Department of Neurology, Post Graduate Institute of Medical Education and Research, Chandigarh 160012, India.
Department of Neurosurgery, Post Graduate Institute of Medical Education and Research, Chandigarh 160012, India.
Asian J Psychiatr. 2017 Oct;29:59-62. doi: 10.1016/j.ajp.2017.04.015. Epub 2017 Apr 22.
A reliable plasma biomarker in differentiating between Alzheimer's disease (AD) and Vascular dementia (VaD) is the need of the hour, in most memory clinics. Even though there is no disease modifying treatment, it is important to know the type of dementia for both symptomatic treatment and prognostication.
Neuropsychological assessment, MRI brain, FDG-PET brain and CSF biomarkers of AD (Aβ42 and total tau) were used for establishing the diagnosis of Mild Cognitive Impairment (MCI), AD or VaD.
68 diagnosed patients of AD/MCI/VaD were included. FDG PET brain, plasma fibrinogen, d dimer, IL6 and CRP were done in all 68 patients while 48 patients underwent CSF biomarker analysis. Sixteen patients had MCI, of which 11 were MCI-AD and 5 were MCI-VaSC. There were 41 patients with AD (Mild AD-9, Mod AD-23, Severe AD-9) and 11 patients with VaD. Alzheimer group (MCI-AD and AD) and Vascular group (MCI VaSC & VaD) consisted of 52 and 16 patients respectively. Alzheimer and Vascular groups did not exhibit significant difference in IL6 and CRP levels. Plasma fibrinogen levels were significantly higher in VaD and vascular group as compared to Alzheimer group. But MCI-VaSC was not significantly different from MCI-AD. Plasma d dimer levels were significantly higher in all vascular subgroups compared to Alzheimer subgroups except between MCI-VaSC and MCI-AD.
Hemostatic biomarkers were higher in Vascular group compared to Alzheimer group whereas there was no difference in inflammatory biomarkers. But the sensitivity and specificity of fibrinogen and d-dimer were not high enough for routine clinical use. Further studies in a larger sample are required to confirm these results.
在大多数记忆诊所,区分阿尔茨海默病(AD)和血管性痴呆(VaD)的可靠血浆生物标志物是当务之急。即使没有疾病修饰治疗,了解痴呆症的类型对于症状治疗和预后也很重要。
使用神经心理学评估、MRI 脑、FDG-PET 脑和 AD 的 CSF 生物标志物(Aβ42 和总tau)来确定轻度认知障碍(MCI)、AD 或 VaD 的诊断。
纳入了 68 例确诊的 AD/MCI/VaD 患者。所有 68 例患者均进行了 FDG PET 脑、血浆纤维蛋白原、D 二聚体、IL6 和 CRP 检查,48 例患者进行了 CSF 生物标志物分析。16 例患者患有 MCI,其中 11 例为 MCI-AD,5 例为 MCI-VaSC。41 例患者患有 AD(轻度 AD-9 例,中度 AD-23 例,重度 AD-9 例),11 例患者患有 VaD。阿尔茨海默病组(MCI-AD 和 AD)和血管组(MCI VaSC 和 VaD)分别由 52 例和 16 例患者组成。阿尔茨海默病组和血管组在 IL6 和 CRP 水平上没有显著差异。与阿尔茨海默病组相比,VaD 和血管组的血浆纤维蛋白原水平显著升高。但 MCI-VaSC 与 MCI-AD 无显著差异。与阿尔茨海默病亚组相比,所有血管亚组的血浆 D 二聚体水平均显著升高,除 MCI-VaSC 与 MCI-AD 之间外。
与阿尔茨海默病组相比,血管组的止血生物标志物较高,而炎症生物标志物没有差异。但是纤维蛋白原和 D-二聚体的敏感性和特异性不足以用于常规临床使用。需要进一步在更大的样本中进行研究以证实这些结果。