본문으로 건너뛰기
← 뒤로

Diabetes secondary to chronic pancreatitis and pancreatic cancer: Observations from the Consortium for the Study of Chronic Pancreatitis, Diabetes, and Pancreatic Cancer (CPDPC).

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2026

Hart PA, Andersen DK, Bellin MD, Kudva YC, Toledo FGS, Goodarzi MO

📝 환자 설명용 한 줄

Diabetes secondary to diseases of the exocrine pancreas, including chronic pancreatitis (CP) and pancreatic cancer (PDAC), is easily confused with type 2 diabetes (T2D).

이 논문을 인용하기

BibTeX ↓ RIS ↓
APA Hart PA, Andersen DK, et al. (2026). Diabetes secondary to chronic pancreatitis and pancreatic cancer: Observations from the Consortium for the Study of Chronic Pancreatitis, Diabetes, and Pancreatic Cancer (CPDPC).. Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]. https://doi.org/10.1016/j.pan.2026.04.001
MLA Hart PA, et al.. "Diabetes secondary to chronic pancreatitis and pancreatic cancer: Observations from the Consortium for the Study of Chronic Pancreatitis, Diabetes, and Pancreatic Cancer (CPDPC).." Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2026.
PMID 41956866

Abstract

Diabetes secondary to diseases of the exocrine pancreas, including chronic pancreatitis (CP) and pancreatic cancer (PDAC), is easily confused with type 2 diabetes (T2D). Misdiagnosis as T2D is common due to poor understanding of the underlying pathophysiology of these diabetes subtypes. In this review, we highlight contributions from our research group to further characterize the distinctions between CP-DM and PDAC-DM as it relates to postprandial response to pancreatic polypeptide (PP) and key metabolic alterations compared to T2D. In general, the PP response is blunted, and there is relatively lower insulin secretion, higher insulin sensitivity, and alpha cell dysregulation in CP-DM and PDAC when compared to T2D. Additionally, we provide updates regarding ongoing work to use clinical and genetic data to model the prediction of incident CP-DM. Lastly, we identify remaining knowledge gaps to further improve the diagnosis and treatment of type 3c diabetes.

같은 제1저자의 인용 많은 논문 (1)