Serena Fasano1,2, Luciana Pierro3,4, Ilenia Pantano3,4, Michele Iudici3,4, Gabriele Valentini3,4. 1. From the Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples, Naples, Italy. serefasa@gmail.com. 2. S. Fasano, MD, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples; L. Pierro, MD, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples; I. Pantano, MD, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples; M. Iudici, PhD, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples; G. Valentini, Professor, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples. serefasa@gmail.com. 3. From the Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples, Naples, Italy. 4. S. Fasano, MD, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples; L. Pierro, MD, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples; I. Pantano, MD, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples; M. Iudici, PhD, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples; G. Valentini, Professor, Department of Clinical and Experimental Medicine, Rheumatology Section, Second University of Naples.
Abstract
OBJECTIVE: Systemic lupus erythematosus (SLE) is associated with an increased risk of cardiovascular disease (CVD). Thromboprophylaxis with low-dose aspirin (ASA) and hydroxychloroquine (HCQ) seems promising in SLE. We investigated the effects of HCQ cumulative dosages (c-HCQ) and the possible synergistic efficacy of ASA and HCQ in preventing a first CV event (CVE) in patients with SLE. METHODS: Patients consecutively admitted to our center who, at admission, satisfied the 1997 American College of Rheumatology and/or 2012 Systemic Lupus Collaborating Clinics classification criteria for SLE, and had not experienced any CVE, were enrolled. The occurrence of a thrombotic event, use of ASA, and c-HCQ were recorded. Kaplan-Meier analysis was performed to determine the c-HCQ associated with a lower incidence of CVE. Cox regression analysis served to identify factors associated with a first CVE. RESULTS: For the study, 189 patients with SLE were enrolled and monitored for 13 years (median). Ten CVE occurred during followup. At Kaplan-Meier analysis, the CVE-free rate was higher in ASA-treated patients administered a c-HCQ > 600 g (standard HCQ dose for at least 5 yrs) than in patients receiving ASA alone, or with a c-HCQ dose < 600 g (log-rank test chi-square = 4.01, p = 0.04). Multivariate analysis showed that antimalarials plus ASA protected against thrombosis (HR 0.041 and HR 0.047, respectively), while antiphospholipid antibodies (HR 17.965) and hypertension (HR 18.054) increased the risk of a first CVE. CONCLUSION: Our results suggest that prolonged use of HCQ plus ASA is thromboprotective in SLE and provides additional evidence for its continued use in patients with SLE.
OBJECTIVE: Systemic lupus erythematosus (SLE) is associated with an increased risk of cardiovascular disease (CVD). Thromboprophylaxis with low-dose aspirin (ASA) and hydroxychloroquine (HCQ) seems promising in SLE. We investigated the effects of HCQ cumulative dosages (c-HCQ) and the possible synergistic efficacy of ASA and HCQ in preventing a first CV event (CVE) in patients with SLE. METHODS:Patients consecutively admitted to our center who, at admission, satisfied the 1997 American College of Rheumatology and/or 2012 Systemic Lupus Collaborating Clinics classification criteria for SLE, and had not experienced any CVE, were enrolled. The occurrence of a thrombotic event, use of ASA, and c-HCQ were recorded. Kaplan-Meier analysis was performed to determine the c-HCQ associated with a lower incidence of CVE. Cox regression analysis served to identify factors associated with a first CVE. RESULTS: For the study, 189 patients with SLE were enrolled and monitored for 13 years (median). Ten CVE occurred during followup. At Kaplan-Meier analysis, the CVE-free rate was higher in ASA-treated patients administered a c-HCQ > 600 g (standard HCQ dose for at least 5 yrs) than in patients receiving ASA alone, or with a c-HCQ dose < 600 g (log-rank test chi-square = 4.01, p = 0.04). Multivariate analysis showed that antimalarials plus ASA protected against thrombosis (HR 0.041 and HR 0.047, respectively), while antiphospholipid antibodies (HR 17.965) and hypertension (HR 18.054) increased the risk of a first CVE. CONCLUSION: Our results suggest that prolonged use of HCQ plus ASA is thromboprotective in SLE and provides additional evidence for its continued use in patients with SLE.
Authors: Joyce C Chang; Rui Xiao; Andrea M Knight; Stephen E Kimmel; Laura M Mercer-Rosa; Pamela F Weiss Journal: Semin Arthritis Rheum Date: 2020-05-03 Impact factor: 5.532