Cerebrospinal Fluid Diagnostics of Alzheimer’s Disease in Patients with Idiopathic Normal Pressure Hydrocephalus

Author:

Vanninen Aleksi12,Lukkarinen Heikki12,Kokkola Tarja3,Koivisto Anne M.3456,Kokki Merja78,Musialowicz Tadeusz8,Hiltunen Mikko9,Zetterberg Henrik1011121314,Leinonen Ville12,Herukka Sanna-Kaisa34,Rauramaa Tuomas1516

Affiliation:

1. Department of Neurosurgery, Kuopio University Hospital, Kuopio, Finland

2. Neurosurgery, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland

3. Neurology, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland

4. Department of Neurology, Kuopio University Hospital, Kuopio, Finland

5. Department of Neurosciences, University of Helsinki, Helsinki, Finland

6. Department of Geriatrics, Helsinki University Hospital, Helsinki, Finland

7. School of Medicine, University of Eastern Finland, Kuopio, Finland

8. Department of Anaesthesia and Intensive Care Medicine, Kuopio University Hospital, Kuopio, Finland

9. Institute of Biomedicine, University of Eastern Finland, Kuopio, Finland

10. Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden

11. Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden

12. Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, UK

13. UK Dementia Research Institute at UCL, London, UK

14. Hong Kong Center for Neurodegenerative Diseases, Clear Water Bay, Hong Kong, China

15. Department of Pathology, Kuopio University Hospital, Kuopio, Finland

16. Pathology, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland

Abstract

Background: Alzheimer’s disease (AD) is the most common cause of dementia worldwide and a frequent comorbidity in idiopathic normal pressure hydrocephalus (iNPH). The presence of AD pathology is associated with worse outcomes after a shunt procedure in iNPH. Preoperative diagnosis of AD is challenging in patients with iNPH, which involves reduced concentrations of the cerebrospinal fluid (CSF) AD biomarkers. Objective: Our aim was to estimate the effect size of iNPH as a factor in CSF levels of AD biomarkers and to test if correction could be used to improve diagnostic value. Methods: Our cohort included 222 iNPH patients with data in the Kuopio NPH registry and brain biopsy and CSF samples available. We divided the patients into groups according to AD pathology per brain biopsy. For control cohorts, we had CSF samples from cognitively healthy individuals (n = 33) and patients with diagnosed AD and no iNPH (n = 39). *-31pt Results: Levels of all investigated biomarkers differed significantly between groups, with the exception of t-Tau levels between healthy individuals and iNPH patients with AD pathology. Applying a correction factor for each biomarker (0.842*Aβ1 - 42, 0.779*t-Tau, and 0.610*P-Tau181) for the effect of iNPH yielded a sensitivity of 2.4% and specificity of 100%. The ratio of P-Tau181 to Aβ1 - 42 was moderately effective in aiding recognition of AD pathology in iNPH patients (sensitivity 0.79, specificity 0.76, area under the curve 0.824). Conclusion: Correcting for iNPH as a factor failed to improve diagnostic effectiveness, but the P-Tau181/Aβ1 - 42 ratio showed some utility in the diagnosis of AD in iNPH patients.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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