Diagnosis of Parkinson's Disease in Patients with and without Dementia
Blood gene transcripts may identify Parkinson's disease patients with and without dementia Project ID : 46-2019-10785
Innovative Products and Technologies
Blood gene transcripts may identify Parkinson's disease patients with and without dementia
Project ID : 46-2019-10785
LifeSciences and BioTechnology
Parkinson’s Disease, PD, Dementia, Diagnostic Kit, Diagnostics, Non-Motor Symptoms, mRNA, Circulating RNA
Current development stage
General list: TRL3 Experimental proof of concept
Parkinson's disease (PD) is the second most common neurodegenerative disease, with an expected 9 million patients worldwide by 2030. Currently, treatment for PD mainly consists of dopamine substitution with L-Dopa, aiming to alleviate the motor symptoms of the disease, which are believed to be caused by the death of dopaminergic neurons in the Substantia Nigra.
The diagnosis of Parkinson's disease relies on expert opinion. Studies, however, have demonstrated that even experienced neurologists misdiagnose Parkinson's disease in about a quarter out of every one hundred cases. Diagnostic accuracy at disease onset, when neuroprotective treatment is purported to be most effective, is even lower; typically, at diagnosis, 70% of dopaminergic neurons have already died and the available treatment can only limit symptoms rather than achieve remission. Thus, there is a crucial need for biomarkers that are disease-specific and which precisely identify the disease course as early as possible. Additionally, part of the PD patients have dementia, but at present there is no objective diagnosis to identify them.
Circulating RNAs have been researched in recent years as an upcoming biomarker in PD. In particular, previous research raised several promising candidates for biomarkers of the disease, however, identifying clinically relevant rare circular RNAs and small non-coding RNA candidates such as microRNAs is rather complex, making the construction of an easy diagnosis tool for clinical use very difficult.
We have discovered novel blood biomarkers that can differentiate between Parkinson’s disease patients with and without dementia. These biomarkers can be used to develop a diagnostic kit that can implicate treatment protocols and can also be used as a tool for companion diagnostics for drug development companies.
The current project is based on the use of mRNA transcripts from nucleated blood cells to differentiate between PD patients with and without dementia and using age-matched controls. It is based on comparing whole blood mRNA transcripts by RNA- sequencing, instead of restricting methods like microarrays and qPCR. This provides accesses to all mRNA transcripts in the blood, as well as to all long non-coding RNAs. Use of technology for clinical diagnostic kit will not require tailored microarrays based on these sequencing results and will be based on the identified biomarkers.
VP Business Development Healthcare
HUJI, Faculty of Science
The Alexander Silberman Institute for Life Sciences
Yissum - Research Development Company of the Hebrew University
Technology Transfer Office from Israel
Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. Founded in 1964 to protect and commercialize the Hebrew University’s intellectual property. Ranked among the top technology transfer companies, Yissum has registered over 8,900 patents covering 2,500 inventions; has licensed out 800 technologies and has spun-off 90 companies. Products that are based on Hebrew University technologies and were commercialized by Yissum generate today over $2 Billion in annual sales.
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