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Personality traits are consistently associated with blood mitochondrial DNA copy number estimated from genome sequences in two genetic cohort studies.
Oppong, Richard F; Terracciano, Antonio; Picard, Martin; Qian, Yong; Butler, Thomas J; Tanaka, Toshiko; Moore, Ann Zenobia; Simonsick, Eleanor M; Opsahl-Ong, Krista; Coletta, Christopher; Sutin, Angelina R; Gorospe, Myriam; Resnick, Susan M; Cucca, Francesco; Scholz, Sonja W; Traynor, Bryan J; Schlessinger, David; Ferrucci, Luigi; Ding, Jun.
Afiliação
  • Oppong RF; Translational Gerontology Branch, National Institute on Aging, Baltimore, United States.
  • Terracciano A; Department of Geriatrics, Florida State University, Tallahassee, United States.
  • Picard M; Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, United States.
  • Qian Y; Division of Behavioral Medicine, Department of Psychiatry; Merritt Center and Columbia Translational Neuroscience initiative, Department of Neurology, Columbia University Irving Medical Center; New York State Psychiatric Institute, New York, United States.
  • Butler TJ; Translational Gerontology Branch, National Institute on Aging, Baltimore, United States.
  • Tanaka T; Translational Gerontology Branch, National Institute on Aging, Baltimore, United States.
  • Moore AZ; Translational Gerontology Branch, National Institute on Aging, Baltimore, United States.
  • Simonsick EM; Translational Gerontology Branch, National Institute on Aging, Baltimore, United States.
  • Opsahl-Ong K; Translational Gerontology Branch, National Institute on Aging, Baltimore, United States.
  • Coletta C; Translational Gerontology Branch, National Institute on Aging, Baltimore, United States.
  • Sutin AR; Laboratory of Genetics and Genomics, National Institute on Aging, Baltimore, United States.
  • Gorospe M; Department of Behavioral Sciences and Social Medicine, College of Medicine, Florida State University, Tallahassee, United States.
  • Resnick SM; Laboratory of Genetics and Genomics, National Institute on Aging, Baltimore, United States.
  • Cucca F; Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, United States.
  • Scholz SW; Istituto di Ricerca Genetica e Biomedica, Consiglio Nazionale delle Ricerche, Monserrato, Italy.
  • Traynor BJ; Neurodegenerative Diseases Research Unit, National Institute of Neurological Disorders and Stroke, Bethesda, United States.
  • Schlessinger D; Department of Neurology, Johns Hopkins University Medical Center, Baltimore, United States.
  • Ferrucci L; Department of Neurology, Johns Hopkins University Medical Center, Baltimore, United States.
  • Ding J; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, United States.
Elife ; 112022 12 20.
Article em En | MEDLINE | ID: mdl-36537669
ABSTRACT

Background:

Mitochondrial DNA copy number (mtDNAcn) in tissues and blood can be altered in conditions like diabetes and major depression and may play a role in aging and longevity. However, little is known about the association between mtDNAcn and personality traits linked to emotional states, metabolic health, and longevity. This study tests the hypothesis that blood mtDNAcn is related to personality traits and mediates the association between personality and mortality.

Methods:

We assessed the big five personality domains and facets using the Revised NEO Personality Inventory (NEO-PI-R), assessed depressive symptoms with the Center for Epidemiologic Studies Depression Scale (CES-D), estimated mtDNAcn levels from whole-genome sequencing, and tracked mortality in participants from the Baltimore Longitudinal Study of Aging. Results were replicated in the SardiNIA Project.

Results:

We found that mtDNAcn was negatively associated with the Neuroticism domain and its facets and positively associated with facets from the other four domains. The direction and size of the effects were replicated in the SardiNIA cohort and were robust to adjustment for potential confounders in both samples. Consistent with the Neuroticism finding, higher depressive symptoms were associated with lower mtDNAcn. Finally, mtDNAcn mediated the association between personality and mortality risk.

Conclusions:

To our knowledge, this is the first study to show a replicable association between mtDNAcn and personality. Furthermore, the results support our hypothesis that mtDNAcn is a biomarker of the biological process that explains part of the association between personality and mortality.

Funding:

Support for this work was provided by the Intramural Research Program of the National Institute on Aging (Z01-AG000693, Z01-AG000970, and Z01-AG000949) and the National Institute of Neurological Disorders and Stroke of the National Institutes of Health. AT was also supported by the National Institute on Aging of the National Institutes of Health Grant R01AG068093.
Cells are powered by internal structures called mitochondria which have their own DNA molecules. How many copies of mitochondrial DNA blood cells contain is one aspect of mitochondrial health and is considered to provide a good indication of an individual's ability to convert glucose into energy. Consequently, changes in the amount of mitochondrial DNA in the blood are linked to conditions like diabetes and cancer, and have also been associated with aging and mortality. A set of well-classified personality traits known as 'the Big Five' have also been shown to affect energy levels and the longevity of individuals. However, it remained unclear if there is a relationship between these characteristics and the number of copies of mitochondrial DNA in the blood. To investigate, Oppong et al. used a specialized test to assess the personality traits of participants from two separate cohorts Baltimore Longitudinal Study of Ageing and the SardiNIA Project. The genomic sequence of each person was then analyzed to calculate the amount of mitochondrial DNA in their blood, and their mortality was recorded based on whether they were alive or dead multiple years later. Oppong et al. found that low levels of mitochondrial DNA were linked with high scores in neuroticism (a trait typically associated with anxiety, depression, and self-doubt). Further statistical tests revealed that mitochondrial DNA levels mediate the relationship between a person's personality and their risk of death. These findings suggest that personality traits impact the number of mitochondrial DNA molecules in a person's blood, which, in turn, influences how long they are likely to live. However, further work is needed to find out what causes this effect.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Transtorno Depressivo Maior Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Elife Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Transtorno Depressivo Maior Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Elife Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
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