About: Genetic variation in key molecules of the Th-17 immune response is not associated with risk for prosthetic joint infection in a Czech population     Goto   Sponge   NotDistinct   Permalink

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  • Background and aims. Prosthetic Joint Infection (PJI) is a serious complication of Total Joint Arthroplasty (TJA). The Th-17 immune response characterised by IL (interleukin)-17A, IL-17F, IL-23, chemotactic cytokines and their receptors, plays a prominent role in the immune response to invading bacteria. In addition, high expression of IL-17A has been reported in PJI. The aim of this study was to investigate whether genetic variation in the key molecules of the Th-17 immune response can affect the risk for PJI. Methods: Altogether ten Single Nucleotide Polymorphisms (SNPs) of IL17A (rs2275913), IL17F (rs763780), IL4 (rs2243250), IL12A (rs583911), IL12B (rs3212227 and (rs17860508), IL23R (rs7517847), CXCL1 (rs4074), CXCL5 (rs425535) and CXCR2 (rs2230054) genes were genotyped by PCR with sequence specific primers (SSP) in 98 patients with PJI and two kontrol groups 1) an aseptic TJA control (253 patients with TJA that did not develop PJI at least 6 yrs. after the surgery) and 2) a population control (185 healthy control subjects without TJA). Results: Allele, genotype and phenotype frequencies of investigated SNPs did not differ between the patients with PJI and control patients with aseptic TJA (P}0.05). There was no difference in the distribution of tested SNPs between patients with PJI and population controls without TJA (P}0.05) or between the two controls groups (P}0.05). Conclusions: We cannot nominate any of studied polymorphisms in IL17A, IL17F, IL4, IL12A, IL12B, IL23R, CXCL1, CXCL5 and CXCR2 genes as risk factors for PJI in the Czech TJA patients examined.
  • Background and aims. Prosthetic Joint Infection (PJI) is a serious complication of Total Joint Arthroplasty (TJA). The Th-17 immune response characterised by IL (interleukin)-17A, IL-17F, IL-23, chemotactic cytokines and their receptors, plays a prominent role in the immune response to invading bacteria. In addition, high expression of IL-17A has been reported in PJI. The aim of this study was to investigate whether genetic variation in the key molecules of the Th-17 immune response can affect the risk for PJI. Methods: Altogether ten Single Nucleotide Polymorphisms (SNPs) of IL17A (rs2275913), IL17F (rs763780), IL4 (rs2243250), IL12A (rs583911), IL12B (rs3212227 and (rs17860508), IL23R (rs7517847), CXCL1 (rs4074), CXCL5 (rs425535) and CXCR2 (rs2230054) genes were genotyped by PCR with sequence specific primers (SSP) in 98 patients with PJI and two kontrol groups 1) an aseptic TJA control (253 patients with TJA that did not develop PJI at least 6 yrs. after the surgery) and 2) a population control (185 healthy control subjects without TJA). Results: Allele, genotype and phenotype frequencies of investigated SNPs did not differ between the patients with PJI and control patients with aseptic TJA (P}0.05). There was no difference in the distribution of tested SNPs between patients with PJI and population controls without TJA (P}0.05) or between the two controls groups (P}0.05). Conclusions: We cannot nominate any of studied polymorphisms in IL17A, IL17F, IL4, IL12A, IL12B, IL23R, CXCL1, CXCL5 and CXCR2 genes as risk factors for PJI in the Czech TJA patients examined. (en)
Title
  • Genetic variation in key molecules of the Th-17 immune response is not associated with risk for prosthetic joint infection in a Czech population
  • Genetic variation in key molecules of the Th-17 immune response is not associated with risk for prosthetic joint infection in a Czech population (en)
skos:prefLabel
  • Genetic variation in key molecules of the Th-17 immune response is not associated with risk for prosthetic joint infection in a Czech population
  • Genetic variation in key molecules of the Th-17 immune response is not associated with risk for prosthetic joint infection in a Czech population (en)
skos:notation
  • RIV/61989592:15110/12:33138726!RIV13-MZ0-15110___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GP310/09/P377), P(NS10260)
http://linked.open...iv/cisloPeriodika
  • 3
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 137926
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15110/12:33138726
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • single nucleotide polymorphisms; chemokine receptors; chemokines; interleukin-17; sepsis; infection; total joint arthroplasty; prosthetic joint infection (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • CZ - Česká republika
http://linked.open...ontrolniKodProRIV
  • [F7DB6815F145]
http://linked.open...i/riv/nazevZdroje
  • Biomedical Papers-Olomouc
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 156
http://linked.open...iv/tvurceVysledku
  • Gallo, Jiří
  • Mrázek, František
  • Navrátilová, Zdenka
  • Petřek, Martin
issn
  • 1213-8118
number of pages
http://bibframe.org/vocab/doi
  • 10.5507/bp.2012.023
http://localhost/t...ganizacniJednotka
  • 15110
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