eISSN: 1509-572x
ISSN: 1641-4640
Folia Neuropathologica
Current issue Archive Manuscripts accepted About the journal Special Issues Editorial board Reviewers Abstracting and indexing Subscription Contact Instructions for authors Ethical standards and procedures
Editorial System
Submit your Manuscript
SCImago Journal & Country Rank
2/2015
vol. 53
 
Share:
Share:

Original article
Analysis of intracranial volume ratios by means of cerebrospinal fluid deployment indicators

Ewa Szczepek
,
Leszek Tomasz Czerwosz
,
Krzysztof Nowiński
,
Zbigniew Czernicki
,
Jerzy Jurkiewicz

Folia Neuropathol 2015; 53 (2): 121-127
Online publish date: 2015/06/30
Article file
Get citation
 
PlumX metrics:
 

Introduction

Advances in the diagnostics of central nervous system (CNS) disorders are connected to a large degree with radiological assessment – the analysis of computed tomographic (CT) and magnetic reson­ance (MRI) images. The largest application is for head examinations, especially the brain. Imaging studies make it possible not only to visualize the general structure of the brain, but also to make precise measurements of brain tissue volume, of the size of individual lobes and their structure (volumetry) [7,15]. The application of specialist software for the analysis of CT and MRI images has made it possible to perform volumetric examinations to obtain non-invasive volume measurements of specific intracranial compartments (i.e., the volume of cerebrospinal fluid [CSF] contained in the subarachnoid space and basal cisterns, in the intracranial ventricular system and the brain tissue volume).
This has been found to be an important clinical application for the non-invasive diagnosis of normal pressure hydrocephalus and various types of brain atrophy. The ageing of society is clearly noticeable in recent years, and the lengthening of life has meant that diseases associated with dementia, the prevalence of which increases with age, currently represent a serious medical and social problem. For this reason, the possibility of early detection of disorders associated with dementia, their diagnosis and differentiation from the symptoms of the development of normal pressure hydrocephalus are of significant importance.
To achieve the intended aim, imaging studies, including CT and MRI volumetric examinations, have made it possible to precisely estimate the volume of the intracranial components of the CNS [16].
From the point of view of differential diagnosis on the basis of CT or MRI studies, we define the intracranial contents as the brain volume and the volume of CSF contained in the intracranial ventricular system and in the subarachnoid space and basal cisterns. According to data from the literature [11], the average brain volume of a healthy person is 1400 cm3 and the average CSF volume is 140 cm3.
Difficulty in the diagnosis of normal pressure hydro­­cephalus (NPH) and differentiating it from brain atrophy (BA) means that normal pressure hydrocephalus is diagnosed in a large percentage of cases that were in fact brain atrophy. It is also possible that brain atrophy is diagnosed in those cases that were in fact hydrocephalus. The commonly applied invasive diagnostic procedure is the infusion test [8], which gives the highest probability of correct diagnosis. This result should always be interpreted together with non-invasive diagnostic procedures, such as neurological examinations, neuropsychological examinations [9], motor and posture parameters [5,6,12], evoked potential, and particularly with CT and/or MRI brain imaging [4].
The Visual Analysis group co-chaired by Dr. Krzy­sztof Nowiński from the Interdisciplinary Centre for Mathematical and Computational Modelling at the University of Warsaw (ICM) has developed special software, VisNow [14], for the visual analysis of data, in particular for the analysis of a three-dimensional tissue density matrix, which is the result of computed tomography. The software allows not only visualization but also spatial morphometric calculations of tissue density specified in Hounsfield units. Szczepek et al. [13] used the VisNow tool for volumetric evaluation of CSF distribution in the intracranial fluid compartments in hydrocephalus and brain atrophy. The real absolute value (in cm3) of the CSF voxels contained in the subarachnoid space and basal cisterns and in the intracranial ventricular system space was determined. The accuracy of volumetric outcomes has been compared to the planimetry paper of Marszałek et al. [9]. Szczepek relied solely on small groups of patients with normal pressure hydrocephalus and with brain atrophy. For both groups the mean value of the volume of CSF in the subarachnoid space and basal cisterns differs at a level of statistical significance from the mean value of CSF volume of normal healthy people. It has also been shown that the ratio of volume of CSF in the ventricles to the volume of CSF in the subarachnoid space and basal cisterns is an important diagnostic indicator for differentiating NPH from brain atrophy.
The aim of this study is to determine the ratio of the intracranial CSF to the brain tissue volume, the volume of CSF contained in the intracranial ventricular system to the brain volume and the volume of CSF in the subarachnoid space and basal cisterns to brain volume.
The aim of the analysis of this study is to answer the question of the clinical relevance of the abovementioned indicators:
– to determine the proportion of the pathologies under study,
– to make it possible to differentiate normal pressure hydrocephalus from brain atrophy with the aid of the abovementioned indicators.

