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Differentiating Childhood Traumas in Inflammatory Bowel Disease

Overview
Specialty Gastroenterology
Date 2023 Oct 9
PMID 37811528
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Abstract

Background: Inflammatory bowel disease is characterized by chronic inflammation of the gastrointestinal tract. Research on inflammatory bowel disease has shown a connection to childhood traumatic events. However, few studies have focused on specific types of traumatic experiences and the impact of confiding in others on disease-related outcomes. This comparative, cross-sectional study expected that: (1) patients would report higher prevalence rates of childhood traumas than healthy controls; (2) healthy controls would report fewer and less severe traumatic experiences than patients and less confiding in others compared to patients; (3) childhood trauma severity would be indirectly related to depressive symptoms through resilience and confiding in others would moderate this relationship.

Methods: Participants completed an online survey; an inflammatory bowel disease patient group ( = 195, = 40.48, 76.4% female) was compared to a similarly recruited sample of healthy controls ( = 190, = 31.16, 59.5% female).

Results: Patients reported a higher prevalence of experiencing sexual traumas ( = .031), major upheavals (i.e., disruptions) ( .048), and violence ( = .050) than controls. Patients had significantly higher total trauma severity odds ratios (OR 0.89, 95% CI[0.81,0.97]) and significantly lower total confiding in other odds ratios than controls (OR 1.09, 95% CI[1.02,1.16]). Childhood trauma severity was indirectly related to depressive symptoms through resilience, .05, SE 0.09, 95% CI[0.01,0.09]; however, confiding did not moderate this relationship.

Conclusions: Patients reported more sexual, disruptive, and violent traumas. Although confiding did not act as a moderator, trauma was related to depressive symptoms through resilience.

Citing Articles

Role of stress and early-life stress in the pathogeny of inflammatory bowel disease.

Bonaz B, Sinniger V, Pellissier S Front Neurosci. 2024; 18:1458918.

PMID: 39319312 PMC: 11420137. DOI: 10.3389/fnins.2024.1458918.

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