Dina Tiniakos

ORCID: 0000-0003-4657-7780
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About
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Research Areas
  • Liver Disease Diagnosis and Treatment
  • Diet, Metabolism, and Disease
  • Liver Disease and Transplantation
  • Liver Diseases and Immunity
  • Alcohol Consumption and Health Effects
  • Hepatitis C virus research
  • Pancreatitis Pathology and Treatment
  • Pancreatic and Hepatic Oncology Research
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Hepatitis B Virus Studies
  • Liver physiology and pathology
  • Endoplasmic Reticulum Stress and Disease
  • Pancreatic function and diabetes
  • Lipid metabolism and disorders
  • Cancer-related Molecular Pathways
  • HER2/EGFR in Cancer Research
  • Diabetes and associated disorders
  • Organ Transplantation Techniques and Outcomes
  • Cancer Immunotherapy and Biomarkers
  • Cancer, Hypoxia, and Metabolism
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Fibroblast Growth Factor Research
  • Immune Cell Function and Interaction
  • Metabolism, Diabetes, and Cancer
  • Drug-Induced Hepatotoxicity and Protection

Newcastle University
2016-2025

Aretaeio Hospital
2020-2025

National and Kapodistrian University of Athens
2015-2024

NIHR Newcastle Biomedical Research Centre
2021-2024

Clinical Research Institute
2023-2024

Newcastle upon Tyne Hospital
2016-2023

Newcastle upon Tyne Hospitals NHS Foundation Trust
2015-2021

Freeman Hospital
2016-2018

Royal Victoria Infirmary
1995-2017

Chinese University of Hong Kong
2017

Dominik Pfister Nicolás Gonzalo Núñez Roser Pinyol Olivier Govaere Matthias Pinter and 95 more Marta Szydlowska Revant Gupta Mengjie Qiu Aleksandra Deczkowska Assaf Weiner Florian L. Müller Ankit Sinha Ekaterina Friebel Thomas Engleitner Daniela Lenggenhager Anja Moncsek Danijela Heide Kristin Stirm Jan Kosla Eleni Kotsiliti Valentina Leone Michael Dudek Suhail Yousuf Donato Inverso Indrabahadur Singh Ana Teijeiro Florian Castet Carla Montironi Philipp K. Haber Dina Tiniakos Pierre Bédossa Simon Cockell Ramy Younes Michèle Vacca Fabio Marra Jörn M. Schattenberg Michael Allison Elisabetta Bugianesi Vlad Ratziu Tiziana Pressiani Antonio D’Alessio Nicola Personeni Lorenza Rimassa Ann K. Daly Bernhard Scheiner Katharina Pomej Martha M. Kirstein Arndt Vogel Markus Peck‐Radosavljevic Florian Hucke Fabian Finkelmeier Oliver Waidmann Jörg Trojan Kornelius Schulze Henning Wege Sandra Koch Arndt Weinmann Marco Bueter Fabian Rössler Alexander Siebenhüner Sara De Dosso Jan‐Philipp Mallm Viktor Umansky Manfred Jugold Tom Luedde Andrea Schietinger Peter Schirmacher Brinda Emu Hellmut G. Augustin Adrian T. Billeter Beat P. Müller‐Stich Hiroto Kikuchi Dan G. Duda Fabian Kütting Dirk-Thomas Waldschmidt Matthias Ebert Nuh N. Rahbari Henrik E. Mei Axel Schulz Marc Ringelhan Nisar P. Malek Stephan Spahn Michael Bitzer Marina Ruiz de Galarreta Amaia Lujambio Jean‐François Dufour Thomas U. Marron Ahmed O. Kaseb Masatoshi Kudo Yi‐Hsiang Huang Nabil Djouder Katharina Wolter Lars Zender Patrice N. Marche Thomas Decaens David J. Pinato Roland Rad Joachim C. Mertens Achim Weber Kristian Unger

Abstract Hepatocellular carcinoma (HCC) can have viral or non-viral causes 1–5 . Non-alcoholic steatohepatitis (NASH) is an important driver of HCC. Immunotherapy has been approved for treating HCC, but biomarker-based stratification patients optimal response to therapy unmet need 6,7 Here we report the progressive accumulation exhausted, unconventionally activated CD8 + PD1 T cells in NASH-affected livers. In preclinical models NASH-induced therapeutic immunotherapy targeted at programmed...

10.1038/s41586-021-03362-0 article EN cc-by Nature 2021-03-24

Abstract The incidence of non-alcoholic fatty liver disease (NAFLD) increases with age. Cellular senescence refers to a state irreversible cell-cycle arrest combined the secretion proinflammatory cytokines and mitochondrial dysfunction. Senescent cells contribute age-related tissue degeneration. Here we show that accumulation senescent promotes hepatic fat steatosis. We report close correlation between markers hepatocyte senescence. elimination by suicide gene-meditated ablation p16 Ink4a...

