Microbiome and Genetic Factors in the Pathogenesis of Liver Diseases
Our genetic background has not changed over the past century, but chronic diseases are on the rise globally. In addition to the genetic component, among the critical factors for many diseases are inhabitants of our intestines (gut microbiota) as a crucial environmental factor. Dysbiosis has been des...
| Published in: | Gastroenterology Insights |
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| Main Authors: | , , , , , , , , , , , |
| Format: | Article |
| Language: | English |
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MDPI AG
2023-11-01
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| Online Access: | https://www.mdpi.com/2036-7422/14/4/41 |
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| author | Dimitrina Miteva Monika Peshevska-Sekulovska Violeta Snegarova Milena Peruhova Georgi H. Vasilev Georgi V. Vasilev Metodija Sekulovski Snezhina Lazova Milena Gulinac Latchezar Tomov Antoaneta Mihova Tsvetelina Velikova |
| author_facet | Dimitrina Miteva Monika Peshevska-Sekulovska Violeta Snegarova Milena Peruhova Georgi H. Vasilev Georgi V. Vasilev Metodija Sekulovski Snezhina Lazova Milena Gulinac Latchezar Tomov Antoaneta Mihova Tsvetelina Velikova |
| author_sort | Dimitrina Miteva |
| collection | DOAJ |
| container_title | Gastroenterology Insights |
| description | Our genetic background has not changed over the past century, but chronic diseases are on the rise globally. In addition to the genetic component, among the critical factors for many diseases are inhabitants of our intestines (gut microbiota) as a crucial environmental factor. Dysbiosis has been described in liver diseases with different etiologies like non-alcoholic fatty liver disease (NAFLD), alcohol-related liver disease (ALD), viral hepatitis, autoimmune hepatitis (AIH), primary sclerosing cholangitis (PSC), primary biliary cholangitis (PBC), cirrhosis, hepatocellular carcinoma (HCC). On the other hand, new technologies have increased our understanding of liver disease genetics and treatment options. Genome-wide association studies (GWAS) identify unknown genetic risk factors, positional cloning of unknown genes associated with different diseases, gene tests for single nucleotide variations (SNVs), and next-generation sequencing (NGS) of selected genes or the complete genome. NGS also allowed studying the microbiome and its role in various liver diseases has begun. These genes have proven their effect on microbiome composition in host genome–microbiome association studies. We focus on altering the intestinal microbiota, and supplementing some bacterial metabolites could be considered a potential therapeutic strategy. The literature data promote probiotics/synbiotics role in reducing proinflammatory cytokines such as TNF-α and the interleukins (IL-1, IL-6, IL-8), therefore improving transaminase levels, hepatic steatosis, and NAFLD activity score. However, even though microbial therapy appears to be risk-free, evaluating side effects related to probiotics or synbiotics is imperative. In addition, safety profiles for long-term usage should be researched. Thus, this review focuses on the human microbiome and liver diseases, recent GWASs on liver disease, the gut-liver axis, and the associations with the microbiome and microbiome during/after liver disease therapy. |
| format | Article |
| id | doaj-art-4b4afe826c2b4efcb47b3e65ea098d8a |
| institution | Directory of Open Access Journals |
| issn | 2036-7414 2036-7422 |
| language | English |
| publishDate | 2023-11-01 |
| publisher | MDPI AG |
| record_format | Article |
