The U.S. blood-based biomarker for alzheimer’s disease diagnostics market size was estimated at USD 59.64 million in 2024 and is expected to grow at a CAGR of 14.60% from 2025 to 2033. This growth is fueled by rising Alzheimer’s prevalence, increasing demand for non-invasive diagnostics, and regulatory approvals such as the FDA’s clearance of blood-based IVD assays. Technological advancements in ultrasensitive immunoassays and multiplex testing further support adoption, positioning blood biomarkers as essential tools in early detection and treatment pathways.
One of the most significant growth drivers for the U.S. blood-based biomarker market is the approval of FDA-cleared IVD assays. A prime example is the Lumipulse G pTau217/β-Amyloid 1-42 Plasma Ratio, which gained marketing authorization in 2025. Regulatory recognition not only lowers clinical adoption barriers but also validates the reliability of blood-based tests in practice. At the same time, advances in ultra-sensitive immunoassays and AI-powered multiplex testing are enhancing diagnostic accuracy. These technologies help reduce dependence on costly, invasive methods such as PET imaging and lumbar punctures. The combination of regulatory approval and innovation is creating strong momentum, boosting confidence among healthcare providers, payers, and patients alike
Demographic trends are another critical driver. As the U.S. population ages, the prevalence of dementia is rising rapidly-about 4% of individuals aged 65+ are affected, and the rate climbs to 13% among those over 85. This has created an urgent need for scalable, early diagnostic solutions. Blood-based biomarkers address this gap by offering less invasive testing, enabling earlier intervention, and streamlining patient care pathways. They also support the shift toward precision medicine, where biologically driven diagnostics guide therapy selection and monitoring. Importantly, anti-amyloid drugs now require biomarker confirmation of pathology, making blood tests an essential first-line triage tool for patients being evaluated for treatment.
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One of the most significant growth drivers for the U.S. blood-based biomarker market is the approval of FDA-cleared IVD assays. A prime example is the Lumipulse G pTau217/β-Amyloid 1-42 Plasma Ratio, which gained marketing authorization in 2025. Regulatory recognition not only lowers clinical adoption barriers but also validates the reliability of blood-based tests in practice. At the same time, advances in ultra-sensitive immunoassays and AI-powered multiplex testing are enhancing diagnostic accuracy. These technologies help reduce dependence on costly, invasive methods such as PET imaging and lumbar punctures. The combination of regulatory approval and innovation is creating strong momentum, boosting confidence among healthcare providers, payers, and patients alike
Demographic trends are another critical driver. As the U.S. population ages, the prevalence of dementia is rising rapidly-about 4% of individuals aged 65+ are affected, and the rate climbs to 13% among those over 85. This has created an urgent need for scalable, early diagnostic solutions. Blood-based biomarkers address this gap by offering less invasive testing, enabling earlier intervention, and streamlining patient care pathways. They also support the shift toward precision medicine, where biologically driven diagnostics guide therapy selection and monitoring. Importantly, anti-amyloid drugs now require biomarker confirmation of pathology, making blood tests an essential first-line triage tool for patients being evaluated for treatment.
U.S. Blood-based Biomarker For Alzheimer’s Disease Diagnostics Market Report Segmentation
This report forecasts revenue growth at country level and provides an analysis on the latest trends in each of the sub-segments from 2021 to 2033. The analyst has segmented the U.S. blood-based biomarker for alzheimer’s disease diagnostics market based on type, technology, and end use:- Type Outlook (USD Million, 2021-2033)
- Amyloid-related markers
- Tau-related markers
- Neurodegeneration
- Others
- Technology Outlook (USD Million, 2021-2033)
- Immunoassays
- Mass spectrometry-based assays
- Next-generation platforms
- Others
- End Use Outlook (USD Million, 2021-2033)
- Clinical laboratories & hospital labs
- Pharma & biotech
- Academic & research institutes
- Others
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Table of Contents
Chapter 1. U.S. Blood-based Biomarker for Alzheimer’s Disease Diagnostics Market: Methodology and Scope
Chapter 2. U.S. Blood-based Biomarker for Alzheimer’s Disease Diagnostics Market: Executive Summary
Chapter 3. U.S. Blood-based Biomarker for Alzheimer’s Disease Diagnostics Market Variables, Trends, & Scope
Chapter 4. U.S. Blood-based Biomarker for Alzheimer’s Disease Diagnostics Market: Type Estimates & Trend Analysis
Chapter 5. U.S. Blood-based Biomarker for Alzheimer’s Disease Diagnostics Market: Technology Estimates & Trend Analysis
Chapter 6. U.S. Blood-based Biomarker for Alzheimer’s Disease Diagnostics Market: End Use Estimates & Trend Analysis
Chapter 7. Competitive Landscape
List of Tables
List of Figures
Companies Mentioned
The major companies profiled in this U.S. Blood-based Biomarker for Alzheimer’s Disease Diagnostics market report include:- F. Hoffmann-La Roche Ltd
- Quanterix
- Fujirebio
- C2N Diagnostics
- Labcorp
- Quest Diagnostics Incorporated
- Siemens Healthineers
- Diadem srl
- Abbott
- BioArctic
- Grifols