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Toll-Like Receptor Polymorphisms and Susceptibility to Urinary Tract Infections in Adult Women
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 a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696082/ https://www.ncbi.nlm.nih.gov/pubmed/19543401 http://dx.doi.org/10.1371/journal.pone.0005990 |
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author | Hawn, Thomas R. Scholes, Delia Li, Shuying S. Wang, Hongwei Yang, Yin Roberts, Pacita L. Stapleton, Ann E. Janer, Marta Aderem, Alan Stamm, Walter E. Zhao, Lue Ping Hooton, Thomas M. |
author_facet | Hawn, Thomas R. Scholes, Delia Li, Shuying S. Wang, Hongwei Yang, Yin Roberts, Pacita L. Stapleton, Ann E. Janer, Marta Aderem, Alan Stamm, Walter E. Zhao, Lue Ping Hooton, Thomas M. |
author_sort | Hawn, Thomas R. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2696082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26960822009-06-22 Toll-Like Receptor Polymorphisms and Susceptibility to Urinary Tract Infections in Adult Women Hawn, Thomas R. Scholes, Delia Li, Shuying S. Wang, Hongwei Yang, Yin Roberts, Pacita L. Stapleton, Ann E. Janer, Marta Aderem, Alan Stamm, Walter E. Zhao, Lue Ping Hooton, Thomas M. PLoS One Research Article 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. Public Library of Science 2009-06-22 /pmc/articles/PMC2696082/ /pubmed/19543401 http://dx.doi.org/10.1371/journal.pone.0005990 Text en Hawn et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hawn, Thomas R. Scholes, Delia Li, Shuying S. Wang, Hongwei Yang, Yin Roberts, Pacita L. Stapleton, Ann E. Janer, Marta Aderem, Alan Stamm, Walter E. Zhao, Lue Ping Hooton, Thomas M. Toll-Like Receptor Polymorphisms and Susceptibility to Urinary Tract Infections in Adult Women |
title | Toll-Like Receptor Polymorphisms and Susceptibility to Urinary Tract Infections in Adult Women |
title_full | Toll-Like Receptor Polymorphisms and Susceptibility to Urinary Tract Infections in Adult Women |
title_fullStr | Toll-Like Receptor Polymorphisms and Susceptibility to Urinary Tract Infections in Adult Women |
title_full_unstemmed | Toll-Like Receptor Polymorphisms and Susceptibility to Urinary Tract Infections in Adult Women |
title_short | Toll-Like Receptor Polymorphisms and Susceptibility to Urinary Tract Infections in Adult Women |
title_sort | toll-like receptor polymorphisms and susceptibility to urinary tract infections in adult women |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696082/ https://www.ncbi.nlm.nih.gov/pubmed/19543401 http://dx.doi.org/10.1371/journal.pone.0005990 |
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