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Background <p>While <sup>18</sup>F-fluorodeoxyglucose (<sup>18</sup>F-FDG) PET supports increased neuronal activity in tinnitus, synaptic density abnormalities via synaptic vesicle protein 2&#xa0;A (SV2A) imaging remain unexplored. This study used <sup>18</sup>F-SynVesT-1 PET to evaluate SV2A changes in tinnitus patients and compared them to <sup>18</sup>F-FDG patterns.</p> Methods <p>28 tinnitus patients (acute/chronic) and 24 healthy controls underwent MRI and static PET with both <sup>18</sup>F-SynVesT-1 and <sup>18</sup>F-FDG. Standardized uptake values (SUV/SUVr) were calculated, followed by brain network analysis and EEG microstate assessment. Correlations with clinical features were examined.</p> Findings <p>Lesions in the brain of chronic tinnitus patients had increased <sup>18</sup>F-SynVesT-1 uptake compared with controls, corresponding to high metabolism detected by <sup>18</sup>F-FDG PET. The patients revealed increased SV2A uptake of 14 brain areas, whereas the left inferior frontal gyrus showed decreased SV2A uptake. However, acute tinnitus patient results revealed a decreased synaptic density in five brain areas as compared to that of HCs. <sup>18</sup>F-SynVesT-1 uptake had a more broaden pattern of induction than <sup>18</sup>F-FDG in tinnitus lesions (<i>P</i> &lt; 0.05). SUVR of these two imaging agents were positively correlated in insula lobe. Tinnitus Handicap Inventory (THI) scores negatively correlated with synaptic density in limbic regions. Brain network anaylsis showed that network connectivity was enhanced in tinnitus, highest acutely. Microstate analysis of EEG showed conserved microstate alternation.</p> Interpretations <p>This first direct evidence demonstrates chronic tinnitus involves synaptic density elevation, while acute phase shows reduction, indicating bidirectional synaptic remodeling. <sup>18</sup>F-SynVesT-1 outperforms <sup>18</sup>F-FDG in detecting tinnitus-linked synaptic reorganization, with abnormality extent correlating to symptom severity, suggesting novel therapeutic targets for synaptic modulation.</p>

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Direct evidence for synaptic density changes in tinnitus: 18F-SynVesT-1 PET reveals novel targets beyond metabolic changes

  • 期刊论文

  • 发表日期：

    2025年11月3日

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  • JiaYu Zhong,
  • Xuping Xiao,
  • Bin Liu,
  • Zhiyou He,
  • Ming Zhou,
  • En Zhou,
  • Shuo Hu

摘要

Background

While 18F-fluorodeoxyglucose (18F-FDG) PET supports increased neuronal activity in tinnitus, synaptic density abnormalities via synaptic vesicle protein 2 A (SV2A) imaging remain unexplored. This study used 18F-SynVesT-1 PET to evaluate SV2A changes in tinnitus patients and compared them to 18F-FDG patterns.

Methods

28 tinnitus patients (acute/chronic) and 24 healthy controls underwent MRI and static PET with both 18F-SynVesT-1 and 18F-FDG. Standardized uptake values (SUV/SUVr) were calculated, followed by brain network analysis and EEG microstate assessment. Correlations with clinical features were examined.

Findings

Lesions in the brain of chronic tinnitus patients had increased 18F-SynVesT-1 uptake compared with controls, corresponding to high metabolism detected by 18F-FDG PET. The patients revealed increased SV2A uptake of 14 brain areas, whereas the left inferior frontal gyrus showed decreased SV2A uptake. However, acute tinnitus patient results revealed a decreased synaptic density in five brain areas as compared to that of HCs. 18F-SynVesT-1 uptake had a more broaden pattern of induction than 18F-FDG in tinnitus lesions (P < 0.05). SUVR of these two imaging agents were positively correlated in insula lobe. Tinnitus Handicap Inventory (THI) scores negatively correlated with synaptic density in limbic regions. Brain network anaylsis showed that network connectivity was enhanced in tinnitus, highest acutely. Microstate analysis of EEG showed conserved microstate alternation.

Interpretations

This first direct evidence demonstrates chronic tinnitus involves synaptic density elevation, while acute phase shows reduction, indicating bidirectional synaptic remodeling. 18F-SynVesT-1 outperforms 18F-FDG in detecting tinnitus-linked synaptic reorganization, with abnormality extent correlating to symptom severity, suggesting novel therapeutic targets for synaptic modulation.