The detection of the cytomegalovirus DNA in the colonic mucosa of patients with ulcerative colitis is associated with increased long-term risk of proctocolectomy: results from an outpatient IBD clinic.


Journal

International journal of colorectal disease
ISSN: 1432-1262
Titre abrégé: Int J Colorectal Dis
Pays: Germany
ID NLM: 8607899

Informations de publication

Date de publication:
Mar 2019
Historique:
accepted: 23 11 2018
pubmed: 7 12 2018
medline: 26 7 2019
entrez: 4 12 2018
Statut: ppublish

Résumé

Cytomegalovirus (CMV) infection has been found to be associated with a reactivation of ulcerative colitis (UC) and with an impaired response to medical therapy. In the past, only limited data were available on the long-term outcome for UC patients with positive tissue CMV-PCR in the colonic mucosa. Between January 2010 and April 2015, we performed a qualitative PCR screening for CMV DNA in one biopsy from most actively inflamed rectal mucosa (tCMV-PCR). All tCMV-PCR-positive patients received 900 mg of valganciclovir b.i.d. for at least 15 days. We analyzed the association of the tCMV-PCR status with the time to steroid-free remission (SFR) and with the risk of proctocolectomy during the further course. One hundred eight consecutive patients (50 women, 58 men, median age 41 years, median UC duration 6 years) with active UC not responding to anti-inflammatory medication were analyzed. Eight of the 24 tCMV-PCR-positive patients (33.3%) compared to ten of the 84 tCMV-PCR-negative patients (11.9%) underwent proctocolectomy during a median follow-up of 52 months (p < 0.005). The median time from CMV diagnosis to colectomy was 501 days (median, interquartile range (IQR): 170, 902 days) in tCMV-PCR-positive and 958 days (IQR: 287, 1328 days) in tCMV-PCR-negative patients (p < 0.01). The median time to SFR was 126 days in tCMV-PCR-positive patients vs. 63 days in tCMV-PCR-negative patients (p < 0.01). The detection of the CMV DNA in the colonic mucosa of patients with active UC is associated with a longer time to steroid-free UC remission and with an increased rate and earlier need of proctocolectomy.

Identifiants

pubmed: 30506156
doi: 10.1007/s00384-018-3210-8
pii: 10.1007/s00384-018-3210-8
doi:

Substances chimiques

DNA, Viral 0
Purines 0
Steroids 0

Types de publication

Journal Article

Langues

eng

Pagination

393-400

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Auteurs

Wiebke Schenk (W)

Internistische Gemeinschaftspraxis für Verdauungs- und Stoffwechselkrankheiten, Leipzig und Schkeuditz, Leipzig, Germany.
Klinik für Innere Medizin IV, Universitätsklinikum Jena, Jena, Germany.

Tobias Klugmann (T)

Internistische Gemeinschaftspraxis für Verdauungs- und Stoffwechselkrankheiten, Leipzig und Schkeuditz, Leipzig, Germany.

Annett Borkenhagen (A)

Internistische Gemeinschaftspraxis für Verdauungs- und Stoffwechselkrankheiten, Leipzig und Schkeuditz, Leipzig, Germany.

Chris Klecker (C)

Internistische Gemeinschaftspraxis für Verdauungs- und Stoffwechselkrankheiten, Leipzig und Schkeuditz, Leipzig, Germany.

Peter Dietel (P)

Internistische Gemeinschaftspraxis für Verdauungs- und Stoffwechselkrankheiten, Leipzig und Schkeuditz, Leipzig, Germany.

Ralf Kirschner (R)

MVZ Labor Dr. Reising-Ackermann und Kollegen, Leipzig, Germany.

Eckhardt Schneider (E)

Gemeinschaftspraxis für Pathologie, Leipzig, Germany.

Tony Bruns (T)

Klinik für Innere Medizin IV, Universitätsklinikum Jena, Jena, Germany.

Andreas Stallmach (A)

Klinik für Innere Medizin IV, Universitätsklinikum Jena, Jena, Germany.

Niels Teich (N)

Internistische Gemeinschaftspraxis für Verdauungs- und Stoffwechselkrankheiten, Leipzig und Schkeuditz, Leipzig, Germany. teich@igvs.de.
Medizinische Fakultät der Friedrich-Schiller-Universität Jena, Jena, Germany. teich@igvs.de.

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Classifications MeSH