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Liver stiffness measurement predicted liver‐related events and all‐cause mortality: A systematic review and nonlinear dose–response meta‐analysis

Numerous studies have investigated the prognosis value of the liver stiffness measurement (LSM) by transient elastography in assessing the risk of liver‐related events (LREs) and all‐cause mortality in patients with chronic liver disease (CLD). However, the shape of the dose–response relationship be...

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Autores principales: Wang, Junna, Li, Jiajun, Zhou, Quan, Zhang, Dandan, Bi, Qiu, Wu, Yulin, Huang, Wenxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880200/
https://www.ncbi.nlm.nih.gov/pubmed/29619424
http://dx.doi.org/10.1002/hep4.1154
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author Wang, Junna
Li, Jiajun
Zhou, Quan
Zhang, Dandan
Bi, Qiu
Wu, Yulin
Huang, Wenxiang
author_facet Wang, Junna
Li, Jiajun
Zhou, Quan
Zhang, Dandan
Bi, Qiu
Wu, Yulin
Huang, Wenxiang
author_sort Wang, Junna
collection PubMed
description Numerous studies have investigated the prognosis value of the liver stiffness measurement (LSM) by transient elastography in assessing the risk of liver‐related events (LREs) and all‐cause mortality in patients with chronic liver disease (CLD). However, the shape of the dose–response relationship between them remains unclear. We searched PubMed, Embase, the Cochrane Library, and reference lists of articles for studies published up to July 1, 2017, that assessed the LSM in predicting LREs and all‐cause mortality among subjects with CLD. Fifty‐four observational cohort studies with 35,249 participants were included. Summary relative risks (RRs) were calculated using a random‐effects model, and a restricted cubic spline function was used to model the dose–response association. LREs and all‐cause mortality were increased in subjects with a high LSM (LRE: RR, 7.90; 95% confidence interval [CI], 5.65, 11.05; I (2) = 71.6%; all‐cause mortality: RR, 4.15; 95% CI, 2.56, 6.72; I (2) = 68.5%). For each unit increment of liver stiffness, the summary RR was 1.06 (95% CI, 1.06, 1.07; I (2) = 74.6%) for LREs and 1.06 (95% CI, 1.04, 1.07; I (2) = 55.7%) for all‐cause mortality. A positive relationship with a nonlinear trend for LSM with LREs and all‐cause mortality was examined by a dose–response meta‐analysis (P < 0.001). When stratified by etiology, a nonlinear association was also found in patients infected with hepatitis C virus and those coinfected with hepatitis C virus and human immunodeficiency virus. In contrast, there was no evidence of departure from linearity among patients with hepatitis B virus infection (P (nonlinearity) = 0.072). Conclusion: LSM is useful in screening LREs and all‐cause mortality in patients with CLD. Further studies are warranted in assessing the application of LSM in monitoring the risk of LREs and all‐cause mortality in clinical practice. (Hepatology Communications 2018;2:467‐476)
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spelling pubmed-58802002018-04-04 Liver stiffness measurement predicted liver‐related events and all‐cause mortality: A systematic review and nonlinear dose–response meta‐analysis Wang, Junna Li, Jiajun Zhou, Quan Zhang, Dandan Bi, Qiu Wu, Yulin Huang, Wenxiang Hepatol Commun Special Article Numerous studies have investigated the prognosis value of the liver stiffness measurement (LSM) by transient elastography in assessing the risk of liver‐related events (LREs) and all‐cause mortality in patients with chronic liver disease (CLD). However, the shape of the dose–response relationship between them remains unclear. We searched PubMed, Embase, the Cochrane Library, and reference lists of articles for studies published up to July 1, 2017, that assessed the LSM in predicting LREs and all‐cause mortality among subjects with CLD. Fifty‐four observational cohort studies with 35,249 participants were included. Summary relative risks (RRs) were calculated using a random‐effects model, and a restricted cubic spline function was used to model the dose–response association. LREs and all‐cause mortality were increased in subjects with a high LSM (LRE: RR, 7.90; 95% confidence interval [CI], 5.65, 11.05; I (2) = 71.6%; all‐cause mortality: RR, 4.15; 95% CI, 2.56, 6.72; I (2) = 68.5%). For each unit increment of liver stiffness, the summary RR was 1.06 (95% CI, 1.06, 1.07; I (2) = 74.6%) for LREs and 1.06 (95% CI, 1.04, 1.07; I (2) = 55.7%) for all‐cause mortality. A positive relationship with a nonlinear trend for LSM with LREs and all‐cause mortality was examined by a dose–response meta‐analysis (P < 0.001). When stratified by etiology, a nonlinear association was also found in patients infected with hepatitis C virus and those coinfected with hepatitis C virus and human immunodeficiency virus. In contrast, there was no evidence of departure from linearity among patients with hepatitis B virus infection (P (nonlinearity) = 0.072). Conclusion: LSM is useful in screening LREs and all‐cause mortality in patients with CLD. Further studies are warranted in assessing the application of LSM in monitoring the risk of LREs and all‐cause mortality in clinical practice. (Hepatology Communications 2018;2:467‐476) John Wiley and Sons Inc. 2018-02-13 /pmc/articles/PMC5880200/ /pubmed/29619424 http://dx.doi.org/10.1002/hep4.1154 Text en © 2018 The Authors. Hepatology Communications published by Wiley Periodicals, Inc., on behalf of the American Association for the Study of Liver Diseases. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Special Article
Wang, Junna
Li, Jiajun
Zhou, Quan
Zhang, Dandan
Bi, Qiu
Wu, Yulin
Huang, Wenxiang
Liver stiffness measurement predicted liver‐related events and all‐cause mortality: A systematic review and nonlinear dose–response meta‐analysis
title Liver stiffness measurement predicted liver‐related events and all‐cause mortality: A systematic review and nonlinear dose–response meta‐analysis
title_full Liver stiffness measurement predicted liver‐related events and all‐cause mortality: A systematic review and nonlinear dose–response meta‐analysis
title_fullStr Liver stiffness measurement predicted liver‐related events and all‐cause mortality: A systematic review and nonlinear dose–response meta‐analysis
title_full_unstemmed Liver stiffness measurement predicted liver‐related events and all‐cause mortality: A systematic review and nonlinear dose–response meta‐analysis
title_short Liver stiffness measurement predicted liver‐related events and all‐cause mortality: A systematic review and nonlinear dose–response meta‐analysis
title_sort liver stiffness measurement predicted liver‐related events and all‐cause mortality: a systematic review and nonlinear dose–response meta‐analysis
topic Special Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880200/
https://www.ncbi.nlm.nih.gov/pubmed/29619424
http://dx.doi.org/10.1002/hep4.1154
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