Risk for hepatic and extra-hepatic outcomes in nonalcoholic fatty liver disease
Open accessAbstract
Nonalcoholic fatty liver disease (NAFLD) is defined by presence of steatosis in more than 5% of liver cells. The gold standard for diagnosis is liver biopsy, but this is seldom achieved due to costs and risk for side effects, and that is why the diagnosis is mostly made based on a combination of radiology and exclusion of other liver diseases. Disease severity staging can be noninvasively achieved with radiological exams such as elastography or blood-based markers that usually have lower sensitivity and specificity. NAFLD is today the most common chronic liver disease globally with a prevalence estimated to be 25%. Fortunately, for many persons NAFLD is an incidental finding with a good prognosis. Whilst a major focus has been on liver-related outcomes in NAFLD, there has recently been an increased interest in extrahepatic consequences of NAFLD. The most commonly studied outcomes include cardiovascular disease and cancer. The risk of adverse outcomes generally differs according to the baseline fibrosis stage. There is a five-time higher risk of liver-related events in NAFLD patients with fibrosis stage 3 as compared to those with no or little fibrosis. Meanwhile, the presence of nonalcoholic steatohepatitis (NASH) does not seem to influence prognosis in addition to fibrosis stage. Patients with NAFLD clearly have a higher risk for cardiovascular outcomes compared to the general population, with a recent meta-analysis indicating a 37% increased hazard for cardiovascular events as opposed to individuals without NAFLD. The risk of liver cancer is increased, which is mostly driven by presence of cirrhosis, but the increased risk is present also in patients without cirrhosis, and to a greater extent than for other chronic liver disease. Around one-third of patients with NAFLD and liver cancer do not have cirrhosis. Additionally, the risk of extrahepatic malignancies is thought to be moderately increased, with most evidence for a link between NAFLD and colorectal cancer where the risk is approximately 50% higher compared to patients without NAFLD. A particularly salient point is if NAFLD can be considered an independent risk factor for outcomes. Many studies have not been able to adjust for key confounders, or suffer from different forms of bias. The clinical problem is nevertheless to identify persons with an increased risk for adverse hepatic and extrahepatic outcomes. We here discuss the evidence linking NAFLD to severe hepatic and extrahepatic outcomes.
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The risk of liver-related outcomes, i.e. mortality, hospitalisation, and HCC, is increased with worsening of liver fibrosis.
“and the risk of liver-related outcomes, i.e. mortality, hospitalisation, and HCC is increased with worsening of liver fi brosis. 23”
From EASL-EASD-EASO Clinical Practice Guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD). (2024) · cites this paper as [23]
The section “Fibrosis as the strongest predictor of end-stage liver disease” reports a stepwise increase in liver-related events with fibrosis stage and an association with mortality. The “Hepatocellular carcinoma” section explicitly says HCC risk increases with fibrosis stage. Our copy does not specifically establish that liver-related hospitalisation increases as fibrosis worsens. (LLM, conf=0.85)
Experimental — accuracy not yet measuredThe stage of liver fibrosis and persistently elevated liver enzymes are associated with liver-related outcomes.
“the stage of liver fi brosis and persistently elevated liver enzymes are associated with liver-related outcomes”
From EASL-EASD-EASO Clinical Practice Guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD). (2024) · cites this paper as [23]
The section “Fibrosis as the strongest predictor of end-stage liver disease” reports a strong association between fibrosis stage and liver-related events in NAFLD. Our copy does not report that persistently elevated liver enzymes are associated with those outcomes; elevated enzymes appear only in cited study titles. (LLM, conf=0.86)
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References 121 · Cited by 52
Research works printed but not linked: 7
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- Authors
- Hagström, H., Kechagias, S., & Ekstedt, M.
- Affiliations
- Karolinska University Hospital (SE)
- Linköping University (SE)
- Corresponding author
- Hagström, Hannes
- Venue
- Journal of Internal Medicine
- Publisher
- Wiley
- Published
- 2021-07-06
- Volume
- 292
- Issue
- 2
- Pages
- 177-189
- ISSN
- 0954-6820 (ISSN-L)
- 1365-2796
- OpenAlex
- W3170703018
- Cited by
- 52
- References
- 121
- Citations by year
- 2026: 14 · 2025: 15 · 2024: 11 · 2023: 4 · 2022: 6 · 2021: 2
- FWCI
- 0.88
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Internal Medicine (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Pathology and Forensic Medicine › Alcohol Consumption and Health Effects
- Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
- Keywords
- non-alcoholic fatty liver disease, nonalcoholic steatohepatitis, liver fibrosis, cardiovascular disease, hepatocellular carcinoma, extrahepatic malignancies, colorectal cancer, liver cirrhosis, disease severity staging
- MeSH terms
- Fibrosis, Humans, Liver, Liver Cirrhosis, Liver Neoplasms, Non-alcoholic Fatty Liver Disease
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