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1.
J Int Neuropsychol Soc ; 25(9): 901-909, 2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-31387659

RESUMO

OBJECTIVES: Low educational attainment is a risk factor for more rapid cognitive aging, but there is substantial variability in cognitive trajectories within educational groups. The aim of this study was to determine the factors that confer resilience to memory decline within educational strata. METHODS: We selected 2573 initially nondemented White, African American, and Hispanic participants from the longitudinal community-based Washington Heights/Inwood Columbia Aging Project who had at least two visits. We estimated initial memory (intercept) and the rate of memory decline (slope) using up to five occasions of measurement. We classified groups according to the educational attainment groups as low (≤5 years), medium (6-11 years), and high (≥12 years). We used a multiple-group latent growth model to identify the baseline predictors of initial memory performance and rate of memory decline across groups. The model specification considered the influence of demographic, socioeconomic, biomedical, and cognitive variables on the intercept and the slope of memory trajectory. RESULTS: Our results indicated that the three educational groups do not benefit from the same factors. When allowed to differ across groups, the predictors were related to cognitive outcomes in the highly educated group, but we found no unique predictor of cognition for the low educated older adults. CONCLUSIONS: These findings highlight that memory-protective factors may differ across older adults with distinct educational backgrounds, and the need to evaluate a broader range of potential resilience factors for older adults with few years of school.


Assuntos
Envelhecimento Cognitivo , Disfunção Cognitiva , Escolaridade , Transtornos da Memória , Memória Episódica , Idoso , Idoso de 80 Anos ou mais , Envelhecimento Cognitivo/fisiologia , Disfunção Cognitiva/etnologia , Disfunção Cognitiva/fisiopatologia , Feminino , Humanos , Estudos Longitudinais , Masculino , Transtornos da Memória/etnologia , Transtornos da Memória/fisiopatologia , Cidade de Nova Iorque/etnologia , Fatores Socioeconômicos
2.
Int Psychogeriatr ; 29(10): 1693-1699, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-28629481

RESUMO

BACKGROUND: This study explored the combined impact of depression and inflammation on memory functioning among Mexican-American adults and elders. METHODS: Data were analyzed from 381 participants of the Health and Aging Brain study among Latino Elders (HABLE). Fasting serum samples were collected and assayed in duplicate using electrochemiluminesce on the SECTOR Imager 2400A from Meso Scale Discovery. Positive DepE (depression endophenotype) was codified as any score >1 on a five-point scale based on the GDS-30. Inflammation was determined by TNFα levels and categorized by tertiles (1st, 2nd, 3rd). WMS-III LMI and LMII as well as CERAD were utilized as measures of memory. ANOVAs examined group differences between positive DepE and inflammation tertiles with neuropsychological scale scores as outcome variables. Logistic regressions were used to examine level of inflammation and DepE positive status on the risk for MCI. RESULTS: Positive DepE as well as higher inflammation were both independently found to be associated with lower memory scores. Among DepE positive, those who were high in inflammation (3rd tertile) were found to perform significantly worse on WMS-III LM I (F = 4.75, p = 0.003), WMS-III LM II (F = 8.18, p < 0.001), and CERAD List Learning (F = 17.37, p < 0.001) when compared to those low on inflammation (1st tertile). The combination of DepE positive and highest tertile of inflammation was associated with increased risk for MCI diagnosis (OR = 6.06; 95% CI = 3.9-11.2, p < 0.001). CONCLUSION: Presence of elevated inflammation and positive DepE scores increased risk for worse memory among Mexican-American older adults. Additionally, the combination of DepE and high inflammation was associated with increased risk for MCI diagnosis. This work suggests that depression and inflammation are independently associated with worse memory among Mexican-American adults and elders; however, the combination of both increases risk for poorer memory beyond either alone.


Assuntos
Disfunção Cognitiva/etnologia , Depressão/etnologia , Inflamação/etnologia , Transtornos da Memória/etnologia , Americanos Mexicanos , Idoso , Disfunção Cognitiva/complicações , Estudos de Coortes , Depressão/complicações , Feminino , Humanos , Inflamação/complicações , Modelos Logísticos , Masculino , Transtornos da Memória/complicações , Pessoa de Meia-Idade , Testes Neuropsicológicos , Fatores de Risco , Estados Unidos/epidemiologia
3.
J Am Geriatr Soc ; 59(4): 628-36, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21480837

