Unraveling the genetics of insulin-dependent type 1A diabetes: the search must go on

Authors
Citation
A. Pugliese, Unraveling the genetics of insulin-dependent type 1A diabetes: the search must go on, DIABET REV, 7(1), 1999, pp. 39-54
Citations number
190
Categorie Soggetti
Endocrynology, Metabolism & Nutrition
Journal title
DIABETES REVIEWS
ISSN journal
10669442 → ACNP
Volume
7
Issue
1
Year of publication
1999
Pages
39 - 54
Database
ISI
SICI code
1066-9442(1999)7:1<39:UTGOIT>2.0.ZU;2-J
Abstract
Insulin-dependent type 1A diabetes results from the autoimmune destruction of pancreatic beta-cells. A targe body of evidence indicates that inherited genetic factors influence both susceptibility and resistance to the diseas e. At least 17 chromosomal regions have been linked to diabetes susceptibil ity, suggesting that type 1A diabetes is a polygenic disorder. Alleles from well-characterized susceptibility loci are commonly observed in the popula tion and appear to have normal sequences. This suggests that susceptibility may simply derive from polymorphisms affecting the function and expression of certain proteins. There is also evidence for the existence of epistatic phenomena involving several loci and of complex parental effects reportedl y modifying the transmission and expression of inherited genes. Moreover, i t is an intriguing but unproven possibility that additional genetic factors or their expression may be acquired after birth, perhaps through environme ntal exposures. Such factors may play a key role in triggering the process leading to beta-cell destruction. This article summarizes the significant p rogress made during the past few years in the identification of several sus ceptibility loci and the understanding of the putative mechanisms by which certain loci modulate susceptibility and resistance to type 1A diabetes. Fu rther studies are expected to lead to the full identification and character ization of susceptibility and perhaps disease genes. Such knowledge may imp rove prediction by genetic testing and deepen our understanding of the key mechanisms leading to the development of type 1A diabetes.