Primary antiphospholipid syndrome: a low-grade auto-inflammatory disease?

Objective. To test the inflammation and immune activation hypothesis in primary thrombotic APS (PAPS) and to identify clinical and laboratory factors related to inflammation and immune activation. Methods. PAPS (n ¼ 41) patients were compared with patients with inherited thrombophilia (IT, n ¼ 44) and controls (CTR, n ¼ 39). IgG aCL, IgG anti-� 2-glycoprotein I (� 2GPI), high-sensitivity CRP (hs-CRP), serum amyloid A (SAA), CRP bound to oxidized low-density lipoprotein– � 2GPI complex (CRP–oxLDL–� 2GPI) (as inflammatory markers) neopterin (NPT), soluble CD14 (sCD14) (as immune activation markers) were measured by ELISA. Results. After correction for confounders, PAPS showed higher plasma levels of hs-CRP (P ¼ 0.0004), SAA (P < 0.01), CRP–oxLDL–� 2GPI (P ¼ 0.0004), NPT (P < 0.0001) and sCD14 (P ¼ 0.007) than IT and CTR. Two regression models were applied to the PAPS group: in the first, IgG aCL and IgG � 2GPI were included amongst the independent variables and in the second they were excluded. In the first model, SAA (as the dependent variable) independently related to thrombosis number (P ¼ 0.003); NPT (as the dependent variable) independently related to thrombosis type (arterial, P ¼ 0.03) and number (P ¼ 0.04); sCD14 (as the dependent variable) independently related to IgG � 2GPI (P ¼ 0.0001), age (0.001) and arterial thrombosis (P ¼ 0.01); CRP–oxLDL–� 2GPI (as the dependent variable) independently related to IgG � 2GPI (P ¼ 0.0001). In the second model, sCD14 and NPT independently related to each other (P ¼ 0.002) (this was noted also in the IT group, P < 0.0001) and CRP–oxLDL–� 2GPI independently predicted SAA (P ¼ 0.002). Conclusion. Low-grade inflammation and immune activation occur in thrombotic PAPS and relate to clinical features and aPL levels.