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Genetic Association Study of Common Mitochondrial Variants on Body Fat Mass

Mitochondria play a central role in ATP production and energy metabolism. Previous studies suggest that common variants in mtDNA are associated with several common complex diseases, including obesity. To test the hypothesis that common mtDNA variants influence obesity-related phenotypes, including B...

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Autores principales: Yang, Tie-Lin, Guo, Yan, Shen, Hui, Lei, Shu-Feng, Liu, Yong-Jun, Li, Jian, Liu, Yao-Zhong, Yu, Na, Chen, Jia, Xu, Ting, Cheng, Yu, Tian, Qing, Yu, Ping, Papasian, Christopher J., Deng, Hong-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3126834/
https://www.ncbi.nlm.nih.gov/pubmed/21747914
http://dx.doi.org/10.1371/journal.pone.0021595
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author Yang, Tie-Lin
Guo, Yan
Shen, Hui
Lei, Shu-Feng
Liu, Yong-Jun
Li, Jian
Liu, Yao-Zhong
Yu, Na
Chen, Jia
Xu, Ting
Cheng, Yu
Tian, Qing
Yu, Ping
Papasian, Christopher J.
Deng, Hong-Wen
author_facet Yang, Tie-Lin
Guo, Yan
Shen, Hui
Lei, Shu-Feng
Liu, Yong-Jun
Li, Jian
Liu, Yao-Zhong
Yu, Na
Chen, Jia
Xu, Ting
Cheng, Yu
Tian, Qing
Yu, Ping
Papasian, Christopher J.
Deng, Hong-Wen
author_sort Yang, Tie-Lin
collection PubMed
description Mitochondria play a central role in ATP production and energy metabolism. Previous studies suggest that common variants in mtDNA are associated with several common complex diseases, including obesity. To test the hypothesis that common mtDNA variants influence obesity-related phenotypes, including BMI and body fat mass, we genotyped a total of 445 mtSNPs across the whole mitochondrial genome in a large sample of 2,286 unrelated Caucasian subjects. 72 of these 445 mtSNPs passed quality control criteria, and were used for subsequent analyses. We also classified all subjects into nine common European haplogroups. Association analyses were conducted for both BMI and body fat mass with single mtSNPs and mtDNA haplogroups. Two mtSNPs, mt4823 and mt8873 were detected to be significantly associated with body fat mass, with adjusted P values of 4.94×10(-3) and 4.58×10(-2), respectively. The minor alleles mt4823 C and mt8873 A were associated with reduced fat mass values and the effect size (β) was estimated to be 3.52 and 3.18, respectively. These two mtSNPs also achieved nominally significant levels for association with BMI. For haplogroup analyses, we found that haplogroup X was strongly associated with both BMI (adjusted P = 8.31×10(-3)) and body fat mass (adjusted P = 5.67×10(-4)) Subjects classified as haplogroup X had lower BMI and fat mass values, with the β estimated to be 2.86 and 6.03, respectively. Our findings suggest that common variants in mitochondria might play a role in variations of body fat mass. Further molecular and functional studies will be needed to clarify the potential mechanism.
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spelling pubmed-31268342011-07-11 Genetic Association Study of Common Mitochondrial Variants on Body Fat Mass Yang, Tie-Lin Guo, Yan Shen, Hui Lei, Shu-Feng Liu, Yong-Jun Li, Jian Liu, Yao-Zhong Yu, Na Chen, Jia Xu, Ting Cheng, Yu Tian, Qing Yu, Ping Papasian, Christopher J. Deng, Hong-Wen PLoS One Research Article Mitochondria play a central role in ATP production and energy metabolism. Previous studies suggest that common variants in mtDNA are associated with several common complex diseases, including obesity. To test the hypothesis that common mtDNA variants influence obesity-related phenotypes, including BMI and body fat mass, we genotyped a total of 445 mtSNPs across the whole mitochondrial genome in a large sample of 2,286 unrelated Caucasian subjects. 72 of these 445 mtSNPs passed quality control criteria, and were used for subsequent analyses. We also classified all subjects into nine common European haplogroups. Association analyses were conducted for both BMI and body fat mass with single mtSNPs and mtDNA haplogroups. Two mtSNPs, mt4823 and mt8873 were detected to be significantly associated with body fat mass, with adjusted P values of 4.94×10(-3) and 4.58×10(-2), respectively. The minor alleles mt4823 C and mt8873 A were associated with reduced fat mass values and the effect size (β) was estimated to be 3.52 and 3.18, respectively. These two mtSNPs also achieved nominally significant levels for association with BMI. For haplogroup analyses, we found that haplogroup X was strongly associated with both BMI (adjusted P = 8.31×10(-3)) and body fat mass (adjusted P = 5.67×10(-4)) Subjects classified as haplogroup X had lower BMI and fat mass values, with the β estimated to be 2.86 and 6.03, respectively. Our findings suggest that common variants in mitochondria might play a role in variations of body fat mass. Further molecular and functional studies will be needed to clarify the potential mechanism. Public Library of Science 2011-06-29 /pmc/articles/PMC3126834/ /pubmed/21747914 http://dx.doi.org/10.1371/journal.pone.0021595 Text en Yang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yang, Tie-Lin
Guo, Yan
Shen, Hui
Lei, Shu-Feng
Liu, Yong-Jun
Li, Jian
Liu, Yao-Zhong
Yu, Na
Chen, Jia
Xu, Ting
Cheng, Yu
Tian, Qing
Yu, Ping
Papasian, Christopher J.
Deng, Hong-Wen
Genetic Association Study of Common Mitochondrial Variants on Body Fat Mass
title Genetic Association Study of Common Mitochondrial Variants on Body Fat Mass
title_full Genetic Association Study of Common Mitochondrial Variants on Body Fat Mass
title_fullStr Genetic Association Study of Common Mitochondrial Variants on Body Fat Mass
title_full_unstemmed Genetic Association Study of Common Mitochondrial Variants on Body Fat Mass
title_short Genetic Association Study of Common Mitochondrial Variants on Body Fat Mass
title_sort genetic association study of common mitochondrial variants on body fat mass
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3126834/
https://www.ncbi.nlm.nih.gov/pubmed/21747914
http://dx.doi.org/10.1371/journal.pone.0021595
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