AUTHOR=Tsugawa Sakiko , Kimura Yuichi , Chikazoe Junichi , Abe Hiroki , Arisawa Tetsu , Hatano Mai , Nakajima Waki , Uchida Hiroyuki , Miyazaki Tomoyuki , Takada Yuuki , Sano Akane , Nakano Kotaro , Eiro Tsuyoshi , Suda Akira , Asami Takeshi , Hishimoto Akitoyo , Tani Hideaki , Nagai Nobuhiro , Koizumi Teruki , Nakajima Shinichiro , Kurokawa Shunya , Ohtani Yohei , Takahashi Kie , Kikuchi Yuhei , Yatomi Taisuke , Mitoma Ryo , Tamura Shunsuke , Baba Shingo , Togao Osamu , Hirano Yoji , Kosaka Hirotaka , Okazawa Hidehiko , Mimura Masaru , Takahashi Takuya TITLE=Differentiation between bipolar disorder and major depressive disorder based on AMPA receptor distribution JOURNAL=Frontiers in Neural Circuits VOLUME=Volume 19 - 2025 YEAR=2025 URL=https://www.frontiersin.org/journals/neural-circuits/articles/10.3389/fncir.2025.1624179 DOI=10.3389/fncir.2025.1624179 ISSN=1662-5110 ABSTRACT=An accurate diagnostic method using biological indicators is critically needed for bipolar disorder (BD) and major depressive disorder (MDD). The excitatory glutamate α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) is a crucial regulator of synaptic function, and its dysregulation may play a central role in the pathophysiology of psychiatric disorders. Our recently developed positron emission tomography (PET) tracer, [11C]K-2, enables the quantitative visualization of AMPAR distribution and is considered useful for characterizing synaptic phenotypes in patients with psychiatric disorders. This study aimed to develop a machine learning-based method to differentiate bipolar disorder from major depressive disorder using AMPAR density. Sixteen patients with BD and 27 patients with MDD, all in depressive episodes, underwent PET scans with [11C]K-2 and structural magnetic resonance imaging. AMPAR density was estimated using the standardized uptake value ratio from 30 to 50 min after tracer injection, normalized to whole brain radioactivity. A partial least squares model was trained to predict diagnoses based on AMPAR density, and its performance was evaluated using a leave-one-pair-out cross-validation. Significant differences in AMPAR density were observed in the parietal lobe, cerebellum, and frontal lobe, notably the dorsolateral prefrontal cortex between patients with BD and patients with MDD during a depressive episode. The model achieved an area under the curve of 0.80, sensitivity of 75.0%, and specificity of 77.8%. These findings suggest that AMPAR density measured with [11C]K-2 can effectively distinguish BD from MDD and may aid diagnosis, especially in patients with ambiguous symptoms or incomplete clinical presentation.