Genetic Determinants of Enterovirus Infections: Polymorphisms in Type 1 Diabetes and Innate Immune Genes in the MIDIA Study

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Genetic Determinants of Enterovirus Infections : Polymorphisms in Type 1 Diabetes and Innate Immune Genes in the MIDIA Study. / Witsø, Elisabet; Cinek, Ondrej; Tapia, German; Brorsson, Caroline A; Stene, Lars C; Gjessing, Håkon K; Rasmussen, Trond; Bergholdt, Regine; Pociot, Flemming M; Rønningen, Kjersti S.

I: Viral Immunology, Bind 28, Nr. 10, 12.2015, s. 556-63.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Witsø, E, Cinek, O, Tapia, G, Brorsson, CA, Stene, LC, Gjessing, HK, Rasmussen, T, Bergholdt, R, Pociot, FM & Rønningen, KS 2015, 'Genetic Determinants of Enterovirus Infections: Polymorphisms in Type 1 Diabetes and Innate Immune Genes in the MIDIA Study', Viral Immunology, bind 28, nr. 10, s. 556-63. https://doi.org/10.1089/vim.2015.0067

APA

Witsø, E., Cinek, O., Tapia, G., Brorsson, C. A., Stene, L. C., Gjessing, H. K., Rasmussen, T., Bergholdt, R., Pociot, F. M., & Rønningen, K. S. (2015). Genetic Determinants of Enterovirus Infections: Polymorphisms in Type 1 Diabetes and Innate Immune Genes in the MIDIA Study. Viral Immunology, 28(10), 556-63. https://doi.org/10.1089/vim.2015.0067

Vancouver

Witsø E, Cinek O, Tapia G, Brorsson CA, Stene LC, Gjessing HK o.a. Genetic Determinants of Enterovirus Infections: Polymorphisms in Type 1 Diabetes and Innate Immune Genes in the MIDIA Study. Viral Immunology. 2015 dec.;28(10):556-63. https://doi.org/10.1089/vim.2015.0067

Author

Witsø, Elisabet ; Cinek, Ondrej ; Tapia, German ; Brorsson, Caroline A ; Stene, Lars C ; Gjessing, Håkon K ; Rasmussen, Trond ; Bergholdt, Regine ; Pociot, Flemming M ; Rønningen, Kjersti S. / Genetic Determinants of Enterovirus Infections : Polymorphisms in Type 1 Diabetes and Innate Immune Genes in the MIDIA Study. I: Viral Immunology. 2015 ; Bind 28, Nr. 10. s. 556-63.

Bibtex

@article{f6df47ce295746db98f7ae6c78342d39,
title = "Genetic Determinants of Enterovirus Infections: Polymorphisms in Type 1 Diabetes and Innate Immune Genes in the MIDIA Study",
abstract = "Enteroviruses have been suggested as triggers of type 1 diabetes (T1D). We aimed to assess whether established T1D susceptibility single nucleotide polymorphisms (SNPs) and candidate SNPs in innate immune genes were associated with the frequency of enterovirus infection in otherwise healthy children. Fifty-six established T1D SNPs and 97 other candidate immunity SNPs were typed in 419 children carrying the T1D high-risk genotype, HLA-DR4-DQ8/DR3-DQ2 genotype, and 373 children without this genotype. Enteroviral RNA was detected using real-time polymerase chain reaction, with primers detecting essentially all enterovirus serotypes, in 7,393 longitudinal stool samples collected monthly (age range 3-36 months). The most significant association was with two T1D SNPs, rs12150079 (ZPBP2/ORMDL3/GSDMB region) (enterovirus frequency: AA 7.3%, AG 8.7%, GG 9.7%, RR = 0.86, overall p = 1.87E-02) and rs229541 (C1QTNF6/SSTR3/RAC2) (enterovirus frequency: CC 7.8%, CT 9.7%, TT 9.4%, RR = 1.13, overall p = 3.6E-02), followed by TLR8 (rs2407992) (p = 3.8E-02), TLR3 (1914926) (p = 4.9E-02), and two other T1D SNPs (IFIH1 rs3747517, p = 4.9E-02 and PTPN22, rs2476601, p = 5.3E-02). However, the quantile-quantile plot of p-values with confidence intervals for all 153 SNPs did not reveal clear evidence for rejection of the complete null hypothesis. Among a number of SNPs in candidate genes, we found no evidence for strong associations with enterovirus presence in stool samples from Norwegian children.",
author = "Elisabet Wits{\o} and Ondrej Cinek and German Tapia and Brorsson, {Caroline A} and Stene, {Lars C} and Gjessing, {H{\aa}kon K} and Trond Rasmussen and Regine Bergholdt and Pociot, {Flemming M} and R{\o}nningen, {Kjersti S}",
year = "2015",
month = dec,
doi = "10.1089/vim.2015.0067",
language = "English",
volume = "28",
pages = "556--63",
journal = "Viral Immunology",
issn = "0882-8245",
publisher = "Mary AnnLiebert, Inc. Publishers",
number = "10",

