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1.
Eur J Nutr ; 62(4): 1755-1765, 2023 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-36820883

RESUMO

PURPOSE: Studies show that dairy fat consumed in the form of cheese reduce LDL-cholesterol concentration (LDL-c) compared to butter and mechanistic suggestions include the calcium content of cheese leading to enhanced faecal fat excretion. The aim of this study was to test the effect of varying the calcium content within a cheese, on faecal fat excretion as a primary outcome, and blood lipid markers, fasting glucose and calcium excretion as secondary outcomes. METHODS: 7 healthy males (BMI 18-25) participated in this randomized, cross-over control intervention, of 3 × 2 week periods. Diets contained 240 g/day cheese; a High Calcium Cheese (HCC) diet, a Reduced Calcium Cheese (RCC) diet, and a control arm: Reduced Calcium Cheese + CaCO3 Supplement (RCC + Supp) diet. Diets differed in calcium content and form but were otherwise controlled for energy and key macronutrients. Blood and 5-day faecal samples were collected. RESULTS: There was no significant difference in faecal fat excretion (g/day) between the diets (P = 0.066). Percent fat of faecel excretion was higher after RCC + Supp (P = 0.016). None of the individual fatty acids were different. Fasting LDL-c was significantly lower following the HCC diet vs. the other arms (P = 0.002). Faecal Ca was different across all diets (P = 0.001), lowest after RCC, and greatest after RCC + Supp. No differences were observed for fasting blood parameters or changes in anthropometry. CONCLUSION: Varying the calcium content within a cheese matrix significantly affected fasting LDL-c values. Results did not support higher faecal fat excretion as an underlying mechanism, but the high attrition rate was a limitation. Trial registerer Trial Registered at ISRCTN.org, registration number ISRCTN11663659 on 12.07.2022. Retrospectively registered.


Assuntos
Carcinoma de Células Renais , Queijo , Neoplasias Renais , Humanos , Masculino , Glicemia , Cálcio , Cálcio da Dieta , HDL-Colesterol , LDL-Colesterol , Estudos Cross-Over , Gorduras na Dieta
2.
J Diet Suppl ; 10(4): 370-80, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24237191

RESUMO

The antioxidant and antiinflammatory properties of polyphenols are well documented in vitro but there are few human studies. A herbal beverage composed of chamomile, meadowsweet, and willow bark (CMW) was developed and tested for its antiinflammatory effect in a cohort of healthy adults (n = 20) during a 4-week intervention. Subjects were randomised to either the treatment (TG) or placebo group (PG). The three herbs under study, which have been used in traditional and alternative medicine, were delivered in a berry extract matrix. This berry extract was used as a control in the experiment. The objective was to assess the herbs' effects on systemic inflammation and joint function by examining circulating cytokines and mechanical joint flexibility. Blood serum was analyzed for cytokines IL-1ß, IL-6, and TNFα. There was an average decrease of 21.7% IL-1ß in the treatment group, whereas the decrease seen in the placebo group was 3% but these were not statistically significant. Quartile analysis based on baseline production of TNFα demonstrated a decrease in the treatment group's IL-6 levels. This group showed improvements in mechanical joint function and pain upon movement of joints specific to the knee and lower back. Overall, no significant antiinflammatory effects were seen. The evidence is therefore inconclusive and further investigations are required using a larger cohort with some degree of elevated inflammatory activity.


Assuntos
Anti-Inflamatórios/farmacologia , Camomila , Citocinas/sangue , Filipendula , Articulações/efeitos dos fármacos , Extratos Vegetais/farmacologia , Salix , Adulto , Dorso , Bebidas , Mirtilos Azuis (Planta) , Frutas , Humanos , Interleucina-1beta/sangue , Interleucina-6/sangue , Joelho , Articulação do Joelho , Fenóis/análise , Fenóis/farmacologia , Fitoterapia , Extratos Vegetais/química , Amplitude de Movimento Articular/efeitos dos fármacos , Fator de Necrose Tumoral alfa/sangue
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