259
Views
7
CrossRef citations to date
0
Altmetric
Original Article

A stool test in patients with active ulcerative colitis helps exclude cytomegalovirus disease

ORCID Icon, , ORCID Icon, ORCID Icon & ORCID Icon
Pages 664-670 | Received 22 Mar 2020, Accepted 17 May 2020, Published online: 19 Jun 2020
 

Abstract

Objectives: In severe ulcerative colitis (UC) bowel biopsy is recommended to detect the cytomegalovirus (CMV) infection capable of complicating the course of the disease. Histopathology with immunohistochemistry (IHC) is time-consuming, and a blood polymerase chain reaction (PCR) for CMV DNA is used as an alternative, notwithstanding nothing more than a moderate correlation between the two. We aimed to detect CMV DNA in the stools of patients with active UC, and to compare the results with CMV IHC in bowel biopsies.

Materials and methods: Measurement of CMV DNA in stools (copies/ml) entailed PCR, while biopsies assessed inflammation activity (Geboes scale), as well as counts of numbers of CMV IHC-positive cells/biopsy. The severity of UC was assessed using the Mayo score, stool calprotectin and concentrations of C-reactive protein in the blood.

Results: 89 of the above pairs of tests for CMV were performed among 75 patients. CMV was detected in 36/89 stool specimens and 19/89 bowel biopsies. The sensitivity of the stool-CMV PCR was thus 84.7%, while specificity was of 71.4%. The negative predictive value was 94.3% and the positive predictive value 44.4%. No difference in the severity of UC was noted between the stool CMV DNA positive and negative groups. Similarly, there was no difference in the severity of UC between the CMV IHC positive and negative groups, except for the Geboes score, more often found to be higher in CMV IHC-positive patients (p = .002).

Conclusions: CMV DNA was detected in the stools of 40.4% of patients with active UC. A negative test result may help to exclude bowel CMV disease.

Correction Statement

This article has been republished with minor changes. These changes do not impact the academic content of the article.

Author contributions

AgM, JS and EZ designed the study. JS and EZ recruited and followed up on the patients. AgM performed the laboratory analyses and drafted the manuscript. AnM performed the histopathological assessment and interpreted the data. PW performed the statistical analysis. All the authors revised the article critically for important intellectual content, and approved the version to be submitted.

Disclosure statement

The authors declared conflicts of interests are as follows: AgM, none; JS, lecture fees: Takeda, other: Takeda, Alfasigma; AnM, lecture fees: Boston Scientific, Janssen; PW, none; EZ, lecture fees: Janssen, Sandoz, Ferring; consultancy: Pfizer, Janssen, Takeda; other: Takeda, Janssen.

Data availability statement

Data collected during the study and analysed for the purpose of preparation of the manuscript are stored by Agnieszka Magdziak, Jakub Szlak and Paulina Wieszczy.

Additional information

Funding

This work was supported by the Medical Centre for Postgraduate Education [Grant No. 501-1-09-12-16] and the Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland [Grant No. SN/GW26/2017].

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.