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Genetic Risk Score in Diabetes Associated With Chronic Pancreatitis Versus Type 2 Diabetes Mellitus
- Goodarzi, Mark O;
- Nagpal, Tanvi;
- Greer, Phil;
- Cui, Jinrui;
- Chen, Yii-Der I;
- Guo, Xiuqing;
- Pankow, James S;
- Rotter, Jerome I;
- Alkaade, Samer;
- Amann, Stephen T;
- Baillie, John;
- Banks, Peter A;
- Brand, Randall E;
- Conwell, Darwin L;
- Cote, Gregory A;
- Forsmark, Christopher E;
- Gardner, Timothy B;
- Gelrud, Andres;
- Guda, Nalini;
- LaRusch, Jessica;
- Lewis, Michele D;
- Money, Mary E;
- Muniraj, Thiruvengadam;
- Papachristou, Georgios I;
- Romagnuolo, Joseph;
- Sandhu, Bimaljit S;
- Sherman, Stuart;
- Singh, Vikesh K;
- Wilcox, C Mel;
- Pandol, Stephen J;
- Park, Walter G;
- Andersen, Dana K;
- Bellin, Melena D;
- Hart, Phil A;
- Yadav, Dhiraj;
- Whitcomb, David C
- et al.
Published Web Location
https://doi.org/10.14309/ctg.0000000000000057Abstract
Introduction
Diabetes mellitus (DM) is a complication of chronic pancreatitis (CP). Whether pancreatogenic diabetes associated with CP-DM represents a discrete pathophysiologic entity from type 2 DM (T2DM) remains uncertain. Addressing this question is needed for development of specific measures to manage CP-DM. We approached this question from a unique standpoint, hypothesizing that if CP-DM and T2DM are separate disorders, they should be genetically distinct. To test this hypothesis, we sought to determine whether a genetic risk score (GRS) based on validated single nucleotide polymorphisms for T2DM could distinguish between groups with CP-DM and T2DM.Methods
We used 60 T2DM single nucleotide polymorphisms to construct a weighted GRS in 1,613 subjects from the North American Pancreatitis Study 2 and 2,685 subjects from the Multi-Ethnic Study of Atherosclerosis, all of European origin.Results
The mean GRS was identical between 321 subjects with CP-DM and 423 subjects with T2DM (66.53 vs 66.42, P = 0.95), and the GRS of both diabetic groups was significantly higher than that of nondiabetic controls (n = 3,554, P < 0.0001). Exploratory analyses attempting to enrich the CP-DM group for pancreatogenic diabetes, such as eliminating diabetes diagnosed before CP, requiring pancreas-specific comorbidities, or removing those with a family history of diabetes, did not improve the ability of the GRS to distinguish between CP-DM and T2DM.Discussion
Recognizing that we lacked a gold standard to define CP-DM, our study suggests that CP-DM may be a subtype of T2DM, a notion that should be tested in future, large prospective studies.Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
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