Identification Of Genetic Mutation May Open Up New Treatment Options For Type 1 Diabetes
"We describe one of the first single gene defects leading to type 1 diabetes, as well as the first human mutation in the SIRT1 gene," says senior study author Marc Donath of University Hospital Basel. "Our findings reveal a potential mechanistic basis for the development of a treatment for type 1 diabetes and other autoimmune diseases."
Type 1 diabetes is a lifelong, potentially fatal disease, typically diagnosed in young individuals, in which beta cells in the pancreas do not produce enough of the hormone insulin, resulting in high levels of blood sugar. Animal studies have shown that a gene called SIRT1, which is well known for its role in promoting longevity and protecting against age-related diseases, also regulates insulin secretion and the development of autoimmune conditions, and activation of this gene can protect against type 1 diabetes. But until now, the role of SIRT1 in human autoimmunity and disease was not known.
In the new study, Donath and his team described a family carrying a mutation in the SIRT1 gene. All five affected members developed an autoimmune disorder, and four developed type 1 diabetes. Using a combination of gene-sequencing techniques, the researchers identified a previously undocumented mutation that caused an amino acid substitution in the SIRT1 protein. Moreover, inactivation of the SIRT1 gene in mice led to the destruction of the insulin-producing region of the pancreas, resulting in high levels of blood sugar.
"The identification of a gene leading to type 1 diabetes should allow us to understand the mechanism responsible for the disease and may open up new treatment options," Donath says. "To follow up on this study, we are creating a mouse that carries the mutation, with the hope of developing an animal model for human type 1 diabetes, and we are exploring the possibility of conducting a clinical study with SIRT1 activators."
Cell Metabolism, Biason-Lauber et al.: "Mutation of SIRT1 in a Family with Type 1 Diabetes."
Source: EurekAlert!, the online, global news service operated by AAAS, the science society
Please use one of the following formats to cite this article in your essay, paper or report:
Press, Cell. "Identification Of Genetic Mutation May Open Up New Treatment Options For Type 1 Diabetes." Medical News Today. MediLexicon, Intl., 7 Mar. 2013. Web.
28 May. 2016. <http://www.medicalnewstoday.com/releases/257235.php>
Press, C. (2013, March 7). "Identification Of Genetic Mutation May Open Up New Treatment Options For Type 1 Diabetes." Medical News Today. Retrieved from
Please note: If no author information is provided, the source is cited instead.
Contact our news editors
For any corrections of factual information, or to contact our editorial team, please see our contact page.
Copyright Medical News Today: Excluding email/sharing services explicitly offered on this website, material published on Medical News Today may not be reproduced, or distributed without the prior written permission of Medilexicon International Ltd. Please contact us for further details.