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  • CSF Flow Dynamics in The Cerebral Aqueduct in An Animal Model of Chronic Communicating Hydrocephalus

    Final Number:
    1231

    Authors:
    Tito Vivas-Buitrago; Armelle Lokossou; Ignacio Jusué-Torres; Gabriel Pinilla-Monsalve; Jamie Robison; Ari Blitz; Daniel Herzka; Jiadi Xu; Hugo Guerrero-Cazares; Susumu Mori; Alfredo Quiñones-Hinojosa; Olivier Baledént; Daniele Rigamonti

    Study Design:
    Laboratory Investigation

    Subject Category:

    Meeting: Congress of Neurological Surgeons 2018 Annual Meeting

    Introduction: iNPH is one of the few causes of dementia that can be reversed when diagnosed opportunely and treated with CSF diversion. Although shunting has shown benefits, it also has well-documented and important rates of complications. New prognostic markers for shunt response are needed to estimate benefit/risk when deciding treatment. Phase-contrast-MRI looking at CSF-flow through the cerebral aqueduct CAQ is a promising prognostic factor; yet, there is a lack of understanding regarding its dynamics during the early stages and throughout the progression of the disease. iNPH identification before symptoms presentation is very challenging, we propose a Phase-contrast-MRI for CSF exploration in the CAQ in a novel rodent model of chronic communicating hydrocephalus.

    Methods: Kaolin was injected over the cerebral convexities bilaterally into the subarachnoid space in Sprague-Dawley Adult Rats. An 11.7T-Bruker MRI was used to acquire Phase Contrast MR with retrospect cardiac gated images, perpendicular to the direction of CSF at the aqueduct. Aqueductal Stroke Volume ASV results were compared with the ventricular volume VV at 15,60,90,120 days.

    Results: Significant ventricular enlargement was found in Kaolin injected animals at 15(p=0.002),60(p=0.001),90(p=<0.001), and 120(p=<0.001) days when compared with control/shams. ASV differed between cases and controls/shams at every time point, (p=0.004,0.001,0.001,and<0.001 at 15,60,90 and 120 days, respectively). After correlation between the ASV and the VV, there was a significant correlation between both measurements at 15(p=0.015),60(p=0.001),90(p<0.001) and 120 days(p<0.001). There was a significant positive linear correlation between the change in ASV and the change in VV for the first period(15-60days).

    Conclusions: This study demonstrates the feasibility of a rodent ASV flow measurement in a controlled fashion at specific time points. There is a high correlation between the ASV and the ventricular volume with a special linear association during the first 60 days. Previous studies from our group have shown symptom onset after 68 days with this model.

    Patient Care: With this work, we aim to identify conditions, values, times and thresholds to predict shunting response in animals; hoping to one day correlate these findings in the iNPH human population, for them to receive a timely treatment with a higher rate of benefit than the known complications.

    Learning Objectives: To elucidate the aqueductal CSF flow dynamics during the early stages and throughout the progression of communicating chronic hydrocephalus.

