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Metabolic profiling of steatotic liver disease by fluorescence lifetime imaging microscopy

Abstract:
BACKGROUND: Metabolic dysfunction-associated steatotic liver disease is defined by hepatic lipid overload resulting in a metabolic shift and subsequent mitochondrial impairment. Diagnosis currently relies on tissue biopsy and non-invasive tests. However, these have drawbacks, including subjective histology scoring and relatively low sensitivity, highlighting the need for more robust and reproducible methodologies. METHODS: Fluorescence lifetime imaging microscopy visualises the metabolic state of cells by measuring the autofluorescence lifetime of metabolites, effectively avoiding the need for exogenous labelling. This technique was applied to a broad range of models, spanning from a hepatocyte cell line to a human tissue slice model, to investigate metabolic changes across disease conditions. RESULTS: Here, by utilising the metabolic dysfunction associated with steatotic liver disease, we propose a time-efficient method and introduce an index as a quantitative output to assess the metabolic state of human liver biopsies. The index encapsulates features of metabolic dysfunction that directly report on the disease state. These findings using lifetime imaging are substantiated by extensive analysis of structural and functional mitochondrial dysfunction. CONCLUSIONS: Measuring fluorescence lifetime can capture features of metabolic change that standard histological methods do not. Correlating the results to established techniques of histological evaluation highlights the potential of this method to enhance characterisation and speed of biopsy results in metabolically implicated diseases.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s43856-026-01605-7

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Institution:
University of Oxford
Role:
Author
ORCID:
0009-0007-0348-5938
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-7891-3825
More by this author
Institution:
University of Oxford
Role:
Author
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-0066-1784


Publisher:
Nature Research
Journal:
communications medicine More from this journal
Publication date:
2026-04-25
Acceptance date:
2026-04-10
DOI:
EISSN:
2730-664X
ISSN:
2730-664X


Language:
English
Keywords:
Pubs id:
2412353
Local pid:
pubs:2412353
Source identifiers:
W7155621474
Deposit date:
2026-04-30
ARK identifier:
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