Genetic variation at ERBB3/IKZF4 and sexual dimorphism in epitope spreading in single autoantibody-positive relatives
Aims/hypothesis We examined whether the non-HLA susceptibility locus ERBB3/IKZF4 influences progression of type 1 diabetes stage specifically according to sex. Methods SNPs of ERBB3 (rs2292239 T/G) and IKZF4 (rs1701704 G/T) were screened by allelic discrimination quantitative PCR assay in first-degr...
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Veröffentlicht in: | Diabetologia 2021-11, Vol.64 (11), p.2511-2516 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Aims/hypothesis
We examined whether the non-HLA susceptibility locus
ERBB3/IKZF4
influences progression of type 1 diabetes stage specifically according to sex.
Methods
SNPs of
ERBB3
(rs2292239 T/G) and
IKZF4
(rs1701704 G/T) were screened by allelic discrimination quantitative PCR assay in first-degree relatives of type 1 diabetes patients who had developed at least one circulating autoantibody. The effect of
ERBB3/IKZF4
genotypes and sex, on the progression of single autoantibody positivity to multiple autoantibody positivity and from multiple autoantibody positivity to diabetes, was studied by Kaplan–Meier analysis and multivariate Cox regression.
Results
In the cohort of autoantibody-positive first-degree relatives, the risk allele frequencies for
ERBB3
rs2292239 (T) and
IKZF4
rs1701704 (G) were increased. There was a significant male excess at the stage of multiple autoantibody positivity (
p
= 0.021). In Kaplan–Meier survival analysis, progression from single to multiple antibody positivity was delayed in female participants with genotype
ERBB3
GG (
p
= 0.018, vs
ERBB3
TG+TT) or
IKZF4
TT (
p
= 0.023, vs
IKZF4
GT+GG), but not in male participants. In multivariate Cox regression models, the interaction effects between female sex and
ERBB3
GG (
p
= 0.012; HR = 0.305 [95% CI 0.120, 0.773]) or between female sex and
IKZF4
TT (
p
= 0.011; HR = 0.329 [95% CI 0.140, 0.777]) emerged as potential determinants of delayed progression to multiple autoantibodies. The progression from multiple autoantibody positivity to type 1 diabetes appeared not to be influenced by
ERBB3/IKZF4
.
Conclusions/interpretation
In siblings and offspring of type 1 diabetes patients, polymorphism in region
ERBB3/IKZF4
may affect disease progression at the level of epitope spreading in female individuals. Our findings suggest that interaction between sex and
ERBB3/IKZF4
may contribute to the post-pubertal male excess in type 1 diabetes.
Graphical abstract |
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ISSN: | 0012-186X 1432-0428 |
DOI: | 10.1007/s00125-021-05546-9 |