Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Inflammation ; 36(1): 15-25, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22865000

RESUMO

Low-grade chronic systemic inflammation is often associated with chronic non-communicable diseases, and its most frequently used marker, the C-reactive protein (CRP), has become an identifier of such diseases as well as an independent predictor for cardiovascular disorders and mortality. CRP is produced in response to pro-inflammatory signaling and to individual and behavioral factors, leading to pathological states. The aim of this study was to rank the predicting factors of high CRP concentrations in free-living adults from a community-based sample. We evaluated 522 adults (40-84 years old; 381 women) for anthropometric characteristics, dietary intake, clinical and physical tests, and blood analysis. Subjects were assigned to groups, according to CRP concentrations, as normal CRP (G1; <3.0 mg/L; n = 269), high CRP (G2; 3.0-6.0 mg/L; n = 139), and very high CRP (G3; >6.0 mg/dL; n = 116). Statistical comparison between groups used one-way ANOVA or Kruskal-Wallis tests, and prediction of altered values in increasing CRP was evaluated by proportional hazard models (odds ratio). CRP distribution was influenced by gender, body mass index, body and abdominal fatness, blood leukocytes, and neutrophil counts. The higher CRP group was discriminated by the above variables in addition to lower VO(2max), serum metabolic syndrome components (triglycerides, glucose, and HDL cholesterol), higher insulin, homeostasis assessment of insulin resistance, uric acid, gamma-GT, and homocysteine. After adjustments, only fatness, blood leukocytes, and hyperglycemia remained as independent predictors for increased serum CRP concentrations. Intervention procedures to treat low-grade chronic inflammation in overweight women would mainly focus on restoring muscle mass and functions in addition to an antioxidant-rich diet.


Assuntos
Proteína C-Reativa/análise , Hiperglicemia , Inflamação/metabolismo , Resistência à Insulina , Obesidade , Gordura Abdominal , Adulto , Idoso , Idoso de 80 Anos ou mais , Antropometria , Glicemia , Índice de Massa Corporal , Brasil , Doenças Cardiovasculares/metabolismo , Doenças Cardiovasculares/mortalidade , HDL-Colesterol/sangue , Estudos Transversais , Comportamento Alimentar , Feminino , Homocisteína/sangue , Humanos , Insulina/sangue , Contagem de Leucócitos , Masculino , Síndrome Metabólica , Pessoa de Meia-Idade , Neutrófilos , Avaliação Nutricional , Modelos de Riscos Proporcionais , Fatores de Risco , Triglicerídeos/sangue , Ácido Úrico/sangue
2.
J Obes ; 2011: 534714, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21822484

RESUMO

Objective. To compare values from predictive equations of resting energy expenditure (REE) with indirect calorimetry (IC) in overweight and obese adults. Methods. Eighty-two participants aged 30 to 60 years old were retrospectively analyzed. The persons had a body mass index ≥25 kg/m(2). REE was estimated by IC and other five equations of the literature (Harris and Benedict, WHO1, WHO2, Owen, Mifflin). Results. All equations had different values when compared to those of IC. The best values were found by Harris and Benedict, WHO1, and WHO2, with high values of intraclass correlation coefficient and low values of mean difference. Furthermore, WHO1 and WHO2 showed lower systematic error and random. Conclusion. No predictive equations had the same values of REE as compared to those of indirect calorimetry, and those which least underestimated REE were the equations of WHO1, WHO2, and Harris and Benedict. The next step would be to validate the new equation proposed.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA