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Associations between early life stress, self-reported traumatic experiences across the lifespan and leukocyte telomere length in elderly adults.
- Source :
-
Biological psychology [Biol Psychol] 2014 Mar; Vol. 97, pp. 35-42. Date of Electronic Publication: 2014 Feb 11. - Publication Year :
- 2014
-
Abstract
- Early life stress (ELS) poses a risk for mental disorders and aging-related diseases. Accelerated biological aging, reflected in shorter leukocyte telomere length (LTL), may underlie these risks. We examined whether objectively recorded ELS and retrospectively self-reported traumatic experiences across the lifespan are associated with LTL in later adulthood. Of 1486 participants, 215 had been exposed to ELS, namely to temporary separation from both parents in childhood. Participants self-reported emotionally or physically traumatic experiences across the lifespan at a mean age of 63.2 years. LTL was measured using a quantitative PCR method at a mean age of 61.5 years. Separation or self-reported traumatic experiences were not associated with LTL. However, separated participants who self-reported traumatic experiences had shorter LTL. Our results suggest that while ELS or self-reported traumatic experiences are not per se associated with LTL measured decades later, ELS may in combination with self-reported traumatic events be associated with accelerated biological aging.<br /> (Copyright © 2014 Elsevier B.V. All rights reserved.)
- Subjects :
- Aged
Anxiety, Separation psychology
Biomarkers
Cellular Senescence
Child, Preschool
Cohort Studies
DNA genetics
Female
Finland
Humans
Male
Mental Disorders psychology
Middle Aged
Parents
Polymerase Chain Reaction
Warfare
Stress, Psychological genetics
Telomere ultrastructure
Telomere Shortening physiology
Wounds and Injuries psychology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-6246
- Volume :
- 97
- Database :
- MEDLINE
- Journal :
- Biological psychology
- Publication Type :
- Academic Journal
- Accession number :
- 24530884
- Full Text :
- https://doi.org/10.1016/j.biopsycho.2014.02.002