Alzheimer’s Disease Biomarker Decision-Making among Patients with Mild Cognitive Impairment and Their Care Partners - 21/11/24

Doi : 10.14283/jpad.2024.10 
Chelsea G. Cox 1, , C.R. Salazar 2, A.I. Birnbaum 3, M. Witbracht 2, S.P. Tam 2, 4, G.T. Thai 2, 5, S.A. Sajjadi 2, 5, D.L. Gillen 2, 3, J.D. Grill 2, 6, 7
1 Department of Health Behavior and Health Education, University of Michigan School of Public Health, 1415 Washington Heights, 48109-2029, Ann Arbor, MI, USA 
2 Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, CA, USA 
3 Department of Statistics, University of California, Irvine, CA, USA 
4 Department of Family Medicine, University of California, Irvine, CA, USA 
5 Department of Neurology, University of California, Irvine, CA, USA 
6 Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA 
7 Department of Neurobiology and Behavior, University of California, Irvine, CA, USA 

a chelseak@umich.edu chelseak@umich.edu

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Abstract

Background

Alzheimer’s disease (AD) biomarker tests can be ordered as part of the diagnostic workup of patients with mild cognitive impairment (MCI). Little is known about how patients with MCI and their care partners decide whether to pursue testing.

Objective

To examine factors that influence AD biomarker testing decisions among patients with MCI and their care partners.

Design

We performed structured research interviews with patients with MCI and their study partners to assess the importance of eight factors in the decision whether to undergo AD biomarker testing (6-point Likert scale; 1-extremely unimportant to 6-extremely important): cost, fear of testing procedures, learning if AD is the cause of cognitive problems, concern about health insurance, instructing future planning, informing treatment decisions, family members’ opinions, and doctor recommendation.

Setting

Two researchers administered interviews with participants in-person (i.e., participant home, research center) or remotely (i.e., telephone, video-conference).

Participants

We completed interviews with 65 patients with a diagnosis of MCI and 57 study partners, referred by dementia specialist clinicians from the University of California, Irvine health system.

Measurements

We used generalized estimating equations (GEE) to examine the mean importance of each factor among patients and study partners, and the mean difference in importance of each factor within dyads.

Results

One third of participants reported the patient had previously undergone AD biomarker testing. Fifty-five percent of patients and 65% of study partners who reported no previous testing indicated a desire for the patient to be tested. GEE analyses found that patients and study partners rated the following factors with highest importance: informing treatment decisions (mean score 5.29, 95% CI: 5.06, 5.52 for patients; mean score 5.56, 95% CI: 5.41, 5.72 for partners); doctor recommendation (4.94, 95% CI: 4.73, 5.15 for patients; 5.16, 95% CI: 4.97, 5.34 for partners); and instructing future planning (4.88, 95% CI: 4.59, 5.16 for patients; 5.11, 95% CI: 4.86, 5.35 for partners). High dyadic agreement was observed for all factors except fear of testing, which patients rated with lower importance than their study partners.

Conclusions

Biomarker testing for AD in patients with MCI is a rapidly evolving practice and limited data exist on patient perspectives. In this study, most patients and their care partners were interested in testing to help inform treatment decisions and to plan for the future. Participants placed high importance on clinician recommendations for biomarker testing, highlighting the need for clear communication and education on the options, limitations, risks, and benefits of testing.

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Key words : Alzheimer’s disease, mild cognitive impairment, biomarkers


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Vol 11 - N° 2

P. 285-293 - mars 2024 Retour au numéro
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