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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;...

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Authors

Katherine Johnson

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

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

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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