1545-P: Characterization of Metabolic Defects in Pancreatic Cancer–Related Diabetes and Type 2 Diabetes in the DETECT Study

Diabetes due to pancreatic ductal adenocarcinoma (PDAC-D) is often difficult to clinically distinguish from type 2 diabetes (T2D) and both insulin resistance and reduced insulin secretion have been implicated in its pathophysiology. Although these metabolic defects are similar to those seen in T2D,...

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Veröffentlicht in:Diabetes (New York, N.Y.) N.Y.), 2023-06, Vol.72 (Supplement_1), p.1
Hauptverfasser: TOLEDO, FREDERICO G.S., LI, YISHENG, WANG, FUCHENCHU, YADAV, DHIRAJ, BELLIN, MELENA, CUSI, KENNETH, FISHER, WILLIAM E., KUDVA, YOGISH C., PARK, WALTER, CONSIDINE, ROBERT V., CHARI, SURESH T., GRAHAM, SARAH C., ANDERSEN, DANA K., ANN RINAUDO, JO, SERRANO, JOSE, GOODARZI, MARK O., HART, PHIL
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Sprache:eng
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Zusammenfassung:Diabetes due to pancreatic ductal adenocarcinoma (PDAC-D) is often difficult to clinically distinguish from type 2 diabetes (T2D) and both insulin resistance and reduced insulin secretion have been implicated in its pathophysiology. Although these metabolic defects are similar to those seen in T2D, the degree to which they relatively contribute to hyperglycemia in PDAC-D has not been established. Additionally, there is a lack of understanding of alpha cell function in PDAC-D. We sought to address these gaps in the DETECT study (NCT03460769). Adults with PDAC-D (n=28) or T2D (n=99) (diabetes diagnosis
ISSN:0012-1797
1939-327X
DOI:10.2337/db23-1545-P