A plasma circulating miRNAs profile predicts type 2 diabetes mellitus and prediabetes: from the CORDIOPREV study

被引:85
作者
Jimenez-Lucena, Rosa [1 ,2 ,3 ]
Camargo, Antonio [1 ,2 ,3 ]
Francisco Alcala-Diaz, Juan [1 ,2 ,3 ]
Romero-Baldonado, Cristina [4 ]
Miguel Luque, Raul [2 ,3 ,5 ]
van Ommen, Ben [6 ]
Delgado-Lista, Javier [1 ,2 ,3 ]
Maria Ordovas, Jose [7 ,8 ,9 ]
Perez-Martinez, Pablo [1 ,2 ,3 ]
Alberto Rangel-Zuniga, Oriol [1 ,2 ,3 ]
Lopez-Miranda, Jose [1 ,2 ,3 ]
机构
[1] Reina Sofia Univ Hosp, Lipids & Atherosclerosis Unit, Cordoba, Spain
[2] Univ Cordoba, Reina Sofia Univ Hosp, IMIBIC, Cordoba, Spain
[3] Inst Salud Carlos III, CIBER Fisiopatol Obesidad & Nutr CIBEROBN, Madrid, Spain
[4] Reina Sofia Univ Hosp, Biochem Lab, Cordoba, Spain
[5] Univ Cordoba, Agrifood Campus Int Excellence CeiA3, Dept Cell Biol Physiol & Immunol, Cordoba, Spain
[6] Netherlands Inst Appl Sci TNO, Res Grp Microbiol & Syst Biol, Zeist, Netherlands
[7] Tufts Univ, Nutr & Genom Lab, USDA, Human Nutr Res Ctr Aging,JM, Boston, MA 02111 USA
[8] Ctr Nacl Invest Cardiovasc, Madrid, Spain
[9] CEI UAM CSIC, IMDEA Food Inst, Madrid, Spain
关键词
IMPAIRED FASTING GLUCOSE; INSULIN SENSITIVITY; MICRORNAS; RESISTANCE; TOLERANCE; SECRETION; INDEXES; DISEASE; GENES; RISK;
D O I
10.1038/s12276-018-0194-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We aimed to explore whether changes in circulating levels of miRNAs according to type 2 diabetes mellitus (T2DM) or prediabetes status could be used as biomarkers to evaluate the risk of developing the disease. The study included 462 patients without T2DM at baseline from the CORDIOPREV trial. After a median follow-up of 60 months, 107 of the subjects developed T2DM, 30 developed prediabetes, 223 maintained prediabetes and 78 remained disease-free. Plasma levels of four miRNAs related to insulin signaling and beta-cell function were measured by RT-PCR. We analyzed the relationship between miRNAs levels and insulin signaling and release indexes at baseline and after the follow-up period. The risk of developing disease based on tertiles (T1-T2-T3) of baseline miRNAs levels was evaluated by COX analysis. Thus, we observed higher miR-150 and miR-30a-5p and lower miR-15a and miR-375 baseline levels in subjects with T2DM than in disease-free subjects. Patients with high miR-150 and miR-30a-5p baseline levels had lower disposition index (p = 0.047 and p = 0.007, respectively). The higher risk of disease was associated with high levels (T3) of miR-150 and miR-30a-5p (HRT3-T1 = 4.218 and HRT3-T1 = 2.527, respectively) and low levels (T1) of miR-15a and miR375 (HRT1-T3 = 3.269 and HRT1-T3 = 1.604, respectively). In conclusion, our study showed that deregulated plasma levels of miR-150, miR-30a-5p, miR-15a, and miR-375 were observed years before the onset of T2DM and pre-DM and could be used to evaluate the risk of developing the disease, which may improve prediction and prevention among individuals at high risk for T2DM.
引用
收藏
页码:1 / 12
页数:12
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