Eidsvaag Vigdis Andersen, Hansson Hans-Arne, Heuser Kjell, Nagelhus Erlend A, Eide Per K
Department of Neurosurgery, Oslo University Hospital - Rikshospitalet, Oslo, Norway; Faculty of Medicine; and Division of Physiology, Department of Molecular Medicine, GliaLab and Letten Centre, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway; Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden; and Department of Neurology, Oslo University Hospital - Rikshospitalet, Oslo, Norway.
J Neuropathol Exp Neurol. 2017 Dec 1;76(12):1034-1045. doi: 10.1093/jnen/nlx091.
Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal cortex biopsies from iNPH patients and related the observations to overnight intracranial pressure (ICP) scores. A biopsy (0.9×10 mm) was taken from where the ICP sensor subsequently was inserted. Brain capillaries were investigated by electron microscopy of biopsies from 27 iNPH patients and 10 reference subjects, i.e. patients (not healthy individuals) without cerebrospinal fluid circulation disturbances, in whom normal brain tissue was removed as part of necessary neurosurgical treatment. Degenerating and degenerated pericyte processes were identified in 23/27 (85%) iNPH and 6/10 (60%) of reference specimens. Extensive disintegration of pericyte processes were recognized in 11/27 (41%) iNPH and 1/10 (10%) reference specimens. There were no differences in basement membrane (BM) thickness or pericyte coverage between iNPH and reference subjects. The pulsatile or static ICP scores did neither correlate with the BM thickness nor with pericyte coverage. We found increased prevalence of degenerating pericytes in iNPH while the BM thickness and pericyte coverage did not differ from the reference individuals. Observations in iNPH may to some extent be age-related since the iNPH patients were significantly older than the reference individuals.
特发性正常压力脑积水(iNPH)是一种病因不明的神经退行性疾病。我们研究了iNPH患者额叶皮质活检组织中毛细血管的形态,并将观察结果与夜间颅内压(ICP)评分相关联。从随后插入ICP传感器的部位取一块活检组织(0.9×10毫米)。通过电子显微镜对27例iNPH患者和10例对照受试者(即无脑脊液循环障碍的患者,而非健康个体,其正常脑组织作为必要神经外科治疗的一部分被切除)的活检组织进行脑毛细血管研究。在23/27(85%)的iNPH患者和6/10(60%)的对照标本中发现了周细胞退化和已退化的过程。在11/27(41%)的iNPH患者和1/10(10%)的对照标本中发现了周细胞过程的广泛解体。iNPH患者和对照受试者之间的基底膜(BM)厚度或周细胞覆盖率没有差异。搏动性或静态ICP评分与BM厚度或周细胞覆盖率均无相关性。我们发现iNPH患者中退化周细胞的患病率增加,而BM厚度和周细胞覆盖率与对照个体无差异。由于iNPH患者的年龄明显大于对照个体,因此iNPH中的观察结果在一定程度上可能与年龄有关。