    References: 1. Abbey P, Singh P, Khandelwal N, Mukherjee KK: Shunt surgery effects on cerebrospinal fluid flow across the aqueduct of Sylvius in patients with communicating hydrocephalus. J Clin Neurosci 16:514-518, 2009 2. Adams RD, Fisher CM, Hakim S, Ojemann RG, Sweet WH: Symptomatic Occult Hydrocephalus with "Normal" Cerebrospinal-Fluid Pressure.A Treatable Syndrome. N Engl J Med 273:117-126, 1965 3. Baledent O, Henry-Feugeas MC, Idy-Peretti I: Cerebrospinal fluid dynamics and relation with blood flow: a magnetic resonance study with semiautomated cerebrospinal fluid segmentation. Invest Radiol 36:368-377, 2001 4. Boon AJ, Tans JT, Delwel EJ, Egeler-Peerdeman SM, Hanlo PW, Wurzer HA, et al: Dutch normal-pressure hydrocephalus study: prediction of outcome after shunting by resistance to outflow of cerebrospinal fluid. Journal of neurosurgery 87:687-693, 1997 5. Bradley WG, Jr.: Magnetic Resonance Imaging of Normal Pressure Hydrocephalus. Semin Ultrasound CT MR 37:120-128, 2016 6. Bradley WG, Jr., Scalzo D, Queralt J, Nitz WN, Atkinson DJ, Wong P: Normal-pressure hydrocephalus: evaluation with cerebrospinal fluid flow measurements at MR imaging. Radiology 198:523-529, 1996 7. Chiang WW, Takoudis CG, Lee SH, Weis-McNulty A, Glick R, Alperin N: Relationship between ventricular morphology and aqueductal cerebrospinal fluid flow in healthy and communicating hydrocephalus. Invest Radiol 44:192-199, 2009 8. Daouk J, Chaarani B, Zmudka J, Capel C, Fichten A, Bouzerar R, et al: Relationship between cerebrospinal fluid flow, ventricles morphology, and DTI properties in internal capsules: differences between Alzheimer's disease and normal-pressure hydrocephalus. Acta Radiol 55:992-999, 2014 9. Dixon GR, Friedman JA, Luetmer PH, Quast LM, McClelland RL, Petersen RC, et al: Use of cerebrospinal fluid flow rates measured by phase-contrast MR to predict outcome of ventriculoperitoneal shunting for idiopathic normal-pressure hydrocephalus. Mayo Clin Proc 77:509-514, 2002 10. Duinkerke A, Williams MA, Rigamonti D, Hillis AE: Cognitive recovery in idiopathic normal pressure hydrocephalus after shunt. Cognitive and Behavioral Neurology 17:179-184, 2004 11. El Sankari S, Fichten A, Gondry-Jouet C, Czosnyka M, Legars D, Deramond H, et al: Correlation between tap test and CSF aqueductal stroke volume in idiopathic normal pressure hydrocephalus. Acta Neurochir Suppl 113:43-46, 2012 12. Forner Giner J, Sanz-Requena R, Florez N, Alberich-Bayarri A, Garcia-Marti G, Ponz A, et al: Quantitative phase-contrast MRI study of cerebrospinal fluid flow: a method for identifying patients with normal-pressure hydrocephalus. Neurologia 29:68-75, 2014 13. Forner J, Florez N, Valero Merino C, Marti-Bonmati L, Moratal D, Piquer J, et al: [Assessment of reliable quantification of the dynamics of cerebrospinal fluid by magnetic resonance imaging in idiopathic normal pressure hydrocephalus]. Neurologia 22:213-220, 2007 14. Hakim S, Adams RD: The special clinical problem of symptomatic hydrocephalus with normal cerebrospinal fluid pressure. Observations on cerebrospinal fluid hydrodynamics. J Neurol Sci 2:307-327, 1965 15. Hebb AO, Cusimano MD: Idiopathic normal pressure hydrocephalus: a systematic review of diagnosis and outcome. Neurosurgery 49:1166-1186, 2001 16. Henry-Feugeas MC, Idy-Peretti I, Baledent O, Cornu P, Lejay H, Bittoun J, et al: Cerebrospinal fluid flow waveforms: MR analysis in chronic adult hydrocephalus. Invest Radiol 36:146-154, 2001 17. Hung AL, Vivas-Buitrago T, Adam A, Lu J, Robison J, Elder BD, et al: Ventriculoatrial versus ventriculoperitoneal