Department of Pediatric Oncology and Hematology, University Children's Hospital of Krakow, 30-663 Krakow, Poland.
Department of Pediatric Oncology and Hematology, Faculty of Medicine, Jagiellonian University Medical College, 30-663 Krakow, Poland.
Nutrients. 2021 May 15;13(5):1683. doi: 10.3390/nu13051683.
The occurrence of childhood obesity is influenced by both genetic and epigenetic factors. ( alpha-ketoglutarate dependent dioxygenase) is a gene of well-established connection with adiposity, while a protooncogene ( zinc finger) has been only recently linked to this condition. We performed a cross-sectional study on a cohort of 16 obese (aged 6.6-17.7) and 10 healthy (aged 11.4-16.9) children. The aim was to evaluate the relationship between methylation and expression of the aforementioned genes and the presence of obesity as well as alterations in anthropometric measurements (including waist circumference (WC), body fat (BF_kg) and body fat percent (BF_%)), metabolic parameters (lipid profile, blood glucose and insulin levels, presence of insulin resistance) and blood pressure. Expression and methylation were measured in peripheral blood mononuclear cells using a microarray technique and a method based on restriction enzymes, respectively. Multiple regression models were constructed to adjust for the possible influence of age and sex on the investigated associations. We showed significantly increased expression of the gene in obese children and in patients with documented insulin resistance. Higher expression was also associated with an increase in WC, BF_kg, and BF_% as well as higher fasting concentration of free fatty acids (FFA). methylation correlated positively with WC and BF_kg. Increase in expression was associated with higher BF%. Our results indicate that the gene is likely to play an important role in the development of childhood adiposity together with coexisting impairment of glucose-lipid metabolism.
儿童肥胖的发生受到遗传和表观遗传因素的影响。(α-酮戊二酸依赖性双加氧酶)是与肥胖密切相关的基因,而原癌基因(锌指)最近才与这种情况有关。我们对 16 名肥胖(年龄 6.6-17.7)和 10 名健康(年龄 11.4-16.9)儿童的队列进行了横断面研究。目的是评估上述基因的甲基化和表达与肥胖以及体重指数(WC)、体脂肪(BF_kg)和体脂肪百分比(BF_%)、血脂谱、血糖和胰岛素水平、胰岛素抵抗等方面的变化之间的关系。采用微阵列技术和基于限制酶的方法分别在外周血单核细胞中测量表达和甲基化。构建多元回归模型,以调整年龄和性别对所研究关联的可能影响。我们发现肥胖儿童和有记录的胰岛素抵抗患者的基因表达显著增加。较高的表达也与 WC、BF_kg 和 BF_%的增加以及空腹游离脂肪酸(FFA)浓度的升高有关。 甲基化与 WC 和 BF_kg 呈正相关。表达的增加与 BF%的增加有关。我们的结果表明,该基因可能在儿童肥胖的发展中与并存的糖脂代谢受损一起发挥重要作用。