| spelling | doaj-art-4b4afe826c2b4efcb47b3e65ea098d8a2025-08-19T22:28:21ZengMDPI AGGastroenterology Insights2036-74142036-74222023-11-0114457559710.3390/gastroent14040041Microbiome and Genetic Factors in the Pathogenesis of Liver DiseasesDimitrina Miteva0Monika Peshevska-Sekulovska1Violeta Snegarova2Milena Peruhova3Georgi H. Vasilev4Georgi V. Vasilev5Metodija Sekulovski6Snezhina Lazova7Milena Gulinac8Latchezar Tomov9Antoaneta Mihova10Tsvetelina Velikova11Department of Genetics, Faculty of Biology, Sofia University St. Kliment Ohridski, 8 Dragan Tzankov Str., 1164 Sofia, BulgariaMedical Faculty, Sofia University St. Kliment Ohridski, 1 Kozyak Str., 1407 Sofia, BulgariaClinic of Internal Diseases, Naval Hospital—Varna, Military Medical Academy, Medical Faculty, Medical University, Blvd. Hristo Smirnenski 3, 9000 Varna, BulgariaDepartment of Gastroenterology, Heart and Brain Hospital, Zdrave 1 Str., 8000 Burgas, BulgariaMedical Faculty, Sofia University St. Kliment Ohridski, 1 Kozyak Str., 1407 Sofia, BulgariaMedical Faculty, Sofia University St. Kliment Ohridski, 1 Kozyak Str., 1407 Sofia, BulgariaMedical Faculty, Sofia University St. Kliment Ohridski, 1 Kozyak Str., 1407 Sofia, BulgariaMedical Faculty, Sofia University St. Kliment Ohridski, 1 Kozyak Str., 1407 Sofia, BulgariaMedical Faculty, Sofia University St. Kliment Ohridski, 1 Kozyak Str., 1407 Sofia, BulgariaMedical Faculty, Sofia University St. Kliment Ohridski, 1 Kozyak Str., 1407 Sofia, BulgariaSMDL Ramus, Department of Immunology, Blvd. Kap. Spisarevski 26, 1527 Sofia, BulgariaMedical Faculty, Sofia University St. Kliment Ohridski, 1 Kozyak Str., 1407 Sofia, BulgariaOur genetic background has not changed over the past century, but chronic diseases are on the rise globally. In addition to the genetic component, among the critical factors for many diseases are inhabitants of our intestines (gut microbiota) as a crucial environmental factor. Dysbiosis has been described in liver diseases with different etiologies like non-alcoholic fatty liver disease (NAFLD), alcohol-related liver disease (ALD), viral hepatitis, autoimmune hepatitis (AIH), primary sclerosing cholangitis (PSC), primary biliary cholangitis (PBC), cirrhosis, hepatocellular carcinoma (HCC). On the other hand, new technologies have increased our understanding of liver disease genetics and treatment options. Genome-wide association studies (GWAS) identify unknown genetic risk factors, positional cloning of unknown genes associated with different diseases, gene tests for single nucleotide variations (SNVs), and next-generation sequencing (NGS) of selected genes or the complete genome. NGS also allowed studying the microbiome and its role in various liver diseases has begun. These genes have proven their effect on microbiome composition in host genome–microbiome association studies. We focus on altering the intestinal microbiota, and supplementing some bacterial metabolites could be considered a potential therapeutic strategy. The literature data promote probiotics/synbiotics role in reducing proinflammatory cytokines such as TNF-α and the interleukins (IL-1, IL-6, IL-8), therefore improving transaminase levels, hepatic steatosis, and NAFLD activity score. However, even though microbial therapy appears to be risk-free, evaluating side effects related to probiotics or synbiotics is imperative. In addition, safety profiles for long-term usage should be researched. Thus, this review focuses on the human microbiome and liver diseases, recent GWASs on liver disease, the gut-liver axis, and the associations with the microbiome and microbiome during/after liver disease therapy.https://www.mdpi.com/2036-7422/14/4/41genomicsliver diseasemicrobiomegut microbiotaNAFLDliver cirrhosis |
| spellingShingle | Dimitrina Miteva Monika Peshevska-Sekulovska Violeta Snegarova Milena Peruhova Georgi H. Vasilev Georgi V. Vasilev Metodija Sekulovski Snezhina Lazova Milena Gulinac Latchezar Tomov Antoaneta Mihova Tsvetelina Velikova Microbiome and Genetic Factors in the Pathogenesis of Liver Diseases genomics liver disease microbiome gut microbiota NAFLD liver cirrhosis |
| title | Microbiome and Genetic Factors in the Pathogenesis of Liver Diseases |
| title_full | Microbiome and Genetic Factors in the Pathogenesis of Liver Diseases |
| title_fullStr | Microbiome and Genetic Factors in the Pathogenesis of Liver Diseases |
| title_full_unstemmed | Microbiome and Genetic Factors in the Pathogenesis of Liver Diseases |
| title_short | Microbiome and Genetic Factors in the Pathogenesis of Liver Diseases |
| title_sort | microbiome and genetic factors in the pathogenesis of liver diseases |
| topic | genomics liver disease microbiome gut microbiota NAFLD liver cirrhosis |
| url | https://www.mdpi.com/2036-7422/14/4/41 |
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