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Genetic polymorphisms associated with urinary tract infection in children and adults: a systematic review and meta-analysis.
Yu, Jiakun; Varella Pereira, Glaucia Miranda; Allen-Brady, Kristina; Cuffolo, Romana; Siddharth, Aditi; Koch, Marianne; Chua, John W F; Sorrentino, Felice; Dytko, Oskar; Ng, Kaa-Yung; Violette, Philippe; Khullar, Vik; Wang, Zhan Tao; Cartwright, Rufus.
Afiliación
  • Yu J; University Hospitals Sussex NHS Foundation Trust, Brighton, United Kingdom. Electronic address: jiakun.yu4@nhs.net.
  • Varella Pereira GM; Department of Epidemiology and Biostatistics, Imperial College London, Norfolk Place, London, United Kingdom; Department of Urogynaecology, LNWH NHS Trust, London, United Kingdom; Department of Obstetrics and Gynaecology, School of Medical Sciences, University of Campinas, Brazil.
  • Allen-Brady K; Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT.
  • Cuffolo R; Department of Obstetrics and Gynaecology, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, United Kingdom.
  • Siddharth A; John Radcliffe Hospital, Headley Way, Headington, Oxford, United Kingdom.
  • Koch M; Department of Obstetrics and Gynecology, Medical University of Vienna, Vienna, Austria.
  • Chua JWF; Frimley Health NHS Foundation Trust, Frimley, United Kingdom.
  • Sorrentino F; Department of Medical and Surgical Sciences, Institute of Obstetrics and Gynecology, University of Foggia, Foggia, Italy.
  • Dytko O; Imperial College School of Medicine, Imperial College London, London, United Kingdom.
  • Ng KY; Imperial College School of Medicine, Imperial College London, London, United Kingdom.
  • Violette P; Department of Health Research Methods, Evidence and Impact (HEI) and Surgery, McMaster University, Hamilton, Ontario, Canada.
  • Khullar V; Department of Urogynaecology, Imperial College London, United Kingdom.
  • Wang ZT; Department of Surgery, Division of Urology, University of Western Ontario, London, Ontario, Canada.
  • Cartwright R; Department of Epidemiology and Biostatistics, Imperial College London, Norfolk Place, London, United Kingdom; Department of Urogynaecology, LNWH NHS Trust, London, United Kingdom; Department of Urogynaecology, Chelsea and Westminster NHS Foundation Trust, London, United Kingdom.
Am J Obstet Gynecol ; 230(6): 600-609.e3, 2024 06.
Article en En | MEDLINE | ID: mdl-38128862
ABSTRACT

INTRODUCTION:

The lifetime risk of urinary tract infection is known from first-degree relative studies to be highly heritable. Associations have also been observed across the life course from pediatric urinary tract infection to recurrent urinary tract infection in adulthood, suggesting lifelong susceptibility factors. Candidate gene studies and genome-wide association studies have tested for genetic associations of urinary tract infection; however, no contemporary systematic synthesis of studies is available.

OBJECTIVE:

We conducted a systematic review to identify all genetic polymorphisms tested for an association with urinary tract infection in children and adults; and to assess their strength, consistency, and risk of bias among reported associations. DATA SOURCES AND STUDY ELIGIBILITY CRITERIA PubMed, HuGE Navigator and Embase were searched from January 1, 2005 to November 16, 2023, using a combination of genetic and phenotype key words. STUDY APPRAISAL AND SYNTHESIS

METHODS:

Fixed and random effects meta-analyses were conducted using codominant models of inheritance in metan. The interim Venice criteria were used to assess their credibility of pooled associations.

RESULTS:

After removing 451 duplicates, 1821 studies reports were screened, with 106 selected for full-text review, 22 were included in the meta-analysis (7 adult studies and 15 pediatric studies). Our meta-analyses demonstrated significant pooled associations for pediatric urinary tract infection with variation in CXCR1, IL8, TGF, TLR4 and VDR; all of which have plausible roles in the pathogenesis of urinary tract infection. Our meta-analyses also demonstrated a significant pooled association for adult urinary tract infection with variation in CXCR1. All significant pooled associations were graded according to their epidemiological credibility, sample sizes, heterogeneity between studies, and risk of bias.

CONCLUSION:

This systematic review provides a current synthesis of the known genetic architecture of urinary tract infection in childhood and adulthood; and should provide important information for researchers analysing future genetic association studies. Although, overall, the credibility of pooled associations was weak, the consistency of findings for rs2234671 single nucleotide polymorphisms of CXCR1 in both populations suggest a key role in the urinary tract infection pathogenesis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Urinarias / Predisposición Genética a la Enfermedad Tipo de estudio: Systematic_reviews Límite: Adult / Child / Humans Idioma: En Revista: Am J Obstet Gynecol Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Urinarias / Predisposición Genética a la Enfermedad Tipo de estudio: Systematic_reviews Límite: Adult / Child / Humans Idioma: En Revista: Am J Obstet Gynecol Año: 2024 Tipo del documento: Article