Related Experiment Video
Updated: Jul 15, 2025

13:32
Recording Human Electrocorticographic ECoG Signals for Neuroscientific Research and Real-time Functional Cortical Mapping
Published on: June 26, 2012
25.8K
Personalized clinical managements through exploring circulating neural cells and electroencephalography
Parvin Mehdipour1, Nima Fathi2, Masoud Nosratabadi3
1Department of Medical Genetics, Tehran University of Medical Sciences, Tehran 14176-1315, Iran. mehdipor@tums.ac.ir.
World Journal of Experimental Medicine
|September 28, 2023
Summary
Early detection of Alzheimer disease (AD) is improved by analyzing protein expression of Ets2 in circulating neural cells. This approach enables a personalized, predictive, preventive, and protective (5xP) management strategy for AD patients and at-risk relatives.
Area of Science:
- Neurogenetics
- Cell Biology
- Personalized Medicine
Background:
- Alzheimer disease (AD) diagnosis lacked early detection methods for 116 years.
- Up-regulation of Ets2 enhances neuronal susceptibility and degeneration in AD.
- Protein expression (PE) of Ets2 significantly impacts AD and Down's syndrome pathogenesis.
Purpose of the Study:
- To integrate cell biology into neuro-genetics for a 5xP (personalized, prognostics, predictive, preventive, predisposing) platform.
- To stratify brain channel behavior in AD patients before and after light music intervention.
- To develop early detection and personalized management strategies for AD.
Main Methods:
- Exploration of protein expression (PE) assays and electroencephalography of brain channels.
- Application of a triangle style using cellular networks and manual/flow-cytometry based PE assay of Ets2 in peripheral blood.
- Inclusion of genetic counseling, pedigree analysis, psychological status, environmental factors, genetic analysis, and complementary tests.
Main Results:
- PE of Ets2 plays a pathogenic role in AD, revealing heterogeneity and evolutionary course.
- Ets2 analysis, alongside polymorphisms in ATM, VEGF, and EGF, identified distinct cellular behaviors.
- An early detection platform was highlighted using circulating neural cells (CNCs) and molecular investigation for individuals predisposed to AD or brain neoplasia.
Conclusions:
- Application of single CNCs and brain channel ratios provides a 5xP personalized clinical management model for early AD detection and therapy.
- Novel findings in brain channels offer personalized markers for health and disease management.
- This approach facilitates early detection and personalized therapy for AD patients and predisposed relatives.

