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Short Term Effects of Infliximab on the Lipid Profile in Patients with Rheumatoid Arthritis
MARIJN VIS, MICHAEL T. NURMOHAMED, GERTJAN WOLBINK, ALEXANDRE E. VOSKUYL, MARGRET H.M.T. de KONING, ROB J. van de STADT, JOS W.R. TWISK, BEN A.C. DIJKMANS, and WILLEM F. LEMS
ABSTRACT. Methods. Infliximab was administered at baseline and at 2 and 6 weeks in patients with active RA. Total cholesterol and HDL-cholesterol concentrations were measured and their ratio, the atherogenic index (an important cardiovascular risk factor indicator), was assessed. Results. Sixty-nine patients were enrolled. The Disease Activity Index score (DAS-28) was 5.9 (SD ± 1.4) at baseline and decreased to 4.6 (± 1.4) after 2 weeks and further to 4.1 (± 1.5) after 6 weeks. Total cholesterol level was 5.2 mmol/l at baseline and increased to 5.7 mmol/l (p < 0.001) at 2 weeks, and was 5.6 mmol/l (p < 0.001 vs baseline) at Week 6. For HDL-cholesterol these values were 1.5, 1.6 (p < 0.001), and 1.6 mmol/l (p < 0.001 vs baseline), respectively. Changes in disease activity were significantly inversely associated with changes in total cholesterol and HDL-cholesterol levels. The atherogenic index, however, remained constant. Corticosteroid use at baseline was associated with significantly higher total cholesterol and HDL-cholesterol levels and a lower (more favorable) atherogenic index at baseline. Conclusion. Infliximab treatment was associated with a significant increase of both total cholesterol and HDL-cholesterol levels, which correlated with decreasing disease activity. However, this was not accompanied by a favorable effect on the atherogenic index. The favorable effect of infliximab on cardiovascular comorbidity might not be mediated by effects on lipid metabolism, but longterm investigations are needed to confirm this. (J Rheumatol 2005;32:25-5) Key Indexing Terms:
RHEUMATOID ARTHRITIS
From the Department of Rheumatology, VU University Medical Centre, Jan van Breemen Institute; and Slotervaart Hospital, Department of Epidemiology, VU University Medical Centre, Amsterdam, The Netherlands. M. Vis, MD, Research Physician, VU University Medical Centre, Slotervaart Hospital; M.T. Nurmohamed, MD, PhD, Rheumatologist, Epidemiologist; G. Wolbink, MD, PhD, Rheumatologist, VU University Medical Centre, Jan van Breemen Institute; A.E. Voskuyl, MD, PhD, Rheumatologist, VU University Medical Centre; M.H.M.T. de Koning, Technician; R.J. van de Stadt, PhD, Clinical Chemist, Jan van Breemen Institute; J.W.R. Twisk, PhD, Statistician, Epidemiologist, Department of Epidemiology, VU University Medical Centre; B.A.C. Dijkmans, MD, PhD, Rheumatologist, Professor of Rheumatology; W.F. Lems, MD, PhD, Rheumatologist, VU University Medical Centre, Jan van Breemen Institute, Slotervaart Hospital. Address reprint requests to Dr. M.T. Nurmohamed, Department of Rheumatology, VU University Medical Centre, Room 4A40, PO Box 7057, Amsterdam, The Netherlands. E-mail:m.nurmohamed@janvanbreemen.nl Submitted February 23, 2004; revision accepted October 13, 2004. |