Time Trends of Cerebrospinal Fluid Biomarkers of Neurodegeneration in Idiopathic Normal Pressure Hydrocephalus

Author:

Lukkarinen Heikki1,Tesseur Ina2,Pemberton Darrel3,Van Der Ark Peter3,Timmers Maarten3,Slemmon Randy4,Janssens Luc3,Streffer Johannes56,Van Nueten Luc3,Bottelbergs Astrid3,Rauramaa Tuomas7,Koivisto Anne M.89,Herukka Sanna-Kaisa8,Korhonen Ville E.1,Junkkari Antti1,Hiltunen Mikko10,Engelborghs Sebastiaan511,Blennow Kaj1213,Zetterberg Henrik12131415,Kolb Hartmuth C.4,Leinonen Ville1

Affiliation:

1. Institute of Clinical Medicine –Neurosurgery, University of Eastern Finland and Department of Neurosurgery, Kuopio University Hospital, Kuopio, Finland

2. UCB, Braine-l’Alleud, Belgium

3. Janssen Research & Development, A Division of Janssen Pharmaceutica NV, Beerse, Belgium

4. Janssen Research & Development, La Jolla, CA, USA

5. Reference Center for Biological Markers of Dementia (BIODEM), Institute Born-Bunge, University of Antwerp, Antwerp, Belgium

6. AC Immune SA, Lausanne, Switzerland

7. Institute of Clinical Medicine –Pathology, University of Eastern Finland and Department of Pathology, Kuopio University Hospital, Kuopio, Finland

8. Institute of Clinical Medicine –Neurology, University of Eastern Finland and Department of Neurology, Kuopio University Hospital, Kuopio, Finland

9. Department of Neurosciences, University of Helsinki, Helsinki, Finland and Department of Geriatrics, Helsinki University Hospital, Helsinki, Finland

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

11. Department of Neurology and Center for Neurosciences, UZ Brussel and Vrije Universiteit Brussel (VUB), Brussels, Belgium

12. Clinical Neurochemistry Laboratory, Sahlgrenska Academy Hospital, Mölndal, Sweden

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

14. UCL Institute of Neurology, Department of Neurodegenerative Disease, University College London, Queen Square, London, United Kingdom

15. UK Dementia Research Institute, London, United Kingdom

Abstract

Background: Longitudinal changes in cerebrospinal fluid (CSF) biomarkers are seldom studied. Furthermore, data on biomarker gradient between lumbar (L-) and ventricular (V-) compartments seems to be discordant. Objective: To examine alteration of CSF biomarkers reflecting Alzheimer’s disease (AD)-related amyloid-β (Aβ) aggregation, tau pathology, neurodegeneration, and early synaptic degeneration by CSF shunt surgery in idiopathic normal pressure hydrocephalus (iNPH) in relation to AD-related changes in brain biopsy. In addition, biomarker levels in L- and V-CSF were compared. Methods: L-CSF was collected prior to shunt placement and, together with V-CSF, 3–73 months after surgery. Thereafter, additional CSF sampling took place at 3, 6, and 18 months after the baseline sample from 26 iNPH patients with confirmed Aβ plaques in frontal cortical brain biopsy and 13 iNPH patients without Aβ pathology. CSF Amyloid-β42 (Aβ42), total tau (T-tau), phosphorylated tau (P-tau181), neurofilament light (NFL), and neurogranin (NRGN) were analyzed with customized ELISAs. Results: All biomarkers but Aβ42 increased notably by 140–810% in L-CSF after CSF diversion and then stabilized. Aβ42 instead showed divergent longitudinal decrease between Aβ-positive and -negative patients in L-CSF, and thereafter increase in Aβ-negative iNPH patients in both L- and V-CSF. All five biomarkers correlated highly between V-CSF and L-CSF (Aβ42 R = 0.87, T-tau R = 0.83, P-tau R = 0.92, NFL R = 0.94, NRGN R = 0.9; all p < 0.0001) but were systematically lower in V-CSF (Aβ42 14 %, T-tau 22%, P-tau 20%, NFL 32%, NRGN 19%). With APOE genotype-grouping, only Aβ42 showed higher concentration in non-carriers of allele ɛ4. Conclusion: Longitudinal follow up shows that after an initial post-surgery increase, T-tau, P-tau, and NRGN are stable in iNPH patients regardless of brain biopsy Aβ pathology, while NFL normalized toward its pre-shunt levels. Aβ42 as biomarker seems to be the least affected by the surgical procedure or shunt and may be the best predictor of AD risk in iNPH patients. All biomarker concentrations were lower in V- than L-CSF yet showing strong correlations.

Publisher

IOS Press

Subject

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

Reference53 articles.

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