Glucotypes reveal new patterns of glucose dysregulation.

Diabetes is an increasing problem worldwide; almost 30 million people, nearly 10% of the population, in the United States are diagnosed with diabetes. Another 84 million are prediabetic, and without intervention, up to 70% of these individuals may progress to type 2 diabetes. Current methods for qua...

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Main Authors: Heather Hall, Dalia Perelman, Alessandra Breschi, Patricia Limcaoco, Ryan Kellogg, Tracey McLaughlin, Michael Snyder
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-07-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC6057684?pdf=render
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spelling doaj-665604ba966e4bdba676e530e732deda2021-07-02T07:24:21ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852018-07-01167e200514310.1371/journal.pbio.2005143Glucotypes reveal new patterns of glucose dysregulation.Heather HallDalia PerelmanAlessandra BreschiPatricia LimcaocoRyan KelloggTracey McLaughlinMichael SnyderDiabetes is an increasing problem worldwide; almost 30 million people, nearly 10% of the population, in the United States are diagnosed with diabetes. Another 84 million are prediabetic, and without intervention, up to 70% of these individuals may progress to type 2 diabetes. Current methods for quantifying blood glucose dysregulation in diabetes and prediabetes are limited by reliance on single-time-point measurements or on average measures of overall glycemia and neglect glucose dynamics. We have used continuous glucose monitoring (CGM) to evaluate the frequency with which individuals demonstrate elevations in postprandial glucose, the types of patterns, and how patterns vary between individuals given an identical nutrient challenge. Measurement of insulin resistance and secretion highlights the fact that the physiology underlying dysglycemia is highly variable between individuals. We developed an analytical framework that can group individuals according to specific patterns of glycemic responses called "glucotypes" that reveal heterogeneity, or subphenotypes, within traditional diagnostic categories of glucose regulation. Importantly, we found that even individuals considered normoglycemic by standard measures exhibit high glucose variability using CGM, with glucose levels reaching prediabetic and diabetic ranges 15% and 2% of the time, respectively. We thus show that glucose dysregulation, as characterized by CGM, is more prevalent and heterogeneous than previously thought and can affect individuals considered normoglycemic by standard measures, and specific patterns of glycemic responses reflect variable underlying physiology. The interindividual variability in glycemic responses to standardized meals also highlights the personal nature of glucose regulation. Through extensive phenotyping, we developed a model for identifying potential mechanisms of personal glucose dysregulation and built a webtool for visualizing a user-uploaded CGM profile and classifying individualized glucose patterns into glucotypes.http://europepmc.org/articles/PMC6057684?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Heather Hall
Dalia Perelman
Alessandra Breschi
Patricia Limcaoco
Ryan Kellogg
Tracey McLaughlin
Michael Snyder
spellingShingle Heather Hall
Dalia Perelman
Alessandra Breschi
Patricia Limcaoco
Ryan Kellogg
Tracey McLaughlin
Michael Snyder
Glucotypes reveal new patterns of glucose dysregulation.
PLoS Biology
author_facet Heather Hall
Dalia Perelman
Alessandra Breschi
Patricia Limcaoco
Ryan Kellogg
Tracey McLaughlin
Michael Snyder
author_sort Heather Hall
title Glucotypes reveal new patterns of glucose dysregulation.
title_short Glucotypes reveal new patterns of glucose dysregulation.
title_full Glucotypes reveal new patterns of glucose dysregulation.
title_fullStr Glucotypes reveal new patterns of glucose dysregulation.
title_full_unstemmed Glucotypes reveal new patterns of glucose dysregulation.
title_sort glucotypes reveal new patterns of glucose dysregulation.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2018-07-01
description Diabetes is an increasing problem worldwide; almost 30 million people, nearly 10% of the population, in the United States are diagnosed with diabetes. Another 84 million are prediabetic, and without intervention, up to 70% of these individuals may progress to type 2 diabetes. Current methods for quantifying blood glucose dysregulation in diabetes and prediabetes are limited by reliance on single-time-point measurements or on average measures of overall glycemia and neglect glucose dynamics. We have used continuous glucose monitoring (CGM) to evaluate the frequency with which individuals demonstrate elevations in postprandial glucose, the types of patterns, and how patterns vary between individuals given an identical nutrient challenge. Measurement of insulin resistance and secretion highlights the fact that the physiology underlying dysglycemia is highly variable between individuals. We developed an analytical framework that can group individuals according to specific patterns of glycemic responses called "glucotypes" that reveal heterogeneity, or subphenotypes, within traditional diagnostic categories of glucose regulation. Importantly, we found that even individuals considered normoglycemic by standard measures exhibit high glucose variability using CGM, with glucose levels reaching prediabetic and diabetic ranges 15% and 2% of the time, respectively. We thus show that glucose dysregulation, as characterized by CGM, is more prevalent and heterogeneous than previously thought and can affect individuals considered normoglycemic by standard measures, and specific patterns of glycemic responses reflect variable underlying physiology. The interindividual variability in glycemic responses to standardized meals also highlights the personal nature of glucose regulation. Through extensive phenotyping, we developed a model for identifying potential mechanisms of personal glucose dysregulation and built a webtool for visualizing a user-uploaded CGM profile and classifying individualized glucose patterns into glucotypes.
url http://europepmc.org/articles/PMC6057684?pdf=render
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