A Lumped Parameter Modelling Study of Idiopathic Intracranial Hypertension Suggests the CSF Formation Rate Varies with the Capillary Transmural Pressure

<b>Background</b>: Idiopathic intracranial hypertension (IIH) is, by definition, of unknown cause. Davson's equation indicates that the increased intracranial pressure (ICP) found in IIH could be due to an increase in the CSF formation rate (CSF<sub>fr</sub>), the CSF outflow resistance (R<sub>out</sub>) or the venous sinus pressure. Studies simultaneously measuring the ICP and sagittal sinus pressures in IIH suggest that there is either a reduction in the R<sub>out</sub> and/or the CSF<sub>fr</sub>. The latter suggests that the increased venous pressure can be the only variable causing this disease process. A study maintaining the ICP at zero showed a significantly elevated CSF<sub>fr</sub> in this disease. The purpose of the current study is to define the most feasible explanation for these findings and to suggest a viable pathophysiology for IIH. <b>Methods</b>: A lumped parameter vascular model, originally developed to study normal pressure hydrocephalus, was extended to investigate IIH. The model used the simultaneously obtained ICP and sagittal sinus pressure measurements from five experiments published in the literature to estimate the CSF<sub>fr</sub> and the capillary transmural pressure (TMP). The assumptions made during this study were those of a normal mean arterial pressure, a normal total R<sub>out</sub> and a normal blood flow rate. <b>Results</b>: When the CSF formation rates were plotted against the estimated capillary transmural pressures, a straight line was returned, suggesting that the CSF<sub>fr</sub> and capillary TMP are related. <b>Conclusions</b>: The novel findings of this study suggest that the CSF<sub>fr</sub> in IIH varies with the capillary TMP. A reduced capillary TMP in IIH can moderate the ICP if there is net CSF absorption across the capillaries. This would require the blood-brain barrier (BBB) to be disrupted. The model suggests that drugs which stabilise the BBB may trigger IIH by blocking CSF absorption across the capillaries, increasing the apparent CSF formation rate back toward normal and increasing the ICP. Anaemia will promote IIH by increasing the cerebral blood flow, the capillary TMP and the CSF<sub>fr</sub>.

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Journal
Brain Sciences
Published
2025-05-20
DOI
https://doi.org/10.3390/brainsci15050527
Citations
2
Primary Topic
Cerebral Venous Sinus Thrombosis
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article
Field-Weighted Citation Impact
2.78
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article

A Lumped Parameter Modelling Study of Idiopathic Intracranial Hypertension Suggests the CSF Formation Rate Varies with the Capillary Transmural Pressure

Alexander Robert Bateman, Grant A. Bateman
2 citations
Brain Sciences
Cerebral Venous Sinus Thrombosis
2.78
article

A Lumped Parameter Modelling Study of Idiopathic Intracranial Hypertension Suggests the CSF Formation Rate Varies with the Capillary Transmural Pressure

Alexander Robert Bateman, Grant A. Bateman
article en
2 citations

Abstract

<b>Background</b>: Idiopathic intracranial hypertension (IIH) is, by definition, of unknown cause. Davson's equation indicates that the increased intracranial pressure (ICP) found in IIH could be due to an increase in the CSF formation rate (CSF<sub>fr</sub>), the CSF outflow resistance (R<sub>out</sub>) or the venous sinus pressure. Studies simultaneously measuring the ICP and sagittal sinus pressures in IIH suggest that there is either a reduction in the R<sub>out</sub> and/or the CSF<sub>fr</sub>. The latter suggests that the increased venous pressure can be the only variable causing this disease process. A study maintaining the ICP at zero showed a significantly elevated CSF<sub>fr</sub> in this disease. The purpose of the current study is to define the most feasible explanation for these findings and to suggest a viable pathophysiology for IIH. <b>Methods</b>: A lumped parameter vascular model, originally developed to study normal pressure hydrocephalus, was extended to investigate IIH. The model used the simultaneously obtained ICP and sagittal sinus pressure measurements from five experiments published in the literature to estimate the CSF<sub>fr</sub> and the capillary transmural pressure (TMP). The assumptions made during this study were those of a normal mean arterial pressure, a normal total R<sub>out</sub> and a normal blood flow rate. <b>Results</b>: When the CSF formation rates were plotted against the estimated capillary transmural pressures, a straight line was returned, suggesting that the CSF<sub>fr</sub> and capillary TMP are related. <b>Conclusions</b>: The novel findings of this study suggest that the CSF<sub>fr</sub> in IIH varies with the capillary TMP. A reduced capillary TMP in IIH can moderate the ICP if there is net CSF absorption across the capillaries. This would require the blood-brain barrier (BBB) to be disrupted. The model suggests that drugs which stabilise the BBB may trigger IIH by blocking CSF absorption across the capillaries, increasing the apparent CSF formation rate back toward normal and increasing the ICP. Anaemia will promote IIH by increasing the cerebral blood flow, the capillary TMP and the CSF<sub>fr</sub>.

Brain SciencesVol. 15(5)
John Hunter Hospital (AU), University of Newcastle Australia (AU)
Good health and well-being
Openalex Percentile: Top 10%
Cerebral Venous Sinus Thrombosis
2.78
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