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Early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting

The gut microbiome has shown promise as a predictive biomarker for various diseases. However, the potential of gut microbiota for prospective risk prediction of liver disease has not been assessed. Here, we utilized shallow shotgun metagenomic sequencing of a large population-based cohort (N > 7,...

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Autores principales: Liu, Yang, Méric, Guillaume, Havulinna, Aki S., Teo, Shu Mei, Åberg, Fredrik, Ruuskanen, Matti, Sanders, Jon, Zhu, Qiyun, Tripathi, Anupriya, Verspoor, Karin, Cheng, Susan, Jain, Mohit, Jousilahti, Pekka, Vázquez-Baeza, Yoshiki, Loomba, Rohit, Lahti, Leo, Niiranen, Teemu, Salomaa, Veikko, Knight, Rob, Inouye, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097589/
https://www.ncbi.nlm.nih.gov/pubmed/35354069
http://dx.doi.org/10.1016/j.cmet.2022.03.002
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author Liu, Yang
Méric, Guillaume
Havulinna, Aki S.
Teo, Shu Mei
Åberg, Fredrik
Ruuskanen, Matti
Sanders, Jon
Zhu, Qiyun
Tripathi, Anupriya
Verspoor, Karin
Cheng, Susan
Jain, Mohit
Jousilahti, Pekka
Vázquez-Baeza, Yoshiki
Loomba, Rohit
Lahti, Leo
Niiranen, Teemu
Salomaa, Veikko
Knight, Rob
Inouye, Michael
author_facet Liu, Yang
Méric, Guillaume
Havulinna, Aki S.
Teo, Shu Mei
Åberg, Fredrik
Ruuskanen, Matti
Sanders, Jon
Zhu, Qiyun
Tripathi, Anupriya
Verspoor, Karin
Cheng, Susan
Jain, Mohit
Jousilahti, Pekka
Vázquez-Baeza, Yoshiki
Loomba, Rohit
Lahti, Leo
Niiranen, Teemu
Salomaa, Veikko
Knight, Rob
Inouye, Michael
author_sort Liu, Yang
collection PubMed
description The gut microbiome has shown promise as a predictive biomarker for various diseases. However, the potential of gut microbiota for prospective risk prediction of liver disease has not been assessed. Here, we utilized shallow shotgun metagenomic sequencing of a large population-based cohort (N > 7,000) with ∼15 years of follow-up in combination with machine learning to investigate the predictive capacity of gut microbial predictors individually and in conjunction with conventional risk factors for incident liver disease. Separately, conventional and microbial factors showed comparable predictive capacity. However, microbiome augmentation of conventional risk factors using machine learning significantly improved the performance. Similarly, disease-free survival analysis showed significantly improved stratification using microbiome-augmented models. Investigation of predictive microbial signatures revealed previously unknown taxa for liver disease, as well as those previously associated with hepatic function and disease. This study supports the potential clinical validity of gut metagenomic sequencing to complement conventional risk factors for prediction of liver diseases.
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spelling pubmed-90975892022-06-14 Early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting Liu, Yang Méric, Guillaume Havulinna, Aki S. Teo, Shu Mei Åberg, Fredrik Ruuskanen, Matti Sanders, Jon Zhu, Qiyun Tripathi, Anupriya Verspoor, Karin Cheng, Susan Jain, Mohit Jousilahti, Pekka Vázquez-Baeza, Yoshiki Loomba, Rohit Lahti, Leo Niiranen, Teemu Salomaa, Veikko Knight, Rob Inouye, Michael Cell Metab Article The gut microbiome has shown promise as a predictive biomarker for various diseases. However, the potential of gut microbiota for prospective risk prediction of liver disease has not been assessed. Here, we utilized shallow shotgun metagenomic sequencing of a large population-based cohort (N > 7,000) with ∼15 years of follow-up in combination with machine learning to investigate the predictive capacity of gut microbial predictors individually and in conjunction with conventional risk factors for incident liver disease. Separately, conventional and microbial factors showed comparable predictive capacity. However, microbiome augmentation of conventional risk factors using machine learning significantly improved the performance. Similarly, disease-free survival analysis showed significantly improved stratification using microbiome-augmented models. Investigation of predictive microbial signatures revealed previously unknown taxa for liver disease, as well as those previously associated with hepatic function and disease. This study supports the potential clinical validity of gut metagenomic sequencing to complement conventional risk factors for prediction of liver diseases. Cell Press 2022-05-03 /pmc/articles/PMC9097589/ /pubmed/35354069 http://dx.doi.org/10.1016/j.cmet.2022.03.002 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Liu, Yang
Méric, Guillaume
Havulinna, Aki S.
Teo, Shu Mei
Åberg, Fredrik
Ruuskanen, Matti
Sanders, Jon
Zhu, Qiyun
Tripathi, Anupriya
Verspoor, Karin
Cheng, Susan
Jain, Mohit
Jousilahti, Pekka
Vázquez-Baeza, Yoshiki
Loomba, Rohit
Lahti, Leo
Niiranen, Teemu
Salomaa, Veikko
Knight, Rob
Inouye, Michael
Early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting
title Early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting
title_full Early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting
title_fullStr Early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting
title_full_unstemmed Early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting
title_short Early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting
title_sort early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097589/
https://www.ncbi.nlm.nih.gov/pubmed/35354069
http://dx.doi.org/10.1016/j.cmet.2022.03.002
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