We have located links that may give you full text access.
Fecal microbiota dynamics and its relation with disease course in Crohn's disease.
Journal of Crohn's & Colitis 2019 Februrary 28
BACKGROUND: Microbial shifts have been associated with disease activity in Crohn's disease (CD), but findings on specific taxa are inconsistent. This may be due to differences in applied methods and cross-sectional study designs. We prospectively examined the fecal microbiota in adult CD patients with changing or stable disease course over time.
METHODS: Feces was collected at two time-points from 15 healthy individuals (HC), 35 CD patients that maintained remission (RR) and 22 during remission and subsequent exacerbation (RA). The microbial composition was assessed by 16S rRNA (V4) gene sequencing.
RESULTS: Compared to HC, CD patients had a lower microbial richness (p=0.0002) and diversity (p=0.005). Moreover, the microbial community structure of a subset of patients clustered apart from HC, characterized by low microbial diversity and Faecalibacterium abundance. Patients within this cluster did not differ with respect to long-term disease course compared to patients with a "healthy-like" microbiota.Over time, microbial richness and diversity did not change in RR versus RA patients. Although the microbial community structure of both RR and RA patients was less stable over time compared to HC, no differences were observed between the patient groups (p=0.17), nor was the stability impacted by Montreal classification, medication use or surgery.
CONCLUSION: The altered microbiota composition and stability in CD was neither associated with disease activity nor long-term disease course, questioning its involvement in the development of an exacerbation. The aberrant microbiota composition in a subset of CD patients, warrants further exploration of a more microbiota-driven etiology in this group.
METHODS: Feces was collected at two time-points from 15 healthy individuals (HC), 35 CD patients that maintained remission (RR) and 22 during remission and subsequent exacerbation (RA). The microbial composition was assessed by 16S rRNA (V4) gene sequencing.
RESULTS: Compared to HC, CD patients had a lower microbial richness (p=0.0002) and diversity (p=0.005). Moreover, the microbial community structure of a subset of patients clustered apart from HC, characterized by low microbial diversity and Faecalibacterium abundance. Patients within this cluster did not differ with respect to long-term disease course compared to patients with a "healthy-like" microbiota.Over time, microbial richness and diversity did not change in RR versus RA patients. Although the microbial community structure of both RR and RA patients was less stable over time compared to HC, no differences were observed between the patient groups (p=0.17), nor was the stability impacted by Montreal classification, medication use or surgery.
CONCLUSION: The altered microbiota composition and stability in CD was neither associated with disease activity nor long-term disease course, questioning its involvement in the development of an exacerbation. The aberrant microbiota composition in a subset of CD patients, warrants further exploration of a more microbiota-driven etiology in this group.
Full text links
Related Resources
Trending Papers
Challenges in Septic Shock: From New Hemodynamics to Blood Purification Therapies.Journal of Personalized Medicine 2024 Februrary 4
Molecular Targets of Novel Therapeutics for Diabetic Kidney Disease: A New Era of Nephroprotection.International Journal of Molecular Sciences 2024 April 4
Perioperative echocardiographic strain analysis: what anesthesiologists should know.Canadian Journal of Anaesthesia 2024 April 11
The 'Ten Commandments' for the 2023 European Society of Cardiology guidelines for the management of endocarditis.European Heart Journal 2024 April 18
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app
All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.
By using this service, you agree to our terms of use and privacy policy.
Your Privacy Choices
You can now claim free CME credits for this literature searchClaim now
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app