}

RIS

TY - JOUR

T1 - Genetic Determinants of Enterovirus Infections

T2 - Polymorphisms in Type 1 Diabetes and Innate Immune Genes in the MIDIA Study

AU - Witsø, Elisabet

AU - Cinek, Ondrej

AU - Tapia, German

AU - Brorsson, Caroline A

AU - Stene, Lars C

AU - Gjessing, Håkon K

AU - Rasmussen, Trond

AU - Bergholdt, Regine

AU - Pociot, Flemming M

AU - Rønningen, Kjersti S

PY - 2015/12

Y1 - 2015/12

N2 - Enteroviruses have been suggested as triggers of type 1 diabetes (T1D). We aimed to assess whether established T1D susceptibility single nucleotide polymorphisms (SNPs) and candidate SNPs in innate immune genes were associated with the frequency of enterovirus infection in otherwise healthy children. Fifty-six established T1D SNPs and 97 other candidate immunity SNPs were typed in 419 children carrying the T1D high-risk genotype, HLA-DR4-DQ8/DR3-DQ2 genotype, and 373 children without this genotype. Enteroviral RNA was detected using real-time polymerase chain reaction, with primers detecting essentially all enterovirus serotypes, in 7,393 longitudinal stool samples collected monthly (age range 3-36 months). The most significant association was with two T1D SNPs, rs12150079 (ZPBP2/ORMDL3/GSDMB region) (enterovirus frequency: AA 7.3%, AG 8.7%, GG 9.7%, RR = 0.86, overall p = 1.87E-02) and rs229541 (C1QTNF6/SSTR3/RAC2) (enterovirus frequency: CC 7.8%, CT 9.7%, TT 9.4%, RR = 1.13, overall p = 3.6E-02), followed by TLR8 (rs2407992) (p = 3.8E-02), TLR3 (1914926) (p = 4.9E-02), and two other T1D SNPs (IFIH1 rs3747517, p = 4.9E-02 and PTPN22, rs2476601, p = 5.3E-02). However, the quantile-quantile plot of p-values with confidence intervals for all 153 SNPs did not reveal clear evidence for rejection of the complete null hypothesis. Among a number of SNPs in candidate genes, we found no evidence for strong associations with enterovirus presence in stool samples from Norwegian children.

AB - Enteroviruses have been suggested as triggers of type 1 diabetes (T1D). We aimed to assess whether established T1D susceptibility single nucleotide polymorphisms (SNPs) and candidate SNPs in innate immune genes were associated with the frequency of enterovirus infection in otherwise healthy children. Fifty-six established T1D SNPs and 97 other candidate immunity SNPs were typed in 419 children carrying the T1D high-risk genotype, HLA-DR4-DQ8/DR3-DQ2 genotype, and 373 children without this genotype. Enteroviral RNA was detected using real-time polymerase chain reaction, with primers detecting essentially all enterovirus serotypes, in 7,393 longitudinal stool samples collected monthly (age range 3-36 months). The most significant association was with two T1D SNPs, rs12150079 (ZPBP2/ORMDL3/GSDMB region) (enterovirus frequency: AA 7.3%, AG 8.7%, GG 9.7%, RR = 0.86, overall p = 1.87E-02) and rs229541 (C1QTNF6/SSTR3/RAC2) (enterovirus frequency: CC 7.8%, CT 9.7%, TT 9.4%, RR = 1.13, overall p = 3.6E-02), followed by TLR8 (rs2407992) (p = 3.8E-02), TLR3 (1914926) (p = 4.9E-02), and two other T1D SNPs (IFIH1 rs3747517, p = 4.9E-02 and PTPN22, rs2476601, p = 5.3E-02). However, the quantile-quantile plot of p-values with confidence intervals for all 153 SNPs did not reveal clear evidence for rejection of the complete null hypothesis. Among a number of SNPs in candidate genes, we found no evidence for strong associations with enterovirus presence in stool samples from Norwegian children.

U2 - 10.1089/vim.2015.0067

DO - 10.1089/vim.2015.0067

M3 - Journal article

C2 - 26485223

VL - 28

SP - 556

EP - 563

JO - Viral Immunology

JF - Viral Immunology

SN - 0882-8245

IS - 10

ER -

ID: 162155680