Department of Neurosurgery, NeuroCenter, Kuopio University Hospital, Kuopio, Finland.
Neurodegener Dis. 2012;10(1-4):166-9. doi: 10.1159/000335155. Epub 2012 Feb 10.
Normal pressure hydrocephalus (NPH) can be alleviated by cerebrospinal fluid shunting but the differential diagnosis and patient selection are challenging. Intraventricular intracranial pressure monitoring as part of the diagnostic workup as well as shunting enable to obtain cortical brain biopsies to detect amyloid-β (Aβ) and hyperphosphorylated tau (HPτ), the hallmark lesions of Alzheimer's disease (AD). In possible NPH, Aβ alone indicates an increased risk of AD and when present with HPτ probable AD, but the effect of those brain lesions on survival is not known. The aim of this study was to evaluate the predictive value of brain biopsy for the long-term outcome of possible NPH. Between 1991 and 2006, the Neurosurgery Department of the Kuopio University Hospital evaluated 468 patients for possible NPH by intraventricular intracranial pressure monitoring and frontal cortical brain biopsy immunostained against Aβ and HPτ. All patients were followed up until the end of 2008 (n = 201) or death (n = 267) with a median follow-up of 4.6 years (range 0-17). Logistic regression analysis with Cox models was applied. Out of the 468 cases, Aβ was detected in 197 (42%) cortical biopsies, and together with HPτ in 44 (9%). Aβ alone indicated increased risk of AD and with HPτ probable AD, but it did not affect survival. Vascular aetiology was the most frequent cause of death. Cortical biopsy findings indicate that NPH is at present a heterogeneous syndrome and has notable overlapping with AD. Brain biopsy did not predict survival but may open a novel research window to study the pathobiology of neurodegeneration.
正常压力脑积水(NPH)可以通过脑脊液分流来缓解,但鉴别诊断和患者选择具有挑战性。作为诊断工作的一部分,脑室内颅内压监测以及分流术可获取皮质脑活检以检测淀粉样蛋白-β(Aβ)和过度磷酸化 tau(HPτ),这是阿尔茨海默病(AD)的标志性病变。在可能的 NPH 中,Aβ 单独表明 AD 的风险增加,当与 HPτ 同时存在时则可能为 AD,但这些脑病变对生存的影响尚不清楚。本研究旨在评估脑活检对可能的 NPH 长期预后的预测价值。1991 年至 2006 年,库奥皮奥大学医院神经外科通过脑室内颅内压监测和对 Aβ 和 HPτ 进行免疫染色的额皮质脑活检评估了 468 例可能的 NPH 患者。所有患者均随访至 2008 年底(n=201)或死亡(n=267),中位随访时间为 4.6 年(范围 0-17 年)。应用逻辑回归分析和 Cox 模型进行分析。在 468 例病例中,197 例(42%)皮质活检中检测到 Aβ,44 例(9%)同时检测到 Aβ 和 HPτ。Aβ 单独提示 AD 的风险增加,与 HPτ 同时存在则提示可能为 AD,但不影响生存。血管病因是最常见的死亡原因。皮质活检结果表明,目前 NPH 是一种异质性综合征,与 AD 有明显重叠。脑活检不能预测生存,但可能为研究神经退行性变的病理生物学开辟新的研究窗口。