RESUMO

OBJECTIVES: To understand how people differentiate normal memory loss from Alzheimer's disease (AD) by investigating cultural models of these conditions. DESIGN: Ethnographic interviews followed by a survey. Cultural consensus analysis was used to test for the presence of group models, derive the "culturally correct" set of beliefs, and compare models of normal memory loss and AD. SETTING: Chicago, Illinois. PARTICIPANTS: One hundred eight individuals from local neighborhoods: African Americans, Mexican Americans, and refugees and immigrants from the former Soviet Union. MEASUREMENTS: Participants responded to yes-or-no questions about the nature and causes of normal memory loss and AD and provided information on ethnicity, age, sex, acculturation, and experience with AD. RESULTS: Groups held a common model of AD as a brain-based disease reflecting irreversible cognitive decline. Higher levels of acculturation predicted greater knowledge of AD. Russian speakers favored biological over psychological models of the disease. Groups also held a common model of normal memory loss, including the important belief that "normal" forgetting involves eventual recall of the forgotten material. CONCLUSION: Popular models of memory loss and AD confirm that patients and clinicians are speaking the same "language" in their discussions of memory loss and AD. Nevertheless, the presence of coherent models of memory loss and AD, and the unequal distribution of that knowledge across groups, suggests that clinicians should include wider circles of patients' families and friends in their consultations. These results frame knowledge as distributed across social groups rather than simply the possession of individual minds.


Assuntos
Doença de Alzheimer/complicações , Negro ou Afro-Americano , Emigrantes e Imigrantes , Transtornos da Memória/etnologia , Memória/fisiologia , Americanos Mexicanos , Refugiados , Adulto , Distribuição por Idade , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/etnologia , Doença de Alzheimer/psicologia , Feminino , Humanos , Illinois/epidemiologia , Incidência , Masculino , Transtornos da Memória/etiologia , Transtornos da Memória/psicologia , Pessoa de Meia-Idade , Distribuição por Sexo , Inquéritos e Questionários , U.R.S.S./etnologia
4.
Genitourin Med ; 73(6): 528-32, 1997 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9582475

RESUMO

OBJECTIVES: To review the management of a cohort of patients with positive treponemal serology and psychiatric and/or neurological disorders. METHODS: A retrospective case note review of 172 patients with positive treponemal serology attending the Patrick Clement's Clinic, Central Middlesex Hospital between December 1990 and November 1995 was performed. RESULTS: 101 men and 71 women were new attenders diagnosed with positive treponemal serology. A neurological problem was identified in 27 patients (12 women and 15 men) with psychiatric and/or neurological disorders, of whom 20 (six women and 14 men) underwent investigation of the cerebrospinal fluid (CSF). With the medical history and results of CSF-RPR and FTA tests, white cell count (WCC), and total protein level in the CSF, 10 patients (eight men and two women) were diagnosed with likely neurosyphilis and 17 with neurological disorders not thought to be caused by syphilis. The clinical features in those having neurosyphilis were sensorineural hearing loss (n = 5) and tabes dorsalis (n = 5). In the seven patients diagnosed with neurosyphilis who underwent CSF examination one patient had a reactive CSF-FTA, elevated protein, and elevated WCC; one patient had a reactive CSF-FTA and RPR with elevated protein; the total protein only was elevated in three cases and the WCC elevated in one case. Nine of the 10 patients with neurosyphilis received adequate neurosyphilitic treatment; one patient was lost to follow up. CONCLUSIONS: The management of patients with positive treponemal serology and psychiatric and/or neurological disorders was consistent. Patients with suspected neurosyphilis or patients with neurological signs compatible with neurosyphilis (who did not undergo CSF examination) were treated with adequate neurosyphilitic therapy.


Assuntos
Neurossífilis/diagnóstico , Adulto , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/etnologia , Doença de Alzheimer/microbiologia , Demência por Múltiplos Infartos/etnologia , Demência por Múltiplos Infartos/microbiologia , Feminino , Perda Auditiva Neurossensorial/etnologia , Perda Auditiva Neurossensorial/microbiologia , Humanos , Londres/epidemiologia , Masculino , Transtornos da Memória/etnologia , Transtornos da Memória/microbiologia , Pessoa de Meia-Idade , Neurossífilis/líquido cefalorraquidiano , Neurossífilis/terapia , Encaminhamento e Consulta , Estudos Retrospectivos , Tabes Dorsal/etnologia , Tabes Dorsal/microbiologia , Índias Ocidentais/etnologia
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