Iacomino Giuseppe, Lauria Fabio, Russo Paola, Venezia Antonella, Iannaccone Nunzia, Marena Pasquale, Ahrens Wolfgang, De Henauw Stefaan, Molnár Dénes, Eiben Gabriele, Foraita Ronja, Hebestreit Antje, Kourides Giannis, Moreno Luis A, Veidebaum Toomas, Siani Alfonso
Institute of Food Sciences, National Research Council, ISA-CNR, via Roma 64, 83100, Avellino, Italy.
Leibniz Institute for Prevention Research and Epidemiology, BIPS, Achterstraße 30, 28359, Bremen, Germany.
Genes Nutr. 2021 Jul 9;16(1):10. doi: 10.1186/s12263-021-00689-1.
In recent years, the exciting emergence of circulating miRNAs as stable, reproducible, and consistent among individuals has opened a promising research opportunity for the detection of non-invasive biomarkers. A firm connection has been established between circulating miRNAs and glycaemic as well as metabolic homeostasis, showing that levels of specific miRNAs vary under different physio-pathological conditions.
In this pilot study, we investigated the expression of candidate miRNAs, hsa-miR-191-3p and hsa-miR-375, in relation to biomarkers associated with insulin sensitivity in a subgroup (n=58) of subjects participating to the European I.Family Study, a project aimed to assess the determinants of eating behaviour in children and adolescents and related health outcomes. The sample included overweight/obese children/adolescents since overweight/obesity is a known risk factor for impaired glucose homeostasis and metabolic disorders. Biological targets of candidate miRNAs were also explored in silico.
We observed a significant association of the two miRNAs and early changes in glycaemic homeostasis, independent of covariates including country of origin, age, BMI z-score, puberty status, highest educational level of parents, total energy intake, energy from fats, energy from carbohydrates, and energy from proteins.
Identification of circulating miRNAs associated with insulin impairment may offer novel approaches of assessing early variations in insulin sensitivity and provide evidence about the molecular mechanisms connected to early changes in glycaemic homeostasis.
ISRCTN, ISRCTN62310987. Retrospectively registered, http://isrctn.com/ISRCTN62310987.
近年来,循环miRNA作为个体间稳定、可重复且一致的物质令人兴奋地出现,为非侵入性生物标志物的检测开辟了一个有前景的研究机会。循环miRNA与血糖以及代谢稳态之间已建立了牢固的联系,表明特定miRNA的水平在不同的生理病理条件下会发生变化。
在这项初步研究中,我们调查了候选miRNA,即hsa-miR-191-3p和hsa-miR-375,在参与欧洲I.Family研究的一个亚组(n = 58)受试者中与胰岛素敏感性相关生物标志物的表达情况。该项目旨在评估儿童和青少年饮食行为的决定因素及相关健康结果。样本包括超重/肥胖儿童/青少年,因为超重/肥胖是已知的葡萄糖稳态受损和代谢紊乱的危险因素。还通过计算机模拟探索了候选miRNA的生物学靶点。
我们观察到这两种miRNA与血糖稳态的早期变化存在显著关联,且不受包括原籍国、年龄、BMI z评分、青春期状态、父母最高教育水平、总能量摄入、脂肪能量、碳水化合物能量和蛋白质能量等协变量的影响。
鉴定与胰岛素损伤相关的循环miRNA可能为评估胰岛素敏感性的早期变化提供新方法,并为与血糖稳态早期变化相关的分子机制提供证据。
ISRCTN,ISRCTN62310987。回顾性注册,http://isrctn.com/ISRCTN62310987。