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Low frequency of cytomegalovirus infection during exacerbations of inflammatory bowel diseases

Authors :
Laurent Andreoletti
Nicolas Lévêque
Fanny Renois
Véronique Brodard
Jean-François Coste
Marie-Danièle Diebold
Thierry Reig
Christophe de Champs
Hedia Brixi-Benmansour
Déborah Talmud
Université de Reims Champagne-Ardenne (URCA)
Laboratoire de Virologie Médicale et Moléculaire - EA 4684 (CardioVir)
Université de Reims Champagne-Ardenne (URCA)-Centre Hospitalier Universitaire de Reims (CHU Reims)-SFR CAP Santé (Champagne-Ardenne Picardie Santé)
Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)
Service de Gastro-entérologie
Centre hospitalier Universitaire
Laboratoire d'Anatomopathologie
Source :
Journal of Medical Virology, Journal of Medical Virology, Wiley-Blackwell, 2010, 82 (10), pp.1694. ⟨10.1002/jmv.21877⟩
Publication Year :
2010
Publisher :
Wiley, 2010.

Abstract

Although numerous reports have described inflammatory bowel diseases (IBDs) complicated with cytomegalovirus (CMV) infection, the virus participation as an exacerbating factor remains unclear. The aim of this study was thus to clarify the clinical significance of CMV infection complicating exacerbation and to correlate CMV detection with various characteristics in IBD patients. Sixty-seven colonic biopsies obtained from 53 patients admitted for IBD exacerbation were retrospectively analyzed by real-time PCR assay. The CMV genome was detected in seven (10.4%) colonic biopsies related to seven patients (three ulcerative colitis and four Crohn's diseases). Among the patients with IBD studied, patients with evidence of CMV infection were older (P = &ethinsp;0.047), were more likely male gender (relative risk [RR] 4.48; 95% confidence interval [CI] 0.94–21.36), received corticosteroids (RR 3.2; CI 0.79–13.02) or azathioprine (RR 3.17; CI 0.80–12.57) treatments, presented more extended lesions (RR for rectum-sigmoid-left colon 3.75 (0.0–69.37) and for pancolitis 2.45 (0.36–16.23)), and had a more severe disease (RR 3.3; CI 0.87–12.48) than those without CMV infection. Viral loads measured in the colonic mucosa of infected patient ranged from 5 to 236961 genome copies by microgram of total extracted DNA. No relationship was observed between the severity of the disease and the viral load level. Furthermore, CMV disappeared in five infected IBD patients in remission without antiviral agents. In conclusion, these results showed infrequent CMV detection in colonic biopsies of IBD patients during exacerbation leaving open the question of the relationship between CMV reactivation and the onset or the severity of IBD exacerbation. J. Med. Virol. 82:1694–1700, 2010. © 2010 Wiley-Liss, Inc.

Details

ISSN :
01466615 and 10969071
Volume :
82
Database :
OpenAIRE
Journal :
Journal of Medical Virology
Accession number :
edsair.doi.dedup.....e40d2404aa0ffb0982560a2f990955e0
Full Text :
https://doi.org/10.1002/jmv.21877