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RECRUITINGINTERVENTIONAL

Effects of Almonds in Glucose-intolerant Adults (AGAMEMNON)

Effects of Almonds in Glucose-intolerant Adults - a Randomised Controlled Study on Muscle Mass and Obesity, Energy Metabolism and Lipidome, NON-alcoholic Fatty Liver and Inflammation (AGAMEMNON)

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Tree nuts - such as almonds - contribute to beneficial effects of the Mediterranean diet on risk for cardiovascular events, type 2 diabetes, dyslipidemia, hypertension, inflammation and non-alcoholic fatty liver disease. Almonds provide few carbohydrates, but lots of unsaturated fat and dietary fiber. But to which extent and by which mechanisms may almonds improve all aspects of the Metabolic Syndrome? Previous clinical trials showed weaker effects than rodent studies, most possibly due to low statistical power and metabolically insusceptible patients. The 3-year AGAMEMNON project aims to investigate, if 16 weeks of supplementation with almonds (vs. no treatment) in 150 patients with prediabetes and NAFLD leads to significant improvements in glycemia and liver fat, lipid metabolism, body composition and inflammation. The isocaloric design will outrule effects of weight loss and will allow the analysis of metabolic pathways between fat depots, inflammation, insulin resistance and gut function. Lipidomics are assessed as novel predictor of disease progression and metabolic response.

Who May Be Eligible (Plain English)

Who May Qualify: - prediabetes (IFG or IGT or IFG-IGT), measured in plasma samples - NAFLD (MR-S: \>5,56 %) - BMI between 25 and 40 kg/m² Who Should NOT Join This Trial: - Treatment with antidiabetic drugs - Overt diabetes mellitus of any kind - Severe cardiovascular or pulmonary disorder - Renal disorder / Renal insufficiency (eGFR \< 60 ml/min/m²) - Severe psychiatric disorder (schizophrenia, severe depression; eating disorders) - Current or recent (\< 5 years) cancer diagnosis - Liver disease other than NAFLD - Use of corticosteroid treatments - Alcohol abuse - Smoking - Ongoing or recently finished (3 months before) weight loss - Current participation in other intervention studies - Pregnancy - Metal implants, claustrophobia - Allergy to almonds Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * prediabetes (IFG or IGT or IFG-IGT), measured in plasma samples * NAFLD (MR-S: \>5,56 %) * BMI between 25 and 40 kg/m² Exclusion Criteria: * Treatment with antidiabetic drugs * Overt diabetes mellitus of any kind * Severe cardiovascular or pulmonary disorder * Renal disorder / Renal insufficiency (eGFR \< 60 ml/min/m²) * Severe psychiatric disorder (schizophrenia, severe depression; eating disorders) * Current or recent (\< 5 years) cancer diagnosis * Liver disease other than NAFLD * Use of corticosteroid treatments * Alcohol abuse * Smoking * Ongoing or recently finished (3 months before) weight loss * Current participation in other intervention studies * Pregnancy * Metal implants, claustrophobia * Allergy to almonds

Treatments Being Tested

DIETARY_SUPPLEMENT

Raw whole almonds

Subjects will be supplemented with 60 grams of almonds (treatment) or left untreated (no-nut group) for 16 weeks. Patients of the no-nut group will receive 6,7 kgs of almonds after finishing the study, supporting their compliance as untreated group.

Locations (1)

Charite University Hospital Berlin
Berlin, Germany