Association between interleukin 8‐receptor gene (CXCR1 and CXCR2) polymorphisms and urinary tract infection: Evidence from 4097 subjects

ABSTRACT Aim The aim of this study was to determine whether a correlation exists between interleukin‐8 receptor polymorphisms and urinary tract infection (UTI) susceptibility. Methods We systematically searched electronic databases including PubMed, Embase, China National Knowledge Infrastructure, a...

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Published inNephrology (Carlton, Vic.) Vol. 24; no. 4; pp. 464 - 471
Main Authors Han, Shi‐Sheng, Lu, Yan, Chen, Min, Xu, Yan‐Qiu, Wang, Yi
Format Journal Article
LanguageEnglish
Published Melbourne John Wiley & Sons Australia, Ltd 01.04.2019
Wiley Subscription Services, Inc
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Online AccessGet full text
ISSN1320-5358
1440-1797
1440-1797
DOI10.1111/nep.13260

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Abstract ABSTRACT Aim The aim of this study was to determine whether a correlation exists between interleukin‐8 receptor polymorphisms and urinary tract infection (UTI) susceptibility. Methods We systematically searched electronic databases including PubMed, Embase, China National Knowledge Infrastructure, and Web of Science up to 5 November 2017 to select appropriate studies that focused on C‐X‐C chemokine receptor type 1 and/or 2 (CXCR1, CXCR2) polymorphisms with susceptibility to UTI. Eight case‐control studies including 2085 patients with UTI and 2012 controls were enrolled in this study. Seven studies of CXCR1 rs2234671 and two studies of rs3138086 were included in the meta‐analyses. Pooled odds ratio (OR) and corresponding 95% confidence interval (CI) were synthesized using fixed‐effects or random‐effects model according to heterogeneity. Results No significant correlations were found between CXCR1 rs2234671 and rs3138086 polymorphisms and UTI susceptibility. However, subgroup analysis showed that rs2234671 was associated with an increased risk of UTI under allelic comparisons (C vs. G, OR = 1.95, 95% CI = 1.07–3.55), heterozygous model (GC vs. GG, OR = 1.93, 95% CI = 1.06–3.50), and dominant model (GC + CC vs. GG, OR = 1.98, 95% CI = 1.07–3.69) in children, especially in paediatric patients with acute pyelonephritis (allelic, OR = 2.43, 95% CI = 1.28–4.60; heterozygous, OR = 2.40, 95% CI = 1.24–4.62; dominant, OR = 2.48, 95% CI = 1.26–4.88). Furthermore, these results remained the same after eliminating paediatric patients with vesicoureteral reflux. Conclusion CXCR1 rs2234671 polymorphism might be associated with an increased risk of UTI in children. Summary at a Glance This meta‐analysis of several case‐control studies showed that polymorphism rs2234671 in the CXCR1 gene may be associated with an increased risk of UTI in Caucasian children, while rs1126579 in the CXCR2 gene may have a protective role in UTI development.
AbstractList The aim of this study was to determine whether a correlation exists between interleukin-8 receptor polymorphisms and urinary tract infection (UTI) susceptibility. We systematically searched electronic databases including PubMed, Embase, China National Knowledge Infrastructure, and Web of Science up to 5 November 2017 to select appropriate studies that focused on C-X-C chemokine receptor type 1 and/or 2 (CXCR1, CXCR2) polymorphisms with susceptibility to UTI. Eight case-control studies including 2085 patients with UTI and 2012 controls were enrolled in this study. Seven studies of CXCR1 rs2234671 and two studies of rs3138086 were included in the meta-analyses. Pooled odds ratio (OR) and corresponding 95% confidence interval (CI) were synthesized using fixed-effects or random-effects model according to heterogeneity. No significant correlations were found between CXCR1 rs2234671 and rs3138086 polymorphisms and UTI susceptibility. However, subgroup analysis showed that rs2234671 was associated with an increased risk of UTI under allelic comparisons (C vs. G, OR = 1.95, 95% CI = 1.07-3.55), heterozygous model (GC vs. GG, OR = 1.93, 95% CI = 1.06-3.50), and dominant model (GC + CC vs. GG, OR = 1.98, 95% CI = 1.07-3.69) in children, especially in paediatric patients with acute pyelonephritis (allelic, OR = 2.43, 95% CI = 1.28-4.60; heterozygous, OR = 2.40, 95% CI = 1.24-4.62; dominant, OR = 2.48, 95% CI = 1.26-4.88). Furthermore, these results remained the same after eliminating paediatric patients with vesicoureteral reflux. CXCR1 rs2234671 polymorphism might be associated with an increased risk of UTI in children.
