Prevalence of cognitive impairment and associated factors in older people.

BACKGROUND: Older people are the fastest-growing age group, with the highest risk of cognitive impairment. This study assessed the prevalence and associated factors with cognitive impairment in community-dwelling older people. METHODS: Older people were interviewed and accomplished through sociodemographic and health questionnaires. The quantitative variables were described by mean and standard deviation or median and interquartile range. The significance level adopted was 5 % (p < 0.05). The association between the quantitative variables was evaluated using the Pearson or Spearman correlation coefficients. RESULTS: The research population comprised 165 long-lived adults aged ≥80. The youngest one was 80, and the oldest one was 94 years old. The participants were 84.8 ± 3.6 years old, female (63 %) with a mean of education of 2.9 ± 1.8 years. A poor performance in the Mini-Mental State Examination (MMSE) was found in 58 (35.2 %) individuals when adjusted for educational level. After adjustment for confounding factors, body mass index (BMI) (p = 0.09), total older adults' income (up to 1 minimum wage [mw], p = 0.023; over 1 to 2 mw, p = 0.023), functional disability (Moderate dependence 75 %, p = 0.038; Moderate dependence 50 %, p = 0.081; Moderate dependence 25 %, p = 0.054), and the anxiety scale (p = 0.032), remained associated with cognitive impairment. CONCLUSIONS: This study showed that BMI, total older adults' income, functional disability, and anxiety are related to cognitive impairment in long-lived adults. This study has some limitations, such as the fact that it is a cross-sectional study, the reduced number of individuals, and the fact that there were no comparisons among different ages and populations.

Folic acid prevents habituation memory impairment and oxidative stress in an aging model induced by D-galactose.

The present study aimed to evaluate the effect of folic acid treatment in an animal model of aging induced by D-galactose (D-gal). For this propose, adult male Wistar rats received D-gal intraperitoneally (100 mg/kg) and/or folic acid orally (5 mg/kg, 10 mg/kg or 50 mg/kg) for 8 weeks. D-gal caused habituation memory impairment, and folic acid (10 mg/kg and 50 mg/kg) reversed this effect. However, folic acid 50 mg/kg per se caused habituation memory impairment. D-gal increased the lipid peroxidation and oxidative damage to proteins in the prefrontal cortex and hippocampus from rats. Folic acid (5 mg/kg, 10 mg/kg, or 50 mg/kg) partially reversed the oxidative damage to lipids in the hippocampus, but not in the prefrontal cortex, and reversed protein oxidative damage in the prefrontal cortex and hippocampus. D-gal induced synaptophysin and BCL-2 decrease in the hippocampus and phosphorylated tau increase in the prefrontal cortex. Folic acid was able to reverse these D-gal-related alterations in the protein content. The present study shows folic acid supplementation as an alternative during the aging to prevent cognitive impairment and brain alterations that can cause neurodegenerative diseases. However, additional studies are necessary to elucidate the effect of folic acid in aging.

Tradução, adaptação e avaliação das propriedades psicométricas da Arousal Predisposition Scale em crianças e adolescentes / Translation, adaptation and evaluation of the psychometric properties of the Arousal Predisposition Scale in children and adolescents / Traducción, adaptación y evaluación de las propiedades psicométricas de la Arousal Predisposition Scale en niños y adolescentes

A Arousal Predisposition Scale (APS) é um instrumento com 12 itens, elaborado para mensurar o nível de arousal de um indivíduo. O termo arousal, traduzido para o português falado no Brasil, significa excitação, isto é, a resposta do organismo frente a um estímulo externo ou estresse ambiental. A escala visa abordar o arousal como uma predisposição ou característica individual de excitação diante de um estressor ambiental. O objetivo deste estudo foi realizar tradução, adaptação e avaliação das propriedades psicométricas da APS para crianças e adolescentes. O estudo foi realizado com 189 alunos, de ambos os sexos, de escolas públicas, com idade entre 10 e 17 anos. A pesquisa foi dividida em duas etapas: a primeira foi a adaptação transcultural e a segunda etapa envolveu a avaliação das propriedades psicométricas da versão final. Os resultados apresentaram uma consistência interna dos itens aceitável para os grupos pré-adolescentes e adolescentes (alfa de Cronbach > 0,700). Não houve diferença significativa entre a escala total em médias de teste-reteste e uma correlação significativa de moderada a forte de validade de critério. A APS foi traduzida, adaptada e validada no Brasil para o grupo etário de 11 anos de idade. Destaca-se ainda a importância da utilização dessa escala por diferentes setores de saúde e da educação, em escolas de ensino fundamental e médio, contribuindo para identificar precocemente problemas de comportamento.

