Pancreatic cancer-related diabetes and type 2 diabetes differ in multiple aspects of glucose homeostasis

Diabetologia. 2025 Dec;68(12):2854-2866. doi: 10.1007/s00125-025-06543-y. Epub 2025 Sep 24.

Abstract

Aims/hypothesis: Pancreatic ductal adenocarcinoma-related diabetes mellitus (PDAC-DM) is a paraneoplastic syndrome with a poorly understood pathophysiology. PDAC-DM is often clinically confused with type 2 diabetes, resulting in delayed cancer detection and poorly individualised hyperglycaemia treatment. We investigated whether these forms of diabetes can be distinguished at the metabolic level.

Methods: Adults with either cancer treatment-naive PDAC-DM (n=28) or type 2 diabetes (n=97), and with diabetes onset within 3 years, underwent mixed-meal tolerance tests to investigate glucose metabolism. Outcomes included insulin sensitivity (Matsuda index), insulin secretion (insulinogenic index), beta cell function (oral disposition index), insulin clearance, and postprandial glucagon, glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP) responses.

Results: Compared with type 2 diabetes, individuals with PDAC-DM showed ~2.5-fold greater insulin sensitivity, ~81% lower insulin secretion and ~40% lower beta cell function. Insulin clearance was higher in the PDAC-DM group than the type 2 diabetes group, with and without adjustment for insulin sensitivity. Glucagon and GLP-1 levels increased after a meal in both groups, but levels were higher in the PDAC-DM group. GIP levels were similar between groups. The metabolic differences between groups persisted after adjustment for age, sex and BMI.

Conclusions/interpretation: PDAC-DM and type 2 diabetes are metabolically distinct, with different defects responsible for hyperglycaemia. PDAC-DM is characterised predominantly by insulin deficiency and displays higher insulin sensitivity than type 2 diabetes. There are also differences in alpha cell regulation and insulin clearance compared with type 2 diabetes. These findings identify biological characteristics that may have implications for individualised treatment of PDAC-DM and guide diagnostic biomarker discovery for early PDAC diagnosis.

Keywords: Diabetes; Insulin secretion; Pancreatic cancer; Pancreatic ductal adenocarcinoma.

MeSH terms

  • Adult
  • Aged
  • Blood Glucose* / metabolism
  • Carcinoma, Pancreatic Ductal* / complications
  • Carcinoma, Pancreatic Ductal* / metabolism
  • Diabetes Mellitus, Type 2* / blood
  • Diabetes Mellitus, Type 2* / metabolism
  • Female
  • Gastric Inhibitory Polypeptide / metabolism
  • Glucagon / blood
  • Glucagon / metabolism
  • Glucagon-Like Peptide 1 / blood
  • Glucagon-Like Peptide 1 / metabolism
  • Glucose Tolerance Test
  • Homeostasis / physiology
  • Humans
  • Insulin / metabolism
  • Insulin Resistance / physiology
  • Insulin Secretion
  • Insulin-Secreting Cells / metabolism
  • Male
  • Middle Aged
  • Pancreatic Neoplasms* / complications
  • Pancreatic Neoplasms* / metabolism

Substances

  • Insulin
  • Blood Glucose
  • Glucagon-Like Peptide 1
  • Glucagon
  • Gastric Inhibitory Polypeptide