AimThe aim of this study was to determine whether a correlation exists between interleukin‐8 receptor polymorphisms and urinary tract infection (UTI) susceptibility.MethodsWe systematically searched electronic databases including PubMed, Embase, China National Knowledge Infrastructure, and Web of Science up to 5 November 2017 to select appropriate studies that focused on C‐X‐C chemokine receptor type 1 and/or 2 (CXCR1, CXCR2) polymorphisms with susceptibility to UTI. Eight case‐control studies including 2085 patients with UTI and 2012 controls were enrolled in this study. Seven studies of CXCR1 rs2234671 and two studies of rs3138086 were included in the meta‐analyses. Pooled odds ratio (OR) and corresponding 95% confidence interval (CI) were synthesized using fixed‐effects or random‐effects model according to heterogeneity.ResultsNo significant correlations were found between CXCR1 rs2234671 and rs3138086 polymorphisms and UTI susceptibility. However, subgroup analysis showed that rs2234671 was associated with an increased risk of UTI under allelic comparisons (C vs. G, OR = 1.95, 95% CI = 1.07–3.55), heterozygous model (GC vs. GG, OR = 1.93, 95% CI = 1.06–3.50), and dominant model (GC + CC vs. GG, OR = 1.98, 95% CI = 1.07–3.69) in children, especially in paediatric patients with acute pyelonephritis (allelic, OR = 2.43, 95% CI = 1.28–4.60; heterozygous, OR = 2.40, 95% CI = 1.24–4.62; dominant, OR = 2.48, 95% CI = 1.26–4.88). Furthermore, these results remained the same after eliminating paediatric patients with vesicoureteral reflux.ConclusionCXCR1 rs2234671 polymorphism might be associated with an increased risk of UTI in children.
ABSTRACT Aim The aim of this study was to determine whether a correlation exists between interleukin‐8 receptor polymorphisms and urinary tract infection (UTI) susceptibility. Methods We systematically searched electronic databases including PubMed, Embase, China National Knowledge Infrastructure, and Web of Science up to 5 November 2017 to select appropriate studies that focused on C‐X‐C chemokine receptor type 1 and/or 2 (CXCR1, CXCR2) polymorphisms with susceptibility to UTI. Eight case‐control studies including 2085 patients with UTI and 2012 controls were enrolled in this study. Seven studies of CXCR1 rs2234671 and two studies of rs3138086 were included in the meta‐analyses. Pooled odds ratio (OR) and corresponding 95% confidence interval (CI) were synthesized using fixed‐effects or random‐effects model according to heterogeneity. Results No significant correlations were found between CXCR1 rs2234671 and rs3138086 polymorphisms and UTI susceptibility. However, subgroup analysis showed that rs2234671 was associated with an increased risk of UTI under allelic comparisons (C vs. G, OR = 1.95, 95% CI = 1.07–3.55), heterozygous model (GC vs. GG, OR = 1.93, 95% CI = 1.06–3.50), and dominant model (GC + CC vs. GG, OR = 1.98, 95% CI = 1.07–3.69) in children, especially in paediatric patients with acute pyelonephritis (allelic, OR = 2.43, 95% CI = 1.28–4.60; heterozygous, OR = 2.40, 95% CI = 1.24–4.62; dominant, OR = 2.48, 95% CI = 1.26–4.88). Furthermore, these results remained the same after eliminating paediatric patients with vesicoureteral reflux. Conclusion CXCR1 rs2234671 polymorphism might be associated with an increased risk of UTI in children. Summary at a Glance This meta‐analysis of several case‐control studies showed that polymorphism rs2234671 in the CXCR1 gene may be associated with an increased risk of UTI in Caucasian children, while rs1126579 in the CXCR2 gene may have a protective role in UTI development.
