pubmed-article:11461950 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11461950 | lifeskim:mentions | umls-concept:C0010825 | lld:lifeskim |
pubmed-article:11461950 | lifeskim:mentions | umls-concept:C0012634 | lld:lifeskim |
pubmed-article:11461950 | lifeskim:mentions | umls-concept:C0022671 | lld:lifeskim |
pubmed-article:11461950 | lifeskim:mentions | umls-concept:C0209368 | lld:lifeskim |
pubmed-article:11461950 | lifeskim:mentions | umls-concept:C0021149 | lld:lifeskim |
pubmed-article:11461950 | lifeskim:mentions | umls-concept:C0205191 | lld:lifeskim |
pubmed-article:11461950 | lifeskim:mentions | umls-concept:C1292733 | lld:lifeskim |
pubmed-article:11461950 | lifeskim:mentions | umls-concept:C1167870 | lld:lifeskim |
pubmed-article:11461950 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:11461950 | pubmed:dateCreated | 2001-7-19 | lld:pubmed |
pubmed-article:11461950 | pubmed:abstractText | Ganciclovir, which is used to treat cytomegalovirus (CMV) infection, has been shown in rodent models to abolish CMV-mediated chronic cellular damage and endothelial cell proliferation; when associated with mycophenolate mofetil (MMF), it has been shown to increase its anti-herpes virus activity. This study tested the hypothesis that kidney graft recipients who received antirejection prophylaxis with MMF and who were treated with ganciclovir for a declared CMV disease could be protected from chronic graft dysfunction. Investigated was the impact of ganciclovir-treated CMV diseases in consecutive first kidney recipients according to their immunosuppressive therapy. The azathioprine (Aza)-treated group (Aza group) included 319 patients. The MMF-treated group (MMF group) included 126 patients. CMV disease was clinically defined and confirmed by virological proof of CMV infection and was treated for at least 14 d with ganciclovir. Despite having the same incidence (21.6% in the Aza group versus 24.6% in the MMF group) and severity, CMV disease was significantly associated with graft loss independent of acute rejection episodes or other factors when tested in a Cox proportional model in the Aza group only (P < 10(-4)). It was shown for the first time that patients whose CMV disease is treated with ganciclovir while they are on MMF therapy are protected from the long-term deleterious consequences of CMV disease on graft survival, independent of acute rejection. It is suggested that the enhanced anti-herpes virus activity of ganciclovir by MMF could contribute to this reported effect, which may represent a significant contribution of MMF efficacy to graft survival. | lld:pubmed |
pubmed-article:11461950 | pubmed:language | eng | lld:pubmed |
pubmed-article:11461950 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11461950 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11461950 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11461950 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11461950 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11461950 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11461950 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11461950 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11461950 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11461950 | pubmed:month | Aug | lld:pubmed |
pubmed-article:11461950 | pubmed:issn | 1046-6673 | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:SoulillouJ... | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:HourmantMM | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:DantalJJ | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:GiralMM | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:BlanchoGG | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:JosienRR | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:CantarovichDD | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:NguyenJ MJM | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:AnceletDD | lld:pubmed |
pubmed-article:11461950 | pubmed:author | pubmed-author:DaguinPP | lld:pubmed |
pubmed-article:11461950 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11461950 | pubmed:volume | 12 | lld:pubmed |
pubmed-article:11461950 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11461950 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11461950 | pubmed:pagination | 1758-63 | lld:pubmed |
pubmed-article:11461950 | pubmed:dateRevised | 2004-11-17 | lld:pubmed |
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pubmed-article:11461950 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11461950 | pubmed:articleTitle | Mycophenolate mofetil does not modify the incidence of cytomegalovirus (CMV) disease after kidney transplantation but prevents CMV-induced chronic graft dysfunction. | lld:pubmed |
pubmed-article:11461950 | pubmed:affiliation | Institut de Transplantation et de Recherche en Transplantation (ITERT) and INSERM U437, 30 Boulevard Jean Monnet, 44093 Nantes Cedex 1, France. | lld:pubmed |
pubmed-article:11461950 | pubmed:publicationType | Journal Article | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11461950 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11461950 | lld:pubmed |