Steen Bønløkke Pedersen

Hepatic exposure of metformin in patients with non-alcoholic fatty liver disease

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

AIM: Metformin is first line treatment of type 2 diabetes mellitus and reduce cardiovascular events in patients with insulin resistance and type 2 diabetes. Target tissue for metformin action is suggested to be the liver, where metformin distribution depends on facilitated transport by polyspecific transmembrane organic cation transporters (OCTs). Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease in the western world with strong associations to insulin resistance and the metabolic syndrome but if NAFLD affects metformin biodistribution to the liver is not known. In this study, the primary aim was to investigate in vivo hepatic uptake of metformin dynamically in humans with variable degrees of liver affection. As secondary aim, we wished to correlate hepatic metformin distribution with OCT gene transcription determined in diagnostic liver biopsies.

METHODS: 18 patients with biopsy-proven NAFLD were investigated using 11C- metformin PET/CT technique. Gene transcripts of OCTs were determined by real time PCR.

RESULTS: We observed similar hepatic volume of distribution of metformin between patients with simple steatosis and NASH (Vd 2.38 ± 0.56 vs 2.10 ± 0.39, p=0.3). There was no association between hepatic exposure to metformin and the degree of inflammation or fibrosis, and no clear correlation between metformin distribution and OCT gene transcription.

CONCLUSION: Metformin is distributed to the liver in patients with NAFLD and the distribution is not impaired by inflammation or fibrosis. The findings implicate that metformin action in liver in patients with NAFLD may be preserved.

OriginalsprogEngelsk
TidsskriftBritish Journal of Clinical Pharmacology
Vol/bind85
Nummer8
Sider (fra-til)1761-1770
Antal sider10
ISSN0306-5251
DOI
StatusUdgivet - 2019

Se relationer på Aarhus Universitet Citationsformater

ID: 150092787