Significance of the rs754635 variant of the cholecystokinin gene in the development of obesity in children

Q4 Medicine
A. Nikulina
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引用次数: 0

Abstract

So far, the possible influence of single nucleotide variants (SNV) of the cholecystokinin (CCK) gene on the likelihood of developing obesity and metabolic disorders in children has not been demonstrated. The aim of the study SNV associations of the CSK gene to predict the probability of obesity and personalize the development trajectory of various metabolic disorders associated with obesity in children. Materials and methods. 252 obese children aged 6-18 years were examined. The main group (n=152) was represented by children with metabolically unhealthy obesity (MUO). The control group (n=100) consolidated of children with metabolically healthy obesity (MHO). Whole genome sequencing (CeGat, Germany) was performed in 31 children of the main and 21 children of the control group. Serum levels of interleukin-1β were measured using a chemiluminescent immunoassay (CLIA) method, interleukin-6 - by enzyme-linked immunosorbent assay (ELISA), Synevo, Ukraine. Results. The G allele of SNV rs754635 of the CCK gene was significantly more frequent among children with both MHO (t=10.93; p<0.05) and MUO (t=12.96; p<0.05) compared to healthy individuals. The G allele of SNV rs754635 of the CCK gene was associated with basal hyperglycemia (r=0.44) and impaired carbohydrate tolerance (r=0.33) in the MHO phenotype and with the atherogenicity index of the lipid spectrum (r=0.40) and was inversely correlated with the level of high-density lipoproteins (HDL) (r=-0.58) in children with MUO phenotype, p<0.05. Conclusions. The G allele SNV rs754635 of the CCK gene is associated with obesity and the development of metabolic disorders. The research was carried out in accordance with the principles of the Declaration of Helsinki. The research protocol was approved by the Local Ethics Committee of the institution mentioned in the work. Informed consent of parents or their guardians was obtained for conducting research. No conflict of interests was declared by the author.
胆囊收缩素基因rs754635变异在儿童肥胖发生中的意义
到目前为止,胆囊收缩素(CCK)基因的单核苷酸变异(SNV)对儿童发生肥胖和代谢紊乱的可能性的可能影响尚未得到证实。研究CSK基因SNV相关性的目的是预测儿童肥胖的发生概率,个性化肥胖症相关的各种代谢性疾病的发展轨迹。材料和方法。对252名6 ~ 18岁的肥胖儿童进行了调查。主要组(n=152)为代谢性不健康肥胖(MUO)儿童。对照组(n=100)合并代谢健康型肥胖(MHO)患儿。对31例主要患儿和21例对照组患儿进行全基因组测序(德国CeGat)。血清白细胞介素-1β水平采用化学发光免疫分析法(CLIA)检测,白细胞介素-6 -采用酶联免疫吸附法(ELISA)检测,乌克兰Synevo。结果。CCK基因SNV rs754635的G等位基因在两种MHO患儿中更为常见(t=10.93;p<0.05)和MUO (t=12.96;p < 0.05)。CCK基因SNV rs754635 G等位基因与MHO表型的基础高血糖(r=0.44)和碳水化合物耐量受损(r=0.33)相关,与脂质谱的动脉粥样硬化指数(r=0.40)相关,与MUO表型儿童高密度脂蛋白(HDL)水平呈负相关(r=-0.58), p < 0.05。结论。CCK基因的G等位基因SNV rs754635与肥胖和代谢性疾病的发生有关。这项研究是按照《赫尔辛基宣言》的原则进行的。研究方案经工作中提到的机构当地伦理委员会批准。在进行研究时获得了父母或其监护人的知情同意。作者未声明存在利益冲突。
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来源期刊
Suchasna pediatriia Ukrayina
Suchasna pediatriia Ukrayina Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
50
审稿时长
8 weeks
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