Ivo J Lutke Schipholt, Gwendolyne G M Scholten-Peeters, Meghan A Koop, Michel W Coppieters, Ronald Boellaard, Elsmarieke van de Giessen, Bastiaan C Ter Meulen, Marieke Coenen, Carmen Vleggeert-Lankamp, Paul R Depaauw, Bart N M van Berckel, Adriaan A Lammerstma, Maqsood Yaqub
{"title":"应用[11C]DPA713 PET/CT定量分析疼痛性颈椎病患者脊髓和神经孔的神经炎症。","authors":"Ivo J Lutke Schipholt, Gwendolyne G M Scholten-Peeters, Meghan A Koop, Michel W Coppieters, Ronald Boellaard, Elsmarieke van de Giessen, Bastiaan C Ter Meulen, Marieke Coenen, Carmen Vleggeert-Lankamp, Paul R Depaauw, Bart N M van Berckel, Adriaan A Lammerstma, Maqsood Yaqub","doi":"10.3389/fnume.2025.1569991","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Animal models of nerve compression have revealed neuroinflammation not only at the entrapment site, but also remotely at the spinal cord. However, there is limited information on the presence of neuroinflammation in human compression neuropathies. The objectives of this study were to: (1) assess which tracer kinetic model most optimally quantified [<sup>11</sup>C]DPA713 uptake in the spinal cord and neuroforamina in patients with painful cervical radiculopathy, (2) evaluate the performance of linearized methods (e.g., Logan) and simplified (e.g., standardized uptake value - SUV) methods, and (3) assess the test-retest reliability of these methods. Microglia activation associated with neuroinflammation was quantified using positron emission tomography (PET) with the radiotracer [<sup>11</sup>C]DPA713, targeting the 18 kDa translocator protein (TSPO). The Akaike information criterion, visual inspection of the fits and number of outliers were used to select the optimal kinetic model. As unaffected tissue, the spinal cord and neuroforamina three cervical levels above the affected target tissue was used.</p><p><strong>Results: </strong>The single tissue (1T2k) compartment model was the preferred model to describe [<sup>11</sup>C]DPA713 kinetics at the spinal cord and neuroforamina. Higher levels of 1T2k <i>V</i> <sub>T</sub> were observed in the affected neuroforamina and spinal cord compared with corresponding unaffected tissues. Logan <i>V</i> <sub>T</sub> (≥0.73) showed high correlation with 1T2k <i>V</i> <sub>T</sub> at both locations. Of the simplified methods, neuroforamina and spinal cord SUV normalized for the metabolite corrected plasma (TBR-PP) exhibited high correlations with 1T2k <i>V</i> <sub>T</sub> (r ≥ 0.84). Test-retest reliability varied between fair to excellent.</p><p><strong>Conclusions: </strong>These results indicate that a 1T2k model with metabolite corrected image derived input function can be used to describe the kinetics of [<sup>11</sup>C]DPA713 in the spinal cord and neuroforamina in humans. 1T2k <i>V</i> <sub>T</sub> or Logan <i>V</i> <sub>T</sub> can be used as binding metric, while TBR-PP is the recommended choice among simplified models.</p>","PeriodicalId":73095,"journal":{"name":"Frontiers in nuclear medicine (Lausanne, Switzerland)","volume":"5 ","pages":"1569991"},"PeriodicalIF":1.4000,"publicationDate":"2025-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12408627/pdf/","citationCount":"0","resultStr":"{\"title\":\"Quantification of neuroinflammation in spinal cord and neuroforamina of patients with painful cervical radiculopathy using [<sup>11</sup>C]DPA713 PET/CT.\",\"authors\":\"Ivo J Lutke Schipholt, Gwendolyne G M Scholten-Peeters, Meghan A Koop, Michel W Coppieters, Ronald Boellaard, Elsmarieke van de Giessen, Bastiaan C Ter Meulen, Marieke Coenen, Carmen Vleggeert-Lankamp, Paul R Depaauw, Bart N M van Berckel, Adriaan A Lammerstma, Maqsood Yaqub\",\"doi\":\"10.3389/fnume.2025.1569991\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Animal models of nerve compression have revealed neuroinflammation not only at the entrapment site, but also remotely at the spinal cord. However, there is limited information on the presence of neuroinflammation in human compression neuropathies. The objectives of this study were to: (1) assess which tracer kinetic model most optimally quantified [<sup>11</sup>C]DPA713 uptake in the spinal cord and neuroforamina in