Evidence map›Paper›PMID 40419118›Full record

ArticleJournal of hepatology2025

Cause-specific mortality in patients with steatotic liver disease in the United States.

Pedro Ochoa-Allemant, Rebecca A Hubbard, David E Kaplan, Marina Serper

Abstract read
In one paragraph

Article in Journal of hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Cardiometabolic Risk Factors Impair Recompensation and Survival in Alcohol-Associated Liver Disease.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2026
    Observational
  6. Review
  7. Selecting Pharmacologic Interventions for MASH.Digestive diseases and sciences · 2026
    Review
  8. Review
  9. Steatosis liver index: A validated machine learning model using clinical data distinguishes steatotic liver disease phenotypes.Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver · 2026
    Article
  10. Review
  11. Time-Varying Impact of Steatosis and Alcohol on Mortality: A Marginal Structural Model of the Canadian Longitudinal Study on Aging.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. The Implications of Lipoprotein(a) in MASLD.Current cardiology reports · 2026
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Pedro Ochoa-AllemantDivision of Gastroenterology and Hepatology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: Pedro.OchoaAllemant@pennmedicine.upenn.edu.
Rebecca A HubbardDepartment of Biostatistics, Brown University School of Public Health, Providence, RI, USA.
David E KaplanDivision of Gastroenterology and Hepatology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Gastroenterology Section, Department of Medicine, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.
Marina SerperDivision of Gastroenterology and Hepatology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Gastroenterology Section, Department of Medicine, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA; Leonard Davis Institute of Health Economics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Funding

CLINICAL EPIDEMIOLOGY TRAINING IN GASTROENTEROLOGYT32DK007740 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI James D Lewis · 1997 to 2026
$9.2M
Cognitive Function, Self-Management, and Health Outcomes among Liver Transplant Recipients: the LivCog CohortR01DK132138 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Marina Serper · 2022 to 2026
$3.5M
Technology Enabled Strategies to Promote Treatment Adherence in Liver Transplant: The TEST TrialR01DK131547 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Marina Serper · 2022 to 2026
$3.4M
2/4-American Consortium of Early Liver Transplantation-Prospective Alcohol-associated liver disease Cohort Evaluation (ACCELERATE-PACE)R01AA030963 · NIAAA · UNIVERSITY OF PENNSYLVANIA · PI Marina Serper · 2023 to 2026
$1.6M
NIAAA NIH HHS R01 AA030963NIDDK NIH HHS R01 DK131547NIDDK NIH HHS R01 DK132138NIDDK NIH HHS T32 DK007740
6 · The paper itself

Abstract

BACKGROUND &

aimsCauses of death across steatotic liver disease (SLD) subtypes remain incompletely characterized in routine clinical practice. We aimed to quantify and compare cause-specific mortality in patients with SLD.

methodsWe conducted a retrospective cohort study of adults with imaging-confirmed hepatic steatosis receiving outpatient care in the national Veterans Health Administration (2010-2021). The primary exposure was SLD subtype, including metabolic dysfunction-associated steatotic liver disease (MASLD), alcohol-associated liver disease (ALD), and their intersection (MetALD). The primary outcome was cause-specific mortality, stratified by baseline cirrhosis.

resultsAmong 366,433 adults (mean age, 60.5 years; 7.7% female; 67.6% non-Hispanic White), 77.9% had MASLD, 17.5% had MetALD, and 4.6% had ALD. Over a median follow-up of 5.4 years, the 10-year cumulative incidences of cardiovascular disease (CVD)- and extrahepatic cancer-related deaths among patients without cirrhosis were 8.1% and 7.5% for MASLD, 7.5% and 7.4% for MetALD, and 8.1% and 7.4% for ALD. Among patients with cirrhosis, the 10-year cumulative incidences of liver- and CVD-related deaths were 9.2% and 17.3% for MASLD, 17.7% and 13.0% for MetALD, and 22.1% and 11.5% for ALD. Compared with non-cirrhotic MASLD (0.04 per 100 person-years), liver-related mortality was higher for MetALD (0.19 per 100 person-years; hazard ratio 3.38; 95% CI 3.02-3.78) and highest for ALD (0.40 per 100 person-years; hazard ratio 6.99; 95% CI 6.08-8.04). This progressive increase persisted in cirrhosis but was less pronounced.

conclusionsCVD and extrahepatic cancer were leading causes of death across SLD subtypes in the absence of cirrhosis, while liver- and CVD-related deaths predominated in patients with cirrhosis. MetALD and ALD were associated with progressively higher risks of liver-related mortality compared with MASLD. These findings underscore the need for integrated strategies addressing alcohol use, cardiovascular risk, and cancer screening to reduce preventable deaths. IMPACT AND IMPLICATIONS: Causes of death across the steatotic liver disease (SLD) spectrum remain incompletely characterized in routine clinical settings. In this large nationwide cohort study, we evaluated cause-specific mortality in patients with MASLD, MetALD, and ALD. We showed that cardiovascular disease and extrahepatic cancer were the primary causes of death in patients without cirrhosis across SLD subtypes, while liver disease and cardiovascular disease were predominant in those with cirrhosis. Importantly, MetALD and ALD were associated with progressively increasing risks of liver-related mortality compared to MASLD. Our findings highlight the need for integrated care models that simultaneously address cardiovascular risk factors, implement strategies to reduce alcohol consumption, and promote cancer screening to mitigate preventable deaths in SLD.

Indexed as

Cardiovascular DiseasesFatty LiverAgedCause of DeathFemaleHumansLiver CirrhosisMaleMiddle AgedRetrospective StudiesRisk FactorsUnited StatesAlcohol-associated liver diseaseMASLDmetabolic dysfunction and alcohol-associated liver diseasemetabolic dysfunction-associated steatotic liver diseaseMetALD

Identifiers

PMID40419118
PMCPMC12227146

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.