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Body mass index trajectory patterns and changes in visceral fat and glucose metabolism before the onset of type 2 diabetes

We investigated BMI trajectory patterns before diabetes diagnosis and examined associated changes in visceral adiposity and glucose metabolism. 23,978 non-diabetic Japanese participants (2,789 women) aged 30–64 years were assessed with a mean follow-up of 7.6 years. Diabetes was diagnosed via fastin...

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Autores principales: Kuwahara, Keisuke, Honda, Toru, Nakagawa, Tohru, Yamamoto, Shuichiro, Hayashi, Takeshi, Mizoue, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339907/
https://www.ncbi.nlm.nih.gov/pubmed/28266592
http://dx.doi.org/10.1038/srep43521
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author Kuwahara, Keisuke
Honda, Toru
Nakagawa, Tohru
Yamamoto, Shuichiro
Hayashi, Takeshi
Mizoue, Tetsuya
author_facet Kuwahara, Keisuke
Honda, Toru
Nakagawa, Tohru
Yamamoto, Shuichiro
Hayashi, Takeshi
Mizoue, Tetsuya
author_sort Kuwahara, Keisuke
collection PubMed
description We investigated BMI trajectory patterns before diabetes diagnosis and examined associated changes in visceral adiposity and glucose metabolism. 23,978 non-diabetic Japanese participants (2,789 women) aged 30–64 years were assessed with a mean follow-up of 7.6 years. Diabetes was diagnosed via fasting glucose, HbA(1c), and self-report. Latent-class trajectory analyses were performed to identify BMI trajectories. Longitudinal changes in BMI, visceral adiposity, and glucose metabolism were estimated using mixed models. 1,892 individuals developed diabetes. Three distinct BMI trajectories were identified in adults developing and not developing diabetes, respectively. Among adults developing diabetes, 47.3% were classified as “medium BMI” (n = 895), and had increased mean BMI within the obesity category before diagnosis. The “low BMI” group (38.4%, n = 726) had an initial mean BMI of 21.9 kg/m(2), and demonstrated small weight gain. The “high BMI” group (n = 271) were severely obese and showed greater increase in BMI until diagnosis. All groups which developed diabetes showed absolute and/or relative increase in visceral fat and impaired β-cell compensation for insulin resistance. All groups not developing diabetes showed measured variables were relatively stable during observation. These data suggest that visceral fat gain may induce β-cell failure in compensation for insulin resistance, resulting in diabetes regardless of obesity level.
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spelling pubmed-53399072017-03-10 Body mass index trajectory patterns and changes in visceral fat and glucose metabolism before the onset of type 2 diabetes Kuwahara, Keisuke Honda, Toru Nakagawa, Tohru Yamamoto, Shuichiro Hayashi, Takeshi Mizoue, Tetsuya Sci Rep Article We investigated BMI trajectory patterns before diabetes diagnosis and examined associated changes in visceral adiposity and glucose metabolism. 23,978 non-diabetic Japanese participants (2,789 women) aged 30–64 years were assessed with a mean follow-up of 7.6 years. Diabetes was diagnosed via fasting glucose, HbA(1c), and self-report. Latent-class trajectory analyses were performed to identify BMI trajectories. Longitudinal changes in BMI, visceral adiposity, and glucose metabolism were estimated using mixed models. 1,892 individuals developed diabetes. Three distinct BMI trajectories were identified in adults developing and not developing diabetes, respectively. Among adults developing diabetes, 47.3% were classified as “medium BMI” (n = 895), and had increased mean BMI within the obesity category before diagnosis. The “low BMI” group (38.4%, n = 726) had an initial mean BMI of 21.9 kg/m(2), and demonstrated small weight gain. The “high BMI” group (n = 271) were severely obese and showed greater increase in BMI until diagnosis. All groups which developed diabetes showed absolute and/or relative increase in visceral fat and impaired β-cell compensation for insulin resistance. All groups not developing diabetes showed measured variables were relatively stable during observation. These data suggest that visceral fat gain may induce β-cell failure in compensation for insulin resistance, resulting in diabetes regardless of obesity level. Nature Publishing Group 2017-03-07 /pmc/articles/PMC5339907/ /pubmed/28266592 http://dx.doi.org/10.1038/srep43521 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kuwahara, Keisuke
Honda, Toru
Nakagawa, Tohru
Yamamoto, Shuichiro
Hayashi, Takeshi
Mizoue, Tetsuya
Body mass index trajectory patterns and changes in visceral fat and glucose metabolism before the onset of type 2 diabetes
title Body mass index trajectory patterns and changes in visceral fat and glucose metabolism before the onset of type 2 diabetes
title_full Body mass index trajectory patterns and changes in visceral fat and glucose metabolism before the onset of type 2 diabetes
title_fullStr Body mass index trajectory patterns and changes in visceral fat and glucose metabolism before the onset of type 2 diabetes
title_full_unstemmed Body mass index trajectory patterns and changes in visceral fat and glucose metabolism before the onset of type 2 diabetes
title_short Body mass index trajectory patterns and changes in visceral fat and glucose metabolism before the onset of type 2 diabetes
title_sort body mass index trajectory patterns and changes in visceral fat and glucose metabolism before the onset of type 2 diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339907/
https://www.ncbi.nlm.nih.gov/pubmed/28266592
http://dx.doi.org/10.1038/srep43521
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