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Case Reports
. 2024 Aug 6;12(8):1776.
doi: 10.3390/biomedicines12081776.

Sustained Cognitive Improvement in Alzheimer's Disease Patients Following a Precision Medicine Protocol: Case Series

Affiliations
Case Reports

Sustained Cognitive Improvement in Alzheimer's Disease Patients Following a Precision Medicine Protocol: Case Series

Dale E Bredesen et al. Biomedicines. .

Abstract

Arguably, the most important parameter in treating cognitive decline associated with Alzheimer's disease is the length of time in which improvement, if achieved at all, is sustained. However, monotherapies such as donepezil and memantine are associated with a more rapid decline than no treatment in patients over multi-year follow-ups. Furthermore, anti-amyloid antibody treatment, which at best simply slows decline, is associated with accelerated cerebral atrophy, resulting in earlier dementia-associated brain volumes for those treated at the MCI stage than untreated patients. In contrast, a precision medicine approach, in which the multiple potential drivers of cognitive decline are identified for each patient and then targeted with a personalized protocol (such as ReCODE), has led to documented improvements in patients with cognitive decline, but long-term follow-up (>5 years) has not been reported previously. Therefore, here, we report sustained cognitive improvement, in some cases for over a decade, in patients treated with a precision medicine protocol-something that has not been reported in patients treated with anti-cholinesterase, glutamate receptor inhibitory, anti-amyloid, or other therapeutic methods. These case studies warrant long-term cohort studies to determine how frequently such sustained cognitive improvements occur in patients treated with precision medicine protocols.

Keywords: anti-amyloid therapy; donepezil; mild cognitive impairment; personalized medicine; treatment.

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Conflict of interest statement

D.E.B. is a consultant for Apollo Health and Life Seasons, neither of which was involved in this study or had any access to the study data. M.K.R. worked for Thorne during some of the time in which she treated some of the patients described in the manuscript, but Thorne was not involved in the management of the patients, and had no access to the data reported in the manuscript.

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