Rapid Elevation in CMPF May Act As a Tipping Point in Diabetes Development
Author(s) -
Ying Liu,
Kacey J. Prentice,
Judith A. Eversley,
Cheng Hu,
Battsetseg Batchuluun,
Katherine Leavey,
Jakob Bondo Hansen,
David Wei,
Brian Cox,
Feihan F. Dai,
Weiping Jia,
Michael B. Wheeler
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.02.079
Subject(s) - prediabetes , medicine , diabetes mellitus , endocrinology , proinsulin , type 2 diabetes , insulin , lipotoxicity , insulin resistance
Prediabetes, a state of mild glucose intolerance, can persist for years before a sudden decline in beta cell function and rapid deterioration to overt diabetes. The mechanism underlying this tipping point of beta cell dysfunction remains unknown. Here, the furan fatty acid metabolite CMPF was evaluated in a prospective cohort. Those who developed overt diabetes had a significant increase in CMPF over time, whereas prediabetics maintained chronically elevated levels, even up to 5 years before diagnosis. To evaluate the effect of increasing CMPF on diabetes progression, we used obese, insulin-resistant models of prediabetes. CMPF accelerated diabetes development by inducing metabolic remodeling, resulting in preferential utilization of fatty acids over glucose. This was associated with diminished glucose-stimulated insulin secretion, increased ROS formation, and accumulation of proinsulin, all characteristics of human diabetes. Thus, an increase in CMPF may represent the tipping point in diabetes development by accelerating beta cell dysfunction.
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