FIELD: medicine.
SUBSTANCE: invention relates to medicine, namely to pediatrics, pediatric endocrinology, medical genetics, and can be used to identify a predisposition to the development of metabolic syndrome in the form of obesity in schoolchildren 7-10 years old. A sample of buccal epithelium is taken from the patient and DNA is isolated. The polymorphism of the TP53 gene (rs1042522) and the IL1β gene (rs1143634) is genotyped. In a child's blood sample, the content of the transcription factor p53 and the level of interleukin 1β are determined. With the simultaneous fulfillment of the following conditions: the presence of a combination of the GG genotype of the TP53 gene (rs1042522) and the CC genotype of the IL1β gene (rs1143634), a decrease in the level of p53 in the blood compared to the lower limit of the physiological norm, equal to 12-18%, by 1.4 or more times, and an increase in the level of interleukin 1β in comparison with the upper limit of the physiological norm equal to 0-5 pg/cm3, by 1.4 or more times, the predisposition to the development of metabolic syndrome in the form of obesity in schoolchildren 7-10 years old is assessed as high.
EFFECT: method ensures the reliability of revealing predisposition to the development of metabolic syndrome in the form of obesity in schoolchildren aged 7-10 years.
1 cl, 1 tbl, 2 ex
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Authors
Dates
2022-08-31—Published
2022-03-02—Filed