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Significance of pancreatic duodenal homeobox-1 (PDX-1) genetic polymorphism in insulin secretion in Japanese patients with type 2 diabetes

INTRODUCTION: Pancreatic and duodenal homeobox factor-1 (PDX-1) is an imperative gene for insulin secretion in maturity-onset diabetes of the young 4. PDX-1 gene polymorphism was associated with lower first-phase insulin secretion in a genome-wide association study of intravenous glucose tolerance t...

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Autores principales: Okura, Tsuyoshi, Nakamura, Risa, Ito, Yuichi, Kitao, Sonoko, Anno, Mari, Endo, Satomi, Taneda, Natsuka, Matsumoto, Kazuhisa, Shoji, Kyoko, Okura, Hiroko, Matsuzawa, Kazuhiko, Izawa, Shoichiro, Ueta, Etsuko, Kato, Masahiko, Imamura, Takeshi, Taniguchi, Shin-ichi, Yamamoto, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462127/
https://www.ncbi.nlm.nih.gov/pubmed/36718853
http://dx.doi.org/10.1136/bmjdrc-2022-002908
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author Okura, Tsuyoshi
Nakamura, Risa
Ito, Yuichi
Kitao, Sonoko
Anno, Mari
Endo, Satomi
Taneda, Natsuka
Matsumoto, Kazuhisa
Shoji, Kyoko
Okura, Hiroko
Matsuzawa, Kazuhiko
Izawa, Shoichiro
Ueta, Etsuko
Kato, Masahiko
Imamura, Takeshi
Taniguchi, Shin-ichi
Yamamoto, Kazuhiro
author_facet Okura, Tsuyoshi
Nakamura, Risa
Ito, Yuichi
Kitao, Sonoko
Anno, Mari
Endo, Satomi
Taneda, Natsuka
Matsumoto, Kazuhisa
Shoji, Kyoko
Okura, Hiroko
Matsuzawa, Kazuhiko
Izawa, Shoichiro
Ueta, Etsuko
Kato, Masahiko
Imamura, Takeshi
Taniguchi, Shin-ichi
Yamamoto, Kazuhiro
author_sort Okura, Tsuyoshi
collection PubMed
description INTRODUCTION: Pancreatic and duodenal homeobox factor-1 (PDX-1) is an imperative gene for insulin secretion in maturity-onset diabetes of the young 4. PDX-1 gene polymorphism was associated with lower first-phase insulin secretion in a genome-wide association study of intravenous glucose tolerance test. It was not associated with type 2 diabetes risk and insulin secretion in a genome-wide oral glucose tolerance test study. However, there have been no reports of overt type 2 diabetes and insulin resistance evaluation using a glucose clamp. We investigated PDX-1 polymorphism, insulin secretion, and insulin resistance in overt type 2 diabetes. RESEARCH DESIGN AND METHODS: We performed a meal tolerance test (MTT) and hyperinsulinemic–euglycemic clamping on 63 Japanese subjects, 30 with type 2 diabetes and 33 non-diabetic. We analyzed the rs1124607 PDX-1 gene polymorphism and defined A/C and C/C as the high-risk group and A/A as the low-risk group. RESULTS: HOMA-beta (homeostatic model assessment beta-cell function) was significantly lower in the high-risk group than in the low-risk group for all subjects (72.9±54.2% vs 107.0±63.5%, p<0.05). Glucose levels and glucose area under the curve (AUC) were not significantly different between both the risk groups. The insulin levels at 60 and 120 min and the insulin AUC after MTT were remarkably lower in the high-risk group than those in the low-risk group for all subjects (AUC 75.7±36.7 vs 112.7±59.5, p<0.05). High-risk subjects with type 2 diabetes had significantly lower insulin levels at 30 and 60 min and insulin AUC than low-risk subjects. Non-diabetic high-risk subjects depicted significantly lower insulin levels at 120 and 180 min. There were negligible differences in insulin resistance between the risk groups. CONCLUSIONS: These results suggest that the PDX-1 genetic polymorphism is crucial for insulin secretion in Japanese patients with type 2 diabetes.
