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"Bernd Schnabl"

Review

Burden of malnutrition and sarcopenia in patients with cirrhosis: pathophysiology, assessment, and management
Takao Miwa, Masahito Shimizu, Bernd Schnabl
Clin Mol Hepatol 2026;32(2):487-510.
Published online December 16, 2025
DOI: https://doi.org/10.3350/cmh.2025.1126
Malnutrition and sarcopenia are highly prevalent and robustly associated with reduced quality of life, disease progression, and poor outcomes, including complications and mortality, in patients with cirrhosis. Their pathophysiology is multifactorial, involving inadequate dietary intake and malabsorption, impaired liver functional reserves, altered energy, protein, and ammonia metabolism, systemic inflammation, hormonal dysregulation, and lifestyle or environmental influences. Despite extensive research, unresolved issues remain regarding optimal diagnostic criteria, as current approaches vary and lack global standardization. Regarding the diagnostic criteria for malnutrition, the usefulness of the Global Leadership Initiative on Malnutrition criteria has been proposed by international nutrition societies. However, evidence supporting their applicability in hepatology remains insufficient. For sarcopenia, differences in disease concept and diagnostic methods among societies indicate that no unified diagnostic standard exists, and clinicians should approach diagnosis with an understanding of the strengths and limitations of each method. Nutritional strategies emphasize adequate energy and protein intake, late evening snacks, and branched-chain amino acid supplementation, while deficiencies in micronutrients require tailored replacement. Nutritional therapy alone has limited effect on sarcopenia, but when combined with exercise it improves muscle mass, physical performance, and outcomes. Comprehensive approaches integrating optimized nutrition, micronutrient support, and structured exercise are essential to alleviate the burden of malnutrition and sarcopenia and to improve prognosis in patients with cirrhosis. This review addresses malnutrition and sarcopenia in cirrhosis by highlighting their prevalence, pathophysiology, clinical impact, and approaches for screening and diagnosis, and by emphasizing personalized nutritional, pharmacological, and exercise interventions to improve patient outcomes.

Citations

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  • Letter: Amino Acid Imbalance Is an Independent Factor for Mortality in Patients With Liver Cirrhosis. Authors' reply
    Yuki Utakata, Takao Miwa, Shinji Unome, Naoya Masuda, Mikita Oi, Masashi Aiba, Kenji Imai, Koji Takai, Makoto Shiraki, Naoki Katsumura, Masahito Shimizu
    Alimentary Pharmacology & Therapeutics.2026; 63(9): 1329.     CrossRef
  • Covert hepatic encephalopathy as a multi-organ syndrome: the gut–liver–muscle–brain axis, diagnosis, treatment, and multidisciplinary care
    Takao Miwa, Cynthia L. Hsu, Masahito Shimizu, Patricia P. Bloom, Bernd Schnabl
    Journal of Gastroenterology.2026; 61(9): 1217.     CrossRef
  • Nutrition in cirrhosis: bridging guidelines and practice in hepatic disease
    Jennifer Jin, Puneeta Tandon, Leah Gramlich
    Current Opinion in Clinical Nutrition & Metabolic Care.2026; 29(5): 494.     CrossRef
  • Letter: Major Adverse Outcomes in Steatotic Liver Disease Subtypes—From Etiological Classification to Biological Phenotyping: Authors' Reply
    Takao Miwa, Bernd Schnabl
    Alimentary Pharmacology & Therapeutics.2026; 64(8): 1171.     CrossRef
  • A 12-week home-based exercise program with nutritional guidance is associated with improved functional capacity in chronic liver disease
    Shinji Unome, Takao Miwa, Yoshihiko Atago, Satomi Nakashima, Kayoko Nishimura, Shinya Hiraoka, Masashi Aiba, Kenji Imai, Yohei Shirakami, Koji Takai, Takaaki Aoki, Masahito Shimizu
    Clinical Nutrition ESPEN.2026; 75: 105073.     CrossRef
  • Editorial: Amino Acid Imbalance and Prognosis in Cirrhosis. Authors' Reply
    Takao Miwa, Yuki Utakata, Masahito Shimizu
    Alimentary Pharmacology & Therapeutics.2026; 64(9): 1314.     CrossRef
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Special topic: Alcoholic liver diseases
The 14th International Symposium on Alcoholic Liver and Pancreatic Diseases and Cirrhosis (ISALPDC)

Alcohol-related liver disease

From intestinal dysbiosis to alcohol-associated liver disease
Beatriz Garcia Mendes, Bernd Schnabl
Clin Mol Hepatol 2020;26(4):595-605.
Published online September 11, 2020
DOI: https://doi.org/10.3350/cmh.2020.0086
Alcohol-associated intestinal dysbiosis and bacterial overgrowth can lead to a dysregulation of tryptophan metabolism and lower production of indoles. Several of these indole derivatives are aryl hydrocarbon receptor ligands that, in turn, are involved in antimicrobial defense via induction of interleukin-22 (IL-22). IL-22 increases the expression of intestinal regenerating islet-derived 3 (Reg3) lectins, which maintain low bacterial colonization of the inner mucus layer and reduce bacterial translocation to the liver. Chronic alcohol consumption is associated with reduced intestinal expression of Reg3β and Reg3γ, increased numbers of mucosa-associated bacteria and bacterial translocation. Translocated microbial products and viable bacteria reach the liver and activate the innate immune system. Release of inflammatory molecules promotes inflammation, contributes to hepatocyte death and results in a fibrotic response. This review summarizes the mechanisms by which chronic alcohol intake changes the gut microbiota and contributes to alcohol-associated liver disease by changing microbial-derived metabolites.

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  • 45 Web of Science
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