AI Article Synopsis

  • This study looks at how the brain folds in people with a condition called intracranial arteriovenous malformations (AVMs).
  • Seven adults with AVMs went through MRI scans to measure brain folding differences between the affected and healthy parts of their brains.
  • The results showed no big differences in brain folding between the AVM patients and healthy people, but there was a link between the size of the AVM and one of the brain folding measurements.

Article Abstract

Background: The pathogenesis of human intracranial arteriovenous malformations (AVMs) is not well understood; this study aims to quantitatively assess cortical folding in patients with these lesions.

Methods: Seven adult participants, 4 male and 3 female, with unruptured, surgically unresectable intracranial AVMs were prospectively enrolled in the study, with a mean age of 42.1 years and Spetzler-Martin grade range of II-IV. High-resolution brain MRI T1 and T2 sequences were obtained. After standard preprocessing, segmentation and registration techniques, three measures of cortical folding, the depth difference index (DDI), coordinate distance index (CDI) and gyrification index (GI)), were calculated for the affected and unaffected hemispheres of each subject as well as a healthy control subject set.

Results: Of the three metrics, CDI, DDI and GI, used for cortical folding assessment, none demonstrated significant differences between the participants and previously studied healthy adults. There was a significant negative correlation between the DDI ratio between affected and unaffected hemispheres and AVM volume (correlation coefficient = -0.74, = 0.04).

Conclusion: This study is the first to quantitatively assess human brain cortical folding in the presence of intracranial AVMs and no significant differences between AVM-affected versus unaffected hemispheres were found in a small dataset. We suggest longitudinal, larger human MRI-based cortical folding studies to assess whether AVMs are congenital lesions of vascular development or , dynamic lesions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167380PMC
http://dx.doi.org/10.1186/s40809-016-0024-3DOI Listing

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