New York State Institute for Basic Research in Developmental Disabilities, Staten Island, New York, NY 10314-6399, USA.
J Alzheimers Dis. 2011;25(3):505-15. doi: 10.3233/JAD-2011-101959.
The role of blood-cerebrospinal fluid barrier (BCB) dysfunction in Alzheimer's disease (AD) has been addressed but not yet established. We evaluated the BCB integrity in 179 samples of cerebrospinal fluid (CSF) retrospectively collected from AD patients and control cases using both CSF/serum albumin ratio (QAlb) and CSF secretory Ca2+-dependent phospholipase A2 (sPLA2) activity. These analyses were supplemented with the measurement of total tau, amyloid-β1-42 (Aβ1-42), and ubiquitin CSF levels. We found that due to its higher sensitivity, CSF sPLA2 activity could 1) discriminate AD from healthy controls and 2) showed BCB impairment in neurological control cases while QAlb could not. Moreover, the CSF sPLA2 activity measurement showed that around half of the AD patients were characterized by a BCB impairment. The BCB dysfunction observed in AD was independent from Mini-Mental State Examination score as well as CSF levels of total tau, Aβ1-42, and ubiquitin. Finally, the BCB dysfunction was not limited to any of the CSF biomarkers-based previously identified subgroups of AD. These results suggest that the BCB damage occurs independent of and probably precedes both Aβ and tau pathologies in a restricted subgroup of AD patients.
血脑屏障(BCB)功能障碍在阿尔茨海默病(AD)中的作用已经得到了研究,但尚未确定。我们使用脑脊液/血清白蛋白比值(QAlb)和脑脊液分泌钙依赖性磷脂酶 A2(sPLA2)活性,对 179 例 AD 患者和对照病例的脑脊液(CSF)样本进行了回顾性评估,以评估 BCB 的完整性。这些分析补充了总 tau、淀粉样蛋白-β1-42(Aβ1-42)和泛素 CSF 水平的测量。我们发现,由于其更高的灵敏度,CSF sPLA2 活性可以 1)将 AD 与健康对照区分开来,2)在神经科对照病例中显示 BCB 损伤,而 QAlb 则不能。此外,CSF sPLA2 活性测量表明,大约一半的 AD 患者存在 BCB 损伤。AD 中观察到的 BCB 功能障碍与 Mini-Mental State Examination 评分以及 CSF 中总 tau、Aβ1-42 和泛素的水平无关。最后,BCB 功能障碍不仅限于以前基于 CSF 生物标志物确定的 AD 亚组。这些结果表明,在 AD 的一个受限亚组中,BCB 损伤独立于 Aβ和 tau 病理学发生,并且可能早于它们发生。