An approach to study population differences in cerebral vasculature is proposed. This is done by 1) extending the concept of encoding cerebral blood vessel networks as spatial graphs and 2) quantifying graph similarity in a kernel-based discriminant classifier setup. We argue that augmenting graph vertices with information about their proximity to selected brain structures adds discriminative information and consequently leads to a more expressive encoding. Using graphkernels then allows us to quantify graph similarity in a principled way. To demonstrate our approach, we assess the hypothesis that gender differences manifest as variations in the architecture of cerebral blood vessels, an observation that previously had only been tested and confirmed for the Circle of Willis. Our results strongly support this hypothesis, i.e, we can demonstrate non-trivial, statistically significant deviations from random gender classification in a cross-validation setup on 40 healthy patients.
MotivationThe human circulatory system, with blood vessels transporting nutrients and waste from one location to another, appears to lend itself naturally to a graph-based representation. A question that immediately arises is whether we can leverage that graph structure to study population differences that manifest as topological changes. In this work, we focus on the cerebrovascular network. Several studies indicate an association between selected mental diseases and irregular cerebral blood vessel topology. Preliminary to our study of such associations, herein we assess the hypothesis that gender-associated differences exist in the architecture of cerebral vessel networks. A recent study [2] demonstrates gender-related differences in local geometry, e.g., radius; however, evidence in support of general architectural differences across genders has only been reported for the Circle of Willis [7]. Beyond serving as a preliminary study, identifying gender-related differences could also help to explain why certain vascular pathologies, such as aneurysms, have a higher incidence rate in women than in men [7].Although it is straight-forward to compare individuals or populations in terms of local vessel network properties, e.g., tortuosity measures or radius estimates [2], a general framework for comparing and characterizing vascular topology at a global scale does not exist. Furthermore, vascular graph comparisons are typically performed using summary statistics in order to circumvent computational complexity issues inherent to many graph similarity metrics. Additionally, while progress has been made in representing cerebral vasculature as graphs [4] and even as graphs that span intracranial space [1], no prior work, to our knowledge, has augmented vascular graph encodings with brain structure information, e.g., hippocampus, thalamic nuclei and so forth.
NIH Public AccessOur contribution is two-fold: First, we augment the spatial graph representation of [1] with brain structure information at each vertex to enhance expressiveness. Secon...