Understanding the Importance of Blood-Brain Barrier Alterations in Brain Arteriovenous Malformations and Implications for Treatment: A Dynamic Contrast-Enhanced-MRI–Based Prospective Study

Author:

Mosteiro Alejandra1,Pedrosa Leire12,Amaro Sergio234,Menéndez-Girón Sebastián5,Reyes Luis1,de Riva Nicolás6,Misis Maite7,Blasco Jordi48,Vert Carla9,Dominguez Carlos J.5,Enseñat Joaquim124,Martín Abraham1011,Rodriguez-Hernández Ana5,Torné Ramon1248ORCID

Affiliation:

1. Department of Neurosurgery, Hospital Clinic of Barcelona, Barcelona, Spain;

2. Instituto de Investigaciones Biomédicas August Pi i Sunyer (IDIBAPS), Barcelona, Spain;

3. Comprehensive Stroke Unit, Neurology, Hospital Clinic of Barcelona, Barcelona, Spain;

4. University of Barcelona, Barcelona, Spain;

5. Department of Neurological Surgery, Germans Trias i Pujol University Hospital, Badalona, Spain;

6. Neuroanesthesia Division, Anesthesiology Department, Hospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain;

7. Intensive Care Department, Germans Trias i Pujol University Hospital, Badalona, Spain;

8. Interventional Neuroradiology Department, Hospital Clínic de Barcelona, Barcelona, Spain;

9. Neuroradiology Department, Germans Trias i Pujol University Hospital, Badalona, Spain;

10. Achucarro Basque Center for Neuroscience, Bizkaia, Spain;

11. Ikerbasque Basque Foundation for Science, Bilbao, Spain

Abstract

BACKGROUND AND OBJECTIVES: The major clinical implication of brain arteriovenous malformations (bAVMs) is spontaneous intracranial hemorrhage. There is a growing body of experimental evidence proving that inflammation and blood-brain barrier (BBB) dysfunction are involved in both the clinical course of the disease and the risk of bleeding. However, how bAVM treatment affects perilesional BBB disturbances is yet unclear. METHODS: We assessed the permeability changes of the BBB using dynamic contrast-enhanced MRI (DCE-MRI) in a series of bAVMs (n = 35), before and at a mean of 5 (±2) days after treatment. A set of cerebral cavernous malformations (CCMs) (n = 16) was used as a control group for the assessment of the surgical-related collateral changes. The extended Tofts pharmacokinetic model was used to extract permeability (Ktrans) values in the lesional, perilesional, and normal brain tissues. RESULTS: In patients with bAVM, the permeability of BBB was higher in the perilesional of bAVM tissue compared with the rest of the brain parenchyma (mean Ktrans 0.145 ± 0.104 vs 0.084 ± 0.035, P = .004). Meanwhile, no significant changes were seen in the perilesional brain of CCM cases (mean Ktrans 0.055 ± 0.056 vs 0.061 ± 0.026, P = .96). A significant decrease in BBB permeability was evident in the perilesional area of bAVM after surgical resection (mean Ktrans 0.145 ± 0.104 vs 0.096 ± 0.059, P = .037). This benefit in BBB permeability reduction after surgery seemed to surpass the relative increase in permeability inherent to the surgical manipulation. CONCLUSION: In contrast to CCMs, BBB permeability in patients with bAVM is increased in the perilesional parenchyma, as assessed using DCE-MRI. However, bAVM surgical resection seems to reduce BBB permeability in the perilesional tissue. No evidence of the so-called breakthrough phenomenon was detected in our series. DCE-MRI could become a valuable tool to follow the longitudinal course of BBB damage throughout the natural history and clinical course of bAVMs.

Funder

Fundacià la Maratà de TV3

Publisher

Ovid Technologies (Wolters Kluwer Health)

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