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
Open accessAbstract
BACKGROUND: Non-alcoholic fatty liver disease (NAFLD) is a common condition that progresses in some patients to steatohepatitis (NASH), cirrhosis and hepatocellular carcinoma (HCC). Here we used healthcare records of 18 million adults to estimate risk of acquiring advanced liver disease diagnoses in patients with NAFLD or NASH compared to individually matched controls. METHODS: Data were extracted from four European primary care databases representing the UK, Netherlands, Italy and Spain. Patients with a recorded diagnosis of NAFLD or NASH (NAFLD/NASH) were followed up for incident cirrhosis and HCC diagnoses. Each coded NAFLD/NASH patient was matched to up to 100 "non-NAFLD" patients by practice site, gender, age ± 5 years and visit recorded within ± 6 months. Hazard ratios (HR) were estimated using Cox models adjusted for age and smoking status and pooled across databases by random effects meta-analyses. RESULTS: Out of 18,782,281 adults, we identified 136,703 patients with coded NAFLD/NASH. Coded NAFLD/NASH patients were more likely to have diabetes, hypertension and obesity than matched controls. HR for cirrhosis in patients compared to controls was 4.73 (95% CI 2.43-9.19) and for HCC, 3.51 (95% CI 1.72-7.16). HR for either outcome was higher in patients with NASH and those with high-risk Fib-4 scores. The strongest independent predictor of a diagnosis of HCC or cirrhosis was baseline diagnosis of diabetes. CONCLUSIONS: Real-world population data show that recorded diagnosis of NAFLD/NASH increases risk of life-threatening liver outcomes. Diabetes is an independent predictor of advanced liver disease diagnosis, emphasising the need to identify specific groups of patients at highest risk.
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T2D was the strongest independent risk factor for the development of HCC in a large European population-based study that included 136,703 individuals with MASLD and a low prevalence of advanced fibrosis as assessed by FIB-4.
“T2D was also found to be the strongest independent risk factor for the development of HCC in a large European population-based study that included 136,703 individuals with MASLD and a low prevalence of advanced fi brosis as assessed by FIB-4.”
From EASL-EASD-EASO Clinical Practice Guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD). (2024) · cites this paper as [56]
The Discussion identifies diabetes as the strongest independent risk factor for a new cirrhosis or HCC diagnosis, and the Abstract reports 136,703 patients with coded NAFLD/NASH. Results Table 2 shows that only 4.7% of patients with available FIB-4 scores were in the high-risk category, but FIB-4 was calculable for only 63,971 patients (Results, ‘Fib-4 predicts disease progression’). The paper does not establish a low prevalence of advanced fibrosis across all 136,703 patients, and it records diabetes without specifying T2D. (LLM, conf=0.86)
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References 30 · Cited by 317
- Authors
- Alexander, M., Loomis, A. K., van der Lei, J., Duarte-Salles, T., Prieto-Alhambra, D., Ansell, D., Pasqua, A., Lapi, F., Rijnbeek, P., Mosseveld, M., Waterworth, D. M., Kendrick, S., Sattar, N., & Alazawi, W.
- Affiliations
- GlaxoSmithKline (United Kingdom) (GB)
- Pfizer (United States) (US)
- IQVIA (United Kingdom) (GB)
- Erasmus MC (NL)
- GlaxoSmithKline (United States) (US)
- University of Glasgow (GB)
- Queen Mary University of London (GB)
- Corresponding author
- Alazawi, William
- ORCID
- Venue
- BMC Medicine
- Published
- 2019-05-20
- Volume
- 17
- Issue
- 1
- Pages
- 95-95
- ISSN
- 1741-7015 (ISSN-L)
- PMC
- PMC6526616
- OpenAlex
- W2947312239
- Cited by
- 317
- References
- 30
- Citations by year
- 2026: 19 · 2025: 35 · 2024: 52 · 2023: 74 · 2022: 44 · 2021: 47 · 2020: 40 · 2019: 5 · 2013: 1
- FWCI
- 25.87
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- BMC Medicine (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion, other-oa)
- ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (acceptedVersion, cc-by-sa)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion, other-oa)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion, other-oa)
- Queen Mary Research Online (Queen Mary University of London) (submittedVersion, cc-by)
- Funders
- Innovative Medicines Initiative (115372)
- Medical Research Council (MR/N00308X/1)
- Topics
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
- Health Sciences › Medicine › Pathology and Forensic Medicine › Alcohol Consumption and Health Effects
- Keywords
- non-alcoholic fatty liver disease, nonalcoholic steatohepatitis, liver cirrhosis, hepatocellular carcinoma, diabetes mellitus, FIB-4, obesity, hypertension, clinical predictors, primary care records
- MeSH terms
- Adult, Aged, Europe, Female, United Kingdom, Carcinoma, Hepatocellular, Humans, Italy, Liver Cirrhosis, Liver Neoplasms, Male, Middle Aged, Netherlands, Prognosis, Risk Factors, Spain, Cohort Studies, Case-Control Studies, Non-alcoholic Fatty Liver Disease
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