Tedeschi E, Hasselbalch S G, Waldemar G, Juhler M, Høgh P, Holm S, Garde L, Knudsen L L, Klinken L, Gjerris F
Department of Neurology, National University Hospital, Rigshospitalet, Copenhagen, Denmark.
J Neurol Neurosurg Psychiatry. 1995 Dec;59(6):608-15. doi: 10.1136/jnnp.59.6.608.
The regional cerebral metabolic rate for glucose (rCMRglu) has never been investigated in large consecutive groups of patients with normal pressure hydrocephalus (NPH), a potentially treatable form of dementia with an unpredictable outcome after shunt surgery. Using PET and 18F-2-fluorodeoxyglucose, rCMRglu was studied in 18 patients who fulfilled hydrodynamic criteria for NPH and in whom a biopsy of the frontal cortex was obtained. When compared with an age matched group of 11 healthy subjects, the patients with NPH showed a significant rCMRglu reduction in all cortical and subcortical regions of interest. Individual metabolic patterns, however, disclosed a large topographical heterogeneity. Furthermore, histopathological examination identified Alzheimer's disease or cerebrovascular disease in six cases, and no parenchymal disease or non-specific degenerative processes in the remaining 12. After separating the patients according to the histological diagnosis, the rCMRglu patterns were still heterogeneous, the abnormalities ranging from focal to diffuse in both subgroups. After shunt operation, 11 patients did not improve or worsened clinically. Six patients improved; of those, two had Alzheimer changes and two cerebrovascular changes in their biopsy. The metabolic pattern of these six patients did not differ from the rest of the NPH group. The results indicate that the NPH syndrome may be non-specifically associated with different degenerative disorders. The metabolic heterogeneity, together with the heterogeneous histopathological findings, indicate the necessity of reevaluating the pathogenesis of the NPH syndrome, and may account for the high variability in the success rate of shunt surgery series.
对于正常压力脑积水(NPH)这一潜在可治疗的痴呆形式,其分流手术后结局不可预测,此前从未对大量连续的NPH患者群体进行过局部脑葡萄糖代谢率(rCMRglu)研究。利用正电子发射断层扫描(PET)和18F - 2 - 氟脱氧葡萄糖,对18例符合NPH流体动力学标准且获取了额叶皮质活检样本的患者进行了rCMRglu研究。与11名年龄匹配的健康受试者组成的对照组相比,NPH患者在所有感兴趣的皮质和皮质下区域均出现显著的rCMRglu降低。然而,个体代谢模式显示出较大的局部异质性。此外,组织病理学检查在6例中发现了阿尔茨海默病或脑血管疾病,其余12例未发现实质性疾病或非特异性退行性病变。根据组织学诊断对患者进行分组后,rCMRglu模式仍然存在异质性,两个亚组的异常范围从局灶性到弥漫性。分流手术后,11例患者临床症状未改善或恶化。6例患者症状改善;其中,2例活检显示有阿尔茨海默病改变,2例有脑血管改变。这6例患者的代谢模式与其他NPH患者组并无差异。结果表明,NPH综合征可能与不同的退行性疾病非特异性相关。代谢异质性以及组织病理学结果的异质性表明,有必要重新评估NPH综合征的发病机制,这可能是分流手术系列成功率差异较大的原因。