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1.
Neurology ; 71(3): 210-6, 2008 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-18625967

RESUMO

OBJECTIVE: To examine the correlation of cardiorespiratory fitness with brain atrophy and cognition in early-stage Alzheimer disease (AD). BACKGROUND: In normal aging physical fitness appears to mitigate functional and structural age-related brain changes. Whether this is observed in AD is not known. METHODS: Subjects without dementia (n = 64) and subjects with early-stage AD (n = 57) had MRI and standard clinical and psychometric evaluations. Peak oxygen consumption (VO(2)(peak)), the standard measure of cardiorespiratory fitness, was assessed during a graded treadmill test. Normalized whole brain volume, a brain atrophy estimate, was determined by MRI. Pearson correlation and linear regression were used to assess fitness in relation to brain volume and cognitive performance. RESULTS: Cardiorespiratory fitness (VO(2)(peak)) was modestly reduced in subjects with AD (34.7 [5.0] mL/kg/min) vs subjects without dementia (38.1 [6.3] mL/kg/min, p = 0.002). In early AD, VO(2)(peak) was associated with whole brain volume (beta = 0.35, p = 0.02) and white matter volume (beta = 0.35, p = 0.04) after controlling for age. Controlling for additional covariates of sex, dementia severity, physical activity, and physical frailty did not attenuate the relationships. VO(2)(peak) was associated with performance on delayed memory and digit symbol in early AD but not after controlling for age. In participants with no dementia, there was no relationship between fitness and brain atrophy. Fitness in participants with no dementia was associated with better global cognitive performance (r = 0.30, p = 0.02) and performance on Trailmaking A and B, Stroop, and delayed logical memory but not after controlling for age. CONCLUSIONS: Increased cardiorespiratory fitness is associated with reduced brain atrophy in Alzheimer disease (AD). Cardiorespiratory fitness may moderate AD-related brain atrophy or a common underlying AD-related process may impact both brain atrophy and cardiorespiratory fitness.


Assuntos
Doença de Alzheimer/patologia , Doença de Alzheimer/fisiopatologia , Encéfalo/patologia , Encéfalo/fisiopatologia , Teste de Esforço , Aptidão Física/fisiologia , Mecânica Respiratória/fisiologia , Idoso , Idoso de 80 Anos ou mais , Envelhecimento/patologia , Envelhecimento/fisiologia , Doença de Alzheimer/psicologia , Atrofia , Cognição/fisiologia , Estudos Transversais , Teste de Esforço/métodos , Feminino , Humanos , Masculino , Fatores de Tempo
2.
Neurology ; 69(11): 1094-104, 2007 Sep 11.
Artigo em Inglês | MEDLINE | ID: mdl-17846409

RESUMO

OBJECTIVE: Accumulating evidence suggests insulin and insulin signaling may be involved in the pathophysiology of Alzheimer disease (AD). The relationship between insulin-mediated glucoregulation and brain structure has not been assessed in individuals with AD. METHODS: Nondemented (Clinical Dementia Rating [CDR] 0, n = 31) and early stage AD (CDR 0.5 and 1, n = 31) participants aged 65 years and older had brain MRI to determine whole brain and hippocampal volume and 3-hour IV glucose tolerance tests to determine glucose and insulin area under the curve (AUC). Linear regression models were used to assess the relationship of insulin and glucose with brain volume, cognition, and dementia severity. RESULTS: In early AD, insulin and glucose AUCs were related to whole brain (insulin beta = 0.66, p < 0.001; glucose beta = 0.45, p < 0.01) and hippocampal volume (insulin beta = 0.42, p < 0.05; glucose beta = 0.46, p < 0.05). These relationships were independent of age, sex, body mass index, body fat, cardiorespiratory fitness, physical activity, cholesterol, and triglycerides. Insulin AUC, but not glucose, was associated with cognitive performance in early AD (beta = 0.40, p = 0.04). Insulin AUC was associated with dementia severity (Pearson r = -0.40, p = 0.03). Glucose and insulin were not related to brain volume or cognitive performance in nondemented individuals. CONCLUSIONS: Increased peripheral insulin is associated with reduced Alzheimer disease (AD)-related brain atrophy, cognitive dysfunction, and dementia severity, suggesting that insulin signaling may play a role in the pathophysiology of AD.


Assuntos
Doença de Alzheimer/metabolismo , Encéfalo/metabolismo , Complicações do Diabetes/metabolismo , Insulina/sangue , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/patologia , Doença de Alzheimer/fisiopatologia , Área Sob a Curva , Atrofia/etiologia , Atrofia/patologia , Atrofia/fisiopatologia , Glicemia/metabolismo , Encéfalo/patologia , Encéfalo/fisiopatologia , Transtornos Cognitivos/metabolismo , Transtornos Cognitivos/patologia , Transtornos Cognitivos/fisiopatologia , Estudos de Coortes , Estudos Transversais , Complicações do Diabetes/patologia , Complicações do Diabetes/fisiopatologia , Progressão da Doença , Feminino , Teste de Tolerância a Glucose , Hipocampo/metabolismo , Hipocampo/patologia , Hipocampo/fisiopatologia , Humanos , Imageamento por Ressonância Magnética , Masculino , Transdução de Sinais/fisiologia , Regulação para Cima
3.
Am Rev Respir Dis ; 123(5): 479-85, 1981 May.
Artigo em Inglês | MEDLINE | ID: mdl-7235369

RESUMO

Using pulmonary function and family respiratory questionnaire data for 16,689 white children 6 to 13 yr of age from 7 geographic areas, the investigators examined the effect of several environmental and other factors on performance, in a standard test of breathing. As expected, FEV0.75 was correlated most strongly with age, height, and sex. A dose-response relationship was observed with maternal smoking habits and explained 0.1% of the variance. No effect caused by the father's smoking habits was observed. A decrease (p = 0.0524) in FEV among older girls was associated with the presence of a gas cooking stove in the home. Although the statistical significance of the decreases was largely attributable to the size of the sample, the decreases in FEV, even though small, were thought to be biologically significant.


Assuntos
Meio Ambiente , Pulmão/fisiologia , Óxido Nitroso/efeitos adversos , Adolescente , Adulto , Fatores Etários , Criança , Pré-Escolar , Feminino , Fluxo Expiratório Forçado , Humanos , Lactente , Recém-Nascido , Masculino , Mães , Transtornos Respiratórios/induzido quimicamente , Testes de Função Respiratória/métodos , Fatores Sexuais , Fumar , Inquéritos e Questionários
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