shunt complications in idiopathic normal pressure hydrocephalus. Clinical Neurology and Neurosurgery 157:1-6, 2017 18. Jusue-Torres I, Jeon LH, Sankey EW, Lu J, Vivas-Buitrago T, Crawford JA, et al: A Novel Experimental Animal Model of Adult Chronic Hydrocephalus. Neurosurgery 79:746-756, 2016 19. Kahlon B, Annertz M, Stahlberg F, Rehncrona S: Is aqueductal stroke volume, measured with cine phase-contrast magnetic resonance imaging scans useful in predicting outcome of shunt surgery in suspected normal pressure hydrocephalus? Neurosurgery 60:124-129; discussion 129-130, 2007 20. Kim DS, Choi JU, Huh R, Yun PH, Kim DI: Quantitative assessment of cerebrospinal fluid hydrodynamics using a phase-contrast cine MR image in hydrocephalus. Childs Nerv Syst 15:461-467, 1999 21. Marmarou A, Bergsneider M, Klinge P, Relkin N, Black PM: The value of supplemental prognostic tests for the preoperative assessment of idiopathic normal-pressure hydrocephalus. Neurosurgery 57:S2-17-S12-28, 2005 22. Marmarou A, Bergsneider M, Klinge P, Relkin N, Black PM: The value of supplemental prognostic tests for the preoperative assessment of idiopathic normal-pressure hydrocephalus. Neurosurgery 57:S17-28; discussion ii-v, 2005 23. McGirt MJ, Woodworth G, Coon AL, Thomas G, Williams MA, Rigamonti D: Diagnosis, treatment, and analysis of long-term outcomes in idiopathic normal-pressure hydrocephalus. Neurosurgery 57:699-705; discussion 699-705, 2005 24. Pujari S, Kharkar S, Metellus P, Shuck J, Williams MA, Rigamonti D: Normal pressure hydrocephalus: long-term outcome after shunt surgery. Journal of Neurology, Neurosurgery & Psychiatry 79:1282-1286, 2008 25. Razay G, Vreugdenhil A, Liddell J: A prospective study of ventriculo-peritoneal shunting for idiopathic normal pressure hydrocephalus. Journal of Clinical Neuroscience 16:1180-1183, 2009 26. Relkin N, Marmarou A, Klinge P, Bergsneider M, Black PM: Diagnosing idiopathic normal-pressure hydrocephalus. Neurosurgery 57:S4-16; discussion ii-v, 2005 27. Saliou G, Baledent O, Lehmann P, Paradot G, Gondry-Jouet C, Bouzerar R, et al: [Acute CSF changes in the mesencephalon aqueduct after subarachnoid hemorrhage as measured by PC-MRI]. J Neuroradiol 36:41-47, 2009 28. Saliou G, Paradot G, Gondry C, Bouzerar R, Lehmann P, Meyers ME, et al: A phase-contrast MRI study of acute and chronic hydrodynamic alterations after hydrocephalus induced by subarachnoid hemorrhage. J Neuroimaging 22:343-350, 2012 29. Scollato A, Gallina P, Gautam B, Pellicano G, Cavallini C, Tenenbaum R, et al: Changes in aqueductal CSF stroke volume in shunted patients with idiopathic normal-pressure hydrocephalus. AJNR Am J Neuroradiol 30:1580-1586, 2009 30. Tawfik AM, Elsorogy L, Abdelghaffar R, Naby AA, Elmenshawi I: Phase-Contrast MRI CSF Flow Measurements for the Diagnosis of Normal-Pressure Hydrocephalus: Observer Agreement of Velocity Versus Volume Parameters. AJR Am J Roentgenol 208:838-843, 2017 31. Vanneste J, Augustijn P, Dirven C, Tan W, Goedhart Z: Shunting normal-pressure hydrocephalus: Do the benefits outweigh the risks? A multicenter study and literature review. Neurology 42:54-54, 1992 32. Williams MA, Thomas G, de Lateur B, Imteyaz H, Rose JG, Shore WS, et al: Objective assessment of gait in normal-pressure hydrocephalus. American journal of physical medicine & rehabilitation 87:39-45, 2008 33. Yin LK, Zheng JJ, Zhao L, Hao XZ, Zhang XX, Tian JQ, et al: Reversed aqueductal cerebrospinal fluid net flow in idiopathic normal pressure hydrocephalus. Acta Neurol Scand 136:434-439, 2017

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