Observational studyInternational journal of colorectal disease2026
Distinct enteric nervous system pattern in obstructed defecation syndrome and slow-transit constipation: a controlled digital pathology study.
Observational study in International journal of colorectal disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05016700 (Correlation of Clinical Symptoms With Neuromorphological Changes of the Colorectal Wall in Patients With a Bowel Evacuation Disorder), which is not on this map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Correlation of Clinical Symptoms With Neuromorphological Changes of the Colorectal Wall in Patients With a Bowel Evacuation Disorder
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeChronic constipation comprises heterogeneous clinical entities, including slow-transit constipation (STC) and functional defecation disorders such as obstructed defecation syndrome (ODS). Although neuroenteric mechanisms are implicated, reproducible histomorphological correlates remain incompletely defined, partly due to methodological heterogeneity and lack of standardized quantification. The study characterizes the myenteric plexus morphology and neuroimmune cell distribution across clinically defined subgroups of functional bowel disorders using a standardized digital pathology approach.
methodsRetrospective observational cohort study at a tertiary colorectal referral center. A total of 100 patients after bowel surgery were included: ODS (n = 17), STC (n = 24), combined ODS + STC (n = 28), and a control cohort without clinically evident bowel motility disorders (n = 31). Digital morphometric assessment of ganglionic density and morphology, neuronal content (immunohistochemistry against MAP2, HuC/D), and the distribution of CD3-positive T-lymphocytes within and around myenteric ganglia were performed.
resultsGanglionic density differed significantly between groups (p = 0.002), with increased density in ODS, whereas STC values were comparable to controls. Neuronal content per ganglion was preserved across all groups as demonstrated by MAP2 and HuC/D analyses. In contrast, the presence of CD3-positive lymphocytes was reduced in all constipation groups, most pronounced in STC, affecting both the intra- and periganglionic compartments.
conclusionFunctional bowel motility and defecation disorders appear to show distinct neuroarchitectural and neuroimmune patterns. Increased ganglionic density in ODS contrasts with preserved neuronal content and reduced presence of T-lymphocytes, particularly in STC. These findings represent associations rather than proven disease mechanisms, derived from comparison with a surgical rather than a healthy control cohort. Standardized digital morphometry nonetheless provides a reproducible framework for phenotypic characterization of chronic constipation and may support future studies linking enteric structure to function.
trial registrationClinicaltrials.gov (NCT05016700; 09/12/2020).
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.