The aim of this study was to determine whether a correlation exists between interleukin-8 receptor polymorphisms and urinary tract infection (UTI) susceptibility.AIMThe aim of this study was to determine whether a correlation exists between interleukin-8 receptor polymorphisms and urinary tract infection (UTI) susceptibility.We systematically searched electronic databases including PubMed, Embase, China National Knowledge Infrastructure, and Web of Science up to 5 November 2017 to select appropriate studies that focused on C-X-C chemokine receptor type 1 and/or 2 (CXCR1, CXCR2) polymorphisms with susceptibility to UTI. Eight case-control studies including 2085 patients with UTI and 2012 controls were enrolled in this study. Seven studies of CXCR1 rs2234671 and two studies of rs3138086 were included in the meta-analyses. Pooled odds ratio (OR) and corresponding 95% confidence interval (CI) were synthesized using fixed-effects or random-effects model according to heterogeneity.METHODSWe systematically searched electronic databases including PubMed, Embase, China National Knowledge Infrastructure, and Web of Science up to 5 November 2017 to select appropriate studies that focused on C-X-C chemokine receptor type 1 and/or 2 (CXCR1, CXCR2) polymorphisms with susceptibility to UTI. Eight case-control studies including 2085 patients with UTI and 2012 controls were enrolled in this study. Seven studies of CXCR1 rs2234671 and two studies of rs3138086 were included in the meta-analyses. Pooled odds ratio (OR) and corresponding 95% confidence interval (CI) were synthesized using fixed-effects or random-effects model according to heterogeneity.No significant correlations were found between CXCR1 rs2234671 and rs3138086 polymorphisms and UTI susceptibility. However, subgroup analysis showed that rs2234671 was associated with an increased risk of UTI under allelic comparisons (C vs. G, OR = 1.95, 95% CI = 1.07-3.55), heterozygous model (GC vs. GG, OR = 1.93, 95% CI = 1.06-3.50), and dominant model (GC + CC vs. GG, OR = 1.98, 95% CI = 1.07-3.69) in children, especially in paediatric patients with acute pyelonephritis (allelic, OR = 2.43, 95% CI = 1.28-4.60; heterozygous, OR = 2.40, 95% CI = 1.24-4.62; dominant, OR = 2.48, 95% CI = 1.26-4.88). Furthermore, these results remained the same after eliminating paediatric patients with vesicoureteral reflux.RESULTSNo significant correlations were found between CXCR1 rs2234671 and rs3138086 polymorphisms and UTI susceptibility. However, subgroup analysis showed that rs2234671 was associated with an increased risk of UTI under allelic comparisons (C vs. G, OR = 1.95, 95% CI = 1.07-3.55), heterozygous model (GC vs. GG, OR = 1.93, 95% CI = 1.06-3.50), and dominant model (GC + CC vs. GG, OR = 1.98, 95% CI = 1.07-3.69) in children, especially in paediatric patients with acute pyelonephritis (allelic, OR = 2.43, 95% CI = 1.28-4.60; heterozygous, OR = 2.40, 95% CI = 1.24-4.62; dominant, OR = 2.48, 95% CI = 1.26-4.88). Furthermore, these results remained the same after eliminating paediatric patients with vesicoureteral reflux.CXCR1 rs2234671 polymorphism might be associated with an increased risk of UTI in children.CONCLUSIONCXCR1 rs2234671 polymorphism might be associated with an increased risk of UTI in children.
This meta‐analysis of several case‐control studies showed that polymorphism rs2234671 in the CXCR1 gene may be associated with an increased risk of UTI in Caucasian children, while rs1126579 in the CXCR2 gene may have a protective role in UTI development.
Author Han, Shi‐Sheng
Wang, Yi
Xu, Yan‐Qiu
Chen, Min
Lu, Yan
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urinary tract infection
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Snippet ABSTRACT Aim The aim of this study was to determine whether a correlation exists between interleukin‐8 receptor polymorphisms and urinary tract infection (UTI)...
This meta‐analysis of several case‐control studies showed that polymorphism rs2234671 in the CXCR1 gene may be associated with an increased risk of UTI in...
The aim of this study was to determine whether a correlation exists between interleukin-8 receptor polymorphisms and urinary tract infection (UTI)...
AimThe aim of this study was to determine whether a correlation exists between interleukin‐8 receptor polymorphisms and urinary tract infection (UTI)...
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SubjectTerms Age Factors
Case-Control Studies
Chemokines
Children
CXCR2 protein
Cytokines
Gene Frequency
Genetic Association Studies
Genetic Predisposition to Disease
Heterozygote
Homozygote
Humans
Interleukin 8
Meta-analysis
Phenotype
polymorphism
Polymorphism, Single Nucleotide
Protective Factors
Pyelonephritis
Pyelonephritis - diagnosis
Pyelonephritis - genetics
Pyelonephritis - prevention & control
Receptors, Interleukin-8A - genetics
Receptors, Interleukin-8B - genetics
Risk Factors
Urinary tract
Urinary tract diseases
urinary tract infection
Urinary tract infections
Urinary Tract Infections - diagnosis
Urinary Tract Infections - genetics
Urinary Tract Infections - prevention & control
Urogenital system
Title Association between interleukin 8‐receptor gene (CXCR1 and CXCR2) polymorphisms and urinary tract infection: Evidence from 4097 subjects
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fnep.13260
https://www.ncbi.nlm.nih.gov/pubmed/29577511
https://www.proquest.com/docview/2198351678
https://www.proquest.com/docview/2018668534
Volume 24
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