Teitsdottir Unnur D, Darreh-Shori Taher, Lund Sigrun H, Jonsdottir Maria K, Snaedal Jon, Petersen Petur H
Faculty of Medicine, Department of Anatomy, Biomedical Center, University of Iceland, Reykjavik, Iceland.
Division of Clinical Geriatrics, Department of Neurobiology, Care Sciences and Society, Center for Alzheimer Research, Karolinska Institutet, Campus Flemingsberg, Stockholm, Sweden.
Front Aging Neurosci. 2022 May 26;14:876019. doi: 10.3389/fnagi.2022.876019. eCollection 2022.
Cholinergic drugs are the most commonly used drugs for the treatment of Alzheimer's disease (AD). Therefore, a better understanding of the cholinergic system and its relation to both AD-related biomarkers and cognitive functions is of high importance.
To evaluate the relationships of cerebrospinal fluid (CSF) cholinergic enzymes with markers of amyloidosis, neurodegeneration, neurofibrillary tangles, inflammation and performance on verbal episodic memory in a memory clinic cohort.
In this cross-sectional study, 46 cholinergic drug-free subjects (median age = 71, 54% female, median MMSE = 28) were recruited from an Icelandic memory clinic cohort targeting early stages of cognitive impairment. Enzyme activity of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) was measured in CSF as well as levels of amyloid-β (Aβ), phosphorylated tau (P-tau), total-tau (T-tau), neurofilament light (NFL), YKL-40, S100 calcium-binding protein B (S100B), and glial fibrillary acidic protein (GFAP). Verbal episodic memory was assessed with the Rey Auditory Verbal Learning (RAVLT) and Story tests.
No significant relationships were found between CSF Aβ levels and AChE or BuChE activity ( > 0.05). In contrast, T-tau ( = 0.46, = 0.001) and P-tau ( = 0.45, = 0.002) levels correlated significantly with AChE activity. Although neurodegeneration markers T-tau and NFL did correlate with each other ( = 0.59, < 0.001), NFL did not correlate with AChE ( = 0.25, = 0.09) or BuChE ( = 0.27, = 0.06). Inflammation markers S100B and YKL-40 both correlated significantly with AChE (S100B: = 0.43, = 0.003; YKL-40: = 0.32, = 0.03) and BuChE (S100B: = 0.47, < 0.001; YKL-40: = 0.38, = 0.009) activity. A weak correlation was detected between AChE activity and the composite score reflecting verbal episodic memory ( = -0.34, = 0.02). LASSO regression analyses with a stability approach were performed for the selection of a set of measures best predicting cholinergic activity and verbal episodic memory score. S100B was the predictor with the highest model selection frequency for both AChE (68%) and BuChE (73%) activity. Age (91%) was the most reliable predictor for verbal episodic memory, with selection frequency of both cholinergic enzymes below 10%.
Results indicate a relationship between higher activity of the ACh-degrading cholinergic enzymes with increased neurodegeneration, neurofibrillary tangles and inflammation in the stages of pre- and early symptomatic dementia, independent of CSF Aβ levels.
胆碱能药物是治疗阿尔茨海默病(AD)最常用的药物。因此,更好地了解胆碱能系统及其与AD相关生物标志物和认知功能的关系至关重要。
在一个记忆门诊队列中,评估脑脊液(CSF)胆碱能酶与淀粉样变性、神经退行性变、神经原纤维缠结、炎症标志物以及言语情景记忆表现之间的关系。
在这项横断面研究中,从冰岛一个针对认知障碍早期阶段的记忆门诊队列中招募了46名未使用胆碱能药物的受试者(年龄中位数 = 71岁,54%为女性,简易精神状态检查表(MMSE)中位数 = 28)。测量了脑脊液中乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BuChE)的酶活性以及淀粉样β蛋白(Aβ)、磷酸化tau蛋白(P-tau)、总tau蛋白(T-tau)、神经丝轻链(NFL)、YKL-40、S100钙结合蛋白B(S100B)和胶质纤维酸性蛋白(GFAP)的水平。用雷伊听觉词语学习测验(RAVLT)和故事测验评估言语情景记忆。
脑脊液Aβ水平与AChE或BuChE活性之间未发现显著相关性(P > 0.05)。相反,T-tau水平(r = 0.46,P = 0.001)和P-tau水平(r = 0.45,P = 0.002)与AChE活性显著相关。虽然神经退行性变标志物T-tau和NFL相互之间存在相关性(r = 0.59,P < 0.001),但NFL与AChE(r = 0.25,P = 0.09)或BuChE(r = 0.27,P = 0.06)均无相关性。炎症标志物S100B和YKL-40均与AChE(S100B:r = 0.43,P = 0.003;YKL-40:r = 0.32,P = 0.03)和BuChE(S100B:r = 0.47,P < 0.001;YKL-40:r = 0.38,P = 0.009)活性显著相关。检测到AChE活性与反映言语情景记忆的综合评分之间存在弱相关性(r = -0.34,P = 0.02)。采用稳定性方法进行套索回归分析,以选择一组最能预测胆碱能活性和言语情景记忆评分的指标。S100B是预测AChE活性(68%)和BuChE活性(73%)时模型选择频率最高的指标。年龄(91%)是言语情景记忆最可靠的预测指标,两种胆碱能酶的选择频率均低于10%。
结果表明,在症状前和症状早期痴呆阶段,ACh降解胆碱能酶活性升高与神经退行性变增加、神经原纤维缠结和炎症之间存在关联,且与脑脊液Aβ水平无关。