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. 2023 Aug 28:16:3889-3906.
doi: 10.2147/IJGM.S413438. eCollection 2023.

Portal Vein Thrombosis in Patients with Liver Cirrhosis: What Went Wrong?

Affiliations

Portal Vein Thrombosis in Patients with Liver Cirrhosis: What Went Wrong?

Doina Georgescu et al. Int J Gen Med. .

Abstract

Purpose: This study aimed to explore inflammatory biomarkers, stool's functional bacterial groups and their possible link to portal vein thrombosis (PVT) in patients with liver cirrhosis (LC).

Materials and methods: An observational study of 300 participants: 200 inhospital cirrhotic patients, who met inclusion criteria, equally assigned into two groups, based on the presence or absence of PVT and 100 healthy controls was carried out.

Results: The PVT group displayed significant differences related to older age, cigarettes smoking history, emergency admission, higher Child-Pugh score, metabolic related disorders and nonalcoholic fatty liver disease, as well as non-obstructive aspects, with chronic thrombi. The PVT group exhibited significant differences related to biomarkers such as tumor necrosis factor (TNF)-alpha, C-reactive protein (CRP), D-dimers (D-D), as well as gut overall dysbiosis (DB) and alteration of different functional bacterial groups of the gut microbiota. Strong positive correlations were observed between PVT severity, and TNF-alpha, CRP, D-D as well as lipopolysaccharide (LPS) positive bacteria. Esophageal varices, age and abdominal pain were independent predictors for PVT severity as well as CRP, TNF-alpha and D-D.

Conclusion: Patients with LC and PVT displayed elevation of TNF-alpha, CRP, D-D alterations of the functional gut microbiota, as well as several morphological and clinical particularities. Although the LPS positive gut microbiota was linked to inflammatory biomarkers and PVT severity, it was not proven to be an independent predictor of the PVT severity like CRP, TNF-alpha and D-D.

Keywords: biomarkers; end stage liver disease; gut functional bacteria; portal vein obstruction.

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Conflict of interest statement

The authors report no conflicts of interest in this work.

Figures

None
Graphical abstract
Figure 1
Figure 1
The study participants inclusion flow-chart.
Figure 2
Figure 2
Distribution of mucosa protective bacteria in patients with LC.
Figure 3
Figure 3
Distribution of neuroactive bacteria in patients with LC.
Figure 4
Figure 4
Distribution of mucin degrading bacteria in patients with LC.
Figure 5
Figure 5
Distribution of LPS (+) bacteria in patients with LC.
Figure 6
Figure 6
Correlations of PVT severity to biomarkers.
Figure 7
Figure 7
Correlations of PVT severity to various clinical aspects.
Figure 8
Figure 8
LPS positive bacteria correlations in PVT group.

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