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Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan
BACKGROUND: The importance of mitochondrial DNA (mtDNA) polymorphism in the prediction of type 2 diabetes (T2D) in men and women is not well understood. We questioned whether mtDNA polymorphism, mitochondrial functions, age and gender influenced the occurrence of T2D with or without ischemic stroke...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108081/ https://www.ncbi.nlm.nih.gov/pubmed/24713204 http://dx.doi.org/10.1186/1756-0500-7-223 |
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author | Loo, Jun-Hun Trejaut, Jean A Yen, Ju-Chen Chen, Zong-Sian Ng, Wai-Mei Huang, Chin-Yuan Hsu, Kuang-Nan Hung, Kuo-Hua Hsiao, Yachun Wei, Yau-Huei Lin, Marie |
author_facet | Loo, Jun-Hun Trejaut, Jean A Yen, Ju-Chen Chen, Zong-Sian Ng, Wai-Mei Huang, Chin-Yuan Hsu, Kuang-Nan Hung, Kuo-Hua Hsiao, Yachun Wei, Yau-Huei Lin, Marie |
author_sort | Loo, Jun-Hun |
collection | PubMed |
description | BACKGROUND: The importance of mitochondrial DNA (mtDNA) polymorphism in the prediction of type 2 diabetes (T2D) in men and women is not well understood. We questioned whether mtDNA polymorphism, mitochondrial functions, age and gender influenced the occurrence of T2D with or without ischemic stroke (IS). METHODS: We first designed a matched case–control study of 373 T2D patients and 327 healthy unrelated individuals without history of IS. MtDNA haplogroups were determined on all participants using sequencing of the control region and relevant SNPs from the coding region. Mitochondria functional tests, systemic biochemical measurements and complete genomic mtDNA sequencing were further determined on 239 participants (73 healthy controls, 33 T2D with IS, 70 T2D only and 63 IS patients without T2D). RESULTS: MtDNA haplogroups B4a1a, and E2b1 showed significant association with T2D (P <0.05), and haplogroup D4 indicated resistance (P <0.05). Mitochondrial and systemic functional tests showed significantly less variance within groups bearing the same mtDNA haplotypes. There was a pronounced male excess among all T2D patients and prevalence of IS was seen only in the older population. Finally, nucleotide variant np 15746, a determinant of haplogroup G3 seen in Japanese and of B4a1a prevalent in Taiwanese was associated with T2D in both populations. CONCLUSIONS: Men appeared more susceptible to T2D than women. Although the significant association of B4a1a and E2b1 with T2D ceased when corrected for multiple testings, these haplogroups are seen only among Taiwan Aborigines, Southeast Asian and the Pacific Ocean islanders where T2D is predominant. The data further suggested that physiological and biochemical measurements were influenced by the mtDNA genetic profile of the individual. More understanding of the function of the mitochondrion in the development of T2D might indicate ways of influencing the early course of the disease. |
format | Online Article Text |
id | pubmed-4108081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41080812014-07-24 Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan Loo, Jun-Hun Trejaut, Jean A Yen, Ju-Chen Chen, Zong-Sian Ng, Wai-Mei Huang, Chin-Yuan Hsu, Kuang-Nan Hung, Kuo-Hua Hsiao, Yachun Wei, Yau-Huei Lin, Marie BMC Res Notes Research Article BACKGROUND: The importance of mitochondrial DNA (mtDNA) polymorphism in the prediction of type 2 diabetes (T2D) in men and women is not well understood. We questioned whether mtDNA polymorphism, mitochondrial functions, age and gender influenced the occurrence of T2D with or without ischemic stroke (IS). METHODS: We first designed a matched case–control study of 373 T2D patients and 327 healthy unrelated individuals without history of IS. MtDNA haplogroups were determined on all participants using sequencing of the control region and relevant SNPs from the coding region. Mitochondria functional tests, systemic biochemical measurements and complete genomic mtDNA sequencing were further determined on 239 participants (73 healthy controls, 33 T2D with IS, 70 T2D only and 63 IS patients without T2D). RESULTS: MtDNA haplogroups B4a1a, and E2b1 showed significant association with T2D (P <0.05), and haplogroup D4 indicated resistance (P <0.05). Mitochondrial and systemic functional tests showed significantly less variance within groups bearing the same mtDNA haplotypes. There was a pronounced male excess among all T2D patients and prevalence of IS was seen only in the older population. Finally, nucleotide variant np 15746, a determinant of haplogroup G3 seen in Japanese and of B4a1a prevalent in Taiwanese was associated with T2D in both populations. CONCLUSIONS: Men appeared more susceptible to T2D than women. Although the significant association of B4a1a and E2b1 with T2D ceased when corrected for multiple testings, these haplogroups are seen only among Taiwan Aborigines, Southeast Asian and the Pacific Ocean islanders where T2D is predominant. The data further suggested that physiological and biochemical measurements were influenced by the mtDNA genetic profile of the individual. More understanding of the function of the mitochondrion in the development of T2D might indicate ways of influencing the early course of the disease. BioMed Central 2014-04-09 /pmc/articles/PMC4108081/ /pubmed/24713204 http://dx.doi.org/10.1186/1756-0500-7-223 Text en Copyright © 2014 Loo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Loo, Jun-Hun Trejaut, Jean A Yen, Ju-Chen Chen, Zong-Sian Ng, Wai-Mei Huang, Chin-Yuan Hsu, Kuang-Nan Hung, Kuo-Hua Hsiao, Yachun Wei, Yau-Huei Lin, Marie Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan |
title | Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan |
title_full | Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan |
title_fullStr | Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan |
title_full_unstemmed | Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan |
title_short | Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan |
title_sort | mitochondrial dna association study of type 2 diabetes with or without ischemic stroke in taiwan |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108081/ https://www.ncbi.nlm.nih.gov/pubmed/24713204 http://dx.doi.org/10.1186/1756-0500-7-223 |
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