Imaging the pro‐coagulant state in Alzheimer’s Disease: Detection of fibrin and platelets accumulation in the brain by PET

利用PET成像技术检测阿尔茨海默病患者的促凝状态:脑内纤维蛋白和血小板聚集的检测

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Abstract

BACKGROUND: Alzheimer's disease (AD) is a multifactorial neurodegenerative disorder with emerging evidence pointing to a pro‐thrombotic environment, supported by increased fibrin content in the brain(1) and an unquestionable role of platelets(2). These mechanisms contribute to hypoperfusion, blood brain barrier disruption, and neurodegeneration, occurring early in the disease but not in all patients. Early diagnosis would be invaluable to identify patients who may benefit from anticoagulant therapies(3). To this end, we have developed two novel PET biomarkers for non‐invasive detection of brain micro‐thrombi in an AD model. METHOD: Vectors (fibrin binding probe ‐FBP(4)‐ and anti‐platelets antibody ‐antiCD41(5)‐) were attached to transcyclooctene (TCO), which reacts via click‐chemistry with tetrazine (TZ). TZ was used to functionalize two probes: 1) (68)Ga‐chelator DOTA for fibrin imaging and 2) (68)Ga‐labeled iron oxide nanoparticles for platelet imaging (Figure 1A). The experimental approach involves two steps: First, AD mice (TgCRND8) and wildtype littermates were injected with either FBP‐TCO or antiCD41‐TCO. 24 hours later, animals received ∼17 MBq IV of (68)Ga‐Tz, and PET/CT studies were acquired with a nanoScan® PET/CT scanner (Mediso, Hungary). Brains were collected for ex vivo biodistribution studies. In vivo validation of both biomarkers was conducted in a carotid crush injury model. RESULT: Studies in the carotid crush injury model confirmed tracers accumulation at the damaged artery, verifying the specificity of both probes. In AD mice, (68)Ga‐Tz uptake was elevated in the brain, independent of the target (fibrin —Figure 1B– or CD41 —Figure 1C—). These findings were confirmed by ex vivo studies. CONCLUSION: We have developed two feasible neuroimaging strategies to assess the pro‐thrombotic state in AD mice, opening a window of opportunity to ameliorate AD’s progression with personalized anticoagulant treatments. Funding: MCV is supported by BrightFocus Foundation, and JDC2022‐048922‐I funded by MCIN/AEI/10.13039/501100011033 and European Union NextGenerationEU/PRTR. This project is funded by the EU Joint Programme – Neurodegenerative Disease Research (JPND). CNIC is a Severo Ochoa Center of Excellence. Bibliography: 1. Cortes‐Canteli, et al. (2015) Neurobiol Aging. doi:10.1016/j.neurobiolaging.2014.10.030 2. Kucheryavykh, et al. (2017) Brain Res Bull. doi:10.1016/j.brainresbull.2016.11.008 3. Cortes‐Canteli, et al. (2019) J Am Coll Cardiol. doi:10.1016/j.jacc.2019.07.081 4. Oliveira & Caravan. (2017) Dalton Transactions. doi:10.1039/c7dt02634j 5. Adrover, et al. (2020) Nanoscale. doi:10.1039/d0nr04538a

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