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. 2025 Jun 19;11(2):e70094.
doi: 10.1002/trc2.70094. eCollection 2025 Apr-Jun.

System readiness and the patient care pathway for Alzheimer's disease diagnosis and treatment

Affiliations

System readiness and the patient care pathway for Alzheimer's disease diagnosis and treatment

B Joy Snider et al. Alzheimers Dement (N Y). .

Abstract

Promising therapeutic interventions that target the underlying pathophysiology are changing the landscape of Alzheimer's disease (AD) research. The AD care pathway must be transformed to meet the challenge of bringing these new therapies to the increasing number of people living with AD within the existing healthcare framework. Challenges include identifying patients who may benefit from treatment interventions early in the course of the disease, ensuring that diagnostic tools are accessible and accurate, and developing capabilities to monitor the effectiveness of interventions over time. These challenges must be addressed at all levels, from primary care settings to tertiary treatment centers; this will require collaborative efforts between health systems, drug manufacturers, and research institutions to navigate this evolving landscape and ensure system readiness for patients and their families with AD. The Spring 2024 Alzheimer's Association Research Roundtable (AARR) meeting gathered industry representatives and clinicians to discuss insights, challenges, and solutions that will help researchers and health systems identify patients in the early stages of AD and deliver emerging therapies efficiently and safely. In this paper, we provide highlights from the Spring 2024 AARR meeting.

Keywords: Alzheimer's disease; amyloid; biomarkers; cognitive testing; diagnostics; disease‐modifying therapy; early diagnosis; early intervention; health systems; real world data; reimbursement; system readiness; treatments.

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Conflict of interest statement

B.J.S. has received grants, contracts, or consulting fees from Eisai, Eli Lilly, and Roche. A.B. is a full‐time employee and minor shareholder at Eli Lilly and Company. S.B. is a full‐time employee of Hoffman–LaRoche. C.C. has received funding from the NIA, ANF, and HRSA, and consulting fees from Braincheck, Otsuka, Eli‐Lilly, and NovoNordisk. G.F. is an employee of GE Healthcare who holds the Marketing Authorisation for VizamylTM.DG. D.G. has received grants or consulting fees from Biogen, Bristol Myers Squibb, Cassava, Eli Lilly, Eisai, Abbvie, Davos Alzheimer's Collaborative, NIA, Alzheimer's Association, Genentech/Roche, Nutricia, NovoNordisk, WIRB‐Copernicus. R.K. is a full‐time employee of Johnson & Johnson Innovative Medicine. S.M. has received research contracts/grants to USC from Biogen, C2N, Eisai, and Roche. M.M. has received grants from the NIH, Alzheimer's Association, Davos Alzheimer's Collaborative, and consulting fees from Athira, Biogen, Eisai, Lilly, Merck, Roche, Siemens Healthineers, and Novo Nordisk. D.M. is a full‐time employee of the Pharmaceutical Care Management Association. J.M. is a full‐time employee of Biogen. H.O. has received grants, contracts, or consulting fees from Biogen, Eisai, Optina, American College of Radiology, NIA/NOH, Alzheimer's Association, Eli Lilly, Woolsey, Ecofibre, Commonwealth Health Research Board. G.D.R. has served on scientific advisory boards and/or as a consultant for Eli Lilly, Genenetech/Roche, GE Healthcare, Alector and Merck, payments from Efficient LLC, JAMA Neurology (Associate Editor), Miller Medical Communications, paid for participation on a Data Safety Monitoring Board or Advisory Board for Johnson & Johnson. D.R. has received honoraria for educational events from Northwestern University, AAAS, IMPACT AD. J.S. has received honoraria from Biogen, Eisai, Eli Lilly, Arrowhead Pharmaceuticals, and Global Learning Collaborative on Alzheimer's Disease Topics. H.S., S.M., G.W., C.J.W., and M.C.C. are full‐time employees of the Alzheimer's Association. Author disclosures are available in the supporting information.

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