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Polymorphism of interleukin-1β gene and susceptibility to chronic adenoiditis development at children of Siberia
Natalia Terskova, Natalia Shnayder, Sergey Vakhrushev
Jazyk angličtina Země Česko
- MeSH
- adenoidy * imunologie MeSH
- dítě MeSH
- ELISA MeSH
- interleukin-1 * analýza genetika krev MeSH
- jednonukleotidový polymorfismus * MeSH
- lidé MeSH
- předškolní dítě MeSH
- riziko MeSH
- rizikové faktory MeSH
- výzkumný projekt MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- předškolní dítě MeSH
The research objective was to establish a role of polymorphism of interleukin-1β gene in the locus 3954 (rs 1143634) on the chromosome 2q13-21 as a risk factor of an adverse course of the inflammatory process at chronic adenoiditis. The research is a part of the complex scientific subject "Translational Otorhinolaryngology" which was carried out in 2010-2012. The results of genotyping of 944 people were received. High total frequency of inheritance of mutant polymorphic allelic variants of interleukin-1β gene, including homozygous (C/C) and heterozygous (С/Т) carriage is revealed at children with chronic adenoiditis. The frequency was 95,5% in sampling. At a homozygous carriage of oligonucleotide replacement of thymine for cytosine in the position 3954 of interleukin-1β gene functional activity of interleukin-1β changed- its pro-inflammatory effect increased by 100%. Children of this group had a heavy current chronic adenoiditis with the frequent aggravations, complications and the interfacing diseases at high concentration in blood serum interleukin-1β (298,4±8,2) pg/ml (control − 65,43 pg/ml) (p˂0,001).
Citace poskytuje Crossref.org
Literatura
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- $a The research objective was to establish a role of polymorphism of interleukin-1β gene in the locus 3954 (rs 1143634) on the chromosome 2q13-21 as a risk factor of an adverse course of the inflammatory process at chronic adenoiditis. The research is a part of the complex scientific subject "Translational Otorhinolaryngology" which was carried out in 2010-2012. The results of genotyping of 944 people were received. High total frequency of inheritance of mutant polymorphic allelic variants of interleukin-1β gene, including homozygous (C/C) and heterozygous (С/Т) carriage is revealed at children with chronic adenoiditis. The frequency was 95,5% in sampling. At a homozygous carriage of oligonucleotide replacement of thymine for cytosine in the position 3954 of interleukin-1β gene functional activity of interleukin-1β changed- its pro-inflammatory effect increased by 100%. Children of this group had a heavy current chronic adenoiditis with the frequent aggravations, complications and the interfacing diseases at high concentration in blood serum interleukin-1β (298,4±8,2) pg/ml (control − 65,43 pg/ml) (p˂0,001).
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