Quanterix Announces Landmark JAMA Study Highlighting Prognostic Value of Multi-Analyte Approach to Blood-Based Alzheimer’s Risk Profiling

Quanterix Corporation (NASDAQ: QTRX), a company transforming healthcare by accelerating biomarker breakthroughs from discovery to diagnostics, today announced publication of a landmark study in the high impact journal JAMA Network Open, https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2842215. The study, led by researchers at Amsterdam UMC, followed a cohort of nearly 300 individuals for up to 15 years. The findings demonstrated that while individual biomarkers provide a baseline snapshot of pathology, the combination of multiple markers at baseline—along with their subsequent longitudinal trajectories—offers a significantly more comprehensive view of clinical risk.

The research utilized ultra-sensitive Simoa technology to measure biomarkers representing the four critical biological axes of Alzheimer’s disease: amyloid (Aβ42/Aβ40 ratio), tau (p-Tau 217), neuroinflammation (GFAP), and neurodegeneration (NfL). A primary conclusion of the study was that the most accurate assessment of clinical progression was achieved through a multi-analyte model, both at baseline as well as through longitudinal monitoring of individual biomarker values. The optimal model achieved a C-index of 0.90 (1.0 being perfect accuracy) for identifying individuals with SCD—the earliest stage where patients notice potential changes that are undetectable in objective cognitive testing–most likely to progress toward clinical impairment. The data showed that even a single baseline measurement of this specific multi-analyte panel offered a distinct prognostic advantage over standalone p-Tau 217 assays.

This JAMA paper highlights how Quanterix’s Simoa ultra-sensitive technology and multiplexed biomarker assays are powering advances in Alzheimer’s disease research, which is becoming increasingly focused on evaluating multiple biomarkers and multiple disease pathways. Quanterix is also leading the way in Alzheimer’s diagnostics with scalable multi-marker laboratory developed tests, such as LucentAD Complete which is designed with same biomarkers evaluated in the JAMA study. As the company’s first algorithmic multi-analyte test for amyloid pathology risk in symptomatic individuals, LucentAD Complete stands alone in providing both an overall amyloid risk score and individual results for these same biomarkers alongside normative reference ranges.