Literature DB >> 31269936

Assessing the disease burden of non-alcoholic fatty liver disease in the real world - big data and big numbers.

Jörn M Schattenberg1, Mattias Ekstedt2.   

Abstract

Entities:  

Keywords:  Advanced fibrosis; Awareness; Epidemiology; Fib-4; Hepatocellular carcinoma; NAFLD; NASH; Real-world data; Screening

Mesh:

Year:  2019        PMID: 31269936      PMCID: PMC6610815          DOI: 10.1186/s12916-019-1357-y

Source DB:  PubMed          Journal:  BMC Med        ISSN: 1741-7015            Impact factor:   8.775


× No keyword cloud information.

Background

Non-alcoholic fatty liver disease (NAFLD) is a growing burden on European healthcare [1], with estimated annual healthcare costs of €19 billion EUR within the EU-5 region (France, Germany, Italy, Spain and the United Kingdom) [2]. In studies with long-term follow-up, excess mortality in people with NAFLD was shown to be dependent on the degree of underlying hepatic fibrosis [3]. Importantly, NAFLD also significantly impairs patients’ quality of life [4]. The histological definition of both the presence of the inflammatory subtype of the disease, which is commonly called non-alcoholic steatohepatitis (NASH), and hepatic fibrosis, causes challenges for all epidemiological studies on the prevalence of the disease in Europe.

Evidence from a real-world study

In a recent article published in BMC Medicine, Alexander et al. [5] undertook an enormous effort to extract data from the European Medical Information Framework in the UK, Netherlands, Italy, and Spain. They analyzed data from the electronic medical records of more than 18 million European patients with codes for NAFLD and (in some countries) for NASH. The control cohort constituted matched cases with up to 100 non-NAFLD patients for each NAFLD/NASH case and took into account GP practice site, age, sex and healthcare utilization habits into account. This represents one of the most comprehensive and largest control populations; for instance, The Health Information Network covers up to 6.2% of the patients cared for in UK-based GP practices. The authors confirm established risk factors that are relevant for NALFD; namely type 2 diabetes, arterial hypertension and obesity [6]. Importantly, the study underlines the relevance of these risk factors in a non-referral based, non-high risk population and expands available knowledge through this very large real-world dataset. The authors observed a hazard ratio for cirrhosis of 4.73 (95% CI: 2.43–9.19) and 3.51 for hepatocellular carcinoma (95% CI: 1.72–7.16), underlining the relevance of liver-related outcomes in patients with NAFLD. The incidences of these diagnoses were even higher when the surrogate score for the presence of advanced fibrosis (in this case Fibrosis-4 score [Fib-4]) was ranked as high-risk. While it is likely that a number of NAFLD/NASH cases were not coded in the available healthcare records, this large real-world study cohort highlights the contribution of diabetes as a strong and independent predictor of advanced liver disease and hepatocellular carcinoma, which is in line with previous data and recent data from the USA [7]. Interestingly, the median time between coding liver disease and cirrhosis was, in general, short, ranging between 0.5 and 2.9 years. This highlights shortcomings in the current practice aiming to identify patients with developing liver disease at an early stage.

Challenges and implications for clinical practice in NAFLD

Considering all available data, including the confirmation arising from this study, the reality of liver disease in metabolically diseased patients is highlighted: diagnosis is made at a late stage. It can take a long time – even several years – to develop advanced liver disease, during which time preventative or even therapeutic approaches could be implemented. However, the fact that many patients are diagnosed at an advanced stage, means that they are prevented from modifying the risk factors responsible for driving the progression of liver disease. This must be highlighted, particularly to primary and secondary care providers. To achieve this, the scientific field urgently needs real-world data from unselected clinical cohorts that represent the disease spectrum of the general population. In the current study, 0.7% of included patients had a diagnosis of NAFLD/NASH; this should be interpreted in light of the 24% estimated global prevalence of NAFLD [8]. Therefore, this study evaluates not the tip of the iceberg, but the tip of the tip of the iceberg. Although this cohort probably represents a selected subtype of NAFLD/NASH, this study gives us a real world insight into the low awareness of NAFLD/NASH in primary care. We also learn that having a code for NAFLD/NASH does not, in itself, significantly raise awareness of this disease. With the advent of medical therapies for the treatment of NAFLD [9], the minimalistic approach to this patient population will be likely to change. It should also be highlighted that, even in the absence of a liver-directed, specific therapy, NAFLD is an ‘indicator disease’, which identifies patients at risk of developing diabetes [10] or cardiovascular disease and complications [8].

Conclusions

In summary, this study, together with many others, has clearly established NAFLD/NASH – with its metabolic comorbidities – as a public health challenge. Now it is time to support patients, advocacy groups and specialists to raise awareness about this liver disease.
  9 in total

1.  Modeling NAFLD disease burden in China, France, Germany, Italy, Japan, Spain, United Kingdom, and United States for the period 2016-2030.

