# Alzheimer’s disease blood-based biomarker testing: A stakeholder-informed assessment of coverage considerations

**Authors:** Patricia A Deverka, Jalayne J Arias, Grace A Lin, Jessica Zwerling, Kathryn A Phillips

PMC · DOI: 10.1177/13872877251329394 · Journal of Alzheimer's disease : JAD · 2025-06-06

## TL;DR

This paper explores how to ensure fair access to blood-based Alzheimer's tests by addressing coverage barriers and stakeholder concerns.

## Contribution

The study identifies key coverage considerations for Alzheimer’s blood tests based on stakeholder input, focusing on equitable access and clinical utility.

## Key findings

- Payers require evidence of clinical validity and utility for blood-based Alzheimer’s tests.
- Evidence gaps exist for minority populations and for screening applications.
- Limiting test coverage to specialists could harm underserved patients.

## Abstract

Recently published clinical studies suggest that blood-based biomarker tests (BBMTs) for Alzheimer’s disease (AD) provide value, but in the U.S., neither public nor private payers currently cover these tests.

To describe considerations for payer coverage of AD BBMTs that would need to be addressed to facilitate timely diagnosis and equitable patient access if clinical utility is demonstrated.

We performed a targeted literature review to characterize predictable coverage barriers for BBMTs and inform the development of an interview guide. We conducted semi-structured interviews with clinicians, researchers, test developers, and a patient advocate and former payer (N = 12) to assess the barriers and refine the proposed key considerations for obtaining payer coverage.

Stakeholders noted that payers will require evidence of clinical validity and utility of BBMTs as part of their coverage determinations contingent on the specific indication for testing, with insufficient evidence for screening applications currently. Stakeholders also agreed that there are evidence gaps for use of BBMTs in patients from ethnic and racial minority communities that must be addressed. Given the shortage of memory specialists, stakeholders noted that limiting testing coverage authorization to specialists could be harmful to patients, particularly the underserved. Interviewees also agreed that patients with mild cognitive impairment or early-stage AD could benefit from earlier diagnosis to avoid progressing to moderate disease and limiting eligibility for new disease-modifying therapies.

If BBMTs meet criteria for clinical utility, anticipating and planning for coverage and reimbursement before widespread implementation will be critical to ensuring broad, equitable access to BBMTs.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Diseases:** AD (MESH:D000544), cognitive impairment (MESH:D003072)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12143641/full.md

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Source: https://tomesphere.com/paper/PMC12143641