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. 2024 Dec 28;17(1):74.
doi: 10.3390/nu17010074.

Plasma Bacterial Metabolites in Crohn's Disease Pathogenesis and Complications

Affiliations

Plasma Bacterial Metabolites in Crohn's Disease Pathogenesis and Complications

Anna Deskur et al. Nutrients. .

Abstract

Background/objectives: Crohn's disease is known for being associated with an abnormal composition of the bacterial flora, dysbiosis and intestinal function disorders. Metabolites produced by gut microbiota play a pivotal role in the pathogenesis of CD, and the presence of unspecific extraintestinal manifestations.

Methods: The aim of this study was a determination of the level of bacterial metabolites in blood plasma in patients with Crohn's disease. CD patients (29) and healthy individuals (30) were recruited for this study. Bacterial metabolites (SCFAs and TMAO panel) were measured by a liquid chromatography-mass spectrometry system.

Results: A significant correlation (p-value < 0.05) between CD and bacterial metabolites was obtained for three of eight tested SCFAs; acetic acid (reduced in CD; FC 1.7; AUC = 0.714), butyric acid (increased; FC 0.68; AUC = 0.717), 2MeBA (FC 1.168; AUC = 0.702), and indoxyl (FC 0.624). The concentration of CA (FC 0.82) and choline (FC 0.78) in plasma was significantly disturbed according to the biological treatment. Choline level (FC 1.28) was also significantly disturbed in the patients treated with glucocorticoids. In total, 68.97% of Crohn's patients presented extraintestinal manifestations (EIMs) of Crohn's disease, mainly osteoarticular complications. The level of BA was statistically significantly elevated in patients with extraintestinal (FC 0.602) manifestations, while in the group of patients with osteoarticular complications, a significant difference in the level of betaine (FC 1.647) was observed.

Conclusions: The analyzed bacterial metabolites of plasma may significantly help in the diagnostic process, and in the monitoring of the disease course and treatment, in a lowly invasive way, as biomarkers after additional research on a larger group of patients.

Keywords: Crohn’s disease; SCFA; TMAO; gut microbiome; inflammatory bowel diseases; metabolites; metabolome.

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Conflict of interest statement

Author Agnieszka Paziewska was employed by the company Warsaw Genomics Inc. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
(a). Analysis of plasma SCFA metabolites in Crohn’s patients and healthy individuals. (b). Analysis of plasma metabolites of TMAO panel in Crohn’s patients and healthy individuals.
Figure 1
Figure 1
(a). Analysis of plasma SCFA metabolites in Crohn’s patients and healthy individuals. (b). Analysis of plasma metabolites of TMAO panel in Crohn’s patients and healthy individuals.
Figure 2
Figure 2
ROC analysis of statistically significantly different metabolites between healthy and Crohn’s patients with AUC > 0.7.
Figure 3
Figure 3
Metabolite correlation analysis (positive correlations are shown in blue; negative correlations in red).
Figure 4
Figure 4
Mucositis in the distal segment of the ileum, with ulcers in a patient with Crohn’s disease.
Figure 5
Figure 5
Ulcerative mucositis in the large intestine of a patient with Crohn’s disease.
Figure 6
Figure 6
Inflammation, swelling and narrowing of the intestinal lumen in a patient with Crohn’s disease.
Figure 7
Figure 7
Violin plots for the analyzed plasma metabolites’ differences between plasma patients CD with (yes) extraintestinal and osteoarticular complications and without (no).

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