91³Ô¹Ï

ISSN: 2161-0460

Journal of Alzheimers Disease & Parkinsonism
91³Ô¹Ï

Our Group organises 3000+ Global Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ 91³Ô¹Ï Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

91³Ô¹Ï Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
Citations : 4334

Indexed In
  • Index Copernicus
  • Google Scholar
  • Sherpa Romeo
  • Open J Gate
  • Genamics JournalSeek
  • Academic Keys
  • JournalTOCs
  • China National Knowledge Infrastructure (CNKI)
  • Electronic Journals Library
  • RefSeek
  • Hamdard University
  • EBSCO A-Z
  • OCLC- WorldCat
  • SWB online catalog
  • Virtual Library of Biology (vifabio)
  • Publons
  • Geneva Foundation for Medical Education and Research
  • Euro Pub
  • ICMJE
Share This Page

Differentiation between normal aging, mild cognitive impairment and Alzheimer�s disease using MRI, neuropsychological, CSF and PET markers: Which are the best contributors?

International Conference on Psychology, Autism and Alzheimers Disease

Ronald J. Killiany

ScientificTracks Abstracts: J Alzheimers Dis Parkinsonism

DOI:

Abstract
Alzheimer�s disease (AD) is a progressive neurodegenerative disease with an insidious onset that is difficult to distinguish from normal aging especially in its earliest stages. It typically begins with a subtle impairment of memory that evolves into the amnestic form of mild cognitive impairment (aMCI). As the disease continues to progress, other cognitive domains become affected and a full dementia state becomes apparent. In order to better understand this disease and to develop effective treatments for it, biomarkers are needed to identify the stages of normal aging, MCI, and AD and predict future cognitive decline. A number of potential biomarkers have been studied in isolation and some have been shown to have reasonable predictive power, but the relationship between the various markers is not well understood making it difficult to understand just what combinations are optimal. We�ve been working to determine the optimal combination of CSF biomarkers, MRI morphometry variable, FDG PET metabolism variables and neuropsychological test scores to differentiate between subjects who are aging normally and those with either MCI or AD. Our results indicate that combining variables from all of the modalities significantly improved the index of discrimination, especially at the earliest stages of the disease when identifying one�s group membership would be expected to be most difficult. MRI variables proved to be highly associated with baseline cognitive function and the best predictor future cognitive decline. These findings suggest that complex approaches will be needed to identify individuals at the earliest stages of this disease.
Biography
Ronald J. Killiany completed his Ph.D. in Physiological Psychology in 1991 from Northeastern University and went on to complete postdoctoral studies where he began working in Neuropsychology and MRI scanning at Boston University School of Medicine, Brigham and Women�s Hospital and Massachusetts General Hospital. He is currently the Director of the Center for Biomedical Imaging at Boston University School of Medicine. He has published more than 70 papers in reputed journals and serves as an ad hoc reviewer for a number of scientific journals.
International Conferences 2025-26
 
Meet Inspiring Speakers and Experts at our 3000+ Global

Conferences by Country

Medical & Clinical Conferences

Conferences By Subject

Top