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Importance of case age in the purported association between phylogenetics and hemolytic uremic syndrome in Escherichia coli O157:H7 infections.
Tarr, G A M; Shringi, S; Oltean, H N; Mayer, J; Rabinowitz, P; Wakefield, J; Tarr, P I; Besser, T E; Phipps, A I.
  • Tarr GAM; Department of Pediatrics,University of Calgary Cumming School of Medicine,Calgary,Alberta,CA.
  • Shringi S; Veterinary Microbiology and Pathology,Washington State University,Pullman,Washington,USA.
  • Oltean HN; Washington State Department of Health,Shoreline, Washington,USA.
  • Mayer J; Department of Epidemiology,University of Washington,Seattle,Washington,USA.
  • Rabinowitz P; Department of Environmental and Occupational Health Sciences and Center for One Health Research,University of Washington,Seattle,Washington,USA.
  • Wakefield J; Departments of Biostatistics and Statistics,University of Washington,Seattle,Washington,USA.
  • Tarr PI; Department of Pediatrics,Washington University in St. Louis School of Medicine,St. Louis,Missouri,USA.
  • Besser TE; Veterinary Microbiology and Pathology,Washington State University,Pullman,Washington,USA.
  • Phipps AI; Department of Epidemiology,University of Washington,Seattle,Washington,USA.
Epidemiol Infect ; 146(12): 1550-1555, 2018 09.
Article en En | MEDLINE | ID: mdl-29914582
ABSTRACT
Escherichia coli O157H7 is the largest cause of hemolytic uremic syndrome (HUS). Previous studies proposed that HUS risk varies across the E. coli O157H7 phylogenetic tree (hypervirulent clade 8), but the role of age in the association is unknown. We determined phylogenetic lineage of E. coli O157H7 isolates from 1160 culture-confirmed E. coli O157H7 cases reported in Washington State, 2004-2015. Using generalised estimating equations, we tested the association between phylogenetic lineage and HUS. Age was evaluated as an effect modifier. Among 1082 E. coli O157H7 cases with both phylogenetic lineage and HUS status (HUS n = 76), stratified analysis suggested effect modification by age. Lineages IIa and IIb, relative to Ib, did not appear associated with HUS in children 0-9-years-old. For cases 10-59-years-old, lineages IIa and IIb appeared to confer increased risk of HUS, relative to lineage Ib. The association reversed in ⩾60-year-olds. Results were similar for clade 8. Phylogenetic lineage appears to be associated with HUS risk only among those ⩾10-years-old. Among children <10, the age group most frequently affected, lineage does not explain progression to HUS. However, lineage frequency varied across age groups, suggesting differences in exposure and/or early disease manifestation.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Escherichia coli O157 / Infecciones por Escherichia coli / Síndrome Hemolítico-Urémico Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País como asunto: America do norte Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Escherichia coli O157 / Infecciones por Escherichia coli / Síndrome Hemolítico-Urémico Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País como asunto: America do norte Idioma: En Año: 2018 Tipo del documento: Article