Material and methods

At this neurosurgical clinic, an evaluation of the volumetric measurements of CT images was undertaken in 23 male and female patients (average age 56.9 ± 6.1) with a diagnosis of normal pressure hydrocephalus and in 27 male and female patients (average age 70.6 ± 5.2) with a diagnosis of brain atrophy. In the CT imaging studies, the total brain tissue volume and the volume of CSF collected in the intracranial fluid compartments were mapped.
The study was undertaken in accordance with the Helsinki Declaration after obtaining the prior agreement of the Bioethical Committee of the Warsaw Medical University. The clinical criteria for the diagnosis of normal pressure hydrocephalus were established based on the following: dilatation of the ventricular system in CT or MRI studies; the Evans indicator with a value > 0.3; the lack of or little evidence of cortical atrophy; Hakim’s triad – at least two symptoms; the value of intracranial pressure measured with the aid of a lumbar puncture NL ≥ 10 cmH2O; resorption resistance R ≥ 11 mmHg/ml/min; and a neuropsychological assessment.
The diagnosis of brain atrophy was established on the basis of the following symptoms: dilatation of the ventricular system in CT or MRI studies of the head; the Evans indicator with a value ≤ 0.3; evidence of cortical and corticobasal atrophy; neurological symptoms; the value of intracranial pressure measured during a lumbar puncture NL < 10 cmH2O; resorption resistance R < 11 mmHg/ml/min; and a neuropsychological assessment.
The results of the neurological examination were maintained in accordance with the set of tests developed and currently applied in this clinic [9].
Volumetric evaluation using the VisNow software, developed from scratch in ICM for volumetric evaluation, is an impartial, quantitative, statistical method for measuring the voxel characteristics in selected CNS regions. The technical data of the software were published by Szczepek et al. in 2015 [13]. A statistical analysis of the voxels was undertaken for the brain tissue volume and the total volume of CSF contained in the intracranial fluid compartments.
In this study, the statistical analysis was based on the volume of the subarachnoid space and basal cisterns, the volume of the intracranial ventricular system and also on the brain tissue volume (BV) in the CT imaging studies of the head (performed at intervals no longer than two months) in patients classified in the group of hydrocephalus and brain atrophy. Total CSF volume (FV) was the sum of the subarachnoid space and basal cisterns and the volume of the intracranial ventricular system.
The following indicators were established:
– VBR (ventricle-to-brain ratio) (expressed as a fraction) – the ratio of the volume of the CSF in the intracranial ventricular system to the brain volume;
– SBR (subarachnoid space and basal cisterns-to-brain ratio) (expressed as a fraction) – the ratio of the volume of CSF in the subarachnoid space and basal cisterns to the brain volume.
The groups were compared by means of the non-parametric Kolmogorov-Smirnov test (K-S) for independent samples. Dependent samples were compared by means of the nonparametric Wilcoxon test.

