TY - JOUR
T1 - Effects of statins on proinflammatory/prothrombotic biomarkers and on disease activity scores in SLE patients
T2 - Data from LUMINA (LXXVI), a multi-ethnic us cohort
AU - Willis, Rohan
AU - Seif, Alan M.
AU - McGwin, Gerald
AU - Martinez-Martinez, Laura Aline
AU - González, Emilio B.
AU - Doan, Ellis
AU - Dang, Neha
AU - Papalardo, Elizabeth
AU - Liu, Jigna
AU - Vilá, Luis M.
AU - Reveille, John D.
AU - Alarcón, Graciela S.
AU - Pierangeli, Silvia S.
PY - 2014
Y1 - 2014
N2 - Objective: We sought to determine the effect of statin therapy on the levels of proinflammatory /prothrombotic markers and disease activity scores in patients with SLE in a multi-ethnic, multi-centre cohort (LUMINA). Methods: Plasma/serum samples from SLE patients placed on statins (n=21) therapy taken before and after at least 6 months of treatment were tested. Disease activity was assessed using SLAM-R scores. Interleukin (IL)-1β, IL-6, IL-8, tumour necrosis factor (TNF)-a, vascular endothelial growth factor (VEGF) and soluble CD40 ligand (sCD40L) levels were determined by a multiplex immunoassay. Soluble intercellular cell adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1 and anticardiolipin (aCL) antibodies were evaluated using ELISA assays while high sensitivity C-reactive protein (hsCRP) was assessed by nephelometry. Plasma/serum samples from frequency-matched healthy donors were used as controls. Results: Levels of IL-6, VEGF, sCD40L and TNF-a were significantly elevated in SLE patients versus controls. Statin therapy resulted in a significant decrease in SLAM-R scores (p=0.0199) but no significant changes in biomarker levels were observed. There was no significant association of biomarkers with SLAM-R scores. Conclusion: Statin therapy resulted in significant clinical improvement in SLE patients, underscoring the use of statins in the treatment of SLE.
AB - Objective: We sought to determine the effect of statin therapy on the levels of proinflammatory /prothrombotic markers and disease activity scores in patients with SLE in a multi-ethnic, multi-centre cohort (LUMINA). Methods: Plasma/serum samples from SLE patients placed on statins (n=21) therapy taken before and after at least 6 months of treatment were tested. Disease activity was assessed using SLAM-R scores. Interleukin (IL)-1β, IL-6, IL-8, tumour necrosis factor (TNF)-a, vascular endothelial growth factor (VEGF) and soluble CD40 ligand (sCD40L) levels were determined by a multiplex immunoassay. Soluble intercellular cell adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1 and anticardiolipin (aCL) antibodies were evaluated using ELISA assays while high sensitivity C-reactive protein (hsCRP) was assessed by nephelometry. Plasma/serum samples from frequency-matched healthy donors were used as controls. Results: Levels of IL-6, VEGF, sCD40L and TNF-a were significantly elevated in SLE patients versus controls. Statin therapy resulted in a significant decrease in SLAM-R scores (p=0.0199) but no significant changes in biomarker levels were observed. There was no significant association of biomarkers with SLAM-R scores. Conclusion: Statin therapy resulted in significant clinical improvement in SLE patients, underscoring the use of statins in the treatment of SLE.
KW - Biomarkers of inflammation
KW - Biomarkers of thrombosis
KW - Lupus
KW - Statins
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M3 - Article
C2 - 24480124
AN - SCOPUS:84904397645
SN - 0392-856X
VL - 32
SP - 162
EP - 167
JO - Clinical and Experimental Rheumatology
JF - Clinical and Experimental Rheumatology
IS - 2
ER -