NTU Undergraduates' research April 2014 - Biosciences | страница 80

Predicting Parkinson’s Disease Abstract Parkinson’s disease (PD) is the second most common neurodegenerative disease in the world behind Alzheimers’s disease (AD). It is most routinely linked with older generations but it is not exclusively a disease for them, as there are early on-set forms. By the time symptoms are clinically recognisable approximately 60% of dopaminergic neurons will have died. This results in treatment options being severely limited. Being able to successfully predict and monitor the progression of the disease would be a significant advance in the prognosis of the disease. Currently mitochondrial proteins (Dj-1, Parkin and PTEN induced kinase 1) are leading the way in identifying a specific biomarker, as they are involved in the maintenance of the mitochondria. The deregulation of mitochondria is known to increase amount of oxidative stress the cell experiences, which is thought to be a prime mechanism in the development of Parkinson’s disease. DJ-1 in the plasma of PD patients was found to decrease in comparison to healthy but this was statistically insignificant. Similarly, the expression of Parkin and PTEN are also reduced in PD patient. These proteins are found in the cerebral spinal fluid (CSF) and are difficult to retrieve from the plasma making them unsuitable biomarkers. The cellular processes these proteins control are proving difficult to link together and this is hindering them being used as specific biomarkers for Parkinson’s disease.