Arousal Predisposition Scale (APS) is a 12-item instrument designed to measure the arousal level of an individual. Translated into Brazilian Portuguese arousal means excitement, that is, the body's response to an external stimulus or environmental stress. The scale aims to address arousal as a predisposition or individual characteristic of excitement when facing an environmental stressor. Hence, this study sought to translate, adapt, and evaluate the psychometric properties of the APS for children and adolescents. Data was collected from 189 students, of all genders, from public schools, aged 10 to 17 years. The research was divided into two stages: first, the cross-cultural adaptation, followed by the evaluation of the psychometric properties in the final version. Results showed an acceptable internal consistency of the items for the pre-adolescent and adolescent groups (Cronbach's alpha > 0.700). The findings presented no significant difference between full-scale test-retest means and a significant moderate to strong correlation of criterion validity. The APS was translated, adapted and validated in Brazil for the 11-year-old age group. APS should be used by different health and education sectors in primary and secondary schools to help identify early behavioral problems.

La Arousal Predisposition Scale (APS) es un instrumento que consta de 12 ítems para estimar el nivel de arousal de un individuo. El término arousal significa excitación en portugués de Brasil, es decir, una respuesta del organismo frente a un estímulo externo o estrés ambiental. La escala pretende abordar el arousal como una predisposición o característica individual de excitación frente a un estrés ambiental. El objetivo de este estudio fue realizar la traducción, la adaptación, la evaluación y la valoración de las propiedades psicométricas de la APS para niños y adolescentes. Se realizó un estudio con 189 alumnos, de ambos sexos, de escuelas públicas, con edades de entre los 10 y 17 años. La investigación constó de dos etapas: la primera realizó la adaptación transcultural; y la segunda, la evaluación de las propiedades psicométricas de la versión final. Los resultados mostraron una consistencia interna de los ítems aceptable para los grupos de preadolescentes y adolescentes (alfa de Cronbach > 0,700). No hubo diferencias significativas entre la escala total en las medias de prueba-reprueba y una correlación significativa de moderada a fuerte como validez de criterio. Se realizó la traducción, la adaptación y la validación de la APS en Brasil para el grupo de edad de los 11 años. Se señala la importancia de la utilización de esta escala para los diferentes sectores de salud y de la educación, en la primaria y la secundaria, al contribuir a la identificación de problemas de comportamiento.

Sodium butyrate improves memory and modulates the activity of histone deacetylases in aged rats after the administration of d-galactose.

Aging is a complex biological process. Epigenetic alterations have been related to both aging and memory decline. Included amongst these alterations is histone acetylation, which may play a crucial role in aging. Thus, the aims of the present study were to standardize the animal model of d-galactose (d-gal), and to evaluate the effects caused by sodium butyrate (SB), which is a histone deacetylase inhibitor on memory, the modulation of histone deacetylases (HDACs), and also DNA damage in 2, 6 or 16-month-old Wistar rats which were subjected to administrations of d-gal. To help choose the best dose of d-gal for the induction of the aging model, we performed a dose-response curve (100, 200 or 300 mg/kg). d-Gal was administered orally to the 2-month-old rats for a period of 30 days. After this, d-gal (200 mg/kg) or water were administered to the 2, 6 or 16-month-old rats for a period of 30 days. On the 24th day, treatment was started with SB (600 mg/kg) intraperitoneally, for a period of 7 days. SB was able to reverse the damage to habituation memory caused by d-gal in the 2 and 6-month-old rats, but was unable to reverse the damage in the 16 month-old animals. In addition, SB was able to reverse the damage caused by natural aging in the 16-month-old animals. In the inhibitory avoidance task, SB improved the damage caused by d-gal in the 2, 6 and 16-month-old animals and had the same result against the effects of natural aging in the 16-month-old rats. Moreover, d-gal caused an increase in the level of HDACs activity in the 16-month-old animals, and SB was able to reverse this effect in the frontal cortex and hippocampus. The 16-month-old animals showed an increase in the frequency of DNA damage in peripheral blood, and SB was able to reduce this damage. Moreover, d-gal caused an increase in the index and frequency of DNA damage in the 2 and 6-month-old animals, and treatment with SB was able to prevent this damage. Thus, the present study showed the protective effects of SB on the memory of naturally aged and d-gal induced aging in rats. Therefore, the present study shows new findings for the use of SB in aging.