Mitochondrial DNA content contributes to healthy aging in Chinese: a study from nonagenarians and centenarians
Abstract Mitochondrial DNA (mtDNA) content plays an important role in energy production and sustaining normal physiological function. A decline in the mtDNA content and subsequent dysfunction cause various senile diseases, with decreasing mtDNA content observed in the elderly individuals with age-re...
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Veröffentlicht in: | Neurobiology of aging 2014-07, Vol.35 (7), p.1779.e1-1779.e4 |
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container_title | Neurobiology of aging |
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creator | He, Yong-Han Lu, Xiang Wu, Huan Cai, Wang-Wei Yang, Li-Qin Xu, Liang-You Sun, Hong-Peng Kong, Qing-Peng |
description | Abstract Mitochondrial DNA (mtDNA) content plays an important role in energy production and sustaining normal physiological function. A decline in the mtDNA content and subsequent dysfunction cause various senile diseases, with decreasing mtDNA content observed in the elderly individuals with age-related diseases. In contrast, the oldest old individuals, for example, centenarians, have a delayed or reduced prevalence of these diseases, suggesting centenarians may have a different pattern of the mtDNA content, enabling them to keep normal mitochondrial functions to help delay or escape senile diseases. To test this hypothesis, a total of 961 subjects, consisting of 424 longevity subjects and 537 younger control subjects from Hainan and Sichuan provinces of China, were recruited for this study. The mtDNA content was found to be inversely associated with age among the age of group 40–70 years. Surprisingly, no reduction of mtDNA content was observed in nonagenarians and centenarians; instead, these oldest old showed a significant increase than the elderly people aged between 50 and 70 years. The results suggest the higher mtDNA content may convey a beneficial effect to the longevity of people through assuring sufficient energy supply. |
doi_str_mv | 10.1016/j.neurobiolaging.2014.01.015 |
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A decline in the mtDNA content and subsequent dysfunction cause various senile diseases, with decreasing mtDNA content observed in the elderly individuals with age-related diseases. In contrast, the oldest old individuals, for example, centenarians, have a delayed or reduced prevalence of these diseases, suggesting centenarians may have a different pattern of the mtDNA content, enabling them to keep normal mitochondrial functions to help delay or escape senile diseases. To test this hypothesis, a total of 961 subjects, consisting of 424 longevity subjects and 537 younger control subjects from Hainan and Sichuan provinces of China, were recruited for this study. The mtDNA content was found to be inversely associated with age among the age of group 40–70 years. Surprisingly, no reduction of mtDNA content was observed in nonagenarians and centenarians; instead, these oldest old showed a significant increase than the elderly people aged between 50 and 70 years. The results suggest the higher mtDNA content may convey a beneficial effect to the longevity of people through assuring sufficient energy supply.</description><identifier>ISSN: 0197-4580</identifier><identifier>EISSN: 1558-1497</identifier><identifier>DOI: 10.1016/j.neurobiolaging.2014.01.015</identifier><identifier>PMID: 24524965</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Aging - genetics ; Asian Continental Ancestry Group - genetics ; DNA, Mitochondrial - metabolism ; DNA, Mitochondrial - physiology ; Energy Metabolism ; Female ; Genetic Association Studies ; Humans ; Internal Medicine ; Longevity - genetics ; Male ; Middle Aged ; Neurology</subject><ispartof>Neurobiology of aging, 2014-07, Vol.35 (7), p.1779.e1-1779.e4</ispartof><rights>Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c617t-a4f289ded59e351fb40e2e73f647a23593a684c3c8086da4a7fde6c595751953</citedby><cites>FETCH-LOGICAL-c617t-a4f289ded59e351fb40e2e73f647a23593a684c3c8086da4a7fde6c595751953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24524965$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>He, Yong-Han</creatorcontrib><creatorcontrib>Lu, Xiang</creatorcontrib><creatorcontrib>Wu, Huan</creatorcontrib><creatorcontrib>Cai, Wang-Wei</creatorcontrib><creatorcontrib>Yang, Li-Qin</creatorcontrib><creatorcontrib>Xu, Liang-You</creatorcontrib><creatorcontrib>Sun, Hong-Peng</creatorcontrib><creatorcontrib>Kong, Qing-Peng</creatorcontrib><title>Mitochondrial DNA content contributes to healthy aging in Chinese: a study from nonagenarians and centenarians</title><title>Neurobiology of aging</title><addtitle>Neurobiol Aging</addtitle><description>Abstract Mitochondrial DNA (mtDNA) content plays an important role in energy production and sustaining normal physiological function. A decline in the mtDNA content and subsequent dysfunction cause various senile diseases, with decreasing mtDNA content observed in the elderly individuals with age-related diseases. In contrast, the oldest old individuals, for example, centenarians, have a delayed or reduced prevalence of these diseases, suggesting centenarians may have a different pattern of the mtDNA content, enabling them to keep normal mitochondrial functions to help delay or escape senile diseases. To test this hypothesis, a total of 961 subjects, consisting of 424 longevity subjects and 537 younger control subjects from Hainan and Sichuan provinces of China, were recruited for this study. The mtDNA content was found to be inversely associated with age among the age of group 40–70 years. Surprisingly, no reduction of mtDNA content was observed in nonagenarians and centenarians; instead, these oldest old showed a significant increase than the elderly people aged between 50 and 70 years. The results suggest the higher mtDNA content may convey a beneficial effect to the longevity of people through assuring sufficient energy supply.