Evidence map›Paper›PMID 41333005›Full record

ArticleInternational journal of hepatology2025

Impact of Age on Mortality and Decompensation Events in Patients With Liver Cirrhosis: A Multicenter, Propensity Score Matched Study.

Muhammad Shabbir, Miguel Salazar, Zeid Kayali

Abstract read
In one paragraph

Article in International journal of hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Muhammad ShabbirDepartment of Gastroenterology and Hepatology, University of California, Riverside, California, USA.ORCID https://orcid.org/0009-0004-1771-535X
Miguel SalazarDepartment of Gastroenterology and Hepatology, University of California, Riverside, California, USA.
Zeid KayaliDepartment of Gastroenterology and Hepatology, University of California, Riverside, California, USA.ORCID https://orcid.org/0009-0006-3893-6690

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The incidence of cirrhosis is increasing in the older population. Limited data are available on the disease progression and mortality in the older population with cirrhosis. This study is aimed at evaluating the impact of age at diagnosis on all-cause mortality and decompensation events in patients with liver cirrhosis. Methods: This is a retrospective cohort study utilizing TriNetX. ICD codes were used to identify individuals with the diagnosis of liver cirrhosis between the ages of 20 and 80. Patients with the diagnosis of congestive heart failure (CHF), end-stage renal disease (ESRD), chronic kidney disease (CKD) Stage IV and V, human immunodeficiency virus (HIV), malignant neoplasm, and psychoactive substance abuse were excluded from the analyses. Patients were divided into two cohorts: Cohort 1 included individuals with the diagnosis of liver cirrhosis between the ages of 51 and 80, and Cohort 2 included individuals with the diagnosis between the ages of 20 and 50. Statistical analyses were conducted using TriNetX Live. A 1:1 propensity score matching was performed for variables including race, gender, ethnicity, comorbidities, laboratory values for MELD 3.0, and etiology of liver cirrhosis. There were 70,983 patients in each cohort after matching. The primary outcome was all-cause mortality, and the composite outcome of decompensation events at 5- and 10-year intervals from the age of diagnosis of liver cirrhosis. Secondary outcomes included the risk of decompensation events, all-cause hospitalization at 5-year intervals, and a subgroup analysis of all-cause mortality and decompensation events among males and females. Results: Older age at diagnosis of liver cirrhosis was associated with increased all-cause mortality at 5 years (aOR 1.378, 95% CI: 1.335-1.422; Conclusion: Older age at diagnosis of liver cirrhosis is associated with increased all-cause mortality and key decompensation events. Certain conditions, like SBP and HRS, are more common in the younger population, likely due to increased alcohol abuse. Early detection of portal hypertension and early appropriate prophylaxis for variceal bleeding can provide benefit in this high-risk population, although the exact impact of such strategies needs further studies. Besides early recognition, alcohol remains a key factor that needs to be concomitantly addressed as it drives life-threatening decompensating events.

Indexed as

agingcirrhosisdecompensation eventsmortality

Identifiers

PMID41333005
PMCPMC12668842

What Socratic holds

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Registered trials

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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 Socratic graph.