Results

The results of the statistical analysis (Kolmogorov-Smirnov) for the two groups – normal pressure hydrocephalus (NPH) and brain atrophy (BA) groups – showed that the brain volumes (BV) are different at a statistically significant level in these groups (Table I). The total volumes of CSF (FV) in the intracranial fluid compartments (CSF contained in the subarachnoid space and basal cisterns as well as the intracranial ventricular system) differ in these groups as well. The volumes of BV and FV differ greatly from each other in both groups; there is no need for a statistical test in this case.
A scatter plot of the value of BV and FV together with the mean values of the BA and NPH groups is shown in Figure 1.
A statistical evaluation for the measurements of the mean values of VBR and SBR indicators in patients with normal pressure hydrocephalus and brain atrophy are presented in Table II. Comparisons of two groups are presented for VBR and SBR independently.
The results of the statistical analysis (Wilcoxon test) for dependent variables proved that SBR and VBR indicators differ significantly and very much within the NPH group as well as within the BA group (Table II).
In the patients classified as the normal pressure hydrocephalus group, a clearly higher value of the VBR can be observed in comparison with patients classified as the brain atrophy group. Analysing the SBR indicator, it was found that there was a higher value of SBR in the group of patients with a diagnosis of brain atrophy than in the group of patients with normal pressure hydrocephalus. There is a very low probability of erroneous outcome of statistical tests (less than 10-12).
A scatter plot of individual VBR and SBR indicators together with the mean values of BA and NPH groups is shown in Figure 2. One can observe a wide gap between the BA and NPH groups. This observation is consistent with the results of statistical tests.

