4.7 Article

MiRNAs pro fi le as biomarkers of nutritional therapy for the prevention of type 2 diabetes mellitus: From the CORDIOPREV study

Journal

CLINICAL NUTRITION
Volume 40, Issue 3, Pages 1028-1038

Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.clnu.2020.06.035

Keywords

Type 2 diabetes mellitus; Diet; microRNAs; Biomarkers; Prevention; CORDIOPREV

Funding

  1. Fundacion Patrimonio Comunal Olivarero
  2. Junta de Andalucia (Consejeria de Salud, Consejeria de Agricultura y Pesca, Consejeria de Innovacion, Ciencia y Empresa)
  3. Diputaciones de Jaen y Cordoba, Centro de Excelencia en Investigacion sobre Aceite de Oliva y Salud
  4. Ministerio de Medio Ambiente, Medio Rural y Marino, Gobierno de Espana
  5. Ministerio de Economia y Competitividad [AGL2012/39615, PIE14/00005, PIE 14/00031, AGL2015-67896-P]
  6. Consejeria de Innovacion, Ciencia y Empresa, Proyectos de Investigacion de Excelencia, Junta de Andalucia [CVI-7450]
  7. Fondo Europeo de Desarrollo Regional (FEDER), JPI HDHL-NutriCog [PCIN-2016-084]
  8. ISCIII research contract (Programa Miguel-Servet) [CP14/00114]
  9. US Department of Agriculture [8050-51000-098-00D]

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The study found that the plasma levels of miRNAs at baseline were associated with the risk of developing T2DM after dietary intervention, with different miRNAs playing different roles depending on the diet. Pathway analysis indicated that miR-126 and miR29a were involved in regulating signaling pathways associated with T2DM development.
Background and aim: The incidence of type 2 diabetes mellitus (T2DM) has increased worldwide. One of the first actions to reduce the risk of this disease is to implement healthy dietary models; however, no universal dietary strategies have so far been established. In addition, MicroRNAs (miRNAs) are emerging as new biomarkers to predict disease. We aimed to study whether miRNAs could be used to select the nutritional therapy to prevent T2DM development in patients with cardiovascular disease. Methods: All patients from the CORDIOPREV study without T2DM at baseline according to the American Diabetes Association (ADA) diagnostic criteria (n 1/4 462) were included in the present study. Of them, after a median dietary intervention period of 60 months with two diets (Low fat or Mediterranean diets), 107 developed T2DM and 355 subjects did not develop the disease. The plasma levels of 24 miRNAs were measured at baseline by qRT-PCR. The risk of T2DM was evaluated by Cox regression analysis based on the plasma levels of the miRNAs at baseline and according to the dietary intervention. Finally, pathways analyses were carried out to identify target genes regulated by the miRNAs studied and cellular processes which could be associated with T2DM development. Results: Cox regression analyses showed that patients with low plasma levels of miR-145 at baseline showed a higher risk of developing T2DM after consumption of an LFHCC diet. In addition, patients with low levels of miR29a, miR-28-3p and miR-126 and high plasma levels of miR-150 at baseline showed a higher risk of developing T2DM after consumption of the Med diet. Finally, pathways analysis showed an interaction of miR-126 and miR29a in the modulation of FoxO, TNF-alpha, PI3K-AKT, p53 and mTOR signaling, associated with T2DM development. Conclusion: Our results suggest that circulating miRNAs could be used in clinical practice as a new tool for selecting the most suitable diet to prevent type 2 diabetes mellitus development in patients with cardiovascular disease. Clinical trials number: NCT00924937. (C) 2020 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.

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