Choi Won Hee, Ahn Jiyun, Um Min Young, Jung Chang Hwa, Jung Sung Eun, Ha Tae Youl
Division of Food Functionality Research, Korea Food Research Institute, Wanju 55365, Korea.
Division of Food Biotechnology, University of Science and Technology, Daejeon 34113, Korea.
Nutr Res Pract. 2020 Aug;14(4):412-422. doi: 10.4162/nrp.2020.14.4.412. Epub 2020 May 4.
BACKGROUND/OBJECTIVES: This study investigates correlations between circulating microRNAs (miRNAs) and obesity-related parameters among young women (aged 20-30 years old) in Korea.
SUBJECTS/METHODS: We analyzed TaqMan low density arrays (TLDAs) of circulating miRNAs in 9 lean (body mass index [BMI] < 25 kg/m) and 15 obese (BMI > 25 kg/m) women. We also performed gene ontology (GO) analyses of the biological functions of predicted miRNA target genes, and clustered the results using the database for annotation, visualization and integrated discovery.
The TLDA cards contain 754 human miRNAs; of these, the levels of 8 circulating miRNAs significantly declined (> 2-fold) in obese subjects compared with those in lean subjects, including miR-1227, miR-144-5p, miR-192, miR-320, miR-320b, miR-484, miR-324-3p, and miR-378. Among them, miR-484 and miR-378 displayed the most significant inverse correlations with BMI (miR-484, r = -0.5484, = 0.0056; miR-378, r = -0.5538, = 0.0050) and visceral fat content (miR-484, r = -0.6141, = 0.0014; miR-378, r = -0.6090, = 0.0017). GO analysis indicated that genes targeted by miR-484 and miR-378 had major roles in carbohydrate and lipid metabolism.
Our result showed the differentially expressed circulating miRNAs in obese subjects compared to lean subjects. Although the mechanistic study to reveal the causal role of miRNAs remains, these miRNAs may be novel biomarkers for obesity.
背景/目的:本研究调查了韩国年轻女性(20 - 30岁)循环微RNA(miRNA)与肥胖相关参数之间的相关性。
对象/方法:我们分析了9名瘦女性(体重指数[BMI]<25kg/m²)和15名肥胖女性(BMI>25kg/m²)循环miRNA的TaqMan低密度阵列(TLDA)。我们还对预测的miRNA靶基因的生物学功能进行了基因本体(GO)分析,并使用注释、可视化和综合发现数据库对结果进行聚类。
TLDA卡包含754种人类miRNA;其中,与瘦受试者相比,8种循环miRNA在肥胖受试者中的水平显著下降(>2倍),包括miR - 1227、miR - 144 - 5p、miR - 192、miR - 320、miR - 320b、miR - 484、miR - 324 - 3p和miR - 378。其中,miR - 484和miR - 378与BMI(miR - 484,r = - 0.5484,P = 0.0056;miR - 378,r = - 0.5538,P = 0.0050)和内脏脂肪含量(miR - 484,r = - 0.6141,P = 0.0014;miR - 378,r = - 0.6090,P = 0.0017)呈现出最显著的负相关。GO分析表明,miR - 484和miR - 378靶向的基因在碳水化合物和脂质代谢中起主要作用。
我们的结果显示肥胖受试者与瘦受试者相比循环miRNA存在差异表达。尽管揭示miRNA因果作用的机制研究仍在进行,但这些miRNA可能是肥胖的新型生物标志物。