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Association of Mitochondrial DNA Haplogroups with Exceptional Longevity in a Chinese Population
BACKGROUND: Longevity is a multifactorial trait with a genetic contribution, and mitochondrial DNA (mtDNA) polymorphisms were found to be involved in the phenomenon of longevity. METHODOLOGY/PRINCIPAL FINDINGS: To explore the effects of mtDNA haplogroups on the prevalence of extreme longevity (EL),...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2713402/ https://www.ncbi.nlm.nih.gov/pubmed/19641616 http://dx.doi.org/10.1371/journal.pone.0006423 |
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author | Cai, Xiao-yun Wang, Xiao-feng Li, Shi-lin Qian, Ji Qian, De-gui Chen, Fei Yang, Ya-jun Yuan, Zi-yu Xu, Jun Bai, Yidong Yu, Shun-zhang Jin, Li |
author_facet | Cai, Xiao-yun Wang, Xiao-feng Li, Shi-lin Qian, Ji Qian, De-gui Chen, Fei Yang, Ya-jun Yuan, Zi-yu Xu, Jun Bai, Yidong Yu, Shun-zhang Jin, Li |
author_sort | Cai, Xiao-yun |
collection | PubMed |
description | BACKGROUND: Longevity is a multifactorial trait with a genetic contribution, and mitochondrial DNA (mtDNA) polymorphisms were found to be involved in the phenomenon of longevity. METHODOLOGY/PRINCIPAL FINDINGS: To explore the effects of mtDNA haplogroups on the prevalence of extreme longevity (EL), a population based case-control study was conducted in Rugao – a prefecture city in Jiangsu, China. Case subjects include 463 individuals aged ≥95 yr (EL group). Control subjects include 926 individuals aged 60–69 years (elderly group) and 463 individuals aged 40–49 years (middle-aged group) randomly recruited from Rugao. We observed significant reduction of M9 haplogroups in longevity subjects (0.2%) when compared with both elderly subjects (2.2%) and middle-aged subjects (1.7%). Linear-by-linear association test revealed a significant decreasing trend of N9 frequency from middle-aged subjects (8.6%), elderly subjects (7.2%) and longevity subjects (4.8%) (p = 0.018). In subsequent analysis stratified by gender, linear-by-linear association test revealed a significant increasing trend of D4 frequency from middle-aged subjects (15.8%), elderly subjects (16.4%) and longevity subjects (21.7%) in females (p = 0.025). Conversely, a significant decreasing trend of B4a frequency was observed from middle-aged subjects (4.2%), elderly subjects (3.8%) and longevity subjects (1.7%) in females (p = 0.045). CONCLUSIONS: Our observations support the association of mitochondrial DNA haplogroups with exceptional longevity in a Chinese population. |
format | Text |
id | pubmed-2713402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27134022009-07-28 Association of Mitochondrial DNA Haplogroups with Exceptional Longevity in a Chinese Population Cai, Xiao-yun Wang, Xiao-feng Li, Shi-lin Qian, Ji Qian, De-gui Chen, Fei Yang, Ya-jun Yuan, Zi-yu Xu, Jun Bai, Yidong Yu, Shun-zhang Jin, Li PLoS One Research Article BACKGROUND: Longevity is a multifactorial trait with a genetic contribution, and mitochondrial DNA (mtDNA) polymorphisms were found to be involved in the phenomenon of longevity. METHODOLOGY/PRINCIPAL FINDINGS: To explore the effects of mtDNA haplogroups on the prevalence of extreme longevity (EL), a population based case-control study was conducted in Rugao – a prefecture city in Jiangsu, China. Case subjects include 463 individuals aged ≥95 yr (EL group). Control subjects include 926 individuals aged 60–69 years (elderly group) and 463 individuals aged 40–49 years (middle-aged group) randomly recruited from Rugao. We observed significant reduction of M9 haplogroups in longevity subjects (0.2%) when compared with both elderly subjects (2.2%) and middle-aged subjects (1.7%). Linear-by-linear association test revealed a significant decreasing trend of N9 frequency from middle-aged subjects (8.6%), elderly subjects (7.2%) and longevity subjects (4.8%) (p = 0.018). In subsequent analysis stratified by gender, linear-by-linear association test revealed a significant increasing trend of D4 frequency from middle-aged subjects (15.8%), elderly subjects (16.4%) and longevity subjects (21.7%) in females (p = 0.025). Conversely, a significant decreasing trend of B4a frequency was observed from middle-aged subjects (4.2%), elderly subjects (3.8%) and longevity subjects (1.7%) in females (p = 0.045). CONCLUSIONS: Our observations support the association of mitochondrial DNA haplogroups with exceptional longevity in a Chinese population. Public Library of Science 2009-07-29 /pmc/articles/PMC2713402/ /pubmed/19641616 http://dx.doi.org/10.1371/journal.pone.0006423 Text en Cai 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 Cai, Xiao-yun Wang, Xiao-feng Li, Shi-lin Qian, Ji Qian, De-gui Chen, Fei Yang, Ya-jun Yuan, Zi-yu Xu, Jun Bai, Yidong Yu, Shun-zhang Jin, Li Association of Mitochondrial DNA Haplogroups with Exceptional Longevity in a Chinese Population |
title | Association of Mitochondrial DNA Haplogroups with Exceptional Longevity in a Chinese Population |
title_full | Association of Mitochondrial DNA Haplogroups with Exceptional Longevity in a Chinese Population |
title_fullStr | Association of Mitochondrial DNA Haplogroups with Exceptional Longevity in a Chinese Population |
title_full_unstemmed | Association of Mitochondrial DNA Haplogroups with Exceptional Longevity in a Chinese Population |
title_short | Association of Mitochondrial DNA Haplogroups with Exceptional Longevity in a Chinese Population |
title_sort | association of mitochondrial dna haplogroups with exceptional longevity in a chinese population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2713402/ https://www.ncbi.nlm.nih.gov/pubmed/19641616 http://dx.doi.org/10.1371/journal.pone.0006423 |
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