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Do Colonic Mucosal Tumor Necrosis Factor Alpha Levels Play a Role in Diverticular Disease? A Systematic Review and Meta-Analysis

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MDPI
DOI: 10.3390/ijms24129934

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diverticular disease (DD); tumor necrosis factor-alpha (TNF-& alpha;); inflammatory markers; biomarkers; irritable bowel syndrome

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In this study, the levels of tumor necrosis factor-alpha (TNF-a) in the colon were evaluated in patients with diverticular disease (DD). The results showed no significant difference in mucosal TNF-a levels between symptomatic uncomplicated DD and asymptomatic DD patients. However, TNF-a levels were significantly higher in DD patients compared to irritable bowel syndrome (IBS) patients. These findings suggest that TNF-a may play a key role in the pathogenesis of DD and could be a potential target for future therapies.
Diverticular disease (DD) is the most frequent condition in the Western world that affects the colon. Although chronic mild inflammatory processes have recently been proposed as a central factor in DD, limited information is currently available regarding the role of inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-a). Therefore, we conducted a systematic review and meta-analysis aiming to assess the mucosal TNF-a levels in DD. We conducted a systematic literature search using PubMed, Embase, and Scopus to identify observational studies assessing the TNF-a levels in DD. Full-text articles that satisfied our inclusion and exclusion criteria were included, and a quality assessment was performed using the Newcastle-Ottawa Scale (NOS). The principal summary outcome was the mean difference (MD). The results were reported as MD (95% confidence interval (CI)). A total of 12 articles involving 883 subjects were included in the qualitative synthesis, out of which 6 studies were included in our quantitative synthesis. We did not observe statistical significance related to the mucosal TNF-a levels in symptomatic uncomplicated diverticular disease (SUDD) vs. the controls (0.517 (95% CI -1.148-2.182)), and symptomatic vs. asymptomatic DD patients (0.657 (95% CI -0.883-2.196)). However, the TNF-a levels were found to be significantly increased in DD compared to irritable bowel disease (IBS) patients (27.368 (95% CI 23.744-30.992)), and segmental colitis associated with diverticulosis (SCAD) vs. IBS patients (25.303 (95% CI 19.823-30.784)). Between SUDD and the controls, as well as symptomatic and asymptomatic DD, there were no significant differences in the mucosal TNF-a levels. However, the TNF-a levels were considerably higher in DD and SCAD patients than IBS patients. Our findings suggest that TNF-a may play a key role in the pathogenesis of DD in specific subgroups and could potentially be a target for future therapies.

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