4% (95% confidence interval=3.5-5.3) and 1.5% (95% confidence interval=1.0-2.0), respectively. Among HCV RNA carriers, genotyping showed that HCV genotypes 2 and 3 were the most prevalent as they were detected in
18 (56.3%) and 5 (15.6%) individuals, respectively. HCV genotypes la and 4 were the least frequent among the blood donors. HCV mixed genotypes 2/3 and 2/4 were also detected among the blood donors. Conclusion. The prevalence of HCV found in this study is lower than previously reported prevalences. Large-scale studies are needed to obtain a better picture of the molecular epidemiology of HCV in Burkina Faso.”
“Background: In published case reports, tocilizumab (TCZ) has PF-00299804 mw shown good efficacy for AA amyloidosis in almost all patients. We investigated the efficacy and BMS-777607 mouse safety of TCZ in AA amyloidosis in a multicentre study of unselected cases. Methods: We e-mailed rheumatology and internal medicine departments in France, Switzerland and North Africa by using the Club Rhumatismes Inflammation (CRI) network and the French TCZ registry, Registry RoAcTEmra (REGATE), to gather data on consecutive patients with histologically proven AA amyloidosis who had received at least one TCZ infusion. Efficacy
was defined as a sustained decrease in proteinuria level and/or stable or improved glomerular filtration rate (GFR) and by TCZ maintenance. Results: We collected 12 cases of AA amyloidosis treated with TCZ as monotherapy (mean age of patients 63 +/- 16.2 years, amyloidosis duration Nepicastat datasheet 20.6 +/- 31.3 months): eight patients had rheumatoid arthritis (RA), six with
previous failure of anti-tumor necrosis factor alpha (anti-TNF-alpha) therapy. In total, 11 patients had renal involvement, with two already on hemodialysis (not included in the renal efficacy assessment). For the nine other patients, baseline GFR and proteinuria level were 53.6 +/- 32.8 mL/min and 5 +/- 3.3 g/24 h, respectively. The mean follow-up was 13.1 +/- 11 months. TCZ was effective for six of the eight RA patients (87.5%) according to European League Against Rheumatism response criteria (four good and two moderate responders). As expected, C-reactive protein (CRP) level decreased with treatment for 11 patients. Renal amyloidosis (n = 9) progressed in three patients and was stabilized in three. Overall, three patients showed improvement, with sustained decrease in proteinuria level (42%, 82% and 96%). Baseline CRP level was higher in subsequent responders to TCZ than other patients (p = 0.02). Among the six RA patients with previous anti-TNF-alpha therapy, amyloidosis was ameliorated in one and stabilized in three. Three serious adverse events occurred (two diverticulitis and one major calciphylaxia due to renal failure). Finally, 7 of 12 (58%) patients continued TCZ. Conclusions: The efficacy of TCZ for AA amyloidosis varies depending on the inflammatory status at treatment onset.