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Alcoholic and Non-Alcoholic Beer Modulate Plasma and Macrophage microRNAs Differently in a Pilot Intervention in Humans with Cardiovascular Risk.
Daimiel, Lidia; Micó, Víctor; Díez-Ricote, Laura; Ruiz-Valderrey, Paloma; Istas, Geoffrey; Rodríguez-Mateos, Ana; Ordovás, José María.
Affiliation
  • Daimiel L; Nutritional Genomics and Epigenomics Group, IMDEA Food, CEI UAM + CSIC, 28049 Madrid, Spain.
  • Micó V; Nutritional Genomics and Epigenomics Group, IMDEA Food, CEI UAM + CSIC, 28049 Madrid, Spain.
  • Díez-Ricote L; Nutritional Genomics and Epigenomics Group, IMDEA Food, CEI UAM + CSIC, 28049 Madrid, Spain.
  • Ruiz-Valderrey P; Nutritional Genomics and Epigenomics Group, IMDEA Food, CEI UAM + CSIC, 28049 Madrid, Spain.
  • Istas G; Department of Nutritional Sciences, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, London WC2R 2LS, UK.
  • Rodríguez-Mateos A; Department of Nutritional Sciences, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, London WC2R 2LS, UK.
  • Ordovás JM; Nutritional Genomics and Epigenomics Group, IMDEA Food, CEI UAM + CSIC, 28049 Madrid, Spain.
Nutrients ; 13(1)2020 Dec 28.
Article in En | MEDLINE | ID: mdl-33379359
ABSTRACT
Beer is a popular beverage and some beneficial effects have been attributed to its moderate consumption. We carried out a pilot study to test if beer and non-alcoholic beer consumption modify the levels of a panel of 53 cardiometabolic microRNAs in plasma and macrophages. Seven non-smoker men aged 30-65 with high cardiovascular risk were recruited for a non-randomised cross-over intervention consisting of the ingestion of 500 mL/day of beer or non-alcoholic beer for 14 days with a 7-day washout period between interventions. Plasma and urine isoxanthohumol were measured to assess compliance with interventions. Monocytes were isolated and differentiated into macrophages, and plasma and macrophage microRNAs were analysed by quantitative real-time PCR. Anthropometric, biochemistry and dietary parameters were also measured. We found an increase in plasma miR-155-5p, miR-328-3p, and miR-92a-3p after beer and a decrease after non-alcoholic beer consumption. Plasma miR-320a-3p levels decreased with both beers. Circulating miR-320a-3p levels correlated with LDL-cholesterol. We found that miR-17-5p, miR-20a-5p, miR-145-5p, miR-26b-5p, and miR-223-3p macrophage levels increased after beer and decreased after non-alcoholic beer consumption. Functional analyses suggested that modulated microRNAs were involved in catabolism, nutrient sensing, Toll-like receptors signalling and inflammation. We concluded that beer and non-alcoholic beer intake modulated differentially plasma and macrophage microRNAs. Specifically, microRNAs related to inflammation increased after beer consumption and decreased after non-alcoholic beer consumption.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasma / Beer / Carbonated Beverages / MicroRNAs / Heart Disease Risk Factors / Macrophages Type of study: Clinical_trials / Etiology_studies / Risk_factors_studies Limits: Adult / Aged / Humans / Male / Middle aged Language: En Journal: Nutrients Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasma / Beer / Carbonated Beverages / MicroRNAs / Heart Disease Risk Factors / Macrophages Type of study: Clinical_trials / Etiology_studies / Risk_factors_studies Limits: Adult / Aged / Humans / Male / Middle aged Language: En Journal: Nutrients Year: 2020 Document type: Article Affiliation country:
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