Katherine Johnson
Increased serum miR-193a-5p during non-alcoholic fatty liver disease progression: Diagnostic and mechanistic relevance
Johnson, Katherine; Leary, Peter J.; Govaere, Olivier; Barter, Matthew J.; Charlton, Sarah H.; Cockell, Simon J.; Tiniakos, Dina; Zatorska, Michalina; Bedossa, Pierre; Brosnan, M. Julia; Cobbold, Jeremy F.; Ekstedt, Mattias; Aithal, Guruprasad P.; Clément, Karine; Schattenberg, Jörn M.; Boursier, Jerome; Ratziu, Vlad; Bugianesi, Elisabetta; Anstee, Quentin M.; Daly, Ann K.; Anstee, Quentin M.; Bedossa, Pierre; Clark, James; Cockell, Simon; Cordell, Heather J.; Daly, Ann K.; Darlay, Rebecca; Day, Christopher P.; Govaere, Olivier; Hardy, Tim; Johnson, Katherine; Liu, Yang-Lin; Oakley, Fiona; Palmer, Jeremy; Queen, Rachel; Tiniakos, Dina; Wonders, Kristy; Zatorska, Michalina; Bossuyt, Patrick M.; Holleboom, Adriaan G.; Zafarmand, Hadi; Vali, Yasaman; Lee, Jenny; Clement, Karine; Pais, Raluca; Ratziu, Vlad; Schattenberg, Jörn M.; Schuppan, Detlef; Allison, Michael; Cuenca, Sergio Rodriguez; Pellegrinelli, Vanessa; Vacca, Michele; Vidal-Puig, Antonio; Hyötyläinen, Tuulia; McGlinchey, Aidan;...
Authors
Peter J. Leary
Olivier Govaere
Matthew J. Barter
Sarah H. Charlton
Simon J. Cockell
Dina Tiniakos
Michalina Zatorska
Pierre Bedossa
M. Julia Brosnan
Jeremy F. Cobbold
Mattias Ekstedt
GURUPRASAD AITHAL Guru.Aithal@nottingham.ac.uk
Professor of Hepatology
Karine Clément
Jörn M. Schattenberg
Jerome Boursier
Vlad Ratziu
Elisabetta Bugianesi
Quentin M. Anstee
Ann K. Daly
Quentin M. Anstee
Pierre Bedossa
James Clark
Simon Cockell
Heather J. Cordell
Ann K. Daly
Rebecca Darlay
Christopher P. Day
Olivier Govaere
Tim Hardy
Katherine Johnson
Yang-Lin Liu
Fiona Oakley
Jeremy Palmer
Rachel Queen
Dina Tiniakos
Kristy Wonders
Michalina Zatorska
Patrick M. Bossuyt
Adriaan G. Holleboom
Hadi Zafarmand
Yasaman Vali
Jenny Lee
Karine Clement
Raluca Pais
Vlad Ratziu
Jörn M. Schattenberg
Detlef Schuppan
Michael Allison
Sergio Rodriguez Cuenca
Vanessa Pellegrinelli
Michele Vacca
Antonio Vidal-Puig
Tuulia Hyötyläinen
Aidan McGlinchey
Matej Orešič
Partho Sen
Jose Mato
Óscar Millet
Jean-Francois Dufour
Jeremy F. Cobbold
Stephen Harrison
Stefan Neubauer
Michael Pavlides
Ferenc Mozes
Salma Akhtar
Rajarshi Banerjee
Matt Kelly
Elizabeth Shumbayawonda
Andrea Dennis
Charlotte Erpicum
Manuel Romero-Gomez
Rocío Gallego-Durán
Isabel Fernández
Morten Karsdal
Diana Leeming
Mette Juul Fisker
Elisabeth Erhardtsen
Daniel Rasmussen
Per Qvist
Antonia Sinisi
Estelle Sandt
Maria Manuela Tonini
Elisabetta Bugianesi
Maurizio Parola
Chiara Rosso
Fabio Marra
Amalia Gastaldelli
Jerome Boursier
Sven Francque
Mattias Ekstedt
Stergios Kechagias
Hannele Yki-Järvinen
Kimmo Porthan
Saskia van Mil
George Papatheodoridis
Helena Cortez-Pinto
Luca Valenti
Salvatore Petta
Luca Miele
Andreas Geier
Christian Trautwein
GURUPRASAD AITHAL Guru.Aithal@nottingham.ac.uk
Professor of Hepatology
Paul Hockings
Phil Newsome
David Wenn
Cecília Maria Pereira Rodrigues
Rémy Hanf
Pierre Chaumat
Christian Rosenquist
Aldo Trylesinski
Pablo Ortiz
Kevin Duffin
Carla Yunis
Melissa Miller
M. Julia Brosnan
Theresa Tuthill
Judith Ertle
Ramy Younes
Leigh Alexander
Rachel Ostroff
Mette Skalshøi Kjær
Lars Friis Mikkelsen
Clifford Brass
Lori Jennings
Maria-Magdalena Balp
Miljen Martic
Guido Hanauer
Sudha Shankar
Richard Torstenson
Céline Fournier
Richard Ehman
Michael Kalutkiewicz
Kay Pepin
Joel Myers
Diane Shevell
Gideon Ho
Henrik Landgren
Rob Myers
Lynda Doward
Diane Whalley
James Twiss
Abstract
