Rauhala Elina, Johansson Jarkko, Karrasch Mira, Eskola Olli, Tolvanen Tuula, Parkkola Riitta, Virtanen Kirsi A, Rinne Juha O
Clinical Neurosciences, Faculty of Medicine, Turku University Hospital, University of Turku and Neurocenter, Turku, Finland.
Turku PET Centre, Turku University Hospital, Turku, Finland.
EJNMMI Res. 2022 Sep 5;12(1):55. doi: 10.1186/s13550-022-00928-5.
Our aim was to investigate the discriminative value of F-Flutemetamol PET in longitudinal assessment of amyloid beta accumulation in amnestic mild cognitive impairment (aMCI) patients, in relation to longitudinal cognitive changes.
We investigated the change in F-Flutemetamol uptake and cognitive impairment in aMCI patients over time up to 3 years which enabled us to investigate possible association between changes in brain amyloid load and cognition over time. Thirty-four patients with aMCI (mean age 73.4 years, SD 6.6) were examined with F-Flutemetamol PET scan, brain MRI and cognitive tests at baseline and after 3-year follow-up or earlier if the patient had converted to Alzheimer´s disease (AD). F-Flutemetamol data were analyzed both with automated region-of-interest analysis and voxel-based statistical parametric mapping.
F-flutemetamol uptake increased during the follow-up, and the increase was significantly higher in patients who were amyloid positive at baseline as compared to the amyloid-negative ones. At follow-up, there was a significant association between F-Flutemetamol uptake and MMSE, logical memory I (immediate recall), logical memory II (delayed recall) and verbal fluency. An association was seen between the increase in F-Flutemetamol uptake and decline in MMSE and logical memory I scores.
In the early phase of aMCI, presence of amyloid pathology at baseline strongly predicted amyloid accumulation during follow-up, which was further paralleled by cognitive declines. Inversely, some of our patients remained amyloid negative also at the end of the study without significant change in F-Flutemetamol uptake or cognition. Future studies with longer follow-up are needed to distinguish whether the underlying pathophysiology of aMCI in such patients is other than AD.
我们的目的是研究¹⁸F-氟替莫尔正电子发射断层扫描(PET)在纵向评估遗忘型轻度认知障碍(aMCI)患者淀粉样蛋白β积累方面的鉴别价值,并探讨其与纵向认知变化的关系。
我们对aMCI患者进行了长达3年的¹⁸F-氟替莫尔摄取变化和认知障碍情况的研究,这使我们能够探究脑淀粉样蛋白负荷变化与认知随时间变化之间的可能关联。34例aMCI患者(平均年龄73.4岁,标准差6.6)在基线时以及3年随访后或如果患者已转化为阿尔茨海默病(AD)则提前进行¹⁸F-氟替莫尔PET扫描、脑磁共振成像(MRI)和认知测试。¹⁸F-氟替莫尔数据采用自动感兴趣区分析和基于体素的统计参数映射两种方法进行分析。
随访期间¹⁸F-氟替莫尔摄取增加,与淀粉样蛋白阴性患者相比,基线时淀粉样蛋白阳性患者的增加更为显著。随访时,¹⁸F-氟替莫尔摄取与简易精神状态检查表(MMSE)、逻辑记忆I(即刻回忆)、逻辑记忆II(延迟回忆)和语言流畅性之间存在显著关联。¹⁸F-氟替莫尔摄取增加与MMSE和逻辑记忆I评分下降之间存在关联。
在aMCI的早期阶段,基线时淀粉样蛋白病理的存在强烈预测随访期间的淀粉样蛋白积累,这进一步与认知下降平行。相反,我们的一些患者在研究结束时仍为淀粉样蛋白阴性,¹⁸F-氟替莫尔摄取或认知无显著变化。需要进行更长时间随访的未来研究,以区分此类患者中aMCI的潜在病理生理学是否不同于AD。