Brigham and Women's Hospital
Ann Romney Center for Neurologic Diseases
Dennis Selkoe MD: Vincent and Stella Coates Professor of Neurologic Diseases, Harvard Medical School; Co-Director of the Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital. Graduated Columbia and University of Virginia, trained at NIH, Harvard/Longwood Neurology and HMS Department of Neuroscience. Selkoe and colleagues isolated the tangles of Alzheimer’s disease and co-discovered their antigenic relationship to tau. His research on amyloid ß-protein and APP led to the “amyloid hypothesis” of AD, showed that Aß is produced by cells throughout life, and that mutations in APP and, later, presenilin, increase Aß. Michael Wolfe and Selkoe identified presenilin as γ-secretase. His lab has applied similar approaches to alpha-synuclein, the key protein of Parkinson’s disease. Selkoe has focused on translating his discoveries on the cause and mechanism of Alzheimer’s disease into therapeutic approaches, and his findings have provided the underpinnings and rationale of numerous disease-modifying trials currently underway worldwide. He is a Fellow of the American Academy of Neurology and Association of American Physicians and a member of the National Academy of Medicine. He was the principal founding scientist of Athena Neurosciences, and is now a founding director of Prothena Biosciences.

Moderator of 1 Session

SPONSORED SYMPOSIUM
Session Type
SPONSORED SYMPOSIUM
Date
Sat, 19.03.2022
Session Time
11:40 AM - 01:25 PM
Room
ONSITE PLENARY: 115-117
Session Description
Amyloid-β Pathway: Evolving Scientific Knowledge and Clinical Implications for Alzheimer’s Disease - Supported by Eisai

Session Description:

Join us for a virtual symposium Amyloid-β Pathway: Evolving Scientific Knowledge and Clinical Implications for Alzheimer’s Disease. In the past 30 years leading up to and since the proposal of the Amyloid Cascade Hypothesis, our understanding of the amyloid pathway in Alzheimer’s disease (AD) has evolved and refined, culminating in therapeutic development based on amyloid-β (Aβ) as a target. Focusing on the dynamic nature of the Aβ pathway across time and space, this symposium will review the clinical evidence and biological rationale of what, when, and where amyloid species may be clinically meaningful and their relevance to AD etiology, diagnosis, and treatment development. The esteemed faculty will discuss the current understanding of Aβ in AD, provide their perspectives on the latest advances, and lay out the foundational concepts linking non-clinical research to disease relevance. They will discuss how Aβ is not a singular entity but exists in various forms and cellular compartments, and how these components may have implications in disease characterization and therapeutic implications. The speakers will also review clinical and nonclinical studies that can explain Aβ related functional changes in the brain in health and AD, and biological underpinnings of Aβ biomarkers that may help track disease progression and guide treatment decision-making.

Presenter of 3 Presentations

Moderated panel discussion (pre-recorded)

Session Type
SPONSORED SYMPOSIUM
Date
Sat, 19.03.2022
Session Time
11:40 AM - 01:25 PM
Room
ONSITE PLENARY: 115-117
Lecture Time
12:55 PM - 01:20 PM

Welcome, introduction, and overview of the Aβ pathway in AD

Session Type
SPONSORED SYMPOSIUM
Date
Sat, 19.03.2022
Session Time
11:40 AM - 01:25 PM
Room
ONSITE PLENARY: 115-117
Lecture Time
11:40 AM - 11:55 AM

PRE-RECORDED: IN MEMORIAM of Dale Schenk

Session Type
OTHER EVENT
Date
Wed, 16.03.2022
Session Time
11:00 AM - 11:30 AM
Room
ONSITE PLENARY: 115-117
Lecture Time
11:15 AM - 11:19 AM