10.1038/ncomms15691 article EN cc-by Nature Communications 2017-06-13

Non-invasive fibrosis scores are widely used to identify/exclude advanced in patients with non-alcoholic fatty liver disease (NAFLD). However, these were principally developed and validated aged between 35 65 years of age. The objective this study was assess the effect age on performance non-invasive tests NAFLD.Patients recruited from European specialist hepatology clinics. cohort divided into five age-based groups: ≤35 (n=74), 36-45 (n=96), 46-55 (n=197), 56-64 (n=191), ≥65 (n=76),...

10.1038/ajg.2016.453 article EN The American Journal of Gastroenterology 2016-10-11

Abstract Non-alcoholic fatty liver disease (NAFLD) is an increasingly common condition, strongly associated with the metabolic syndrome, that can lead to progressive hepatic fibrosis, cirrhosis and failure. Subtle inter-patient genetic variation environmental factors combine determine in progression. A non-synonymous polymorphism TM6SF2 (rs58542926 c.449 C>T, p.Glu167Lys) was recently increased triglyceride content, but whether this variant promotes clinically relevant fibrosis unknown....

10.1038/ncomms5309 article EN cc-by Nature Communications 2014-06-30

•Genome-wide association study involved 1,483 biopsied NAFLD cases and 17,781 controls.•Main analysis shows genome-wide significance for PNPLA3, TM6SF2, HSD17B13 GCKR.•Sub-analyses show near LEPR NASH PYGO1 steatosis.•Except GCKR, the significant signals were replicated. Background & AimsGenetic factors associated with non-alcoholic fatty liver disease (NAFLD) remain incompletely understood. To date, most studies (GWASs) have adopted radiologically assessed hepatic triglyceride content as...

10.1016/j.jhep.2020.04.003 article EN cc-by-nc-nd Journal of Hepatology 2020-04-14

Primary biliary cholangitis (formerly known as primary cirrhosis, PBC) is an autoimmune liver disease in which a cycle of immune mediated epithelial cell injury, cholestasis and progressive fibrosis can culminate over time end-stage cirrhosis. Both genetic environmental influences are presumed relevant to initiation. PBC most prevalent women those the age 50, but spectrum recognised adult patients globally; male sex, younger at onset (<45) advanced presentation baseline predictors poorer...

10.1136/gutjnl-2017-315259 article EN cc-by Gut 2018-03-28

Liver biopsy is currently the most reliable way of evaluating liver fibrosis in patients with non-alcoholic fatty disease (NAFLD). Its inherent risks limit its widespread use. Differential DNA methylation peroxisome proliferator-activated receptor gamma (PPARγ) gene promoter has recently been shown to stratify terms severity but requires access tissue. The aim this study was assess whether circulating could be detected human plasma and potentially used NAFLD.Patients biopsy-proven NAFLD...

10.1136/gutjnl-2016-311526 article EN cc-by Gut 2016-03-21

Background & AimsPharmacologic treatments for nonalcoholic steatohepatitis (NASH) are limited. Lifestyle interventions believed to be effective in reducing features of NASH, although the effect regular exercise, independent dietary change, is unclear. We performed a randomized controlled trial study exercise on hepatic triglyceride content (HTGC) and biomarkers fibrosis patients with NASH.MethodsTwenty-four (mean age, 52 ± 14 y; body mass index, 33 6 kg/m2) sedentary lifestyles (<60 min/wk...

10.1016/j.cgh.2016.07.031 article EN cc-by Clinical Gastroenterology and Hepatology 2016-08-11

Objective The full phenotypic expression of non-alcoholic fatty liver disease (NAFLD) in lean subjects is incompletely characterised. We aimed to investigate prevalence, characteristics and long-term prognosis Caucasian with NAFLD. Design study cohort comprises 1339 biopsy-proven NAFLD from four countries (Italy, UK, Spain Australia), stratified into non-lean (body mass index (BMI) &lt;/≥25 kg/m 2 ). Liver/non-liver-related events survival free transplantation were recorded during the...

10.1136/gutjnl-2020-322564 article EN Gut 2021-02-04

•Hepatocyte ballooning identification underpins regulatory-approved drug efficacy endpoints in clinical trials.•We report substantial variation ballooned cell by expert hepatopathologists.•Our data suggest that is too subjective for its presence or complete absence to be used as a trial endpoint.•A ‘concordance atlas’ of cells identified multiple pathologists can train AI-based image analysis.•AI-based approaches may provide more reliable way assess the range injury recorded hepatocyte...

