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Published on: July 27, 2011
Characteristics of the Cajal interstitial cells and intestinal microbiota in children with refractory constipation
Yi Yuan1, Yan Lu2, Zhihua Zhang2
1Department of Pediatrics, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210011, China.
Insights
Children with refractory constipation exhibit reduced colonic motility and altered interstitial cells of Cajal (ICCs). Intestinal microbiota composition significantly differs in these patients, suggesting new therapeutic targets for this condition.
Area of Science:
- Pediatric Gastroenterology
- Colorectal Surgery
- Microbiome Research
Background:
- Refractory constipation significantly impacts children's quality of life.
- The underlying pathophysiology of pediatric refractory constipation is not fully understood.
Purpose of the Study:
- To investigate colonic motor patterns, interstitial cells of Cajal (ICCs), and intestinal microbiota in children with refractory constipation.
Main Methods:
- Colonic manometry (CM) assessed motility in 30 children.
- Colon biopsies analyzed ICCs via immunohistochemistry.
- 16S rRNA sequencing profiled fecal microbiota in 14 patients and 28 controls.
Main Results:
- Dysmotility group (n=20) showed lower colonic motility and impaired postprandial response compared to the normal group (n=10).
- ICCs exhibited altered number, distribution, and morphology in refractory constipation patients.
- Significant differences in intestinal microbiota composition were observed, with decreased Faecalibacterium and increased Parabacteroides and Alistipes in affected children.
Conclusions:
- Reduced colonic motility and ICC abnormalities contribute to refractory constipation pathogenesis.
- Distinct gut microbiota profiles in affected children offer potential therapeutic avenues.
- Findings provide insights for novel treatment strategies for pediatric refractory constipation.
Background:
Children with refractory constipation experience intense and persistent symptoms that greatly diminish their quality of life. However, the underlying pathophysiological mechanism responsible for this condition remains uncertain. Our objective was to evaluate characteristics of colonic motor patterns and interstitial cells of Cajal (ICCs) to refractory constipation children, as well as intestinal microbiota compositions.
Methods:
Colonic manometry (CM) was conducted on a cohort of 30 patients with refractory constipation to assess colonic motility, and 7 of them underwent full-thickness colon biopsy specimens. Another 5 colonic specimens from nonconstipation patients were collected to identify the ICCs by immunohistochemistry. Fecal samples from 14 children diagnosed with refractory constipation and subjecting 28 age-matched healthy children to analysis using high-throughput sequencing of 16S rRNA.
Results:
According to CM results, dividing 30 children with refractory constipation into 2 groups: normal group (n = 10) and dysmotility group (n = 20). Dysmotility subjects showed lower colonic motility. Antegrade propagating pressure waves, retrograde propagating pressure waves, and periodic colonic motor activity were common in normal subjects and rare in dysmotility subjects (32.7 ± 8.9 vs 20.7 ± 13.0/17 h, P < 0.05, 11.5 ± 2.3 vs 9.6 ± 2.3/17 h, P < 0.05, and 5.2 ± 8.9 vs 3.5 ± 6.8 cpm, P < 0.005, respectively), whereas periodic rectal motor activity was more common in dysmotility subjects (3.4 ± 4.8 vs 3.0 ± 3.1 cpm, P < 0.05). Dysmotility subjects exhibited a significantly greater number of preprandial simultaneous pressure waves compared to the normal subjects (32.3 ± 25.0 vs 23.6 ± 13.2/1 h, P < 0.005). Dysmotility subjects displayed a notable decrease in postprandial count of antegrade propagating pressure waves and high amplitude propagating pressure waves when compared to normal subjects (3.9 ± 2.9 vs 6.9 ± 3.5/1 h and 2.3 ± 1.5 vs 5.4 ± 2.9/1 h, respectively, P < 0.05). The number, distribution, and morphology of ICCs were markedly altered in refractory constipation compared children to the controls (P < 0.05). Children diagnosed with refractory constipation displayed a distinct dissimilarity in composition of their intestinal microbiota comparing with control group (P < 0.005). In genus level, Bacteroidetes represented 34.34% and 43.78% in the refractory constipation and control groups, respectively. Faecalibacterium accounted for 3.35% and 12.56%, respectively (P < 0.005). Furthermore, the relative abundances of Faecalibacterium (P < 0.005), Lachnospira (P < 0.05), and Haemophilus (P < 0.05) significantly decreased, whereas those of Parabacteroides (P < 0.05), Alistipes (P < 0.005), Prevotella_2 (P < 0.005), [Ruminococcus]_torques_group (P < 0.005), Barnesiella (P < 0.05), Ruminococcaceae_UCG-002 (P < 0.005), and Christensensenellaceae_R-7_group (P < 0.05) were markedly increased in children with refractory constipation.
Conclusions:
Dysmotility subjects showed lower colonic motility and an impaired postprandial colonic response. The decreased number and abnormal morphology of colonic ICCs may contribute to the pathogenesis of refractory constipation. Children with refractory constipation exhibited significant variations in microbiota composition across various taxonomic levels compared to the healthy control group. Our findings contribute valuable insights into pathophysiological mechanism underlying refractory constipation and provide evidence to support the exploration of novel therapeutic strategies for affected children.
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