Authors:  Chris Estes; Quentin M Anstee; Maria Teresa Arias-Loste; Heike Bantel; Stefano Bellentani; Joan Caballeria; Massimo Colombo; Antonio Craxi; Javier Crespo; Christopher P Day; Yuichiro Eguchi; Andreas Geier; Loreta A Kondili; Daniela C Kroy; Jeffrey V Lazarus; Rohit Loomba; Michael P Manns; Giulio Marchesini; Atsushi Nakajima; Francesco Negro; Salvatore Petta; Vlad Ratziu; Manuel Romero-Gomez; Arun Sanyal; Jörn M Schattenberg; Frank Tacke; Junko Tanaka; Christian Trautwein; Lai Wei; Stefan Zeuzem; Homie Razavi
Journal:  J Hepatol       Date:  2018-06-08       Impact factor: 25.083

2.  Fibrosis stage but not NASH predicts mortality and time to development of severe liver disease in biopsy-proven NAFLD.

Authors:  Hannes Hagström; Patrik Nasr; Mattias Ekstedt; Ulf Hammar; Per Stål; Rolf Hultcrantz; Stergios Kechagias
Journal:  J Hepatol       Date:  2017-08-10       Impact factor: 25.083

3.  Health-related Quality of Life in Nonalcoholic Fatty Liver Disease Associates With Hepatic Inflammation.

Authors:  Yvonne Huber; Marie Boyle; Kate Hallsworth; Dina Tiniakos; Beate K Straub; Christian Labenz; Christian Ruckes; Peter R Galle; Manuel Romero-Gómez; Quentin M Anstee; Jörn M Schattenberg
Journal:  Clin Gastroenterol Hepatol       Date:  2018-12-20       Impact factor: 11.382

Review 4.  Non-alcoholic fatty liver disease - A global public health perspective.

Authors:  Zobair M Younossi
Journal:  J Hepatol       Date:  2018-11-09       Impact factor: 25.083

Review 5.  Global burden of NAFLD and NASH: trends, predictions, risk factors and prevention.

Authors:  Zobair Younossi; Quentin M Anstee; Milena Marietti; Timothy Hardy; Linda Henry; Mohammed Eslam; Jacob George; Elisabetta Bugianesi
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2017-09-20       Impact factor: 46.802

6.  Risk of Hepatocellular Cancer in Patients With Non-Alcoholic Fatty Liver Disease.

Authors:  Fasiha Kanwal; Jennifer R Kramer; Srikar Mapakshi; Yamini Natarajan; Maneerat Chayanupatkul; Peter A Richardson; Liang Li; Roxanne Desiderio; Aaron P Thrift; Steven M Asch; Jinna Chu; Hashem B El-Serag
Journal:  Gastroenterology       Date:  2018-08-23       Impact factor: 22.682

7.  Predictors of advanced fibrosis in non-cirrhotic non-alcoholic fatty liver disease in Germany.

Authors:  Christian Labenz; Yvonne Huber; Eva Kalliga; Michael Nagel; Christian Ruckes; Beate K Straub; Peter R Galle; Marcus-Alexander Wörns; Quentin M Anstee; Detlef Schuppan; Jörn M Schattenberg
Journal:  Aliment Pharmacol Ther       Date:  2018-10-04       Impact factor: 8.171

8.  Cohort study of non-alcoholic fatty liver disease, NAFLD fibrosis score, and the risk of incident diabetes in a Korean population.

Authors:  Yoosoo Chang; Hyun-Suk Jung; Kyung Eun Yun; Juhee Cho; Yong Kyun Cho; Seungho Ryu
Journal:  Am J Gastroenterol       Date:  2013-10-08       Impact factor: 10.864

9.  Risks and clinical predictors of cirrhosis and hepatocellular carcinoma diagnoses in adults with diagnosed NAFLD: real-world study of 18 million patients in four European cohorts.

Authors:  Myriam Alexander; A Katrina Loomis; Johan van der Lei; Talita Duarte-Salles; Daniel Prieto-Alhambra; David Ansell; Alessandro Pasqua; Francesco Lapi; Peter Rijnbeek; Mees Mosseveld; Dawn M Waterworth; Stuart Kendrick; Naveed Sattar; William Alazawi
Journal:  BMC Med       Date:  2019-05-20       Impact factor: 8.775

  9 in total
  3 in total

1.  Incident Dementia in Elderly Patients with Nonalcoholic Fatty Liver Disease in Germany.

Authors:  Christian Labenz; Karel Kostev; Leonard Kaps; Peter R Galle; Jörn M Schattenberg
Journal:  Dig Dis Sci       Date:  2020-10-10       Impact factor: 3.199

Review 2.  Effects of Thyroid Hormones on Lipid Metabolism Pathologies in Non-Alcoholic Fatty Liver Disease.

Authors:  Chia-Jung Liao; Po-Shuan Huang; Hui-Tzu Chien; Tzu-Kang Lin; Chau-Ting Yeh; Kwang-Huei Lin
Journal:  Biomedicines       Date:  2022-05-25

3.  Nonalcoholic Fatty Liver Disease Increases the Risk of Anxiety and Depression.

Authors:  Christian Labenz; Yvonne Huber; Maurice Michel; Michael Nagel; Peter R Galle; Karel Kostev; Jörn M Schattenberg
Journal:  Hepatol Commun       Date:  2020-06-22
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.