Background & Aims: Serum microRNA (miRNA) levels are known to change in non-alcoholic fatty liver disease (NAFLD) and may serve as useful biomarkers. This study aimed to profile miRNAs comprehensively at all NAFLD stages. Methods: We profiled 2,083 serum miRNAs in a discovery cohort (183 cases with NAFLD representing the complete NAFLD spectrum and 10 population controls). miRNA libraries generated by HTG EdgeSeq were sequenced by Illumina NextSeq. Selected serum miRNAs were profiled in 372 additional cases with NAFLD and 15 population controls by quantitative reverse transcriptase PCR. Results: Levels of 275 miRNAs differed between cases and population controls. Fewer differences were seen within individual NAFLD stages, but miR-193a-5p consistently showed increased levels in all comparisons. Relative to NAFL/non-alcoholic steatohepatitis (NASH) with mild fibrosis (stage 0/1), 3 miRNAs (miR-193a-5p, miR-378d, and miR378d) were increased in cases with NASH and clinically significant fibrosis (stages 2–4), 7 (miR193a-5p, miR-378d, miR-378e, miR-320b, miR-320c, miR-320d, and miR-320e) increased in cases with NAFLD activity score (NAS) 5–8 compared with lower NAS, and 3 (miR-193a-5p, miR-378d, and miR-378e) increased but 1 (miR-19b-3p) decreased in steatosis, activity, and fibrosis (SAF) activity score 2–4 compared with lower SAF activity. The significant findings for miR-193a-5p were replicated in the additional cohort with NAFLD. Studies in Hep G2 cells showed that following palmitic acid treatment, miR-193a-5p expression decreased significantly. Gene targets for miR-193a-5p were investigated in liver RNAseq data for a case subgroup (n = 80); liver GPX8 levels correlated positively with serum miR-193a-5p. Conclusions: Serum miR-193a-5p levels correlate strongly with NAFLD activity grade and fibrosis stage. MiR-193a-5p may have a role in the hepatic response to oxidative stress and is a potential clinically tractable circulating biomarker for progressive NAFLD. Lay summary: MicroRNAs (miRNAs) are small pieces of nucleic acid that may turn expression of genes on or off. These molecules can be detected in the blood circulation, and their levels in blood may change in liver disease including non-alcoholic fatty liver disease (NAFLD). To see if we could detect specific miRNA associated with advanced stages of NAFLD, we carried out miRNA sequencing in a group of 183 patients with NAFLD of varying severity together with 10 population controls. We found that a number of miRNAs showed changes, mainly increases, in serum levels but that 1 particular miRNA miR-193a-5p consistently increased. We confirmed this increase in a second group of cases with NAFLD. Measuring this miRNA in a blood sample may be a useful way to determine whether a patient has advanced NAFLD without an invasive liver biopsy.
Citation
Johnson, K., Leary, P. J., Govaere, O., Barter, M. J., Charlton, S. H., Cockell, S. J., …Twiss, J. (2022). Increased serum miR-193a-5p during non-alcoholic fatty liver disease progression: Diagnostic and mechanistic relevance. JHEP Reports, 4(2), Article 100409. https://doi.org/10.1016/j.jhepr.2021.100409
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 9, 2021 |
Online Publication Date | Nov 25, 2021 |
Publication Date | Feb 1, 2022 |
Deposit Date | Dec 7, 2021 |
Publicly Available Date | Dec 8, 2021 |
Journal | JHEP Reports |
Electronic ISSN | 2589-5559 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 4 |
Issue | 2 |
Article Number | 100409 |
DOI | https://doi.org/10.1016/j.jhepr.2021.100409 |
Keywords | Gastroenterology; Hepatology; Immunology and Allergy; Internal Medicine |
Public URL | https://nottingham-repository.worktribe.com/output/6911030 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S2589555921001853 |
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