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Ventricular volume in relation to lumbar CSF levels of amyloid-β 1–42, tau and phosphorylated tau in iNPH, is there a dilution effect?
Department of Medical Sciences, Neurology, Uppsala University, Uppsala, Sweden.ORCID iD: 0000-0002-5137-2782
Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.ORCID iD: 0000-0003-3254-286X
Department of Medical Sciences, Neurology, Uppsala University, Uppsala, Sweden.ORCID iD: 0000-0002-7504-8354
2022 (English)In: Fluids and Barriers of the CNS, E-ISSN 2045-8118, Vol. 19, no 1Article in journal (Refereed) Published
Abstract [en]

Background

Levels of the biomarkers amyloid-β 1–42 (Aβ42), tau and phosphorylated tau (p-tau) are decreased in the cerebrospinal fluid (CSF) of patients with idiopathic normal pressure hydrocephalus (iNPH). The mechanism behind this is unknown, but one potential explanation is dilution by excessive CSF volumes. The aim of this study was to investigate the presence of a dilution effect, by studying the relationship between ventricular volume (VV) and the levels of the CSF biomarkers.

Methods

In this cross-sectional observational study, preoperative magnetic resonance imaging (MRI) and lumbar CSF was acquired from 136 patients with a median age of 76 years, 89 men and 47 females, selected for surgical treatment for iNPH. The CSF volume of the lateral and third ventricles was segmented on MRI and related to preoperative concentrations of Aβ42, tau and p-tau.

Results

In the total sample VV (Median 140.7 mL) correlated weakly (rs = − 0.17) with Aβ42 (Median 534 pg/mL), but not with tau (Median 216 pg/mL) nor p-tau (Median 31 pg/mL). In a subgroup analysis, the correlation between VV and Aβ42 was only present in the male group (rs = − 0.22, p = 0.038). Further, Aβ42 correlated positively with tau (rs = 0.30, p = 0.004) and p-tau (rs = 0.26, p = 0.012) in males but not in females.

Conclusions

The findings did not support a major dilution effect in iNPH, at least not in females. The only result in favor for dilution was a weak negative correlation between VV and Aβ42 but not with the other lumbar CSF biomarkers. The different results between males and females suggest that future investigations of the CSF pattern in iNPH would gain from sex-based subgroup analysis.

Place, publisher, year, edition, pages
Springer Nature, 2022. Vol. 19, no 1
National Category
Neurosciences
Identifiers
URN: urn:nbn:se:liu:diva-223186DOI: 10.1186/s12987-022-00353-9ISI: 000826478000001PubMedID: 35843939Scopus ID: 2-s2.0-85134460278OAI: oai:DiVA.org:liu-223186DiVA, id: diva2:2054795
Note

Funding: Open access funding provided by Uppsala University. The study received governmental funding from Uppsala University and Region Jämtland Härjedalen as well as donations from the following foundations: Forskningsfonden för klinisk neurovetenskap Norrlands Universitetssjukhus, Jämtlands läns cancer- och omvårdnadsfond, Syskonen Perssons Donationsfond.

Available from: 2026-04-22 Created: 2026-04-22 Last updated: 2026-04-22Bibliographically approved
In thesis
1. Ventricular volume in normal pressure hydrocephalus: Associations with shunt settings, clinical symptoms, and cerebrospinal fluid biomarkers
Open this publication in new window or tab >>Ventricular volume in normal pressure hydrocephalus: Associations with shunt settings, clinical symptoms, and cerebrospinal fluid biomarkers
2026 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Background: Idiopathic Normal Pressure Hydrocephalus (iNPH) is a disease mainly affecting the elderly with the core symptoms of incontinence, gait and cognitive impairment. The standard treatment is cerebrospinal fluid diversion, with ventriculoperitoneal shunts being the most common choice. The main radiological finding in iNPH is the expansion of the cerebral ventricles. Recent radiological and computational advances have made the measurement of ventricular volume increasingly feasible. This thesis, comprising of four papers, focuses on the potential use of ventricular volume as a clinical tool in the postsurgical setting in iNPH. Primarily for assessing suspected shunt malfunction (paper II), but also the individualization of shunt opening pressure settings (paper IV). Additional aims were to investigate associations between ventricular volume and cerebrospinal fluid biomarkers to assess whether there is a dilution effect (paper I), and investigating improvement in excessive daytime sleepiness after surgery (paper III).

Methods: For Paper I, participants with iNPH were examined (n=136). Lumbar CSF was sampled as a part of routine care and concentrations of Amyloid β 1-42, total tau and phosphorylated tau results extracted from medical charts. Ventricular volume for the lateral and third ventricles was manually segmented on presurgical MRI using ITK-SNAP. Papers II-IV were based on one study population of participants with iNPH (n=36). All participants received Strata II shunts with adjustable performance levels (PL) corresponding to different opening pressures. Clinical evaluation and MRI were performed repeatedly: before surgery and at one, two, three months as well as three months plus one day after surgery. At surgery, all shunts were set at PL 1.5. After the first follow-up, participants were randomly assigned to either PL 1.0 or 2.5. After the two months follow-up, the assignments were crossed over. At the third follow-up, all shunts were set to PL 0.5 for the final 24 hours. Clinical assessment included the Timed Up and Go test, 10-meter walking test, Mini-Mental State Examination, continence scale, gait scale, balance scale, modified Rankin scale, and Epworth Sleepiness Scale. Ventricular volume was manually segmented using SyMRI.

Results: Ventricular volume and Amyloid β 1-42 were weakly associated (β=-0.20 p=0.027). Ventricular volume was not significantly associated with the tau forms, though the estimates were positive. Ventricular volume decreased gradually according to lower opening pressures of the shunts: the median change from presurgical to PL 2.5 was 6.9 mL (p<0.001), from PL 2.5 was PL 1.5 of 3.5 mL (p=0.01), from PL 1.5 was PL 1.0 of 9.6 mL (p<0.001). Daytime sleepiness significantly improved following surgery with a median change of -1.5 points, p=0.026, though it did not change further at subsequent follow-ups. Clinical outcomes did not change following randomization to PL 1.0 versus PL 2.5, despite an overall significant clinical improvement following surgery. Clinical outcomes were not consistently associated with change in ventricular volume. There was an increased incidence of subdural effusion after randomization to PL 1.0, occurring in eight participants (p=0.005).

Conclusions: In this thesis, ventricular volume shows substantial and predictable change with shunt adjustments, supporting its usefulness as a marker of shunt patency. In contrast, the pattern of associations between ventricular volume and CSF biomarkers does not support dilution as a primary cause of lower biomarker concentrations in iNPH, and ventricular volume does not meaningfully relate to clinical outcomes within a one-month time frame. Lower shunt opening pressures increase risk without providing clinical benefit. Another key finding was that excessive daytime sleepiness appears to be a symptom of iNPH that is amenable to treatment.

Place, publisher, year, edition, pages
Linköping: Linköping University Electronic Press, 2026. p. 95
Series
Linköping University Medical Dissertations, ISSN 0345-0082 ; 2031
Keywords
Normal Pressure Hydrocephalus, Ventricular Volume, Randomized Trial, Ventriculoperitoneal Shunt, Excessive Daytime Sleepiness
National Category
Neurology
Identifiers
urn:nbn:se:liu:diva-223187 (URN)10.3384/9789181184662 (DOI)9789181184655 (ISBN)9789181184662 (ISBN)
Public defence
2026-05-22, Granitsalen, building 440, Campus US, Linköping, 09:00
Opponent
Supervisors
Available from: 2026-04-22 Created: 2026-04-22 Last updated: 2026-04-29Bibliographically approved

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