Department of Neuroscience (DINOGMI), University of Genoa, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Mov Disord. 2022 Jan;37(1):52-61. doi: 10.1002/mds.28785. Epub 2021 Sep 17.
Dopamine transporter single photon-emission computed tomography (DAT-SPECT) is the strongest risk factor for phenoconversion in patients with idiopathic rapid eye movement (REM)-sleep behavior disorder (iRBD). However, it might be used as a second-line stratification tool in clinical trials, because it is expensive and mini-invasive.
Aim of the study is to investigate whether other cost-effective and non-invasive biomarkers may be proposed as first-line stratification tools.
Forty-seven consecutive iRBD patients (68.53 ± 7.16 years, 40 males) underwent baseline clinical and neuropsychological assessment, olfaction test, resting electroencephalogram (EEG), and DAT-SPECT. All patients underwent 6 month-based clinical follow-up to investigate the emergence of parkinsonism and/or dementia. Survival analysis and Cox regression were used to estimate conversion risk.
Seventeen patients developed an overt synucleinopathy (eight Parkinsonism and nine dementia) 32.8 ± 22 months after diagnosis. The strongest risk factors were putamen specific to non-displaceable binding ratio (SBR) (hazard ratio [HR], 7.3), attention/working memory cognitive function (NPS-AT/WM) (HR, 5.9), EEG occipital mean frequency (HR, 2.7) and clinical motor assessment (HR, 2.3). On multivariate Cox-regression analysis, only putamen SBR and NPS-AT/WM significantly contributed to the model (HR, 6.2, 95% confidence interval [CI], 1.9-19.8). At post-hoc analysis, the trail-making test B (TMT-B) was the single most efficient first-line stratification tool that allowed to reduce the number of eligible subjects to 76.6% (sensitivity 1, specificity 0.37). Combining TMT-B and DAT-SPECT further reduced the sample to 66% (sensitivity 0.88, specificity 0.47).
The TMT-B seems to be a cost-effective and efficient first-line screening tool, to be used to select patients that deserve DAT-SPECT as second-line screening tool for disease-modifying clinical trials. © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
多巴胺转运体单光子发射计算机断层扫描(DAT-SPECT)是特发性快速眼动睡眠行为障碍(iRBD)患者出现表型转化的最强风险因素。然而,由于其昂贵且微创,它可能被用作临床试验中的二线分层工具。
本研究旨在探讨是否可以提出其他具有成本效益且非侵入性的生物标志物作为一线分层工具。
47 例连续的 iRBD 患者(68.53±7.16 岁,40 名男性)接受基线临床和神经心理学评估、嗅觉测试、静息脑电图(EEG)和 DAT-SPECT。所有患者均接受 6 个月的临床随访,以调查帕金森病和/或痴呆的发生情况。生存分析和 Cox 回归用于估计转化风险。
17 例患者在诊断后 32.8±22 个月出现显性神经突触核病(8 例帕金森病和 9 例痴呆)。最强的风险因素是纹状体特定的不可置换结合率(SBR)(危险比[HR],7.3)、注意力/工作记忆认知功能(NPS-AT/WM)(HR,5.9)、脑电图枕部平均频率(HR,2.7)和临床运动评估(HR,2.3)。在多变量 Cox 回归分析中,只有纹状体 SBR 和 NPS-AT/WM 对模型有显著贡献(HR,6.2,95%置信区间[CI],1.9-19.8)。在事后分析中,连线测试 B(TMT-B)是唯一最有效的一线分层工具,可将合格受试者的数量减少到 76.6%(敏感性 1,特异性 0.37)。将 TMT-B 和 DAT-SPECT 结合使用可进一步将样本减少至 66%(敏感性 0.88,特异性 0.47)。
TMT-B 似乎是一种具有成本效益且高效的一线筛查工具,可用于选择需要 DAT-SPECT 作为疾病修饰临床试验二线筛查工具的患者。