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持续性谵妄与神经元损伤的脑脊液标志物有关。

Persistent delirium is associated with cerebrospinal fluid markers of neuronal injury.

作者信息

Tsui Alex, Johnstone Benjamin, Heslegrave Amanda, Zetterberg Henrik, Watne Leiv Otto, Neerland Bjørn Erik, Krogseth Maria, Cunningham Colm, MacLullich Alasdair, Muniz Terrera Graciela, Davis Daniel, Caplan Gideon

机构信息

Department of Population Science and Experimental Medicine, MRC Unit for Lifelong Health and Ageing at University College London (UCL), 1-19 Torrington Place, London WC1E 7HB, UK.

St Pancras Rehabilitation Unit, Central and North West London NHS Foundation Trust, London NW1 0PE, UK.

出版信息

Brain Commun. 2024 Sep 18;6(5):fcae319. doi: 10.1093/braincomms/fcae319. eCollection 2024.

Abstract

Delirium is associated with the risk of future long-term cognitive impairment, but the degree to which markers of neuronal injury may be distinct or shared with dementia has yet to be comprehensively described. We investigated CSF biomarkers of dementia, astrocytosis and neuronal damage in a clinical cohort with persistent delirium, comparing them with an outpatient memory clinic sample. Our aim was to determine if different patterns of biomarker changes could implicate specific mechanisms for delirium-related neuronal injury over and above that attributable to comorbid dementia. We recruited 35 participants from the Prince of Wales Hospital, Sydney, Australia. We included inpatients with delirium persisting for at least 5 days ( = 15, 10 with underlying dementia) and participants from outpatient memory clinics ( = 20, 17 with dementia). CSF assays were as follows: amyloid-β, amyloid-β, phosphorylated tau181, neurofilament light chain and glial fibrillary acidic protein. We used propensity score matching to estimate effect sizes for each standardized CSF biomarker separately for persistent delirium (irrespective of underlying dementia) and dementia (irrespective of superimposed delirium). Compared with individuals without delirium, persistent delirium was associated with elevated glial fibrillary acidic protein (normalized coefficient per transformed standard deviation, = 0.85; 95% confidence interval: 0.03-1.68) and neurofilament light chain ( = 1.1; 95% confidence interval: 0.5-1.6), but not phosphorylated tau181. Compared with individuals without dementia, glial fibrillary acidic protein, neurofilament light chain and phosphorylated tau181 were all increased to expected levels in dementia cases, with the former two biomarkers at levels comparable to those seen in persistent delirium [glial fibrillary acidic protein ( = 1.54; 95% confidence interval: 1.05-2.0) and neurofilament light chain ( = 0.65; 95% confidence interval: 0.24-1.1)]. Persistent delirium was linked with changes in CSF biomarkers not necessarily attributable to dementia. These findings support the potential that delirium is associated with direct neuronal injury independent of dementia pathophysiology. Whether this neuronal injury involves astrocyte dysfunction or direct axonal damage are both possibilities. Future work examining acute brain injury in delirium is needed.

摘要

谵妄与未来长期认知障碍的风险相关,但神经元损伤标志物与痴呆症可能不同或共享的程度尚未得到全面描述。我们调查了一组持续性谵妄临床队列中的痴呆症、星形细胞增多和神经元损伤的脑脊液生物标志物,并将其与门诊记忆诊所样本进行比较。我们的目的是确定生物标志物变化的不同模式是否能暗示除合并痴呆症之外的与谵妄相关的神经元损伤的特定机制。我们从澳大利亚悉尼威尔士亲王医院招募了35名参与者。我们纳入了谵妄持续至少5天的住院患者(n = 15,其中10人患有潜在痴呆症)和门诊记忆诊所的参与者(n = 20,其中17人患有痴呆症)。脑脊液检测项目如下:淀粉样蛋白-β、淀粉样蛋白-β、磷酸化tau181、神经丝轻链和胶质纤维酸性蛋白。我们使用倾向得分匹配法分别估计持续性谵妄(无论是否存在潜在痴呆症)和痴呆症(无论是否叠加谵妄)中每种标准化脑脊液生物标志物的效应大小。与无谵妄的个体相比,持续性谵妄与胶质纤维酸性蛋白升高(每转换标准差的标准化系数,β = 0.85;95%置信区间:0.03 - 1.68)和神经丝轻链升高(β = 1.1;95%置信区间:0.5 - 1.6)相关,但与磷酸化tau181无关。与无痴呆症的个体相比,痴呆症患者的胶质纤维酸性蛋白、神经丝轻链和磷酸化tau181均升高至预期水平,前两种生物标志物的水平与持续性谵妄中的水平相当[胶质纤维酸性蛋白(β = 1.54;95%置信区间:1.05 - 2.0)和神经丝轻链(β = 0.65;95%置信区间:0.24 - 1.1)]。持续性谵妄与脑脊液生物标志物的变化有关,这些变化不一定归因于痴呆症。这些发现支持了谵妄可能与独立于痴呆症病理生理学的直接神经元损伤相关的可能性。这种神经元损伤是涉及星形胶质细胞功能障碍还是直接轴突损伤都有可能。未来需要开展研究来检查谵妄中的急性脑损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7708/11443447/27ba80a264ee/fcae319_ga.jpg

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