PROJECT SUMMARY
Chiari Malformation type 1 (CM1) is a pathology characterized by structural defects in the cerebellum and a vast
associated symptomatology which can include recurrent headaches, muscle weakness, sleep disorders and, in
the most extreme cases, even paralysis. So far, diagnosis is based on an assessment of the patient's
neurological history combined with an MRI or CT examination. However, the lack of a uniform and clear
symptomatology among patients is so pronounced that an estimated 3.2 million of the patients affected do not
show symptoms significant enough to lead to a diagnosis. Increasing diagnostic accuracy would therefore be of
crucial importance, given that early diagnosis of Chiari malformation and subsequent surgical treatment can lead
to highly improved clinical outcomes. One overlooked element that is thought of as a prime candidate for
diagnosing obstructive brain disorders such as Chiari Malformation is brain motion. As the heart contracts and
relaxes during the cardiac cycle, periodic variations in arterial blood pressure are transmitted along the
vasculature, resulting in relatively localized motions and deformations of the brain, which are very subtle and
difficult to see and quantify on traditional cine MRI images. Such motions, however, are expected to follow
different spatial and temporal patterns in patients suffering from obstructive brain malformations. We have
recently developed a novel method called amplified Magnetic Resonance Imaging (aMRI), which uses a
video magnification algorithm to amplify the subtle spatial variations in cardiac-gated brain MRI scans. This
approach reveals deformations of the brain parenchyma, and displacements of arteries and CSF due to cardiac
pulsatility. We hypothesize that the anatomy of CM1 patients causes an increased cerebellar, spinal cord, and
pons motion which cannot be reliably captured with standard imaging methods but can be assessed with our
aMRI technique. To test this hypothesis, we propose to extend our aMRI method to to capture and quantitatively
track 3D brain motion during the cardiac cycle. We will first validate the 3D-aMRI method with computational
phantom models, consisting of deformable solids of varying properties. In parallel, we will test the 3D-aMRI
method in a healthy adult population and obtain age and gender specific normal ranges of brain motion in
different regions of the brain. Finally, the potential diagnostic value of aMRI will be tested in patients with CM1,
where we will compare the aMRI-derived CM1 brain motion data against those of healthy volunteers. aMRI has
the potential for widespread clinical use and significant impact since it can amplify and characterize small, often
barely perceptible motion and can visualize the biomechanical response of tissues using the heartbeat as an
endogenous mechanical driver. Further development of this method could enable earlier diagnosis and
intervention of brain pathologies other than CM1 such as traumatic brain injury, hydrocephalus, Alzheimer's
disease, and other neurodegenerative diseases; may remove the need for unnecessary invasive brain surgery;
and may provide a reliable method to monitor progress following therapeutic intervention.
