Institute of Neuroscience, Université Catholique de Louvain, Brussels, Belgium.
Neurology Department, Saint-Luc University Hospital, Av. Hippocrate, 10, 1200, Brussels, Belgium.
Eur J Nucl Med Mol Imaging. 2021 Jan;48(1):302-310. doi: 10.1007/s00259-020-04942-4. Epub 2020 Jun 29.
To evaluate cerebral amyloid-β(Aβ) pathology in older adults with cognitive complaints, visual assessment of PET images is approved as the routine method for image interpretation. In research studies however, Aβ-PET semi-quantitative measures are associated with greater risk of progression to dementia; but until recently, these measures lacked standardization. Therefore, the Centiloid scale, providing standardized Aβ-PET semi-quantitation, was recently validated. We aimed to determine the predictive values of visual assessments and Centiloids in non-demented patients, using long-term progression to dementia as our standard of truth.
One hundred sixty non-demented participants (age, 54-86) were enrolled in a monocentric [F] flutemetamol Aβ-PET study. Flutemetamol images were interpreted visually following the manufacturers recommendations. SUVr values were converted to the Centiloid scale using the GAAIN guidelines. Ninety-eight persons were followed until dementia diagnosis or were clinically stable for a median of 6 years (min = 4.0; max = 8.0). Twenty-five patients with short follow-up (median = 2.0 years; min = 0.8; max = 3.9) and 37 patients with no follow-up were excluded. We computed ROC curves predicting subsequent dementia using baseline PET data and calculated negative (NPV) and positive (PPV) predictive values.
In the 98 participants with long follow-up, Centiloid = 26 provided the highest overall predictive value = 87% (NPV = 85%, PPV = 88%). Visual assessment corresponded to Centiloid = 40, which predicted dementia with an overall predictive value = 86% (NPV = 81%, PPV = 92%). Inclusion of the 25 patients who only had a 2-year follow-up decreased the PPV = 67% (NPV = 88%), reflecting the many positive cases that did not progress to dementia after short follow-ups.
A Centiloid threshold = 26 optimally predicts progression to dementia 6 years after PET. Visual assessment provides similar predictive value, with higher specificity and lower sensitivity.
Eudra-CT number: 2011-001756-12.
评估有认知主诉的老年患者大脑淀粉样蛋白-β(Aβ)病理学。目前,视觉评估 PET 图像已被批准为图像解释的常规方法。然而,在研究中,Aβ-PET 半定量测量与向痴呆进展的风险增加相关;但直到最近,这些测量方法还缺乏标准化。因此,最近验证了 Centiloid 量表,该量表提供了标准化的 Aβ-PET 半定量测量。我们的目的是确定视觉评估和 Centiloids 在非痴呆患者中的预测值,以长期进展为痴呆作为我们的标准。
160 名非痴呆参与者(年龄 54-86 岁)被纳入单中心[F] flutemetamol Aβ-PET 研究。根据制造商的建议,对 flutemetamol 图像进行视觉评估。使用 GAAIN 指南将 SUVr 值转换为 Centiloid 量表。98 人随访至痴呆诊断或临床稳定中位时间为 6 年(min = 4.0;max = 8.0)。排除 25 名随访时间短(中位时间 = 2.0 年;min = 0.8;max = 3.9)和 37 名无随访的患者。我们计算了使用基线 PET 数据预测随后痴呆的 ROC 曲线,并计算了阴性(NPV)和阳性(PPV)预测值。
在 98 名有长期随访的参与者中,Centiloid = 26 提供了最高的整体预测值 = 87%(NPV = 85%,PPV = 88%)。视觉评估与 Centiloid = 40 相对应,预测痴呆的整体预测值 = 86%(NPV = 81%,PPV = 92%)。纳入仅随访 2 年的 25 名患者降低了 PPV = 67%(NPV = 88%),这反映了许多阳性病例在短期随访后并未进展为痴呆。
Centiloid 阈值 = 26 可最佳预测 PET 后 6 年向痴呆的进展。视觉评估提供了类似的预测值,具有更高的特异性和更低的敏感性。
Eudra-CT 编号:2011-001756-12。