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spelling pubmed-94621272022-09-14 Significance of pancreatic duodenal homeobox-1 (PDX-1) genetic polymorphism in insulin secretion in Japanese patients with type 2 diabetes Okura, Tsuyoshi Nakamura, Risa Ito, Yuichi Kitao, Sonoko Anno, Mari Endo, Satomi Taneda, Natsuka Matsumoto, Kazuhisa Shoji, Kyoko Okura, Hiroko Matsuzawa, Kazuhiko Izawa, Shoichiro Ueta, Etsuko Kato, Masahiko Imamura, Takeshi Taniguchi, Shin-ichi Yamamoto, Kazuhiro BMJ Open Diabetes Res Care Genetics/Genomes/Proteomics/Metabolomics INTRODUCTION: Pancreatic and duodenal homeobox factor-1 (PDX-1) is an imperative gene for insulin secretion in maturity-onset diabetes of the young 4. PDX-1 gene polymorphism was associated with lower first-phase insulin secretion in a genome-wide association study of intravenous glucose tolerance test. It was not associated with type 2 diabetes risk and insulin secretion in a genome-wide oral glucose tolerance test study. However, there have been no reports of overt type 2 diabetes and insulin resistance evaluation using a glucose clamp. We investigated PDX-1 polymorphism, insulin secretion, and insulin resistance in overt type 2 diabetes. RESEARCH DESIGN AND METHODS: We performed a meal tolerance test (MTT) and hyperinsulinemic–euglycemic clamping on 63 Japanese subjects, 30 with type 2 diabetes and 33 non-diabetic. We analyzed the rs1124607 PDX-1 gene polymorphism and defined A/C and C/C as the high-risk group and A/A as the low-risk group. RESULTS: HOMA-beta (homeostatic model assessment beta-cell function) was significantly lower in the high-risk group than in the low-risk group for all subjects (72.9±54.2% vs 107.0±63.5%, p<0.05). Glucose levels and glucose area under the curve (AUC) were not significantly different between both the risk groups. The insulin levels at 60 and 120 min and the insulin AUC after MTT were remarkably lower in the high-risk group than those in the low-risk group for all subjects (AUC 75.7±36.7 vs 112.7±59.5, p<0.05). High-risk subjects with type 2 diabetes had significantly lower insulin levels at 30 and 60 min and insulin AUC than low-risk subjects. Non-diabetic high-risk subjects depicted significantly lower insulin levels at 120 and 180 min. There were negligible differences in insulin resistance between the risk groups. CONCLUSIONS: These results suggest that the PDX-1 genetic polymorphism is crucial for insulin secretion in Japanese patients with type 2 diabetes. BMJ Publishing Group 2022-09-07 /pmc/articles/PMC9462127/ /pubmed/36718853 http://dx.doi.org/10.1136/bmjdrc-2022-002908 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Genetics/Genomes/Proteomics/Metabolomics
Okura, Tsuyoshi
Nakamura, Risa
Ito, Yuichi
Kitao, Sonoko
Anno, Mari
Endo, Satomi
Taneda, Natsuka
Matsumoto, Kazuhisa
Shoji, Kyoko
Okura, Hiroko
Matsuzawa, Kazuhiko
Izawa, Shoichiro
Ueta, Etsuko
Kato, Masahiko
Imamura, Takeshi
Taniguchi, Shin-ichi
Yamamoto, Kazuhiro
Significance of pancreatic duodenal homeobox-1 (PDX-1) genetic polymorphism in insulin secretion in Japanese patients with type 2 diabetes
title Significance of pancreatic duodenal homeobox-1 (PDX-1) genetic polymorphism in insulin secretion in Japanese patients with type 2 diabetes
title_full Significance of pancreatic duodenal homeobox-1 (PDX-1) genetic polymorphism in insulin secretion in Japanese patients with type 2 diabetes
title_fullStr Significance of pancreatic duodenal homeobox-1 (PDX-1) genetic polymorphism in insulin secretion in Japanese patients with type 2 diabetes
title_full_unstemmed Significance of pancreatic duodenal homeobox-1 (PDX-1) genetic polymorphism in insulin secretion in Japanese patients with type 2 diabetes
title_short Significance of pancreatic duodenal homeobox-1 (PDX-1) genetic polymorphism in insulin secretion in Japanese patients with type 2 diabetes
title_sort significance of pancreatic duodenal homeobox-1 (pdx-1) genetic polymorphism in insulin secretion in japanese patients with type 2 diabetes
topic Genetics/Genomes/Proteomics/Metabolomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462127/
https://www.ncbi.nlm.nih.gov/pubmed/36718853
http://dx.doi.org/10.1136/bmjdrc-2022-002908
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