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging - genetics</subject><subject>Asian Continental Ancestry Group - genetics</subject><subject>DNA, Mitochondrial - metabolism</subject><subject>DNA, Mitochondrial - physiology</subject><subject>Energy Metabolism</subject><subject>Female</subject><subject>Genetic Association Studies</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Longevity - genetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neurology</subject><issn>0197-4580</issn><issn>1558-1497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU2LFDEQhoMo7rj6FyQHD156THW-OiLCMn7Cqgf3HjLp6pmMPcmadAvz703vrII3oaAgPHmrqIeQF8DWwEC9OqwjzjltQxrdLsTdumUg1gxqyQdkBVJ2DQijH5IVA6MbITt2QZ6UcmCMaaHVY3LRCtkKo-SKxC9hSn6fYp-DG-m7r1fUpzhhnO56Dtt5wkKnRPfoxml_ondDaYh0sw8RC76mjpZp7k90yOlIY4puh9HVuFioiz31uOSdH56SR4MbCz6775fk5sP7m82n5vrbx8-bq-vGK9BT48TQdqbHXhrkEoatYNii5oMS2rVcGu5UJzz3HetU74TTQ4_KSyO1BCP5JXl5jr3N6eeMZbLHUDyOo4uY5mJBctExwzv1HygIwQWDtqJvzqjPqZSMg73N4ejyyQKzixt7sP-6sYsby6DWstTz-0nz9oj9389_ZFTg7RnAeplfAbP1Y4jBu_EHnrAc0pxjPZoFW1rL7PdF72IXRDULNeA3LXOl5g</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>He, Yong-Han</creator><creator>Lu, Xiang</creator><creator>Wu, Huan</creator><creator>Cai, Wang-Wei</creator><creator>Yang, Li-Qin</creator><creator>Xu, Liang-You</creator><creator>Sun, Hong-Peng</creator><creator>Kong, Qing-Peng</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20140701</creationdate><title>Mitochondrial DNA content contributes to healthy aging in Chinese: a study from nonagenarians and centenarians</title><author>He, Yong-Han ; Lu, Xiang ; Wu, Huan ; Cai, Wang-Wei ; Yang, Li-Qin ; Xu, Liang-You ; Sun, Hong-Peng ; Kong, Qing-Peng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c617t-a4f289ded59e351fb40e2e73f647a23593a684c3c8086da4a7fde6c595751953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging - genetics</topic><topic>Asian Continental Ancestry Group - genetics</topic><topic>DNA, Mitochondrial - metabolism</topic><topic>DNA, Mitochondrial - physiology</topic><topic>Energy Metabolism</topic><topic>Female</topic><topic>Genetic Association Studies</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Longevity - genetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neurology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>He, Yong-Han</creatorcontrib><creatorcontrib>Lu, Xiang</creatorcontrib><creatorcontrib>Wu, Huan</creatorcontrib><creatorcontrib>Cai, Wang-Wei</creatorcontrib><creatorcontrib>Yang, Li-Qin</creatorcontrib><creatorcontrib>Xu, Liang-You</creatorcontrib><creatorcontrib>Sun, Hong-Peng</creatorcontrib><creatorcontrib>Kong, Qing-Peng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Neurobiology of aging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, Yong-Han</au><au>Lu, Xiang</au><au>Wu, Huan</au><au>Cai, Wang-Wei</au><au>Yang, Li-Qin</au><au>Xu, Liang-You</au><au>Sun, Hong-Peng</au><au>Kong, Qing-Peng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mitochondrial DNA content contributes to healthy aging in Chinese: a study from nonagenarians and centenarians</atitle><jtitle>Neurobiology of aging</jtitle><addtitle>Neurobiol Aging</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>35</volume><issue>7</issue><spage>1779.e1</spage><epage>1779.e4</epage><pages>1779.e1-1779.e4</pages><issn>0197-4580</issn><eissn>1558-1497</eissn><abstract>Abstract Mitochondrial DNA (mtDNA) content plays an important role in energy production and sustaining normal physiological function. A decline in the mtDNA content and subsequent dysfunction cause various senile diseases, with decreasing mtDNA content observed in the elderly individuals with age-related diseases. In contrast, the oldest old individuals, for example, centenarians, have a delayed or reduced prevalence of these diseases, suggesting centenarians may have a different pattern of the mtDNA content, enabling them to keep normal mitochondrial functions to help delay or escape senile diseases. To test this hypothesis, a total of 961 subjects, consisting of 424 longevity subjects and 537 younger control subjects from Hainan and Sichuan provinces of China, were recruited for this study. The mtDNA content was found to be inversely associated with age among the age of group 40–70 years. Surprisingly, no reduction of mtDNA content was observed in nonagenarians and centenarians; instead, these oldest old showed a significant increase than the elderly people aged between 50 and 70 years. The results suggest the higher mtDNA content may convey a beneficial effect to the longevity of people through assuring sufficient energy supply.</abstract><cop>United States</cop><pmid>24524965</pmid><doi>10.1016/j.neurobiolaging.2014.01.015</doi></addata></record> |
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subjects | Adult Aged Aged, 80 and over Aging - genetics Asian Continental Ancestry Group - genetics DNA, Mitochondrial - metabolism DNA, Mitochondrial - physiology Energy Metabolism Female Genetic Association Studies Humans Internal Medicine Longevity - genetics Male Middle Aged Neurology |
title | Mitochondrial DNA content contributes to healthy aging in Chinese: a study from nonagenarians and centenarians |
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