The chromosome 6q22.33 region is associated with age at diagnosis of type 1 diabetes and disease risk in those diagnosed under 5 years of age
Aims/hypothesis The genetic risk of type 1 diabetes has been extensively studied. However, the genetic determinants of age at diagnosis (AAD) of type 1 diabetes remain relatively unexplained. Identification of AAD genes and pathways could provide insight into the earliest events in the disease proce...
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Veröffentlicht in: | Diabetologia 2018-01, Vol.61 (1), p.147-157 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | Aims/hypothesis
The genetic risk of type 1 diabetes has been extensively studied. However, the genetic determinants of age at diagnosis (AAD) of type 1 diabetes remain relatively unexplained. Identification of AAD genes and pathways could provide insight into the earliest events in the disease process.
Methods
Using ImmunoChip data from 15,696 cases, we aimed to identify regions in the genome associated with AAD.
Results
Two regions were convincingly associated with AAD (
p
0.001), the SNP most associated with AAD, rs72975913, was associated with susceptibility to type 1 diabetes in those individuals diagnosed at less than 5 years old (
p
= 2.3 × 10
−9
).
Conclusion/interpretation
PTPRK
and its neighbour
THEMIS
are required for early development of the thymus, which we can assume influences the initiation of autoimmunity. Non-HLA genes may only be detectable as risk factors for the disease in individuals diagnosed under the age 5 years because, after that period of immune development, their role in disease susceptibility has become redundant. |
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ISSN: | 0012-186X 1432-0428 |
DOI: | 10.1007/s00125-017-4440-y |