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Mapping of Metabolic Liver Functions in Patients With Non-alcoholic Fatty Liver Disease

Mapping of Metabolic Liver Functions in Patients With Non-alcoholic Fatty Liver Disease

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02488941
Enrollment
30
Registered
2015-07-02
Start date
2015-06-30
Completion date
2018-05-31
Last updated
2015-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-alcoholic Fatty Liver Disease

Keywords

Liver Function Tests, Blood Coagulation

Brief summary

Background: Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease in the western world and an important cause of morbidity and mortality including risk of cardiovascular disease. A ruling dogma is that a fatty liver is well-functioning. Recent studies imply the contrary but quantitative measurements of metabolic liver function have not been systematically investigated in NAFLD. Objectives: To study and quantify specific metabolic liver functions in varying degrees of NAFLD. Furthermore to map the coagulation system of patients with NAFLD. Methods: A human clinical study. Metabolic liver functions are studied by a series of functional tests (Galactose elimination capacity (GEC), Aminopyrine breath test (ABT), Indocyanine green plasma disappearance rate (ICG-PDR), Functional hepatic nitrogen clearance (FHNC)). Regional liver function evaluated by 2-\[18F\]fluoro-2-deoxy-D-galactose (FDGal) PET/CT is compared to fat infiltration assessed by Magnetic resonance imaging (MRI). Primary and secondary hemostasis, natural anti-coagulants and fibrinolysis are evaluated. Perspectives: To challenge the dogma, that hepatic metabolic function is not affected in NAFLD, improving the understanding of the relationship between the clinical degree of NAFLD, histology, metabolic functions, and imaging. Furthermore to disclose a proposed procoagulant imbalance in NAFLD.

Interventions

None listed

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 * Hepatic steatosis found on ultrasound * Clinical indication for liver biopsy (typically persistently elevated alanine transaminase (ALT) levels)

Exclusion criteria

* Other liver pathology * Alcohol consumption \> 20g/day * Chronic inflammatory disease, current infection or cancer * Diabetes mellitus type I, II or HbA1c ≥ 48 mmol/mol (6.5 %) * Prednisolone treatment within last 8 weeks * Pregnancy within last 12 months * Contraindication for MRI

Design outcomes

Primary

MeasureTime frameDescription
Regional fat infiltration assessed by MRIBaseline
Metabolic Liver Function assessed by FHNCBaseline
Metabolic Liver Function assessed by ABTBaseline
Metabolic Liver Function assessed by ICG-PDRBaseline
Regional metabolic liver function evaluated by FDGal PET/CTBaseline100 megabecquerel FDGal is injected intravenously in the beginning of a 20 min PET recording and 3D images of regional metabolic liver function expressed in terms of hepatic metabolic clearance of FDGal is created.
Metabolic Liver Function assessed by GECBaseline

Secondary

MeasureTime frame
FibrinolysisBaseline
Primary hemostasisBaseline
Secondary hemostasisBaseline
Natural anti-coagulantsBaseline

Countries

Denmark

Contacts

Primary ContactPeter Lykke Eriksen, MD
ple@clin.au.dk+45 7846 4076

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026