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Gut dysbiosis is associated with poorer long-term prognosis in cirrhosis

BACKGROUND: Gut dysbiosis is common in cirrhosis. AIM: To study the influence of gut dysbiosis on prognosis in cirrhosis. METHODS: The case-control study included 48 in-patients with cirrhosis and 21 healthy controls. Stool microbiome was assessed using 16S ribosomal ribonucleic acid gene sequencing...

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Autores principales: Maslennikov, Roman, Ivashkin, Vladimir, Efremova, Irina, Alieva, Aliya, Kashuh, Ekaterina, Tsvetaeva, Ekaterina, Poluektova, Elena, Shirokova, Elena, Ivashkin, Konstantin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173342/
https://www.ncbi.nlm.nih.gov/pubmed/34131470
http://dx.doi.org/10.4254/wjh.v13.i5.557
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author Maslennikov, Roman
Ivashkin, Vladimir
Efremova, Irina
Alieva, Aliya
Kashuh, Ekaterina
Tsvetaeva, Ekaterina
Poluektova, Elena
Shirokova, Elena
Ivashkin, Konstantin
author_facet Maslennikov, Roman
Ivashkin, Vladimir
Efremova, Irina
Alieva, Aliya
Kashuh, Ekaterina
Tsvetaeva, Ekaterina
Poluektova, Elena
Shirokova, Elena
Ivashkin, Konstantin
author_sort Maslennikov, Roman
collection PubMed
description BACKGROUND: Gut dysbiosis is common in cirrhosis. AIM: To study the influence of gut dysbiosis on prognosis in cirrhosis. METHODS: The case-control study included 48 in-patients with cirrhosis and 21 healthy controls. Stool microbiome was assessed using 16S ribosomal ribonucleic acid gene sequencing. We used modified dysbiosis ratio (MDR): [Bacilli (%) + Proteobacteria (%)]/[Clostridia (%) + Bacteroidetes (%)]. Patients with MDR more the median made up the group with severe dysbiosis, others did the group with non-severe dysbiosis. The follow-up period was 4 years. RESULTS: The mortality rate of patients with severe dysbiosis was significantly higher than that of patients with non-severe dysbiosis (54.2% vs 12.5%; P = 0.001). The presence of severe dysbiosis was independent risk factors for death [hazard ratio = 8.6 × (1.9-38.0); P = 0.005]. The abundance of Enterobacteriaceae (P = 0.002), Proteobacteria (P = 0.002), and Lactobacillaceae (P = 0.025) was increased and the abundance of Firmicutes (P = 0.025) and Clostridia (P = 0.045) was decreased in the deceased patients compared with the survivors. The deceased patients had a higher MDR value than the survivors [0.131 × (0.069-0.234) vs 0.034 × (0.009-0.096); P = 0.004]. If we applied an MDR value of 0.14 as the cutoff point, then it predicted patient death within the next year with a sensitivity of 71.4% and a specificity of 82.9% [area under the curve = 0.767 × (0.559-0.974)]. MDR was higher in patients with cirrhosis than in health controls [0.064 × (0.017-0.131) vs 0.005 × (0.002-0.007); P < 0.001], and in patients with decompensated cirrhosis than in patients with compensated cirrhosis [0.106 × (0.023-0.211) vs 0.033 × (0.012-0.074); P = 0.031]. MDR correlated negatively with prothrombin (r = -0.295; P = 0.042), cholinesterase (r = -0.466; P = 0.014) and serum albumin (r = -0.449; P = 0.001) level and positively with Child–Turcotte–Pugh scale value (r = 0.360; P = 0.012). CONCLUSION: Gut dysbiosis is associated with a poorer long-term prognosis in cirrhosis.
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spelling pubmed-81733422021-06-14 Gut dysbiosis is associated with poorer long-term prognosis in cirrhosis Maslennikov, Roman Ivashkin, Vladimir Efremova, Irina Alieva, Aliya Kashuh, Ekaterina Tsvetaeva, Ekaterina Poluektova, Elena Shirokova, Elena Ivashkin, Konstantin World J Hepatol Case Control Study BACKGROUND: Gut dysbiosis is common in cirrhosis. AIM: To study the influence of gut dysbiosis on prognosis in cirrhosis. METHODS: The case-control study included 48 in-patients with cirrhosis and 21 healthy controls. Stool microbiome was assessed using 16S ribosomal ribonucleic acid gene sequencing. We used modified dysbiosis ratio (MDR): [Bacilli (%) + Proteobacteria (%)]/[Clostridia (%) + Bacteroidetes (%)]. Patients with MDR more the median made up the group with severe dysbiosis, others did the group with non-severe dysbiosis. The follow-up period was 4 years. RESULTS: The mortality rate of patients with severe dysbiosis was significantly higher than that of patients with non-severe dysbiosis (54.2% vs 12.5%; P = 0.001). The presence of severe dysbiosis was independent risk factors for death [hazard ratio = 8.6 × (1.9-38.0); P = 0.005]. The abundance of Enterobacteriaceae (P = 0.002), Proteobacteria (P = 0.002), and Lactobacillaceae (P = 0.025) was increased and the abundance of Firmicutes (P = 0.025) and Clostridia (P = 0.045) was decreased in the deceased patients compared with the survivors. The deceased patients had a higher MDR value than the survivors [0.131 × (0.069-0.234) vs 0.034 × (0.009-0.096); P = 0.004]. If we applied an MDR value of 0.14 as the cutoff point, then it predicted patient death within the next year with a sensitivity of 71.4% and a specificity of 82.9% [area under the curve = 0.767 × (0.559-0.974)]. MDR was higher in patients with cirrhosis than in health controls [0.064 × (0.017-0.131) vs 0.005 × (0.002-0.007); P < 0.001], and in patients with decompensated cirrhosis than in patients with compensated cirrhosis [0.106 × (0.023-0.211) vs 0.033 × (0.012-0.074); P = 0.031]. MDR correlated negatively with prothrombin (r = -0.295; P = 0.042), cholinesterase (r = -0.466; P = 0.014) and serum albumin (r = -0.449; P = 0.001) level and positively with Child–Turcotte–Pugh scale value (r = 0.360; P = 0.012). CONCLUSION: Gut dysbiosis is associated with a poorer long-term prognosis in cirrhosis. Baishideng Publishing Group Inc 2021-05-27 2021-05-27 /pmc/articles/PMC8173342/ /pubmed/34131470 http://dx.doi.org/10.4254/wjh.v13.i5.557 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Control Study
Maslennikov, Roman
Ivashkin, Vladimir
Efremova, Irina
Alieva, Aliya
Kashuh, Ekaterina
Tsvetaeva, Ekaterina
Poluektova, Elena
Shirokova, Elena
Ivashkin, Konstantin
Gut dysbiosis is associated with poorer long-term prognosis in cirrhosis
title Gut dysbiosis is associated with poorer long-term prognosis in cirrhosis
title_full Gut dysbiosis is associated with poorer long-term prognosis in cirrhosis
title_fullStr Gut dysbiosis is associated with poorer long-term prognosis in cirrhosis
title_full_unstemmed Gut dysbiosis is associated with poorer long-term prognosis in cirrhosis
title_short Gut dysbiosis is associated with poorer long-term prognosis in cirrhosis
title_sort gut dysbiosis is associated with poorer long-term prognosis in cirrhosis
topic Case Control Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173342/
https://www.ncbi.nlm.nih.gov/pubmed/34131470
http://dx.doi.org/10.4254/wjh.v13.i5.557
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