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Updated: Nov 17, 2025

Microbiota Analysis Using Two-step PCR and Next-generation 16S rRNA Gene Sequencing
Published on: October 15, 2019
Gut Microbiota Profile in Pediatric Patients With Inflammatory Bowel Disease: A Systematic Review
Xiaojun Zhuang1, Caiguang Liu1, Shukai Zhan1
1Department of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Insights
Gut microbiota alterations are linked to pediatric inflammatory bowel disease (IBD). While some bacterial changes were noted, inconsistent findings in pediatric IBD microbiota highlight the need for standardized research.
Area of Science:
- Microbiome research
- Pediatric gastroenterology
- Inflammatory Bowel Disease (IBD)
Background:
- Gut microbiota dysbiosis is implicated in pediatric and adult inflammatory bowel disease (IBD).
- Early-onset, treatment-naïve pediatric IBD may offer clearer insights into microbial changes.
- This systematic review focuses on identifying gut microbiota biomarkers in pediatric IBD.
Approach:
- Systematic review of original studies on pediatric IBD gut microbiota.
- Searched electronic databases from inception to July 31, 2020.
- Assessed study quality using the Newcastle-Ottawa scale.
Key Points:
- 41 studies revealed decreased alpha-diversity and altered beta-diversity in pediatric IBD.
- Increased Enterococcus and decreased Anaerostipes, Blautia, Coprococcus, Faecalibacterium, Roseburia, Ruminococcus, and Lachnospira were observed.
- Insufficient data exists to link specific microbiota to disease activity, location, or behavior in pediatric IBD.
Conclusions:
- Evidence suggests bacterial abundance differences in pediatric IBD patients compared to controls.
- Inconsistent results and methodologies prevent definitive conclusions.
- Further large-scale studies with standardized methods are required for clarity.
Abstract:
Background and Aim: Accumulating evidence have implicated gut microbiota alterations in pediatric and adult patients with inflammatory bowel disease (IBD); however, the results of different studies are often inconsistent and even contradictory. It is believed that early changes in new-onset and treatment-naïve pediatric patients are more informative. We performed a systematic review to investigate the gut microbiota profiles in pediatric IBD and identify specific microbiota biomarkers associated with this disorder. Methods: Electronic databases were searched from inception to 31 July 2020 for studies that observed gut microbiota alterations in pediatric patients with IBD. Study quality was assessed using the Newcastle-Ottawa scale. Results: A total of 41 original studies investigating gut microbiota profiles in pediatric patients with IBD were included in this review. Several studies have reported a decrease in α-diversity and an overall difference in β-diversity. Although no specific gut microbiota alterations were consistently reported, a gain in Enterococcus and a significant decrease in Anaerostipes, Blautia, Coprococcus, Faecalibacterium, Roseburia, Ruminococcus, and Lachnospira were found in the majority of the included articles. Moreover, there is insufficient data to show specific microbiota bacteria associated with disease activity, location, and behavior in pediatric IBD. Conclusions: This systematic review identified evidence for differences in the abundance of some bacteria in pediatric patients with IBD when compared to patients without IBD; however, no clear overall conclusion could be drawn from the included studies due to inconsistent results and heterogeneous methodologies. Further studies with large samples that follow more rigorous and standardized methodologies are needed.
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