Department of Clinical Neurosciences, Division of Neurology, Geneva University Hospitals and Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Institute of Bioengineering, Center of Neuroprosthetics, École Polytechnique Fédérale De Lausanne (EPFL), Geneva, Switzerland.
Hum Brain Mapp. 2021 Apr 1;42(5):1485-1502. doi: 10.1002/hbm.25308. Epub 2020 Dec 9.
Idiopathic Normal Pressure Hydrocephalus (iNPH)-the leading cause of reversible dementia in aging-is characterized by ventriculomegaly and gait, cognitive and urinary impairments. Despite its high prevalence estimated at 6% among the elderlies, iNPH remains underdiagnosed and undertreated due to the lack of iNPH-specific diagnostic markers and limited understanding of pathophysiological mechanisms. INPH diagnosis is also complicated by the frequent occurrence of comorbidities, the most common one being Alzheimer's disease (AD). Here we investigate the resting-state functional magnetic resonance imaging dynamics of 26 iNPH patients before and after a CSF tap test, and of 48 normal older adults. Alzheimer's pathology was evaluated by CSF biomarkers. We show that the interactions between the default mode, and the executive-control, salience and attention networks are impaired in iNPH, explain gait and executive disturbances in patients, and are not driven by AD-pathology. In particular, AD molecular biomarkers are associated with functional changes distinct from iNPH functional alterations. Finally, we demonstrate a partial normalization of brain dynamics 24 hr after a CSF tap test, indicating functional plasticity mechanisms. We conclude that functional changes involving the default mode cross-network interactions reflect iNPH pathophysiological mechanisms and track treatment response, possibly contributing to iNPH differential diagnosis and better clinical management.
特发性正常压力脑积水(iNPH)是衰老导致可逆转痴呆的主要原因,其特征是脑室扩大以及步态、认知和排尿功能障碍。尽管估计老年人中 iNPH 的患病率高达 6%,但由于缺乏 iNPH 特异性诊断标志物和对病理生理机制的认识有限,iNPH 的诊断仍然不足且治疗不足。iNPH 诊断还因合并症的频繁发生而变得复杂,最常见的合并症是阿尔茨海默病(AD)。在这里,我们研究了 26 名 iNPH 患者在腰椎穿刺试验前后以及 48 名正常老年人的静息态功能磁共振成像动力学。通过脑脊液生物标志物评估阿尔茨海默病病理。我们表明,默认模式与执行控制、突显和注意力网络之间的相互作用在 iNPH 中受损,解释了患者的步态和执行障碍,并且不受 AD 病理的驱动。特别是,AD 分子生物标志物与与 iNPH 功能改变不同的功能变化相关。最后,我们证明腰椎穿刺后 24 小时脑脊液动力学有部分正常化,表明存在功能可塑性机制。我们得出结论,涉及默认模式跨网络相互作用的功能变化反映了 iNPH 的病理生理机制,并可跟踪治疗反应,可能有助于 iNPH 的鉴别诊断和更好的临床管理。