4.5 Article

Serum procalcitonin levels associate with Clostridioides difficile infection in patients with inflammatory bowel disease

期刊

BMC INFECTIOUS DISEASES
卷 21, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12879-021-06804-2

关键词

Clostridioides difficile infection; Inflammatory bowel disease; Procalcitonin level; IBD flare; Predictive biomarker; CD; ROC curve analysis

资金

  1. Foodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran [RIGLD 1063]

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This study evaluated the utility of measuring serum procalcitonin levels to detect CDI in IBD patients, showing a positive correlation between procalcitonin levels and the presence of CDI. Procalcitonin may be a good candidate biomarker for assessing CDI in IBD patients, and further research is needed to determine its predictive value for CDI therapy or recurrence.
Background Clostridioides difficile infection (CDI) is a major cause of morbidity among patients with inflammatory bowel disease (IBD). Diagnostic biomarkers for early detection of CDI are needed in clinical practice. The relationship between serum procalcitonin and CDI in IBD patients has not been investigated so far. Therefore, we aimed to evaluate the usefulness of measuring serum procalcitonin level to detect CDI in patients with the flare of IBD. Methods One hundred twenty patients with IBD were enrolled in this study. Bacterial identification was performed using standard microbiological and molecular methods. The serum procalcitonin levels were measured in all patients. Receiver operating characteristic (ROC) curve analysis was applied to assess the value of procalcitonin for the prediction of CDI among IBD patients. Results The median serum procalcitonin level was significantly increased in IBD patients with CDI compared to non-CDI IBD patients (0.69 ng/mL vs 0.32 ng/mL). In univariate analysis, log(10) procalcitonin was associated with CDI (OR 2.81, 95% CI 1.54-4.09, P-value < 0.001). Procalcitonin 1.1 ng/mL was 85% sensitive and 88% specific for the prediction of CDI. In the multivariable model including the covariates log(10) procalcitonin, age, hospitalization, type of IBD, duration of the disease, and antibiotic usage, procalcitonin showed a robust association with CDI (OR 4.59, 95% CI 2.49-6.70, P-value < 0.001). An elevated procalcitonin level was associated with the presence of CDI among IBD patients. Conclusions Our results indicate that procalcitonin level can be a good candidate biomarker for assessing the CDI in IBD patients. Further studies are required to decipher whether procalcitonin can predict CDI therapy or its recurrence.

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