Brisson Mélanie, Brodeur Catherine, Létourneau-Guillon Laurent, Masellis Mario, Stoessl Jon, Tamm Alex, Zukotynski Katherine, Ismail Zahinoor, Gauthier Serge, Rosa-Neto Pedro, Soucy Jean-Paul
Centre hospitalier de l'université de Québec Quebec City Canada.
Institut universiatire de gériatrie de Montréal Montreal Canada.
Alzheimers Dement (N Y). 2021 Jan 22;6(1):e12098. doi: 10.1002/trc2.12098. eCollection 2020.
Since 1989, four Canadian Consensus Conferences on the Diagnosis and Treatment of Dementia (CCCDTDs) have provided evidence-based dementia diagnostic and treatment guidelines for Canadian clinicians and researchers. We present the results from the Neuroimaging and Fluid Biomarkers Group of the 5th CCCDTD (CCCDTD5), which addressed topics chosen by the steering committee to reflect advances in the field and build on our previous guidelines. Recommendations on Imaging and Fluid Biomarker Use from this Conference cover a series of different fields. Prior structural imaging recommendations for both computerized tomography (CT) and magnetic resonance imaging (MRI) remain largely unchanged, but MRI is now more central to the evaluation than before, with suggested sequences described here. The use of visual rating scales for both atrophy and white matter anomalies is now included in our recommendations. Molecular imaging with [F]-fluorodeoxyglucose ([18F]-FDG) Positron Emisson Tomography (PET) or [Tc]-hexamethylpropyleneamine oxime/ethylene cysteinate dimer ([Tc]-HMPAO/ECD) Single Photon Emission Tomography (SPECT), should now decidedly favor PET. The value of [F]-FDG PET in the assessment of neurodegenerative conditions has been established with greater certainty since the previous conference, and it has now been recognized as a useful biomarker to establish the presence of neurodegeneration by a number of professional organizations around the world. Furthermore, the role of amyloid PET has been clarified and our recommendations follow those from other groups in multiple countries. SPECT with [I]-ioflupane (DaTscan) is now included as a useful study in differentiating Alzheimer's disease (AD) from Lewy body disease. Finally, liquid biomarkers are in a rapid phase of development and, could lead to a revolution in the assessment AD and other neurodegenerative conditions at a reasonable cost. We hope these guidelines will be useful for clinicians, researchers, policy makers, and the lay public, to inform a current and evidence-based approach to the use of neuroimaging and liquid biomarkers in clinical dementia evaluation and management.
自1989年以来,四届加拿大痴呆症诊断与治疗共识会议(CCCDTDs)为加拿大临床医生和研究人员提供了基于证据的痴呆症诊断和治疗指南。我们展示了第五届CCCDTD(CCCDTD5)神经影像学和液体生物标志物小组的结果,该小组讨论了指导委员会选定的主题,以反映该领域的进展并基于我们之前的指南。本次会议关于影像学和液体生物标志物使用的建议涵盖了一系列不同领域。之前关于计算机断层扫描(CT)和磁共振成像(MRI)的结构成像建议基本保持不变,但现在MRI在评估中比以前更为核心,此处描述了建议的序列。我们的建议现在包括使用视觉评定量表评估萎缩和白质异常。使用[F]-氟脱氧葡萄糖([18F]-FDG)正电子发射断层扫描(PET)或[锝]-六甲基丙烯胺肟/半胱氨酸二聚体([Tc]-HMPAO/ECD)单光子发射断层扫描(SPECT)进行分子成像,现在应明确倾向于PET。自上次会议以来,[F]-FDG PET在神经退行性疾病评估中的价值已得到更确切的证实,现在它已被全球多个专业组织认可为一种有用的生物标志物,用于确定神经退行性变的存在。此外,淀粉样蛋白PET的作用已得到明确,我们的建议遵循多个国家其他小组的建议。使用[碘]-碘氟潘(DaTscan)进行SPECT现在被纳入一项有用的研究,用于区分阿尔茨海默病(AD)和路易体病。最后,液体生物标志物正处于快速发展阶段,可能会以合理的成本给AD和其他神经退行性疾病的评估带来变革。我们希望这些指南对临床医生、研究人员、政策制定者和普通公众有用,为临床痴呆症评估和管理中使用神经影像学和液体生物标志物提供一种当前的、基于证据的方法。