Abstract

BackgroundAbnormalities in cerebrospinal fluid (CSF) production and turnover, seen in normal pressure hydrocephalus (NPH) and in Alzheimer's disease (AD), may be an important cause of amyloid retention in the brain and may relate the two diseases. There is a high incidence of AD pathology in patients being shunted for NPH, the AD-NPH syndrome. We now report elevated CSF pressure (CSFP), consistent with very early hydrocephalus, in a subset of AD patients enrolled in a clinical trial of chronic low-flow CSF drainage. Our objective was to determine the frequency of elevated CSFP in subjects meeting National Institutes of Neurological and Communicative Diseases and Stroke – Alzheimer's Disease and Related Disorders Association (NINCDS-ADRDA) criteria for AD, excluding those with signs of concomitant NPH.MethodsAD subjects by NINCDS-ADRDA criteria (n = 222), were screened by history, neurological examination, and radiographic imaging to exclude those with clinical or radiographic signs of NPH. As part of this exclusion process, opening CSFP was measured supine under general anesthesia during device implantation surgery at a controlled pCO2 of 40 Torr (40 mmHg).ResultsOf the 222 AD subjects 181 had pressure measurements recorded. Seven subjects (3.9%) enrolled in the study had CSFP of 220 mmH20 or greater, mean 249 ± 20 mmH20 which was significantly higher than 103 ± 47 mmH2O for the AD-only group. AD-NPH patients were significantly younger and significantly less demented on the Mattis Dementia Rating Scale (MDRS).ConclusionOf the AD subjects who were carefully screened to exclude those with clinical NPH, 4% had elevated CSFP. These subjects were presumed to have the AD-NPH syndrome and were withdrawn from the remainder of the study.

Highlights

  • Abnormalities in cerebrospinal fluid (CSF) production and turnover, seen in normal pressure hydrocephalus (NPH) and in Alzheimer's disease (AD), may be an important cause of amyloid retention in the brain and may relate the two diseases

  • The data from the clinical trial will be the subject of a separate communication. The subjects in this trial were enrolled at 25 medical centers in the USA in an FDA (Federal Drug Administration) approved clinical trial of low-flow CSF shunting for AD, FDA Investigational device exemption (IDE) # G 970117, protocol # 2000–01

  • As observed in previous series, an important subgroup of patients with NPH meets pathological criteria for AD and exhibit features of both diseases. This series represents the first set of observations documenting evidence of raised CSF pressure (CSFP), suggesting early NPH, among carefully selected AD subjects

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Summary

Introduction

Abnormalities in cerebrospinal fluid (CSF) production and turnover, seen in normal pressure hydrocephalus (NPH) and in Alzheimer's disease (AD), may be an important cause of amyloid retention in the brain and may relate the two diseases. Alzheimer's disease (AD) and adult-onset, idiopathic chronic hydrocephalus, or normal pressure hydrocephalus (NPH), are age-related disorders involving various degrees of dementia. Patients with both diseases have reduced cerebrospinal fluid (CSF) production and (page number not for citation purposes). In a more recent series, 23 of 55 patients (42%) biopsied at the time of shunt placement for NPH met CERAD (Consortium to establish a registry for Alzheimer's disease) criteria for AD [5], including 75% of those with severe dementia [6]. There have been no corollary studies addressing the occurrence of raised CSFP among patients with clinical AD, who have not yet developed the clinical syndrome or radiographic features of NPH

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