Lipids & metabolic liver disease

Hepatic steatosis is associated with impaired hepatic glucose uptake under hyperglycemic conditions, a dynamic whole-body 18F-FDG PET approach

Diabetes Res Clin PractPublished Cross-sectional study

Authors' conclusion

We show that another aspect of hepatic insulin resistance, namely the ability of insulin to stimulate hepatic glucose uptake under hyperglycemic conditions, is negatively associated with hepatic fat content. This suggests that hepatic glucose uptake is another factor that may be important in Metabolic dysfunction Associated Steatotic Liver Disease (MASLD) and the risk for type 2 diabetes, and needs further investigation.

Study context

Population
Participants with a range of liver fat content (0.9–18 %) assessed by 1H-MRS
Participants
15 participants
Outcome
Hepatic glucose uptake under hyperglycemia and hyperinsulinemia in relation to hepatic steatosis
Methodological detailsdynamic whole-body 18F-FDG PET, two-step euglycemic-hyperinsulinemic clamp, hyperglycemic-hyperinsulinemic clamp
  • Dynamic whole-body 18F-FDG PET
  • Two-step euglycemic-hyperinsulinemic clamp
  • Hyperglycemic-hyperinsulinemic clamp

Main finding

As reported in the abstract

Hepatic glucose uptake vs liver fat content (hyperglycemic-hyperinsulinemic clamp)

Strong inverse correlation of hepatic glucose uptake with liver fat content

r = −0.756

p < 0.001

Observational data: associations, not effects.

Further findings

Hepatic glucose uptake vs insulin-stimulated endogenous glucose production (EGP) suppression

Correlation of hepatic glucose uptake with insulin-stimulated EGP suppression
r = 0.616, p = 0.015

Adipose tissue insulin sensitivity

Negatively associated with liver fat content and positively with hepatic, skeletal muscle and adipose tissue glucose uptake

Original publication

Hepatic steatosis is associated with impaired hepatic glucose uptake under hyperglycemic conditions, a dynamic whole-body 18F-FDG PET approach. Diabetes Res Clin Pract. Published 29 May 2025. doi:10.1016/j.diabres.2025.112288

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.