Pancreatic steatosis is not associated with impaired insulin secretion among individuals with diabetes

Aims We aimed to assess pancreatic and hepatic steatosis (PS/HS) association with residual insulin secretion and insulin resistance in individuals with diabetes. Methods Pancreatic/liver fat fractions (PFF/LFF) in magnetic resonance imaging (MRI) were used as a proxy for PS and HS in 170 participants. Insulin secretion was estimated by HOMA2-B, C-peptide response 6 minutes after an i.v. bolus of 0.5 mg glucagon (ΔC-Pe), and fasting proinsulin to C-peptide ratio (PI:C). Insulin resistance was estimated by HOMA2-IR, Adipo-IR and i.v. insulin (0.05 IU/kg) tolerance test. Results PFF did not correlate with measures of insulin secretion but it correlated with fasting indices of insulin resistance among women (HOMA2-IR, R = 0.26, p = 0.017; Adipo-IR, R = 0.29, p = 0.007). Both LFF and PFF correlated with BMI (R = 0.43 & R = 0.34, respectively, p < 0.001) but not with each other (R = 0.10, p = 0.215). Unlike PS, HS was associated with higher HOMA2-IR, Adipo-IR, HOMA2-B, PI:C and glucagon, after adjustment with confounders. Participants with PS without HS had lower fasting C-peptide, HOMA2-IR, HOMA2-B, Adipo-IR, glucagon and triglycerides (p < 0.05) compared to those having HS without PS. Cluster-based subgroups of diabetes did not differ in PF (p = 0.071). Conclusions Within this cohort, pancreatic fat was more strongly associated with adiposity than with the investigated measures of β-cell function or insulin resistance.

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Journal
The Journal of Clinical Endocrinology & Metabolism
Published
2026-10-15
DOI
https://doi.org/10.1210/clinem/dgag416
Primary Topic
Pancreatic function and diabetes
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article
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article

Pancreatic steatosis is not associated with impaired insulin secretion among individuals with diabetes

Kaj Lahti, Emma Ahlqvist, A LAITINEN, Liisa Hakaste et al.
The Journal of Clinical Endocrinology & Metabolism
Pancreatic function and diabetes
article

Pancreatic steatosis is not associated with impaired insulin secretion among individuals with diabetes

Kaj Lahti, Emma Ahlqvist, A LAITINEN, Liisa Hakaste, Annemari Käräjämäki, Aki Juhani Käräjämäki, Katarina Johansson, Samu H. Kurki, Jaakko Tuomilehto, Jenny Häggblom
article en

Abstract

Aims We aimed to assess pancreatic and hepatic steatosis (PS/HS) association with residual insulin secretion and insulin resistance in individuals with diabetes. Methods Pancreatic/liver fat fractions (PFF/LFF) in magnetic resonance imaging (MRI) were used as a proxy for PS and HS in 170 participants. Insulin secretion was estimated by HOMA2-B, C-peptide response 6 minutes after an i.v. bolus of 0.5 mg glucagon (ΔC-Pe), and fasting proinsulin to C-peptide ratio (PI:C). Insulin resistance was estimated by HOMA2-IR, Adipo-IR and i.v. insulin (0.05 IU/kg) tolerance test. Results PFF did not correlate with measures of insulin secretion but it correlated with fasting indices of insulin resistance among women (HOMA2-IR, R = 0.26, p = 0.017; Adipo-IR, R = 0.29, p = 0.007). Both LFF and PFF correlated with BMI (R = 0.43 & R = 0.34, respectively, p < 0.001) but not with each other (R = 0.10, p = 0.215). Unlike PS, HS was associated with higher HOMA2-IR, Adipo-IR, HOMA2-B, PI:C and glucagon, after adjustment with confounders. Participants with PS without HS had lower fasting C-peptide, HOMA2-IR, HOMA2-B, Adipo-IR, glucagon and triglycerides (p < 0.05) compared to those having HS without PS. Cluster-based subgroups of diabetes did not differ in PF (p = 0.071). Conclusions Within this cohort, pancreatic fat was more strongly associated with adiposity than with the investigated measures of β-cell function or insulin resistance.

The Journal of Clinical Endocrinology & Metabolism
University of Helsinki (FI), Lund University (SE), Helsinki University Hospital (FI), Turku University Hospital (FI), Vaasa Central Hospital (FI), Institute for Molecular Medicine Finland (FI), Folkhälsans Forskningscentrum (FI), Hospital District of Helsinki and Uusimaa (FI)
Openalex Percentile: Top 10%
Pancreatic function and diabetes
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