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MASLD Under the Umbrella of the Microbiota: A Narrative Review on Ecological Risk and Functional Transmissibility
Javier Crespo1,2, Paula Argos Vélez2, Marta Alonso-Peña2,3
1School of Medicine, University of Cantabria, 39005 Santander, Spain.
Abstract:
Metabolic dysfunction-associated steatotic liver disease (MASLD) is the leading cause of chronic liver disease worldwide, distinguished by pronounced clinical heterogeneity and a frequent dissociation between metabolic risk factors and the degree of hepatic injury. These observations, together with the limited contribution of genetic heritability, have prompted a re-evaluation of the traditional conceptual framework of the disease. In this context, the question has emerged as to whether MASLD could be, at least in part, a transmissible condition. While there is no evidence to suggest that MASLD is contagious in humans, as no data support person-to-person transmission, gnotobiotic animal studies demonstrate that human gut microbiota can transfer susceptibility to steatosis, inflammation, and systemic metabolic disturbances through immunometabolic mechanisms, independent of host genetics. In parallel, human studies involving microbiota-targeted interventions support the concept that the gut ecosystem is a modifiable determinant of metabolic and hepatic phenotypes. Crucially, these findings do not imply natural transmission of disease, but rather underscore the functional plasticity of microbiota-host interactions. This narrative review integrates epidemiological, experimental, and clinical data to explore the hypothesis that MASLD may be functionally transmissible. MASLD is increasingly recognized as an eco-biological disease, where liver disease risk is not only shaped by host genetics and environment, but also by the ecological configuration and functional outputs of the gut microbiome. This perspective redefines disease susceptibility as, in part, context-dependent and microbiota-mediated, without implying infectiousness in the traditional sense.
Insights
Metabolic dysfunction-associated steatotic liver disease (MASLD) may be functionally transmissible, not contagious. Gut microbiota transfer MASLD susceptibility via immunometabolic mechanisms, independent of host genetics.
Area of Science:
- Gastroenterology and Hepatology
- Microbiome Research
- Metabolic Disease Research
Background:
- Metabolic dysfunction-associated steatotic liver disease (MASLD) is a global health concern with variable clinical presentations.
- Limited genetic heritability suggests environmental and other factors influence MASLD development.
- The traditional view of MASLD is being challenged, prompting investigation into novel transmission pathways.
Purpose of the Study:
- To explore the hypothesis that MASLD might be functionally transmissible.
- To integrate epidemiological, experimental, and clinical data regarding MASLD's eco-biological nature.
- To re-evaluate MASLD susceptibility in the context of gut microbiome interactions.
Main Methods:
- Literature review integrating epidemiological, experimental, and clinical data.
- Analysis of gnotobiotic animal studies on gut microbiota transfer.
- Examination of human studies on microbiota-targeted interventions.
Main Results:
- Human gut microbiota can transfer MASLD susceptibility (steatosis, inflammation, metabolic disturbances) in animal models, independent of host genetics.
- Gut microbiome interventions demonstrate its role as a modifiable determinant of metabolic and hepatic health.
- MASLD is increasingly viewed as an eco-biological disease influenced by the gut microbiome's ecological state and function.
Conclusions:
- MASLD susceptibility is partly context-dependent and mediated by the gut microbiome.
- While not contagious, MASLD exhibits functional transmissibility through microbiota-host interactions.
- This perspective highlights the gut microbiome as a critical factor in MASLD pathogenesis and risk.