10.1016/j.jhep.2022.01.011 article EN cc-by Journal of Hepatology 2022-01-25

Abstract Background &amp; Aims Diagnostic histological criteria for autoimmune hepatitis (AIH) have not been clearly established. Previously published focused mainly on chronic AIH, in which inflammatory changes occur portal/periportal regions and may be applicable to acute presentation of are typically predominantly lobular location. International consensus the diagnosis assessment disease severity both AIH thus urgently needed. Methods Seventeen expert liver pathologists convened at an...

10.1111/liv.15217 article EN cc-by-nc-nd Liver International 2022-03-01

Abstract Non-alcoholic fatty liver disease (NAFLD) is a common, progressive strongly associated with the metabolic syndrome. It unclear how progression of NAFLD towards cirrhosis translates into systematic changes in circulating proteins. Here, we provide detailed proteo-transcriptomic map steatohepatitis and fibrosis during NAFLD. In this multicentre proteomic study, characterize 4,730 proteins 306 patients histologically characterized integrate transcriptomic analysis paired tissue. We...

10.1038/s42255-023-00775-1 article EN cc-by Nature Metabolism 2023-04-10
Michèle Vacca Ioannis Kamzolas Lea Mørch Harder Fiona Oakley Christian Trautwein and 95 more Maximilian Hatting Trenton T. Ross Barbara Bernardo Anouk Oldenburger Sara Toftegaard Hjuler Iwona Ksiazek Daniel Lindén Detlef Schuppan Sergio Rodríguez‐Cuenca Maria Manuela Tonini Tamara R. Castañeda Aimo Kannt Cecília M. P. Rodrigues Simon Cockell Olivier Govaere Ann K. Daly Michael Allison Kristian Honnens de Lichtenberg Yong Ook Kim Anna Lindblom Stephanie Oldham Anne‐Christine Andréasson Franklin Schlerman Jonathon Marioneaux Arun J. Sanyal Marta B. Afonso Ramy Younes Yuichiro Amano Scott L. Friedman Shuang Wang Dipankar Bhattacharya Eric J. Simon Valérie Paradis Alastair D. Burt Ioanna Maria Grypari Susan Davies Ann Driessen Hiroaki Yashiro Susanne Elisabeth Pors M Andersen Michael Feigh Carla Yunis Pierre Bédossa Michelle Stewart Heather Cater Sara Wells Jörn M. Schattenberg Quentin M. Anstee Quentin M. Anstee Ann K. Daly Simon Cockell Dina Tiniakos Pierre Bédossa Alastair D. Burt Fiona Oakley Heather J. Cordell Christopher P. Day Kristy Wonders Paolo Missier Matthew McTeer Luke Vale Yemi Oluboyede Matt Breckons Jo Boyle Patrick M. Bossuyt Hadi Zafarmand Yasaman Vali Jenny Lee Max Nieuwdorp Adriaan G. Holleboom Athanasios Angelakis Joanne Verheij Vlad Ratziu Karine Clément Rafael Patiño‐Navarrete Raluca Pais Valérie Paradis Detlef Schuppan Jörn M. Schattenberg Rambabu Surabattula Sudha Rani Myneni Yong Ook Kim Beate K. Straub Antonio Vidal‐Puig Michèle Vacca Sergio Rodrigues-Cuenca Mike Allison Ioannis Kamzolas Evangelia Petsalaki Mark Campbell Chris Lelliott Nathan Davies Matej Orešič Tuulia Hyötyläinen Aidan McGlinchey

Abstract Metabolic dysfunction-associated steatotic liver disease (MASLD), previously known as non-alcoholic fatty disease, encompasses steatosis and metabolic steatohepatitis (MASH), leading to cirrhosis hepatocellular carcinoma. Preclinical MASLD research is mainly performed in rodents; however, the model that best recapitulates human yet be defined. We conducted a wide-ranging retrospective review (metabolic phenotype, histopathology, transcriptome benchmarked against humans) of murine...

10.1038/s42255-024-01043-6 article EN cc-by Nature Metabolism 2024-06-12

Objective Hyperferritinaemia is associated with liver fibrosis severity in patients metabolic dysfunction-associated steatotic disease (MASLD), but the longitudinal implications have not been thoroughly investigated. We assessed role of serum ferritin predicting long-term outcomes or death. Design evaluated relationship between baseline and events a multicentre cohort 1342 patients. Four survival models considering confounders non-invasive scoring systems were applied repeated five-fold...

10.1136/gutjnl-2023-330815 article EN Gut 2024-01-10
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