patients with painful cervical radiculopathy, (2) evaluate the performance of linearized methods (e.g., Logan) and simplified (e.g., standardized uptake value - SUV) methods, and (3) assess the test-retest reliability of these methods. Microglia activation associated with neuroinflammation was quantified using positron emission tomography (PET) with the radiotracer [<sup>11</sup>C]DPA713, targeting the 18 kDa translocator protein (TSPO). The Akaike information criterion, visual inspection of the fits and number of outliers were used to select the optimal kinetic model. As unaffected tissue, the spinal cord and neuroforamina three cervical levels above the affected target tissue was used.</p><p><strong>Results: </strong>The single tissue (1T2k) compartment model was the preferred model to describe [<sup>11</sup>C]DPA713 kinetics at the spinal cord and neuroforamina. Higher levels of 1T2k <i>V</i> <sub>T</sub> were observed in the affected neuroforamina and spinal cord compared with corresponding unaffected tissues. Logan <i>V</i> <sub>T</sub> (≥0.73) showed high correlation with 1T2k <i>V</i> <sub>T</sub> at both locations. Of the simplified methods, neuroforamina and spinal cord SUV normalized for the metabolite corrected plasma (TBR-PP) exhibited high correlations with 1T2k <i>V</i> <sub>T</sub> (r ≥ 0.84). 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引用次数: 0
摘要
背景:神经压迫动物模型显示神经炎症不仅发生在压迫部位,而且远端发生在脊髓。然而,关于人类压迫性神经病中存在神经炎症的信息有限。本研究的目的是:(1)评估哪种示踪动力学模型最能量化疼痛性颈椎病患者脊髓和神经孔中[11C]DPA713的摄取,(2)评估线性化方法(如Logan)和简化方法(如标准化摄取值- SUV)的性能,以及(3)评估这些方法的重测可靠性。使用正电子发射断层扫描(PET)和放射性示踪剂[11C]DPA713,量化与神经炎症相关的小胶质细胞激活,靶向18 kDa转运蛋白(TSPO)。采用赤池信息准则、目视拟合检验和离群值数等方法选择最优动力学模型。作为未受影响的组织,脊髓和神经孔比受影响的目标组织高三个颈椎水平。结果:单组织(1T2k)室模型是描述脊髓和神经孔[11C]DPA713动力学的首选模型。与未受影响的相应组织相比,在受影响的神经孔和脊髓中观察到较高水平的1T2k V T。Logan V T(≥0.73)与两个部位的1T2k V T高度相关。在简化方法中,神经孔和脊髓SUV标准化代谢物校正血浆(TBR-PP)与1T2k V T呈高度相关(r≥0.84)。重测信度在一般到优异之间变化。结论:这些结果表明,具有代谢物校正图像衍生输入功能的1T2k模型可用于描述人类脊髓和神经孔中[11C]DPA713的动力学。可以使用1T2k V T或Logan V T作为绑定度量,简化模型中推荐选择TBR-PP。
Quantification of neuroinflammation in spinal cord and neuroforamina of patients with painful cervical radiculopathy using [11C]DPA713 PET/CT.
Background: Animal models of nerve compression have revealed neuroinflammation not only at the entrapment site, but also remotely at the spinal cord. However, there is limited information on the presence of neuroinflammation in human compression neuropathies. The objectives of this study were to: (1) assess which tracer kinetic model most optimally quantified [11C]DPA713 uptake in the spinal cord and neuroforamina in patients with painful cervical radiculopathy, (2) evaluate the performance of linearized methods (e.g., Logan) and simplified (e.g., standardized uptake value - SUV) methods, and (3) assess the test-retest reliability of these methods. Microglia activation associated with neuroinflammation was quantified using positron emission tomography (PET) with the radiotracer [11C]DPA713, targeting the 18 kDa translocator protein (TSPO). The Akaike information criterion, visual inspection of the fits and number of outliers were used to select the optimal kinetic model. As unaffected tissue, the spinal cord and neuroforamina three cervical levels above the affected target tissue was used.
Results: The single tissue (1T2k) compartment model was the preferred model to describe [11C]DPA713 kinetics at the spinal cord and neuroforamina. Higher levels of 1T2k VT were observed in the affected neuroforamina and spinal cord compared with corresponding unaffected tissues. Logan VT (≥0.73) showed high correlation with 1T2k VT at both locations. Of the simplified methods, neuroforamina and spinal cord SUV normalized for the metabolite corrected plasma (TBR-PP) exhibited high correlations with 1T2k VT (r ≥ 0.84). Test-retest reliability varied between fair to excellent.
Conclusions: These results indicate that a 1T2k model with metabolite corrected image derived input function can be used to describe the kinetics of [11C]DPA713 in the spinal cord and neuroforamina in humans. 1T2k VT or Logan VT can be used as binding metric, while TBR-PP is the recommended choice among simplified models.