Discussion

The variety of diagnostic procedures for differentiating normal pressure hydrocephalus and brain atrophy is proof of the difficulty in differentiating the two pathological syndromes. In spite of the fact that invasive procedures carry a risk of development of complications, they are still necessary in the diagnosis of hydrocephalus. For this reason, we attempted to develop a non-invasive differential diagnostic procedure for normal pressure hydrocephalus and brain atrophy. The presented observations are a further attempt to introduce into clinical practice a non-invasive diagnostic procedure – the evaluation of intracranial volumetric indicators of the distribution of the volume of CSF and brain tissue volume.
The volumetric evaluation undertaken in this study using CT imaging studies of the head showed that there were changes in the distribution of the volume of CSF and brain tissue volume in the intracranial compartments of the CNS for both hydrocephalus (NPH) and BA groups of patients. The scope of these changes differed in each particular group.
The new indicators VBR and SBR, identified in the study, made it possible to estimate the value of the volume of CSF in relation to the brain tissue volume in specific intracranial spaces of the CNS in the groups of patients with NPH and BA.
The results obtained in our study are similar to the results obtained by Blatter et al. [3]. The authors presented a quantitative evaluation of the volumetric intracranial parameters of volume ratios using MRI imaging studies in a control group. One hundred ninety-four healthy persons, including men and women in the age range from 16 to 65 years old, were divided into five ten-year age groups. The analysis included the total volume of CSF in the intracranial ventricular system and in the subarachnoid space, the total brain volume and the total intracranial volume.
A highly significant change was noticed with age. The authors found that the mean brain volume decreases with age, and the smallest value of brain volume was noted in the 5th decade of life (56-65 years old). The mean volume of CSF increases with age, and the highest value of CSF volume was recorded in the 5th decade of life (56-65 years old).
In the abovementioned study, in the group of healthy persons, the VBR indicator was also identified – the ratio of the volume of CSF in the intracranial ventricular system to the total brain volume. In healthy people in the age range of 56-65 years, the VBR for women was 2.08 ± 1.11 and for men 2.07 ± 0.88. The presented range of the VBR index in the control group in the specified age range should be compared with the VBR results obtained in our publication. It can also be noted that the value of VBR obtained in our study clearly differs from the norms in both of the discussed CNS pathologies. In our study, the VBR coefficient in the BA group (9.9 ± 1.3) is at a lower level than in the volumetric studies of the NPH group (13.9 ± 1.3). An explanation for this could be that in the BA group loss of brain tissue (i.e., brain volume) occurs with increasing age and with the progression of atrophy of the neural pathways. It should be noted that the CSF distribution in the intracranial fluid compartments is different in the group of patients with BA than in the group with NPH. It was observed that a higher value of CSF in the intracranial ventricular system was obtained in the patients with NPH, whereas a higher value of CSF in the subarachnoid space was obtained with patients diagnosed with BA.
The use of volumetric evaluation for tracking the volume changes in the intracranial compartments of the CNS in neurodegenerative disorders is also found in the study by Bigler et al. [2]. The authors performed an analysis of the volume parameters in patients with various types of dementia over the age of 65 years (i.e., Alzheimer’s disease, vascular dementia). The VBR coefficient was identified. The results of the volumetric parameters presented by the authors in the study in patients with Alzheimer’s disease or with vascular dementia are similar to the results of the study obtained in our publication with patients classified to the group of brain atrophy – a reduction in brain volume and an increase in the volume of CSF in the intracranial fluid compartments.
Akdogan et al. [1] undertook to use volumetric evaluation to highlight the relationship between TVV (total ventricle volume) and TBV (total brain volume). For their analysis, 40 men (average age 40.9 ± 3.7 years) and 40 women (average age 41.4 ± 3.6 years) were selected. Patients were excluded from the study if a CT imaging study of the head presented intracranial bleeding or traumatic brain injury. It was found that the ratio TVV/TBV in the group of patients in the first decade was only 1.27%, whereas for the group of patients in the third decade the ratio rose to as much as 3.37%. The results were connected with increasing volume of CSF in the intracranial ventricular system and with decreasing brain volume together with age and the associated ageing process of the brain.
The authors observed that the volume ratio TVV/TBV turned out to be an important indicator for diseases, i.e., hydrocephalus, Alzheimer’s, and disorders of a neurodegenerative nature.
In the study of Nestor et al. [10], semi-automatic software was presented that enabled the volumetric evaluation of MRI imaging studies for the early detection of dementia disorders. The authors found that the volume of CSF in the intracranial ventricular system can constitute an explanation for Alzheimer’s disease or mild cognitive impairments. In the analysed group of patients, the volume of CSF in the brain ventricles was evaluated at an early stage of the illness and after 6 months for control purposes. It was noticed that patients with a diagnosis of Alzheimer’s have clearly a larger volume of the ventricles than is the case in the group of patients with mild cognitive impairments. In Nestor’s study, the possibility of evaluating the progression of changes of the volume ratios was also mentioned (i.e., a clear increase of the volume in the intracranial ventricular system was noted after 6 months in patients with mild cognitive impairments).
The results obtained in Nestor’s study concur with the data from the literature. It should be underlined at this point that all of the abovementioned indicators can be used with success for the evaluation of the development of intracranial pathologies, but they do not give an unambiguous answer whether a specific examined case should be classified as brain atrophy or as hydrocephalus. For differentiating these pathological processes, the best indicator is in our opinion [13] an indicator highlighting the ratio of the volume of CSF in the brain ventricles to the volume of CSF contained in the subarachnoid space and basal cisterns.
It should be emphasized that the simultaneous use of the two indicators VBR and SBR on a study group of 50 patients enabled the total separation of NPH and BA groups. This differentiation can have real diagnostic value. Thus the volumetric assessment of the volume of CSF and brain tissue based on CT of the head can become an important part of the differential diagnosis of hydrocephalus and brain atrophy.

Acknowledgments

The research support was partially provided by the project POIG.02.03.00-00-003/09 “Applications of digital technologies in medicine”, which was carried out based on a common project of the Polish Academy of Sciences research institutions – “Biocentrum Ochota – information infrastructure for the strategic areas of biology and medicine”.

Disclosure

Authors report no conflict of interest.

