Jongbloed Wesley, Bruggink Kim A, Kester Maartje I, Visser Pieter-Jelle, Scheltens Philip, Blankenstein Marinus A, Verbeek Marcel M, Teunissen Charlotte E, Veerhuis Robert
Department of Clinical Chemistry, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands Alzheimer Center & Department of Neurology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.
Department of Neurology, Department of Laboratory Medicine, Donders Institute for Brain, Cognition and behaviour, Alzheimer Centre Nijmegen, Radboud University Medical Centre, Nijmegen, The Netherlands.
J Alzheimers Dis. 2015;45(1):35-43. doi: 10.3233/JAD-142136.
Amyloid-β (Aβ)-oligomers are neurotoxic isoforms of Aβ and are a potential diagnostic biomarker for Alzheimer's disease (AD).
24 non-demented, 61 mild cognitive impairment (MCI), and 64 AD patients who underwent lumbar puncture and cognitive testing at baseline and follow-up were selected from the memory clinic based Amsterdam Dementia Cohort. CSF samples were analyzed for standard AD-biomarkers and Aβ-oligomer levels using a validated in-house Aβ-oligomer specific enzyme-linked immunosorbent assay. Aβ-oligomer levels were analyzed as indicators of disease progression (follow-up AD diagnosis) and cognitive decline, respectively.
Patient groups did not differ in Aβ-oligomer concentrations at baseline or follow-up. Baseline CSF Aβ-oligomer levels were similar in MCI patients that develop AD as in stable MCI patients. MCI and AD patients showed an annual decrease in Aβ-oligomer levels of 9.4% and 6.8%, respectively. A decrease in Aβ-oligomer levels over time was strongly associated with more severe cognitive decline in AD patients.
Despite the limited diagnostic potential of Aβ-oligomer levels in CSF to differentiate between patient groups, and between MCI-AD and MCI-stable patients, changes in CSF Aβ-oligomer levels were related to cognitive decline. Therefore, CSF Aβ-oligomers may aid in the selection of patients with a more aggressive disease course.
淀粉样β蛋白(Aβ)寡聚体是Aβ的神经毒性异构体,是阿尔茨海默病(AD)潜在的诊断生物标志物。
1)在一个大型临床研究样本中分析脑脊液(CSF)中Aβ寡聚体浓度对AD的诊断及预测疾病进展的潜力。2)在AD的早期和晚期阶段监测Aβ寡聚体浓度随时间的变化。3)研究CSF中Aβ寡聚体水平与认知功能之间的关系。
从基于阿姆斯特丹痴呆队列的记忆门诊中选取24名非痴呆患者、61名轻度认知障碍(MCI)患者和64名AD患者,这些患者在基线和随访时接受了腰椎穿刺和认知测试。使用经过验证的内部Aβ寡聚体特异性酶联免疫吸附测定法分析CSF样本中的标准AD生物标志物和Aβ寡聚体水平。分别将Aβ寡聚体水平作为疾病进展(随访AD诊断)和认知衰退的指标进行分析。
患者组在基线或随访时的Aβ寡聚体浓度无差异。发展为AD的MCI患者与稳定的MCI患者的基线CSF Aβ寡聚体水平相似。MCI和AD患者的Aβ寡聚体水平每年分别下降9.4%和6.8%。随着时间推移,Aβ寡聚体水平的下降与AD患者更严重的认知衰退密切相关。
尽管CSF中Aβ寡聚体水平在区分患者组之间以及MCI-AD和MCI稳定患者之间的诊断潜力有限,但CSF中Aβ寡聚体水平的变化与认知衰退有关。因此,CSF Aβ寡聚体可能有助于选择疾病进程更具侵袭性的患者。