Abstract
Several neurological and psychiatric disorders have been associated with neuroinflammation, defined by the activation of microglia and astrocytes in the brain. PET radioligands that target microglial and astrocytic proteins allow in vivo quantification of neuroimmune responses. To date, the 18 kDa translocator protein (TSPO) and monoamine oxidase B, proteins predominantly expressed by microglia and astrocytes, respectively, are the most commonly used targets of neuroinflammation PET radioligands. Several TSPO radioligands have been developed; however, TSPO PET has only been extensively studied in a few disorders, and results of these studies have not always been consistent. Evidence suggests that PET imaging can detect neuroinflammatory changes in Alzheimer’s disease, major depressive disorder, and traumatic brain injury. In Alzheimer’s disease, TSPO signal increases with disease progression, suggesting that PET imaging could be used to monitor inflammatory changes in patients with this disorder. In major depressive disorder, unmedicated patients have greater TSPO signal, and greater amounts of TSPO binding are associated with reduction of mood symptoms after treatment with celecoxib. Therefore, TSPO PET may be useful predictor of response to anti-inflammatory therapies in depression.
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Kreisl, W.C. (2022). Microglial Activation and Neuroinflammation. In: Franceschi, A.M., Franceschi, D. (eds) Hybrid PET/MR Neuroimaging. Springer, Cham. https://doi.org/10.1007/978-3-030-82367-2_17
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DOI: https://doi.org/10.1007/978-3-030-82367-2_17
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