tetano
Editor, Senior Moderator
J Med Virol. 2017 Oct 20. doi: 10.1002/jmv.24975. [Epub ahead of print]
[h=1]Pilot screening study of targeted genetic polymorphisms for association with seasonal influenza hospital admission.[/h] Carter TC[SUP]1[/SUP], Hebbring SJ[SUP]1[/SUP], Liu J[SUP]1[/SUP], Mosley JD[SUP]2[/SUP], Shaffer CM[SUP]2[/SUP], Ivacic LC[SUP]3[/SUP], Kopitzke S[SUP]4[/SUP], Stefanski EL[SUP]3[/SUP], Strenn R[SUP]5[/SUP], Sundaram ME[SUP]4[/SUP], Meece J[SUP]3[/SUP], Brilliant MH[SUP]1[/SUP], Ferdinands JM[SUP]6[/SUP], Belongia EA[SUP]4[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Host response to influenza is highly variable, suggesting a potential role of host genetic variation. To investigate the host genetics of severe influenza in a targeted fashion, 32 single nucleotide polymorphisms (SNPs) within viral immune response genes were evaluated for association with seasonal influenza hospitalization in an adult study population with European ancestry. SNP allele and genotype frequencies were compared between hospitalized influenza patients (cases) and population controls in a case-control study that included a discovery group (26 cases and 993 controls) and two independent, validation groups (one with 84 cases and 4,076 controls; the other with 128 cases and 9,187 controls). Cases and controls had similar allele frequencies for variant rs12252 in interferon-inducible transmembrane protein 3 (IFITM3) (P > 0.05), and the study did not replicate the previously reported association of rs12252 with hospitalized influenza. In the discovery group, the preliminary finding of an association with a nonsense polymorphism (rs8072510) within the schlafen family member 13 (SFLN13) gene (P = 0.0099) was not confirmed in either validation group. Neither rs12252 nor rs8072510 showed an association according to the presence of clinical risk factors for influenza complications (P > 0.05), suggesting that these factors did not modify associations between the SNPs and hospitalized influenza. No other SNPs showed a statistically significant association with hospitalized influenza. Further research is needed to identify genetic factors involved in host response to seasonal influenza infection and to assess whether rs12252, a low-frequency variant in Europeans, contributes to influenza severity in populations with European ancestry. This article is protected by copyright. All rights reserved.
This article is protected by copyright. All rights reserved.
[h=4]KEYWORDS:[/h] IFITM3; host susceptibility; influenza; polymorphisms; virus
PMID: 29053189 DOI: 10.1002/jmv.24975
[h=1]Pilot screening study of targeted genetic polymorphisms for association with seasonal influenza hospital admission.[/h] Carter TC[SUP]1[/SUP], Hebbring SJ[SUP]1[/SUP], Liu J[SUP]1[/SUP], Mosley JD[SUP]2[/SUP], Shaffer CM[SUP]2[/SUP], Ivacic LC[SUP]3[/SUP], Kopitzke S[SUP]4[/SUP], Stefanski EL[SUP]3[/SUP], Strenn R[SUP]5[/SUP], Sundaram ME[SUP]4[/SUP], Meece J[SUP]3[/SUP], Brilliant MH[SUP]1[/SUP], Ferdinands JM[SUP]6[/SUP], Belongia EA[SUP]4[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Host response to influenza is highly variable, suggesting a potential role of host genetic variation. To investigate the host genetics of severe influenza in a targeted fashion, 32 single nucleotide polymorphisms (SNPs) within viral immune response genes were evaluated for association with seasonal influenza hospitalization in an adult study population with European ancestry. SNP allele and genotype frequencies were compared between hospitalized influenza patients (cases) and population controls in a case-control study that included a discovery group (26 cases and 993 controls) and two independent, validation groups (one with 84 cases and 4,076 controls; the other with 128 cases and 9,187 controls). Cases and controls had similar allele frequencies for variant rs12252 in interferon-inducible transmembrane protein 3 (IFITM3) (P > 0.05), and the study did not replicate the previously reported association of rs12252 with hospitalized influenza. In the discovery group, the preliminary finding of an association with a nonsense polymorphism (rs8072510) within the schlafen family member 13 (SFLN13) gene (P = 0.0099) was not confirmed in either validation group. Neither rs12252 nor rs8072510 showed an association according to the presence of clinical risk factors for influenza complications (P > 0.05), suggesting that these factors did not modify associations between the SNPs and hospitalized influenza. No other SNPs showed a statistically significant association with hospitalized influenza. Further research is needed to identify genetic factors involved in host response to seasonal influenza infection and to assess whether rs12252, a low-frequency variant in Europeans, contributes to influenza severity in populations with European ancestry. This article is protected by copyright. All rights reserved.
This article is protected by copyright. All rights reserved.
[h=4]KEYWORDS:[/h] IFITM3; host susceptibility; influenza; polymorphisms; virus
PMID: 29053189 DOI: 10.1002/jmv.24975