References

1. Akdogan I, Kiroglu Y, Onur S, Karabulut N. The volume fraction of brain ventricles to total brain volume: a computed tomo­graphy stereological study. Folia Morphologica 2010; 69: 193-200.
2. Bigler ED, Lowry CM, Anderson CV, Johnson SC, Terry J, Steed M. Dementia, quantitative neuroimaging and apolipoprotein E ge­no­type. AJNR Am J Neuroradiol 2000; 21: 1857-1868.
3. Blatter DD, Bigler ED, Gale SD, Johnson SC, Anderson CV, Burnett BM, Parker N, Kurth S, Horn SD. Quantitative volumetric analysis of brain MR: normative database spanning 5 decades of life. AJNR Am J Neuroradiol 1995; 16: 241-251.
4. Czernicki Z, Walecki J, Jurkiewicz J, Grochowski W, Tychmanowicz K. Intracranial volume reserve determination using CT images, numerical analysis and lumbar infusion tests. An expe­rimental study. Acta Neurochir 1992; 115: 43-46.
5. Czerwosz L, Szczepek E. Hydrocephalus. In: Recognition of Posture and Gait Disturbances in Patients with Normal Pressure Hydrocephalus Using a Posturography and Computer Dynography Systems. Czerwosz L, Szczepek E, Sokołowska B, Jurkiewicz J, Czernicki Z. InTech 2012; 12, pp. 189-214.
6. Czerwosz L, Szczepek E, Sokołowska B, Jurkiewicz J, Czernicki Z. Posturography in differential diagnosis of normal pressure hydrocephalus and brain atrophy. Adv Exp Med Biol 2013; 755: 311-324.
7. Duning T, Kloska S, Steinsträter O, Kugel H, Heindel W, Knecht S. Dehydration complicates the assessment of brain atrophy. Neurology 2005; 64: 876-879.
8. Juniewicz H, Kasprowicz M, Czosnyka M, Czosnyka Z, Gizewski S, Dzik M, Pickard JD. Analysis of intracranial pressure during and after the infusion test in patients with communicating hydrocephalus. Physiol Meas 2005; 26: 1039-1048.
9. Marszałek P, Jurkiewicz J, Fersten E, Luczywek E, Czernicki Z, Gielecki J, Bogucki J. Multi-stage method for the diagnosis of low-pressure hydrocephalus. Neurol Neurochir Pol 1997; 31: 527-539.
10. Nestor SM, Rupsingh R, Borrie M, Smith M, Accomazzi V, Wells JL, Fogarty J, Bartha R; Alzheimer’s Disease Neuroimaging Initiative. Ventricular enlargement as a possible measure of Alzheimer’s disease progression validated using the Alzheimer’s disease neuroimaging initiative database. Brain 2008; 131: 2443-2454.
11. Rengachary SS, Ellenbogen RG. Principles of Neurosurgery. Elsevier Mosby, Edinburgh 2005; pp. 99-115.
12. Szczepek E, Czerwosz L, Dąbrowski P, Dudziński K, Jurkiewicz J, Czernicki Z. Posturography and computerized gait analysis in the Computer Dyno Graphy system as non-invasive methods for evaluation of normal pressure hydrocephalus progression. Neurol Neurochir Pol 2008; 42: 139-152.
13. Szczepek E, Czerwosz L, Nowiński K, Jurkiewicz J, Czernicki Z. Evaluation of volumetric changes in differential diagnosis of brain atrophy and active hydrocephalus. Adv Exp Med Biol 2015; 840: 59-67.
14. VisNow visualization software developed at Laboratory of Visual Analysis at Interdisciplinary Center of Mathematical and Computational Modeling (2011). http://visnow.icm.edu.pl. Accessed 18 Apr 2015.
15. Walecki J, Ziemiański A. Magnetic Resonance Imaging and Computed Tomography in clinical practice. Springer PWN, Warsaw 1997; pp. 215-225.
16. Whitwell JL, Crum WR, Watt HC, Fox NC. Normalization of cerebral volumes by use of intracranial volume: implications for longitudinal quantitative MR imaging. AJNR Am J Neuroradiol 2001; 22: 1483-1489.
Copyright: © 2015 Mossakowski Medical Research Centre Polish Academy of Sciences and the Polish Association of Neuropathologists. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.