Evidence map›Paper›PMID 41523421›Full record

ArticleCureus2025

Dysgeusia-Driven Nutritional Decline in Cirrhosis: A Case of Autoimmune Hepatitis and Primary Biliary Cholangitis.

Newton Rahming, Stephan Corcho, Oluwasegun Olowe, Leila Falls, Murali K Manikkavelu, Frederick Tiesenga

Abstract readCase Reports
In one paragraph

Article in Cureus, 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

6 authors.

Newton RahmingSurgery, Caribbean Medical University, Willemstad, CUW.
Stephan CorchoSurgery, St George's University, West Indies, GRD.
Oluwasegun OloweSurgery, St George's University, West Indies, GRD.
Leila FallsSurgery, Windsor University School of Medicine, West Indies, KNA.
Murali K ManikkaveluGeneral Surgery, American University of Antigua, St. John, ATG.
Frederick TiesengaGeneral Surgery, West Suburban Medical Center, Chicago, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysgeusia, or altered taste perception, is characterized by metallic, sweet, sour, or bitter sensations that can significantly impair oral intake and contribute to malnutrition, particularly in patients with chronic illness. This report describes a 75-year-old woman with decompensated cirrhosis secondary to autoimmune hepatitis and primary biliary cholangitis (PBC), who presented with a persistent metallic taste and an unintentional 25-pound weight loss over three months. Dysgeusia began shortly after the initiation of mycophenolate mofetil (MMF) and led to reduced caloric intake, early satiety, and progressive sarcopenia. Laboratory evaluation demonstrated pancytopenia, hypoalbuminemia, and hyperbilirubinemia, consistent with decompensated cirrhosis. Zinc levels were normal (82 mcg/dL), and the patient remained compliant with supplementation, making isolated zinc deficiency an unlikely cause of her symptoms. Longitudinal assessment demonstrated parallel declines in weight, nutritional intake, and hepatic synthetic function. Imaging and alpha-fetoprotein (AFP) testing excluded hepatocellular carcinoma, and no acute complications of cirrhosis were identified. The overall clinical picture suggested that dysgeusia-associated malnutrition, likely exacerbated by medication exposure in the context of portal hypertension, contributed substantially to hepatic decompensation. This case underscores the overlooked impact of taste disturbances in cirrhotic patients and highlights the importance of early identification, medication review, and nutritional intervention to mitigate malnutrition-related complications.

Indexed as

autoimmune hepatitischild-pugh scorecirrhosisdysgeusiahepatic decompensationmalnutritionmycophenolate mofetilprimary biliary cholangitistaste disorderszinc deficiency

Identifiers

PMID41523421
PMCPMC12782885

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