Evidence map›Paper›PMID 41493845›Full record

ArticleHepatology communications2026

Low serum pseudocholinesterase levels are associated with mortality in patients with hepatocellular carcinoma.

Karina Sato-Espinoza, Marie-Lise Chrysostome, Robert A Vierkant, Hunter B Miller, Perapa Chotiprasidhi, Sumera I Ilyas, Lewis R Roberts, Kirk J Wangensteen

Abstract read
In one paragraph

Article in Hepatology communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Karina Sato-EspinozaDepartment of Medicine, Division of Gastroenterology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-1725-5865
Marie-Lise ChrysostomeDepartment of Medicine, Division of Gastroenterology, Mayo Clinic, Rochester, Minnesota, USA.
Robert A VierkantDepartment of Quantitative Health Sciences, Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota, USA.
Hunter B MillerDepartment of Medicine, Division of Gastroenterology, Mayo Clinic, Rochester, Minnesota, USA.
Perapa ChotiprasidhiDepartment of Medicine, Division of Gastroenterology, Mayo Clinic, Rochester, Minnesota, USA.
Sumera I IlyasDepartment of Medicine, Division of Gastroenterology, Mayo Clinic, Rochester, Minnesota, USA.
Lewis R RobertsDepartment of Medicine, Division of Gastroenterology, Mayo Clinic, Rochester, Minnesota, USA.
Kirk J WangensteenDepartment of Medicine, Division of Gastroenterology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0001-6042-6490

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is no consensus scoring system for staging and prognosis in hepatocellular carcinoma (HCC), which is the fourth leading cause of cancer-related mortality worldwide. Commonly used systems include the albumin-bilirubin (ALBI) score, the Barcelona staging classification (Barcelona Clinic Liver Cancer, BCLC), the Model for End-Stage Liver Disease (MELD), and the model to estimate survival in ambulatory HCC patients (MESIAH). Liver secretion of pseudocholinesterase (PCHE) has been linked to liver function but is poorly studied in the natural history of HCC. We evaluated whether serum PCHE level predicts HCC mortality and whether it enhances existing scoring systems.

methodsWe conducted a retrospective cohort study of individuals diagnosed with HCC. We collected variables including PCHE level, clinical data used in scoring systems, and time to mortality or liver transplant. We then analyzed the association between these variables and survival using Kaplan-Meier curves, Cox proportional hazards regression models, receiver operating characteristic (ROC) curves, and area under the curve (AUC) calculations.

resultsWe identified 420 individuals with HCC who were tested for PCHE levels, with a follow-up time of more than 20 years. There was a strong inverse relationship between PCHE level and overall survival, with the lowest quartile having high mortality and poor outcomes. Low PCHE level was associated with hepatitis C virus (HCV) infection, vascular invasion, poor liver function, and a high likelihood of liver transplant. In contrast, the highest quartile was associated with metabolic dysfunction-associated steatotic liver disease (MASLD) as the underlying cause. Compared with validated scoring systems, ALBI, BCLC, MELD 3.0, and MESIAH, the PCHE level was an independent predictor of mortality. PCHE levels could predict 3-month survival as well as or better than the other scoring systems, with an AUC of 0.74. PCHE level could also predict mortality related to hepatectomy. The addition of PCHE level to MESIAH and ALBI scoring systems could further improve the ability to predict overall mortality in HCC.

conclusionsPCHE is a reliable stand-alone biomarker of HCC prognosis. It is an independent predictor of mortality and can improve the accuracy of existing scoring systems. Improved risk stratification could improve outcomes by informing treatment decisions regarding hepatectomy or other interventions.

Indexed as

ButyrylcholinesteraseCarcinoma, HepatocellularLiver NeoplasmsAgedFemaleHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisProportional Hazards ModelsRetrospective StudiesROC CurveButyrylcholinesterasehepatectomyhepatitis C virushepatocellular carcinomaprognosispseudocholinesterase

Identifiers

PMID41493845
PMCPMC12772465

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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.