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Revised temperament and character inventory factors predict neuropsychiatric symptoms and aging-related cognitive decline across 25 years
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk och translationell biologi. Umeå universitet, Medicinska fakulteten, Umeå centrum för funktionell hjärnavbildning (UFBI). Centre de Recherche de l’Institut Universitaire de Gériatrie de Montréal, Neuroimaging of Emotions Lab, Montreal, QC; Canada Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, QC, Canada.
Umeå universitet, Samhällsvetenskapliga fakulteten, Institutionen för psykologi.ORCID-id: 0000-0001-5726-4101
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk vetenskap, Psykiatri.ORCID-id: 0000-0001-9785-8473
Centre de Recherche de l’Institut Universitaire de Gériatrie de Montréal, Neuroimaging of Emotions Lab, Montreal, QC, Canada; Department of Psychology, Faculty of Arts and Sciences, University of Montreal, Montreal, QC, Canada.
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2024 (Engelska)Ingår i: Frontiers in Aging Neuroscience, E-ISSN 1663-4365, Vol. 16, artikel-id 1335336Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Introduction: Personality traits and neuropsychiatric symptoms such as neuroticism and depression share genetic overlap and have both been identified as risks factors for development of aging-related neurocognitive decline and Alzheimer’s disease (AD). This study aimed to examine revised personality factors derived from the Temperament and Character Inventory, previously shown to be associated with psychiatric disorders, as predictors of neuropsychiatric, cognitive, and brain trajectories of participants from a population-based aging study.

Methods: Mixed-effect linear regression analyses were conducted on data for the full sample (Nmax = 1,286), and a healthy subsample not converting to AD-dementia during 25-year follow-up (Nmax = 1,145), complemented with Cox proportional regression models to determine risk factors for conversion to clinical AD.

Results: Two personality factors, Closeness to Experience (CE: avoidance of new stimuli, high anxiety, pessimistic anticipation, low reward seeking) and Tendence to Liabilities (TL: inability to change, low autonomy, unaware of the value of their existence) were associated with higher levels of depressive symptoms, stress (CE), sleep disturbance (TL), as well as greater decline in memory, vocabulary and verbal fluency in the full sample. Higher CE was additionally associated with greater memory decline across 25 years in the healthy subsample, and faster right hippocampal volume reduction across 8 years in a neuroimaging subsample (N = 216). Most, but not all, personality-cognition associations persisted after controlling for diabetes, hypertension and cardiovascular disease. Concerning risks for conversion to AD, higher age, and APOE-ε4, but none of the personality measures, were significant predictors.

Conclusion: The results indicate that personality traits associated with psychiatric symptoms predict accelerated age-related neurocognitive declines even in the absence of neurodegenerative disease. The attenuation of some personality effects on cognition after adjustment for health indicators suggests that those effects may be partly mediated by somatic health. Taken together, the results further emphasize the importance of personality traits in neurocognitive aging and underscore the need for an integrative (biopsychosocial) perspective of normal and pathological age-related cognitive decline.

Ort, förlag, år, upplaga, sidor
Frontiers Media S.A., 2024. Vol. 16, artikel-id 1335336
Nyckelord [en]
personality, cognitive decline, neuropsychiatric symptoms, Alzheimer’s dementia, MRI, longitudinal study
Nationell ämneskategori
Psykologi (exklusive tillämpad psykologi) Neurovetenskaper
Identifikatorer
URN: urn:nbn:se:umu:diva-221338DOI: 10.3389/fnagi.2024.1335336Scopus ID: 2-s2.0-85186625892OAI: oai:DiVA.org:umu-221338DiVA, id: diva2:1839510
Forskningsfinansiär
Riksbankens Jubileumsfond, 1988-0082:17Riksbankens Jubileumsfond, 2001-0682Vetenskapsrådet, D1988-0092Vetenskapsrådet, D1989-0115Vetenskapsrådet, D1990-0074Vetenskapsrådet, D1991-0258Vetenskapsrådet, D1992-0143Vetenskapsrådet, D1997-0756Vetenskapsrådet, D1997-1841Vetenskapsrådet, D1999-0739Vetenskapsrådet, B1999-474Vetenskapsrådet, F377/1988-2000Vetenskapsrådet, 1988-1990:88-0082Vetenskapsrådet, 311/1991-2000Vetenskapsrådet, 345-2003-3883Vetenskapsrådet, 315-2004-6977Tillgänglig från: 2024-02-21 Skapad: 2024-02-21 Senast uppdaterad: 2024-07-04Bibliografiskt granskad

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Ronat, LucasRönnlund, MichaelAdolfsson, RolfPudas, Sara

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Institutionen för medicinsk och translationell biologiUmeå centrum för funktionell hjärnavbildning (UFBI)Institutionen för psykologiPsykiatri
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Frontiers in Aging Neuroscience
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