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Latest developments in Alzheimer’s disease research

  • February 26, 2024
  • 12:00 PM - 1:00 PM
  • 2100 E. 71st St., Indianapolis, IN 46220

Speaker: Sophia Wang, MD, Associate Professor of Clinical Psychiatry, IUSM

Introduced By: Russell Judd

Attendance: NESC: 88, Zoom: 48

Guest(s): Josh Matthews, Marinelle Morgan, Rich Peine

Scribe: Benny Ko

Editor: Carl Warner

View a recording of today’s Zoom presentation at: 

Today's Program 022624

When viewing the recording, please advance the video to the 33 minute mark to see the start of the program. We were testing the recording function during our setup and forgot to turn it off until the meeting started.

With the recent FDA approval of the new drug Lecanemab (Lequembi), we are on the verge of a new era in the treatment of Alzheimer's disease. While the drug does not cure the disease, it has been shown to slow its progression by about 20-30% while the patients were on an 18-month therapy. The drug is given intravenously every two weeks in a 45-60 minute session. The mechanism of action of Lecanemab is thought to be its binding with protofibrils and preventing the latter from becoming fibrils, the main component of amyloid plaques. Currently, the treatment is recommended for patients with very mild to mild symptoms of Alzheimer's disease. A similar class of therapeutic agents is currently on trial.

Before this new drug, Alzheimer's disease treatment was palliative, i.e., moderating symptoms. Such symptom reducing drugs include acetylcholinesterase inhibitors, rivastigmine, and donepezil. Other drugs such as memantine target NMDA receptors at the neuronal level. Unlike Lecanemab, they do not slow disease progression.

In Alzheimer's disease, early detection is important. CSF biomarkers, APOE genetic testing, amyloid PET scans, cognitive testing, and clinical history are all important diagnostic tools.

Lecanemab has to be intravenous-delivered because it has to cross the blood-brain barrier. The therapy is not without some known complications such as allergic reactions. ARIA stands for amyloid-related imaging abnormalities observed in patients' serial imaging studies during their therapy period. These observed abnormalities are sometimes asymptomatic and transient while at other times they are not. ARIA with severe symptoms and complications occurs in less than 1%.

ARIA-E represents brain edema and ARIA-H represents hemosiderin, a sign of hemorrhage. These vascular pathologies happen because the drug removes the amyloid accumulated in an infiltrated blood vessel and hence compromises its integrity. The drug should not be given in conjunction with anticoagulative and TPA therapy.

The cost is substantial but Medicare will pay for the major portion.

What is DICE in non-drug management of behavioral symptoms? The DICE approach includes describe, investigate, create, and evaluate. Behavioral symptoms include aggression, agitation, anxiety, apathy, delusions, hallucinations, disinhibition, irritability, motor disturbances, and nighttime behaviors. A "behavioral triad" involves three components: the caregiver, the environment, and the person with dementia. Together, they have a role in the behavioral status of the patient. To establish a routine and a safe environment are important for the patient.


Sophia Wang


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