HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

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

AbstractOBJECTIVE:
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 = 41) patients were compared with patients with inherited thrombophilia (IT, n = 44) and controls (CTR, n = 39). IgG aCL, IgG anti-beta2-glycoprotein I (beta(2)GPI), high-sensitivity CRP (hs-CRP), serum amyloid A (SAA), CRP bound to oxidized low-density lipoprotein-beta(2)GPI complex (CRP-oxLDL-beta(2)GPI) (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 = 0.0004), SAA (P < 0.01), CRP-oxLDL-beta(2)GPI (P = 0.0004), NPT (P < 0.0001) and sCD14 (P = 0.007) than IT and CTR. Two regression models were applied to the PAPS group: in the first, IgG aCL and IgG beta(2)GPI 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 = 0.003); NPT (as the dependent variable) independently related to thrombosis type (arterial, P = 0.03) and number (P = 0.04); sCD14 (as the dependent variable) independently related to IgG beta(2)GPI (P = 0.0001), age (0.001) and arterial thrombosis (P = 0.01); CRP-oxLDL-beta(2)GPI (as the dependent variable) independently related to IgG beta(2)GPI (P = 0.0001). In the second model, sCD14 and NPT independently related to each other (P = 0.002) (this was noted also in the IT group, P < 0.0001) and CRP-oxLDL-beta(2)GPI independently predicted SAA (P = 0.002).
CONCLUSION:
Low-grade inflammation and immune activation occur in thrombotic PAPS and relate to clinical features and aPL levels.
AuthorsP R J Ames, I Antinolfi, A Ciampa, J Batuca, G Scenna, L R Lopez, J Delgado Alves, L Iannaccone, E Matsuura
JournalRheumatology (Oxford, England) (Rheumatology (Oxford)) Vol. 47 Issue 12 Pg. 1832-7 (Dec 2008) ISSN: 1462-0332 [Electronic] England
PMID18930964 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Autoantibodies
  • Biomarkers
  • Immunoglobulin G
  • Lipopolysaccharide Receptors
  • Serum Amyloid A Protein
  • beta 2-Glycoprotein I
  • Neopterin
  • C-Reactive Protein
Topics
  • Adult
  • Aged
  • Antiphospholipid Syndrome (immunology)
  • Autoantibodies (blood)
  • Biomarkers (blood)
  • C-Reactive Protein (analysis)
  • Cross-Sectional Studies
  • Enzyme-Linked Immunosorbent Assay (methods)
  • Female
  • Humans
  • Immunoglobulin G (blood)
  • Inflammation (immunology)
  • Lipopolysaccharide Receptors (blood)
  • Male
  • Middle Aged
  • Neopterin (blood)
  • Serum Amyloid A Protein (analysis)
  • Thrombophilia (immunology)
  • beta 2-Glycoprotein I (blood)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: