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Title: | A preliminary study on efficacy of rupatadine for the treatment of acute dengue infection | Authors: | Malavige, G.N Wijewickrama, A Fernando, S Jeewandara, C Ginneliya, A Samarasekara, S Madushanka, P Punchihewa, C Paranavitane, S Idampitiya, D Wanigatunga, C Dissanayake, H Prathapan, S Gomes, L Aman, S.A.B John, A.S Ogg, G.S |
Keywords: | antiallergic agent antihistaminic agent cyproheptadine histamine H1 receptor antagonist rupatadine acute disease adult animal C57BL mouse dengue Dengue virus disease model double blind procedure drug effect endothelium female human male metabolism mouse pathogenicity preliminary data Sri Lanka thrombocyte treatment outcome umbilical vein endothelial cell Acute Disease Adult Animals Anti-Allergic Agents Blood Platelets Cyproheptadine Dengue Dengue Virus Disease Models, Animal Double-Blind Method Endothelium Female Histamine Antagonists Histamine H1 Antagonists, Non-Sedating Human Umbilical Vein Endothelial Cells Humans Male Mice Mice, Inbred C57BL Preliminary Data Sri Lanka Treatment Outcome |
Issue Date: | 2018 | Publisher: | Nature Publishing Group | Citation: | Malavige, G.N, Wijewickrama, A, Fernando, S, Jeewandara, C, Ginneliya, A, Samarasekara, S, Madushanka, P, Punchihewa, C, Paranavitane, S, Idampitiya, D, Wanigatunga, C, Dissanayake, H, Prathapan, S, Gomes, L, Aman, S.A.B, John, A.S, Ogg, G.S (2018). A preliminary study on efficacy of rupatadine for the treatment of acute dengue infection. Scientific Reports 8 (1) : 3857. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-018-22285-x | Rights: | Attribution 4.0 International | Abstract: | Currently there are no specific treatments available for acute dengue infection. We considered that rupatadine, a platelet-activating factor receptor inhibitor, might modulate dengue-associated vascular leak. The effects of rupatadine were assessed in vitro, and in a dengue model, which showed that rupatadine significantly reduced endothelial permeability by dengue sera in vitro, and significantly inhibited the increased haematocrit in dengue-infected mice with dose-dependency. We conducted a randomised, placebo-controlled trial in 183 adult patients in Sri Lanka with acute dengue, which showed that rupatadine up to 40 mg daily appeared safe and well-tolerated with similar proportions of adverse events with rupatadine and placebo. Although the primary end-point of a significant reduction in fluid leakage (development of pleural effusions or ascites) was not met, post-hoc analyses revealed small but significant differences in several parameters on individual illness days - higher platelet counts and lower aspartate-aminotransferase levels on day 7 in the rupatadine group compared to the placebo group, and smaller effusions on day 8 in the subgroup of patients with pleural effusions. However, due to the small sample size and range of recruitment time, the potential beneficial effects of rupatadine require further evaluation in large studies focused on recruitment during the early febrile phase. © 2018 The Author(s). | Source Title: | Scientific Reports | URI: | https://scholarbank.nus.edu.sg/handle/10635/178426 | ISSN: | 2045-2322 | DOI: | 10.1038/s41598-018-22285-x | Rights: | Attribution 4.0 International |
Appears in Collections: | Staff Publications Elements |
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