Davidsson P, Blennow K, Andreasen N, Eriksson B, Minthon L, Hesse C
Department of Clinical Neuroscience, Experimental Neuroscience section, Göteborg University, Sahlgrenska University Hospital, S-431 80, Mölndal, Sweden.
Neurosci Lett. 2001 Mar 16;300(3):157-60. doi: 10.1016/s0304-3940(01)01586-5.
The clinical significance and the effects of pharmacological treatment of patients with Alzheimer's disease (AD) were evaluated by measurement of acetylcholinesterase (AChE) in the cerebrospinal fluid (CSF). CSF-AChE of AD patients was lower, not significantly, compared with controls. However, CSF-AChE was significantly increased after treatment of AD patients with AChE inhibitors (donepezil and galantamine). The increase was higher in patients treated with donezepil than in those treated with galantamine, which might be related to different mechanisms for the substances. The increase was also dose-dependent, and was especially marked in patients showing a clinical response. These data suggest that CSF biomarkers are capable not only of identifying a biochemical effect of drugs, but also of differentiating between different compounds in a dose-dependent manner.
通过测量脑脊液(CSF)中的乙酰胆碱酯酶(AChE)来评估阿尔茨海默病(AD)患者的临床意义及药物治疗效果。与对照组相比,AD患者的脑脊液AChE较低,但差异不显著。然而,用AChE抑制剂(多奈哌齐和加兰他敏)治疗AD患者后,脑脊液AChE显著升高。多奈哌齐治疗的患者升高幅度高于加兰他敏治疗的患者,这可能与这些物质的不同作用机制有关。这种升高也是剂量依赖性的,在有临床反应的患者中尤为明显。这些数据表明,脑脊液生物标志物不仅能够识别药物的生化作用,还能够以剂量依赖性方式区分不同的化合物。