de Souza Aline Morais, Pitombeira Milena Sales, de Souza Larissa Estessi, Marques Fabio Luiz Navarro, Buchpiguel Carlos Alberto, Real Caroline Cristiano, de Paula Faria Daniele
Laboratory of Nuclear Medicine (LIM43), Department of Radiology and Oncology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Department of Neurology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Neural Regen Res. 2021 Dec;16(12):2494-2498. doi: 10.4103/1673-5374.313062.
C-PK11195 is a positron emitter tracer used for Positron Emission Tomography (PET) imaging of innate immune cell activation in studies of neuroinflammatory diseases. For the image quantitative analysis, it is necessary to quantify the intact fraction of this tracer in the arterial plasma during imaging acquisition (plasma intact fraction). Due to the complexity and costs involved in this analysis it is important to evaluate the real necessity of individual analysis in each C-PK11195 PET imaging acquisition. The purpose of this study is to compare C-PK11195 plasma metabolization rate between healthy controls and multiple sclerosis (MS) patients and evaluate the interference of sex, age, treatment, and disease phenotype in the tracer intact fraction measured in arterial plasma samples. C-PK11195 metabolization rate in arterial plasma was quantified by high performance liquid chromatography in samples from MS patients (n = 50) and healthy controls (n = 23) at 20, 45, and 60 minutes after C-PK11195 injection. Analyses were also stratified by sex, age, treatment type, and MS phenotype. The results showed no significant differences in the metabolization rate of healthy controls and MS patients, or in the stratified samples. In conclusion, C-PK11195 metabolization has the same rate in patients with MS and healthy controls, which is not affected by sex, age, treatment, and disease phenotype. Thus, these findings could contribute to exempting the necessity for tracer metabolization determination in all C-PK11195 PET imaging acquisition, by using a population metabolization rate average. The study procedures were approved by the Ethics Committee for Research Projects Analysis of the Hospital das Clinicas of the University of Sao Paulo Medical School (approval No. 624.065) on April 23, 2014.
C-PK11195是一种正电子发射体示踪剂,用于在神经炎症性疾病研究中对先天性免疫细胞激活进行正电子发射断层扫描(PET)成像。对于图像定量分析,有必要在成像采集期间对动脉血浆中该示踪剂的完整部分进行定量(血浆完整部分)。由于该分析涉及的复杂性和成本,评估每次C-PK11195 PET成像采集中个体分析的实际必要性很重要。本研究的目的是比较健康对照者和多发性硬化症(MS)患者之间C-PK11195血浆代谢率,并评估性别、年龄、治疗和疾病表型对动脉血浆样本中测量的示踪剂完整部分的干扰。在注射C-PK11195后20、45和60分钟,通过高效液相色谱法对MS患者(n = 50)和健康对照者(n = 23)的样本中动脉血浆中的C-PK11195代谢率进行定量。分析也按性别、年龄、治疗类型和MS表型进行分层。结果显示,健康对照者和MS患者的代谢率或分层样本之间没有显著差异。总之,MS患者和健康对照者的C-PK11195代谢率相同,不受性别、年龄、治疗和疾病表型的影响。因此,这些发现有助于通过使用总体代谢率平均值,免除在所有C-PK11195 PET成像采集中测定示踪剂代谢的必要性。该研究程序于2014年4月23日获得圣保罗大学医学院临床医院研究项目分析伦理委员会的批准(批准号624.065)。