4.0 Article

High performance older adults in a population-based sample with low education: Pieta study

Journal

ARQUIVOS DE NEURO-PSIQUIATRIA
Volume 81, Issue 2, Pages 112-118

Publisher

ASSOC ARQUIVOS NEURO- PSIQUIATRIA
DOI: 10.1055/s-0042-1759760

Keywords

Aging; Memory; Healthy Aging; Depression; Aged; Educational Status

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This study investigated the presence of high-performance older adults (HPOA) in an oldest-old population with low education and explored associations with sociodemographic, clinical, and lifestyle variables. Results showed that 18 individuals fulfilled HPOA criteria, with an average age of 77.4 years and education level of 4.6 years. Younger age and lower scores on the Geriatric Depression Scale were associated with HPOA.
Background Healthy brain aging can be defined as aging without neurological or psychiatric disorders, sustaining functional independence. In addition to the absence of disease and preserved functionality, there are individuals who stand out for their superior performance to that considered normal for their age in cognitive tests. These individuals are called high-performance older adults (HPOA). Objectives To investigate the presence of HPOA in an oldest-old population with low education, and if present, to investigate associations with sociodemographic, clinical, and lifestyle variables. Methods We evaluated 132 cognitively healthy individuals from the Pieta Study, a population-based investigation with 639 participants. We used the delayed recall from the Rey Auditory- Verbal Learning Test to verify the existence of HPOA and to classify participants based on their performance. Sociodemographic, clinical, and lifestyle variables associated with HPOA were investigated. Results We identified 18 individuals fulfilling HPOA criteria (age: 77.4 +/- 2.6 years old; 14 women; education: 4.6 +/- 3.4 years). The other participants, 114 total (age: 79.8 +/- 4.5 years old; 69 women; education: 3.0 +/- 2.7 years) were classified as standard performance older adults (SPOA). In multivariate analysis, younger age (odds ratio [OR] = 0.672; 95% confidence interval [CI]: 0.462-0.979; p = 0.037) and lower scores on the Geriatric Depression Scale (OR = 0.831; 95%CI: 0.688-0.989; p = 0.038) were associated with HPOA. Conclusions The present study identifies for the first time HPOA with low educational level, thereby reinforcing the existence of biological substrates related to this condition. Furthermore, the data suggest an association between younger age and less depressive symptoms with HPOA.

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