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Novel Alzheimer’s disease risk gene among Icelanders discovered
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Novel Alzheimer’s disease risk gene among Icelanders discovered

Novel Alzheimer’s disease risk gene among Icelanders discovered
News

Novel Alzheimer’s disease risk gene among Icelanders discovered

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Scientists at Baylor College of Medicine and the Jan and Dan Duncan Neurological Research Institute (NRI) at Texas Children's Hospital are part of a multicenter collaborative study that has identified a novel genetic risk factor for late-onset Alzheimer's disease. The study appears in the journal PLoS Genetics.


Alzheimer's disease is the most common cause of dementia among older adults, and the presence of certain genetic variants increases an individual's risk for developing this disease.


See Also: Epigenomics of Alzheimer’s disease progression


Baylor researchers Dr. Shinya Yamamoto, assistant professor of molecular and human genetics; Dr. Joshua M. Shulman, assistant professor of neurology, neuroscience, and molecular and human genetics, and Dr. Hugo J. Bellen, professor and director of the program in developmental biology and also an investigator at the Howard Hughes Medical Institute, were part of an international team that analyzed samples from 1,393 subjects with late-onset Alzheimer's disease and compared the results with those of 8,141 neurologically healthy individuals.


The consortium found a variant in TM2D3, a gene that has never been studied in human or other vertebrate species. Interestingly, while the probability of this variant was very rare among people of European ancestry, it was significantly enriched among Icelanders (but still less than 1 percent frequency). The researchers estimated that carriers of this variant would have an approximately six-fold increased risk of developing Alzheimer's disease.


To further understand the impact of the discovered mutation and its potential link to processes that lead to Alzheimer's disease, the Baylor researchers studied the function of TM2D3 in the fruit fly model system.


They found that loss-of-function of theTM2D3 gene causes abnormal development of the fly's nervous system. They next showed that human normal TM2D3 could functionally substitute for its fly counterpart and rescue the neurodevelopmental defect, whereas introduction of the Alzheimer's disease-associated variant was unable to restore the normal function.


Learn More: New mechanism discovered for Alzheimer's risk gene


In summary, this study has identified a novel, rare genetic variant in the TM2D3 gene to be a risk factor in the development of late-onset Alzheimer's disease among Icelanders. This gene has not been previously linked to Alzheimer's, and researchers are hopeful that further investigations may lead to new and more effective therapies.


Note: Material may have been edited for length and content. For further information, please contact the cited source.


Baylor College of Medicine   Original reporting by: Allison Huseman


Publication

Jakobsdottir J et al. Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.   PLoS Genetics, Published October 20 2016. doi: 10.1371/journal.pgen.1006327


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