Cited 11 times in
Combined Impact of Telomere Length and Mitochondrial DNA Copy Number on Cognitive Function in Community-Dwelling Very Old Adults
DC Field | Value | Language |
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dc.contributor.author | 이덕철 | - |
dc.date.accessioned | 2018-07-20T11:52:57Z | - |
dc.date.available | 2018-07-20T11:52:57Z | - |
dc.date.issued | 2017 | - |
dc.identifier.issn | 1420-8008 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/161445 | - |
dc.description.abstract | BACKGROUND: This study was conducted to investigate the combined impact of telomere length and mitochondrial DNA (mtDNA) copy number on cognitive function in community-dwelling very old adults. METHODS: In total, 186 subjects over 75 years participated in this study. Cognitive function was assessed using the Korean Mini-Mental State Examination, and leukocyte telomere length and mtDNA copy number were measured using real-time polymerase chain reaction methods. RESULTS: Both the fourth quartile of telomere length and mtDNA copy number were associated with cognitive dysfunction with an adjusted odds ratio of 0.23 (95% confidence interval (CI), 0.10-0.75) and 0.18 (95% CI, 0.03-0.54), respectively. Participants in the high telomere length/high mtDNA copy number group were more likely to have cognitive dysfunction than participants in the low telomere/low mtDNA copy number group with an adjusted odds ratio of 0.19 (95% CI, 0.07-0.58). CONCLUSION: Our results collectively suggest that the combination of telomere length and mtDNA copy number may be useful for monitoring cognitive decline in older adults. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Karger | - |
dc.relation.isPartOf | DEMENTIA AND GERIATRIC COGNITIVE DISORDERS | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.title | Combined Impact of Telomere Length and Mitochondrial DNA Copy Number on Cognitive Function in Community-Dwelling Very Old Adults | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Family Medicine | - |
dc.contributor.googleauthor | Lee J.-Y. | - |
dc.contributor.googleauthor | Kim J.-H. | - |
dc.contributor.googleauthor | Lee D.-C. | - |
dc.identifier.doi | 10.1159/000480427 | - |
dc.contributor.localId | A02716 | - |
dc.relation.journalcode | J00696 | - |
dc.identifier.eissn | 1421-9824 | - |
dc.identifier.pmid | 28982094 | - |
dc.identifier.url | https://www.karger.com/Article/Abstract/480427 | - |
dc.subject.keyword | Aging | - |
dc.subject.keyword | Cognitive decline | - |
dc.subject.keyword | Mitochondrial DNA copy number | - |
dc.subject.keyword | Telomere length | - |
dc.subject.keyword | Very old adults | - |
dc.contributor.alternativeName | Lee, Duk Chul | - |
dc.contributor.affiliatedAuthor | Lee, Duk Chul | - |
dc.citation.volume | 44 | - |
dc.citation.number | 3~4 | - |
dc.citation.startPage | 232 | - |
dc.citation.endPage | 243 | - |
dc.identifier.bibliographicCitation | DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, Vol.44(3~4) : 232-243, 2017 | - |
dc.identifier.rimsid | 61354 | - |
dc.type.rims | ART | - |
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