Intervention for Cognitive Reserve Enhancement in Delaying the Onset of Alzheimer’s Symptomatic Expression (INCREASE) Study: Results from a Randomized Controlled Study of Medication Therapy Management Targeting a Delay in Prodromal Dementia Symptom Progression - 21/11/24

Doi : 10.14283/jpad.2022.55 
Daniela C. Moga 1, 2, 3, 10, , E.L. Abner 2, 3, F.A. Schmitt 2, 4, L. Eckmann 5, M. Huffmyer 5, 6, A.I. Martinez 1, 7, B.F. Beech 2, 8, R. George 2, R.H. El Khouli 9, D. Ali 2, G.A. Jicha 2, 4
1 Department of Pharmacy Practice and Science, University of Kentucky College of College of Pharmacy, Lexington, KY, USA 
2 Sanders-Brown Center on Aging, Lexington, KY, USA 
3 Department of Epidemiology, University of Kentucky College of Public Health, Lexington, KY, USA 
4 Department of Neurology, University of Kentucky College of Medicine, Lexington, KY, USA 
5 PRO2RX LLC Pharmacy Consulting Services, Lexington, KY, USA 
6 University of Kentucky Healthcare, Lexington, KY, USA 
7 Harvard Pilgrim Health Care Institute and Harvard Medical School, Boston, MA, USA 
8 Washington State University, Pullman, WA, USA 
9 Department of Radiology, University of Kentucky College of Medicine, Lexington, KY, USA 
10 241 Lee T. Todd Jr. Building, 789 S. Limestone, 40536, Lexington, KY, USA 

a daniela.moga@uky.edu daniela.moga@uky.edu

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Abstract

Background

Cognitive reserve has been hypothesized as a mechanism to explain differences in individual risk for symptomatic expression of Alzheimer’s Disease (AD). Inappropriate medications may diminish cognitive reserve, precipitating the transition from preclinical AD (pAD) to a symptomatic state. To date, there is limited data on the potential impact of medication optimization as a potential tool for slowing the symptomatic expression of AD.

Objectives

(1) To test the efficacy of a medication therapy management intervention designed to bolster cognitive reserve in community-dwelling older adults without dementia. (2) To evaluate the efficacy of intervention by baseline pAD status.

Design

A 1-year randomized controlled trial was conducted in community-dwelling older adults without dementia. Randomization was stratified by amyloid β positron emission tomography levels.

Setting

Community-based, Lexington, Kentucky.

Participants

Adults 65 years or older with no evidence of dementia and reporting at least one potentially inappropriate medication as listed in the Beers 2015 criteria were recruited. The study aimed to enroll 90 participants based on the a priori sample size calculation.

Intervention

Medication therapy management versus standard of care.

Measurements

Primary outcomes were: (1) one-year changes in the Medication Appropriateness Index; (2) one-year changes in Trail Making Test B under scopolamine challenge.

Results

The medication therapy management intervention resulted in significant improvement in Medication Appropriateness Index scores. Overall, there was no beneficial effect of the medication therapy management on Trail Making Test B scores, however stratified analysis demonstrated improvement in Trail Making Test B challenged scores associated with the medication therapy management for those with elevated amyloid β positron emission tomography levels consistent with pAD.

Conclusions

Medication therapy management can reduce inappropriate medication use in older adults at risk for AD. Our study indicated beneficial cognitive effects in those with preclinical Alzheimer’s Disease. No statistically significant effects were evident in the study group as a whole, or in those without preclinical cerebral amyloidosis. Further work designed to improve the effectiveness of the medication therapy management approach and defining other preclinical pathologic states that may benefit from medication optimization are readily achievable goals for promoting improved cognitive health and potentially delaying the onset of symptomatic AD.

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Key words : Medication therapy management, cognitive reserve, randomized controlled trial, Beers criteria, deprescribing


Plan


 Trial registration number: ClinicalTrials.gov, NCT02849639. Registered on 29 July 2016.


© 2022  THE AUTHORS. Published by Elsevier Masson SAS on behalf of SERDI Publisher.. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 9 - N° 4

P. 646-654 - octobre 2022 Retour au numéro
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