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rs73185306 C/T Is Not a Predisposing Risk Factor for Inherited Chromosomally Integrated Human Herpesvirus 6A/B.
Mouammine, Annabelle; Gravel, Annie; Dubuc, Isabelle; Feroz Zada, Yassamin; Provost, Sylvie; Busseuil, David; Tardif, Jean-Claude; Dubé, Marie-Pierre; Flamand, Louis.
Afiliación
  • Mouammine A; Division of Infectious and Immune Diseases, Centre Hospitalier Universitaire de Quebec Research Center, Laval University, Quebec City, Quebec, Canada.
  • Gravel A; Division of Infectious and Immune Diseases, Centre Hospitalier Universitaire de Quebec Research Center, Laval University, Quebec City, Quebec, Canada.
  • Dubuc I; Division of Infectious and Immune Diseases, Centre Hospitalier Universitaire de Quebec Research Center, Laval University, Quebec City, Quebec, Canada.
  • Feroz Zada Y; Montreal Heart Institute, Montreal, Quebec, Canada.
  • Provost S; Montreal Heart Institute, Montreal, Quebec, Canada.
  • Busseuil D; Montreal Heart Institute, Montreal, Quebec, Canada.
  • Tardif JC; Montreal Heart Institute, Montreal, Quebec, Canada.
  • Dubé MP; Faculty of Medicine, Department of Medicine, University of Montreal, Montreal, Quebec, Canada.
  • Flamand L; Montreal Heart Institute, Montreal, Quebec, Canada.
J Infect Dis ; 221(6): 878-881, 2020 03 02.
Article en En | MEDLINE | ID: mdl-31621866
ABSTRACT
Approximately 1% of people worldwide carry a copy of the human herpesvirus 6A or 6B (HHV-6A/B) in every cell of their body. This condition is referred to as inherited chromosomally integrated HHV-6A/B (iciHHV-6A/B). The mechanisms leading to iciHHV-6A/B chromosomal integration are yet to be identified. A recent report suggested that the rs73185306 C/T single-nucleotide polymorphism (SNP) represents a favorable predisposing factor leading to HHV-6A/B integration. After genotype analysis of an independent cohort (N = 11 967), we report no association between the rs73185306 C/T SNP and HHV-6A/B chromosomal integration (odds ratio, 0.90 [95% confidence interval, .54-1.51]; P = .69).
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Mutación Puntual / Herpesvirus Humano 6 / Predisposición Genética a la Enfermedad Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Infect Dis Año: 2020 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Mutación Puntual / Herpesvirus Humano 6 / Predisposición Genética a la Enfermedad Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Infect Dis Año: 2020 Tipo del documento: Article País de afiliación: Canadá