Dr. N.A. Aziz
ZonMw
The Netherlands
Triplet repeat polymorphisms as modifiers of health and disease
ZonMw
250,000
01/01/15
4.0
Huntington's disease
Triplet repeat polymorphisms | polyglutamine diseases | Huntington disease | depression | dementia
Diseases such as dementia, depression and diabetes are among the leading causes of
disability and exert a dramatic burden on societys social, economic and health care
systems. In order to understand their pathophysiology and devise more effective
therapies it is essential to elucidate their genetic basis. However, to date genetic
association studies have only identified a small fraction of the genetic determinants,
possibly because of the focus on single-nucleotide polymorphisms and consequently
neglect of other important genomic variations, especially DNA repeat expansions.
Expanded DNA repeats above a certain threshold are associated with many hereditary
neurological disorders, the most common of which are polyglutamine diseases caused by
intronic triplet (cytosine-adenine-guanine (CAG)) repeat expansions leading to a range of
cognitive, psychiatric, motor and metabolic abnormalities. Emerging findings, including
our own pilot data, suggest that even CAG repeat length variations in the normal range