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Progressive Supranuclear Palsy in India: Past, Present, and Future
Srinivas Raju1, Kuldeep Shetty2, Lulup Sahoo3
1Department of Neurology, Manipal Hospital, Hebbal, Bengaluru, Karnataka, India.
Indian research on Progressive Supranuclear Palsy (PSP) has evolved from single-center studies to collaborative, pan-India projects. Future research should focus on genetics, risk factors, and treatments for this neurodegenerative disorder.
Area of Science:
- Neuroscience
- Neurology
- Medical Research
Background:
- Progressive Supranuclear Palsy (PSP) is a significant neurodegenerative disorder with growing research interest globally, particularly in India.
- Decades of Indian research have contributed to understanding PSP, with over 80 publications since 1974.
Purpose of the Study:
- To review the landscape of Progressive Supranuclear Palsy (PSP) research conducted in India.
- To analyze historical research trends and highlight current initiatives and future directions for PSP management in the region.
Main Methods:
- A comprehensive review of Indian research publications on PSP from 1974 to 2023.
- Analysis of study themes, methodologies, phenotypes (predominantly PSP-Richardson's syndrome), and patient demographics.
- Identification of the shift towards collaborative, multicentric research models, exemplified by the PAn India Registry for PSP (PAIR-PSP) project.
Main Results:
- Historical research predominantly involved single-center studies with varied recruitment numbers.
- PSP-Richardson's syndrome is the most common phenotype observed, with patients typically diagnosed around age 64.
- A recent trend shows a move towards large-scale, multicentric, and pan-India collaborative projects.
Conclusions:
- Indian research on PSP has transitioned from isolated efforts to coordinated, nationwide initiatives.
- There is a critical need for further research into genetic factors, risk identification, and the development of effective treatments and preventive strategies for PSP.
- India's large population positions it to make pivotal contributions to understanding PSP and other tauopathies.
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