AI Article Synopsis

  • The study investigates the genetic factors, specifically polymorphisms in Toll-like receptor (TLR) pathway genes, in relation to urinary tract infections (UTIs) among women aged 18-49.
  • Results show that the TLR4_A896G variant may provide protection against recurrent cystitis, while TLR5_C1174T is linked to an increased risk of recurrent infections; TLR1_G1805T offers protection against pyelonephritis.
  • These findings point to the potential role of TLR gene variants in UTI susceptibility, but further research is needed for confirmation due to the modest statistical significance of results.

Article Abstract

Background: Although behavioral risk factors are strongly associated with urinary tract infection (UTI) risk, the role of genetics in acquiring this disease is poorly understood.

Methodology/principal Findings: To test the hypothesis that polymorphisms in Toll-like receptor (TLR) pathway genes are associated with susceptibility to UTIs, we conducted a population-based case-control study of women ages 18-49 years. We examined DNA variants in 9 TLR pathway genes in 431 recurrent cystitis (rUTI) cases, 400 pyelonephritis cases, and 430 controls with no history of UTIs. In the Caucasian subgroup of 987 women, polymorphism TLR4_A896G was associated with protection from rUTI, but not pyelonephritis, with an odds ratio (OR) of 0.54 and a 95% confidence interval (CI) of 0.31 to 0.96. Polymorphism TLR5_C1174T, which encodes a variant that abrogates flagellin-induced signaling, was associated with an increased risk of rUTI (OR(95%CI): 1.81 (1.00-3.08)), but not pyelonephritis. Polymorphism TLR1_G1805T was associated with protection from pyelonephritis (OR(95%CI): 0.53 (0.29-0.96)).

Conclusions: These results provide the first evidence of associations of TLR5 and TLR1 variants with altered risks of acquiring rUTI and pyelonephritis, respectively. Although these data suggest that TLR polymorphisms are associated with adult susceptibility to UTIs, the statistical significance was modest and will require further study including validation with independent cohorts.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696082PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0005990PLOS

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