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1.
BMC Public Health ; 16: 93, 2016 Jan 30.
Artigo em Inglês | MEDLINE | ID: mdl-26829928

RESUMO

BACKGROUND: Obesity is growing at an alarming rate in Latin America. Lifestyle behaviours such as physical activity and dietary intake have been largely associated with obesity in many countries; however studies that combine nutrition and physical activity assessment in representative samples of Latin American countries are lacking. The aim of this study is to present the design rationale of the Latin American Study of Nutrition and Health/Estudio Latinoamericano de Nutrición y Salud (ELANS) with a particular focus on its quality control procedures and recruitment processes. METHODS/DESIGN: The ELANS is a multicenter cross-sectional nutrition and health surveillance study of a nationally representative sample of urban populations from eight Latin American countries (Argentina, Brazil, Chile, Colombia, Costa Rica, Ecuador, Perú and Venezuela). A standard study protocol was designed to evaluate the nutritional intakes, physical activity levels, and anthropometric measurements of 9000 enrolled participants. The study was based on a complex, multistage sample design and the sample was stratified by gender, age (15 to 65 years old) and socioeconomic level. A small-scale pilot study was performed in each country to test the procedures and tools. DISCUSSION: This study will provide valuable information and a unique dataset regarding Latin America that will enable cross-country comparisons of nutritional statuses that focus on energy and macro- and micronutrient intakes, food patterns, and energy expenditure. TRIAL REGISTRATION: Clinical Trials NCT02226627.


Assuntos
Dieta/etnologia , Comportamento Alimentar/etnologia , Inquéritos Nutricionais/estatística & dados numéricos , Estado Nutricional/etnologia , Adulto , Idoso , Argentina/epidemiologia , Brasil/epidemiologia , Chile/epidemiologia , Estudos Transversais , Ingestão de Alimentos/etnologia , Equador/epidemiologia , Feminino , Nível de Saúde , Humanos , América Latina/epidemiologia , Masculino , Pessoa de Meia-Idade , Inquéritos Nutricionais/normas , Peru/epidemiologia , Projetos Piloto , Venezuela/epidemiologia
2.
Braz. j. med. biol. res ; 44(10): 992-999, Oct. 2011.
Artigo em Inglês | LILACS | ID: lil-600690

RESUMO

The present review evaluates the role of sleep and its alteration in triggering problems of glucose metabolism and the possible involvement of adipokines in this process. A reduction in the amount of time spent sleeping has become an endemic condition in modern society, and a search of the current literature has found important associations between sleep loss and alterations of nutritional and metabolic contexts. Studies suggest that sleep loss is associated with problems in glucose metabolism and a higher risk for the development of insulin resistance and type 2 diabetes mellitus. The mechanism involved may be associated with the decreased efficacy of regulation of the hypothalamus-pituitary-adrenal axis by negative feedback mechanisms in sleep-deprivation conditions. In addition, changes in the circadian pattern of growth hormone (GH) secretion might also contribute to the alterations in glucose regulation observed during sleep loss. On the other hand, sleep deprivation stress affects adipokines - increasing tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) and decreasing leptin and adiponectin -, thus establishing a possible association between sleep-debt, adipokines and glucose metabolism. Thus, a modified release of adipokines resulting from sleep deprivation could lead to a chronic sub-inflammatory state that could play a central role in the development of insulin resistance and type 2 diabetes mellitus. Further studies are necessary to investigate the role of sleep loss in adipokine release and its relationship with glucose metabolism.


Assuntos
Humanos , Adipocinas/metabolismo , /etiologia , Intolerância à Glucose/metabolismo , Resistência à Insulina/fisiologia , Privação do Sono/complicações , Adiponectina/metabolismo , /metabolismo , /metabolismo , Leptina/metabolismo , Privação do Sono/metabolismo , Fator de Necrose Tumoral alfa/metabolismo
3.
Braz J Med Biol Res ; 44(10): 992-9, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21881808

RESUMO

The present review evaluates the role of sleep and its alteration in triggering problems of glucose metabolism and the possible involvement of adipokines in this process. A reduction in the amount of time spent sleeping has become an endemic condition in modern society, and a search of the current literature has found important associations between sleep loss and alterations of nutritional and metabolic contexts. Studies suggest that sleep loss is associated with problems in glucose metabolism and a higher risk for the development of insulin resistance and type 2 diabetes mellitus. The mechanism involved may be associated with the decreased efficacy of regulation of the hypothalamus-pituitary-adrenal axis by negative feedback mechanisms in sleep-deprivation conditions. In addition, changes in the circadian pattern of growth hormone (GH) secretion might also contribute to the alterations in glucose regulation observed during sleep loss. On the other hand, sleep deprivation stress affects adipokines - increasing tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) and decreasing leptin and adiponectin -, thus establishing a possible association between sleep-debt, adipokines and glucose metabolism. Thus, a modified release of adipokines resulting from sleep deprivation could lead to a chronic sub-inflammatory state that could play a central role in the development of insulin resistance and type 2 diabetes mellitus. Further studies are necessary to investigate the role of sleep loss in adipokine release and its relationship with glucose metabolism.


Assuntos
Adipocinas/metabolismo , Diabetes Mellitus Tipo 2/etiologia , Intolerância à Glucose/metabolismo , Resistência à Insulina/fisiologia , Privação do Sono/complicações , Adiponectina/metabolismo , Diabetes Mellitus Tipo 2/metabolismo , Humanos , Interleucina-6/metabolismo , Leptina/metabolismo , Privação do Sono/metabolismo , Fator de Necrose Tumoral alfa/metabolismo
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