Univ Alicante, Alicante, Spain

Freire-Gonzalez, M:
 Hosp Univ Juan Canalejo, La Coruna, Spain

Soler, GS:
 Hosp Marina Baixa, Alicante, Spain

Ruiz-Lucea, E:
 Hosp Univ Basurto, Bilbao, Spain

Ibanez-Barcelo, M:
 Hosp Univ Son Llatzer, Palma De Mallorca, Spain

Castellvi, I:
 Hosp Santa Creu & Sant Pau, Barcelona, Spain

Galisteo, C:
 Hosp Univ Parc Tauli, Barcelona, Spain

Vila, VQ:
 Hosp Comarcal Monforte, Lugo, Spain

Raya, E:
 Hosp Univ Clin San Cecilio, Granada, Spain

Narvaez, J:
 Hosp Univ Bellvitge, Barcelona, Spain

Exposito, L:
 Hosp Univ Canarias, Tenerife, Spain

Hernandez-Beriain, JA:
 Hosp Insular Univ Gran Canaria, Las Palmas Gran Canaria, Spain

Horcada, L:
 Complejo Hosp Univ Navarra, Navarra, Spain

Aurrecoechea, E:
 Hosp Sierrallana, IDIVAL, Dept Rheumatol, Torrelavega, Spain

Pego-Reigosa, JM:
 Univ Vigo IRIDIS Grp, Inst Invest Sanitaria Galicia IISGS, Complejo Hosp, Vigo, Spain
ISSN: 0392856X





CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
Editorial
CLINICAL & EXPER RHEUMATOLOGY, VIA SANTA MARIA 31, 56126 PISA, ITALY, Italia
Tipo de documento: Article
Volumen: 39 Número: 3
Páginas: 555-563
WOS Id: 000653640600014
ID de PubMed: 32828148
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