Méndez-Mancilla A, Lima-Rogel V, Toro-Ortíz J C, Escalante-Padrón F, Monsiváis-Urenda A E, Noyola D E, Salgado-Bustamante M
Biochemistry Department, Faculty of Medicine, Universidad Autónoma de San Luis Potosí, San Luis Potosí, Mexico.
Pediatrics Department, Hospital Central "Dr. Ignacio Morones Prieto", San Luis Potosi, Mexico.
Pediatr Obes. 2018 Mar;13(3):168-174. doi: 10.1111/ijpo.12247. Epub 2017 Oct 17.
The perinatal environment has a role in the establishment of altered metabolic and inflammatory responses, and could be modulated by microRNAs regulating immune and metabolic processes.
To analyze the expression profile of four circulating microRNAs and cytokine serum concentrations in neonates born to overweight and obese women.
Pregnant women were included and grouped by pregestational body mass index (21 with normal weight, 10 overweight and 10 obese women). A peripheral blood sample was obtained from newborn infants and used to determine circulating miRNAs expression and cytokine serum concentrations.
There were significant differences in the expression of three microRNAs between newborns of pregestational obese women and newborns from pregestational normal weight women: miR-155 (p = 0.03), miR-181a (p = 0.02) and miR-221 (p = 0.04). A significant reduction in IL-1β (p = 0.005) expression was also found in newborns of overweight women; although this cytokine was also diminished in newborns of obese women, this was not statistically significant. An association between IL-1β concentrations and miR-146a and miR-221 expression was also observed.
Expression of miR-155, miR-181a and miR-221 differs in infants born to obese women compared with infants born to normal weight women. Changes in microRNA expression could participate in the epigenetic foetal programming of metabolic disorders in children born to obese women.
围产期环境在改变代谢和炎症反应的建立过程中发挥作用,并且可能受到调节免疫和代谢过程的微小RNA的调控。
分析超重和肥胖女性所生新生儿中四种循环微小RNA的表达谱及细胞因子血清浓度。
纳入孕妇并根据孕前体重指数进行分组(21例体重正常、10例超重和10例肥胖女性)。采集新生儿外周血样本,用于测定循环微小RNA表达及细胞因子血清浓度。
孕前肥胖女性所生新生儿与孕前体重正常女性所生新生儿之间,三种微小RNA的表达存在显著差异:miR-155(p = 0.03)、miR-181a(p = 0.02)和miR-221(p = 0.04)。超重女性所生新生儿中IL-1β(p = 0.005)表达也显著降低;尽管肥胖女性所生新生儿中该细胞因子也有所减少,但差异无统计学意义。还观察到IL-1β浓度与miR-146a和miR-221表达之间存在关联。
与体重正常女性所生婴儿相比,肥胖女性所生婴儿中miR-155、miR-181a和miR-221的表达存在差异。微小RNA表达的变化可能参与肥胖女性所生孩子代谢紊乱的表观遗传胎儿编程。