FIELD: medicine.
SUBSTANCE: invention refers to medicine, namely to paediatrics, and can be used for prediction of progressive clinical course of glomerulonephritis in children. Single-nucleotide polymorphism of endothelin-1 (Lys198Asn), interleukin-4 (C-589T) and tumour necrosis factor (G308A) genes is determined in peripheral blood cells. When detecting allele 198Asn of the endothelin-1 gene, the allele -589T of the interleukin-4 gene and allele 308A of the tumour necrosis factor gene; allele 198Asn of endothelin-1 gene and allele -589T of interleukin-4 gene; allele 198Asn of endothelin-1 gene and allele 308A of tumour necrosis factor gene; allele -589T of interleukin-4 gene; allele -589T of interleukin-4 gene and allele 308A of tumour necrosis factor gene; allele 198Asn of endothelin-1 gene, predict progressive clinical course of glomerulonephritis in children.
EFFECT: method provides high reliability of predicting the progressive clinical course of glomerulonephritis in children by determining single-nucleotide polymorphisms of endothelin-1 (Lys198Asn), interleukin-4 (C-589T) and tumour necrosis factor (G308A) genes.
1 cl, 3 ex
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Authors
Dates
2025-01-13—Published
2024-02-27—Filed