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1.
Parasitol Res ; 120(2): 743-746, 2021 Feb.
Article in English | MEDLINE | ID: mdl-33409625

ABSTRACT

The probiotic medicinal product TSO (Trichuris suis ova) is administered to patients with active ulcerative colitis in an ongoing clinical phase IIb trial where the typical co-medications are steroids (prednisolone or budesonide) and antibiotics (e.g., phenoxymethylpenicillin). The present pre-clinical study evaluates the effects of these co-medications on the biological activity of TSO in Göttingen Minipigs. This translationally relevant pre-clinical model allows administration of TSO with and without oral steroids or antibiotics in a manner similar to the administration to patients, followed by quantification of the biological activity of TSO. The biological activity of TSO was not affected by oral steroids but was reduced by oral antibiotics. Fecal calprotectin, the common marker of intestinal inflammation in patients with UC, did not differ between groups.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Probiotics/therapeutic use , Steroids/therapeutic use , Trichuris , Animals , Anti-Bacterial Agents/pharmacology , Colitis, Ulcerative/therapy , Disease Models, Animal , Female , Ovum/drug effects , Steroids/pharmacology , Swine , Swine, Miniature , Trichuris/drug effects
2.
Sci Rep ; 9(1): 13473, 2019 09 17.
Article in English | MEDLINE | ID: mdl-31530835

ABSTRACT

Intestinal dysbiosis in inflammatory bowel disease (IBD) patients depend on disease activity. We aimed to characterize the microbiota after 7 years of follow-up in an unselected cohort of IBD patients according to disease activity and disease severity. Fifty eight Crohn's disease (CD) and 82 ulcerative colitis (UC) patients were included. Disease activity was assessed by the Harvey-Bradshaw Index for CD and Simple Clinical Colitis Activity Index for UC. Microbiota diversity was assessed by 16S rDNA MiSeq sequencing. In UC patients with active disease and in CD patients with aggressive disease the richness (number of OTUs, p = 0.018 and p = 0.013, respectively) and diversity (Shannons index, p = 0.017 and p = 0.023, respectively) were significantly decreased. In the active UC group there was a significant decrease in abundance of the phylum Firmicutes (p = 0.018). The same was found in CD patients with aggressive disease (p = 0.05) while the abundance of Proteobacteria phylum showed a significant increase (p = 0.03) in CD patients. We found a change in the microbial abundance in UC patients with active disease and in CD patients with aggressive disease. These results suggest that dysbiosis of the gut in IBD patients is not only related to current activity but also to the course of the disease.


Subject(s)
Crohn Disease/etiology , Crohn Disease/pathology , Dysbiosis , Gastrointestinal Microbiome , Proteobacteria , Biodiversity , Case-Control Studies , Crohn Disease/diagnosis , Disease Progression , Disease Susceptibility , Feces/microbiology , Humans , Inflammatory Bowel Diseases/etiology , Inflammatory Bowel Diseases/pathology , Metagenomics/methods , RNA, Ribosomal, 16S/genetics , Severity of Illness Index
3.
J Crohns Colitis ; 12(3): 265-272, 2018 Feb 28.
Article in English | MEDLINE | ID: mdl-29506105

ABSTRACT

BACKGROUND AND AIM: Crohn's disease [CD] is a progressive inflammatory bowel disease that can lead to complications such as strictures or penetrating disease, and ultimately surgery. Few population-based studies have investigated the predictors for disease progression and surgery in CD according to the Montreal classification. We aimed to identify clinical predictors associated with complicated CD in a Danish population-based inception cohort during the biologic era. METHODS: All incident patients with CD in a well-defined Copenhagen area, between 2003 and 2004, were followed prospectively until 2011. Disease progression was defined as the development of bowel stricture [B2] or penetrating disease [B3] in patients initially diagnosed with non-stricturing/non-penetrating disease [B1]. Associations between disease progression and/or resection, and multiple covariates, were investigated by Cox regression analyses. RESULTS: In total, 213 CD patients were followed. A total of 177 [83%] patients had B1 at diagnosis. Patients who changed location had increased risk of disease progression (hazard ratio [HR] = 3.1, 95% CI: 1.12,8.52). Biologic treatment was associated with lower risk of change in location [HR = 0.3, 95% CI: 0.1-0.7]. Colonic involvement [L2 or L3 vs L1] was associated with a lower risk of surgery (HR = 0.34/0.22, 95% CI: [0.13,0.86]/[0.08,0.60]). All CD patients who progressed in behaviour or changed location had an increased risk of surgery [p < 0.05]. CONCLUSIONS: This population-based inception cohort study demonstrates that changes in disease location or behaviour in patients with CD increase their risk of resection. Our findings highlight the protective effect of biologic treatment with regard to change in disease location, which might ultimately improve the disease course for CD patients.


Subject(s)
Abdominal Abscess/etiology , Crohn Disease/complications , Crohn Disease/surgery , Intestines/pathology , Rectal Fistula/etiology , Adult , Biological Products/therapeutic use , Colon/pathology , Constriction, Pathologic/etiology , Crohn Disease/drug therapy , Crohn Disease/pathology , Denmark , Disease Progression , Follow-Up Studies , Humans , Intestines/surgery , Middle Aged , Proportional Hazards Models , Prospective Studies , Young Adult
4.
Aliment Pharmacol Ther ; 47(1): 6-15, 2018 Jan.
Article in English | MEDLINE | ID: mdl-28994131

ABSTRACT

BACKGROUND: The Inflammatory Bowel Disease Disability Index (IBD-DI) has recently been developed for patients with Crohn's disease (CD) and ulcerative colitis (UC). AIM: To assess the severity of disability and associated factors using the IBD-DI, and review the validity of the IBD-DI as a tool. METHOD: Systematic review of cross-sectional studies. Patients included had UC or CD and were classified as active, in remission, or needing surgery, biological and/or steroid treatment. We included studies assessing disability using the IBD-DI and that were captured by electronic and manual searches (January 2017). The possibility of bias was evaluated with the Newcastle-Ottawa Scale. RESULTS: Nine studies were included with 3167 patients. Comparatively, patients with active disease had higher disability rates than those in remission (SMD [CI95] = 1.49[1.11, 1.88], I2  = 94%, P<.01), while patients on biological treatment had lower disability rates than those receiving corticosteroid treatment (SMD [CI95] = -0.22[-0.36, -0.08], I2  = 0%, P<.01). Disease activity and unemployment were found to be associated factors. The IBD-DI scored "good" for internal consistency, "fair" to "excellent" for intra-rater reliability and "excellent" for inter-rater reliability. Construct validity was "moderately strong" to "very strong" and structural validity was found to be mainly unidimensional. The IBD-DI had excellent responsiveness, while its interpretability was only useful on a group level. CONCLUSIONS: This systematic review and meta-analysis found a significant association between disease activity, treatment received and disability; although significant heterogeneity was found. The IBD-DI is reliable and valid, but further studies are needed to measure its interpretability.


Subject(s)
Colitis, Ulcerative/physiopathology , Crohn Disease/physiopathology , Disabled Persons , Cross-Sectional Studies , Humans , Reproducibility of Results
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