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Systemic inflammation and family history in relation to the prevalence of type 2 diabetes based on an alternating decision tree

To investigate unknown patterns associated with type 2 diabetes in the Japanese population, we first used an alternating decision tree (ADTree) algorithm, a powerful classification algorithm from data mining, for the data from 1,102 subjects aged 35–69 years. On the basis of the investigated pattern...

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Autores principales: Uemura, Hirokazu, Ghaibeh, A. Ammar, Katsuura-Kamano, Sakurako, Yamaguchi, Miwa, Bahari, Tirani, Ishizu, Masashi, Moriguchi, Hiroki, Arisawa, Kokichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374531/
https://www.ncbi.nlm.nih.gov/pubmed/28361994
http://dx.doi.org/10.1038/srep45502
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author Uemura, Hirokazu
Ghaibeh, A. Ammar
Katsuura-Kamano, Sakurako
Yamaguchi, Miwa
Bahari, Tirani
Ishizu, Masashi
Moriguchi, Hiroki
Arisawa, Kokichi
author_facet Uemura, Hirokazu
Ghaibeh, A. Ammar
Katsuura-Kamano, Sakurako
Yamaguchi, Miwa
Bahari, Tirani
Ishizu, Masashi
Moriguchi, Hiroki
Arisawa, Kokichi
author_sort Uemura, Hirokazu
collection PubMed
description To investigate unknown patterns associated with type 2 diabetes in the Japanese population, we first used an alternating decision tree (ADTree) algorithm, a powerful classification algorithm from data mining, for the data from 1,102 subjects aged 35–69 years. On the basis of the investigated patterns, we then evaluated the associations of serum high-sensitivity C-reactive protein (hs-CRP) as a biomarker of systemic inflammation and family history of diabetes (negative, positive or unknown) with the prevalence of type 2 diabetes because their detailed associations have been scarcely reported. Elevated serum hs-CRP levels were proportionally associated with the increased prevalence of type 2 diabetes after adjusting for probable covariates, including body mass index and family history of diabetes (P for trend = 0.016). Stratified analyses revealed that elevated serum hs-CRP levels were proportionally associated with increased prevalence of diabetes in subjects without a family history of diabetes (P for trend = 0.020) but not in those with a family history or with an unknown family history of diabetes. Our study demonstrates that systemic inflammation was proportionally associated with increased prevalence of type 2 diabetes even after adjusting for body mass index, especially in subjects without a family history of diabetes.
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spelling pubmed-53745312017-04-03 Systemic inflammation and family history in relation to the prevalence of type 2 diabetes based on an alternating decision tree Uemura, Hirokazu Ghaibeh, A. Ammar Katsuura-Kamano, Sakurako Yamaguchi, Miwa Bahari, Tirani Ishizu, Masashi Moriguchi, Hiroki Arisawa, Kokichi Sci Rep Article To investigate unknown patterns associated with type 2 diabetes in the Japanese population, we first used an alternating decision tree (ADTree) algorithm, a powerful classification algorithm from data mining, for the data from 1,102 subjects aged 35–69 years. On the basis of the investigated patterns, we then evaluated the associations of serum high-sensitivity C-reactive protein (hs-CRP) as a biomarker of systemic inflammation and family history of diabetes (negative, positive or unknown) with the prevalence of type 2 diabetes because their detailed associations have been scarcely reported. Elevated serum hs-CRP levels were proportionally associated with the increased prevalence of type 2 diabetes after adjusting for probable covariates, including body mass index and family history of diabetes (P for trend = 0.016). Stratified analyses revealed that elevated serum hs-CRP levels were proportionally associated with increased prevalence of diabetes in subjects without a family history of diabetes (P for trend = 0.020) but not in those with a family history or with an unknown family history of diabetes. Our study demonstrates that systemic inflammation was proportionally associated with increased prevalence of type 2 diabetes even after adjusting for body mass index, especially in subjects without a family history of diabetes. Nature Publishing Group 2017-03-31 /pmc/articles/PMC5374531/ /pubmed/28361994 http://dx.doi.org/10.1038/srep45502 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
Uemura, Hirokazu
Ghaibeh, A. Ammar
Katsuura-Kamano, Sakurako
Yamaguchi, Miwa
Bahari, Tirani
Ishizu, Masashi
Moriguchi, Hiroki
Arisawa, Kokichi
Systemic inflammation and family history in relation to the prevalence of type 2 diabetes based on an alternating decision tree
title Systemic inflammation and family history in relation to the prevalence of type 2 diabetes based on an alternating decision tree
title_full Systemic inflammation and family history in relation to the prevalence of type 2 diabetes based on an alternating decision tree
title_fullStr Systemic inflammation and family history in relation to the prevalence of type 2 diabetes based on an alternating decision tree
title_full_unstemmed Systemic inflammation and family history in relation to the prevalence of type 2 diabetes based on an alternating decision tree
title_short Systemic inflammation and family history in relation to the prevalence of type 2 diabetes based on an alternating decision tree
title_sort systemic inflammation and family history in relation to the prevalence of type 2 diabetes based on an alternating decision tree
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374531/
https://www.ncbi.nlm.nih.gov/pubmed/28361994
http://dx.doi.org/10.1038/srep45502
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