Naganawa Mika, Zheng Ming-Qiang, Gallezot Jean-Dominique, Bonomi Robin, Gu Jiwei, Gao Hong, Jacutin-Porte Swanee, Nabulsi Nabeel B, Koole Michel, Van Laere Koen, Matuskey David, Huang Yiyun, Carson Richard E
Yale PET Center, Yale School of Medicine, PO Box 208408, New Haven, 06520-8048, USA.
Nuclear Medicine and Molecular Imaging, Department of Imaging & Pathology, KU Leuven, Leuven, Belgium.
EJNMMI Res. 2025 Jun 21;15(1):76. doi: 10.1186/s13550-025-01268-w.
Histone deacetylase 6 (HDAC6) is an enzyme pivotal for gene regulation, influencing cellular pathways through protein deacetylation. HDAC6 is a potential therapeutic target in diseases such as cancer and neurodegenerative disorders. Koole et al. investigated brain binding of [F]Bavarostat, an HDAC6 inhibitor, in healthy participants, revealing an absolute test-retest variability (aTRV) of 7.7% (n = 4) for the distribution volume (V) with a 1-day interscan interval. This study aims to evaluate test-retest reproducibility with a more extended interscan interval.
Six participants (3 M/3F) underwent a test-retest scan, each lasting for 120 min using a 4-ring Biograph mCT PET/CT scanner. Arterial blood sampling and metabolite analysis were performed to derive the input function. The two scans were 28 ± 12 days apart (14-43 days, n = 6). Regional time-activity curves (TACs) were generated for 15 regions of interest (ROIs). Kinetic analysis of the 120-min TACs was performed using one-tissue and two-tissue compartment models (1TC, 2TC) and multilinear analysis-1 (MA1) to quantify V values and compute absolute test-retest variability (aTRV). The effects of scan duration (60 to 120 min) and MA1 t* setting on aTRV and bias were investigated. Careful analysis of the plasma HPLC data was needed since metabolites eluted close in time to the parent. The MA1 model (t* = 40 min) adequately described regional TACs and produced stable kinetic parameters with good agreement to 2TC (MA1 V=0.98 × 2TC V + 0.48, bias: -0.1%) while 1TC underestimated V by 5.1%. Regional V values exhibited a relatively uniform pattern, highest in the amygdala and lowest in the centrum semiovale. Individual aTRV values ranged from 2 to 9%. Scan durations between 100 and 120 min provided the most consistent results, with minimal bias and acceptable aTRV across all tested t* values. Although a 90-minute scan with t*=10 or 20-minute balanced scan time and aTRV, optimal parameters varied by brain region. Smaller regions (e.g., amygdala) required longer scans to achieve reliable V quantification.
The test-retest variability of [F]Bavarostat V values demonstrated favorable results for a one-month scan interval, comparable to the reported values.
组蛋白去乙酰化酶6(HDAC6)是一种对基因调控至关重要的酶,通过蛋白质去乙酰化影响细胞途径。HDAC6是癌症和神经退行性疾病等疾病的潜在治疗靶点。库勒等人研究了HDAC6抑制剂[F]巴伐他汀在健康参与者大脑中的结合情况,发现在扫描间隔为1天的情况下,分布容积(V)的绝对重测变异性(aTRV)为7.7%(n = 4)。本研究旨在评估更长扫描间隔下的重测可重复性。
六名参与者(3名男性/3名女性)接受了重测扫描,每次扫描使用4环Biograph mCT PET/CT扫描仪,持续120分钟。进行动脉血采样和代谢物分析以获取输入函数。两次扫描间隔28±12天(14 - 43天,n = 6)。为15个感兴趣区域(ROI)生成了区域时间 - 活度曲线(TAC)。使用单组织和双组织隔室模型(1TC、2TC)以及多线性分析 - 1(MA1)对120分钟的TAC进行动力学分析,以量化V值并计算绝对重测变异性(aTRV)。研究了扫描持续时间(60至120分钟)和MA1 t设置对aTRV和偏差的影响。由于代谢物与母体在时间上洗脱接近,因此需要仔细分析血浆HPLC数据。MA1模型(t = 40分钟)充分描述了区域TAC,并产生了稳定的动力学参数,与2TC具有良好的一致性(MA1 V = 0.98×2TC V + 0.48,偏差: - 0.1%),而1TC低估V达5.1%。区域V值呈现相对均匀的模式,在杏仁核中最高,在半卵圆中心最低。个体aTRV值范围为2%至9%。100至120分钟的扫描持续时间提供了最一致的结果,在所有测试的t值下偏差最小且aTRV可接受。尽管90分钟扫描(t = 10或20分钟平衡扫描时间)以及aTRV的最佳参数因脑区而异。较小的区域(如杏仁核)需要更长的扫描时间来实现可靠的V量化。
[F]巴伐他汀V值的重测变异性在一个月的扫描间隔内显示出良好的结果,与报告值相当。