» Articles » PMID: 37546181

A Multiphysics Model to Predict Periventricular White Matter Hyperintensity Growth During Healthy Brain Aging

Overview
Journal Brain Multiphys
Specialty Neurology
Date 2023 Aug 7
PMID 37546181
Authors
Affiliations
Soon will be listed here.
Abstract

Periventricular white matter hyperintensities (WMH) are a common finding in medical images of the aging brain and are associated with white matter damage resulting from cerebral small vessel disease, white matter inflammation, and a degeneration of the lateral ventricular wall. Despite extensive work, the etiology of periventricular WMHs remains unclear. We pose that there is a strong coupling between age-related ventricular expansion and the degeneration of the ventricular wall which leads to a dysregulated fluid exchange across this brain-fluid barrier. Here, we present a multiphysics model that couples cerebral atrophy-driven ventricular wall loading with periventricular WMH formation and progression. We use patient data to create eight 2D finite element models and demonstrate the predictive capabilities of our damage model. Our simulations show that we accurately capture the spatiotemporal features of periventricular WMH growth. For one, we observe that damage appears first in both the anterior and posterior horns and then spreads into deeper white matter tissue. For the other, we note that it takes up to 12 years before periventricular WMHs first appear and derive an average annualized periventricular WMH damage growth rate of 15.2 ± 12.7 mm/year across our models. A sensitivity analysis demonstrated that our model parameters provide sufficient sensitivity to rationalize subject-specific differences with respect to onset time and damage growth. Moreover, we show that the septum pellucidum, a membrane that separates the left and right lateral ventricles, delays the onset of periventricular WMHs at first, but leads to a higher WMH load in the long-term.

Citing Articles

Single-nucleus RNA sequencing of human periventricular white matter in vascular dementia.

Diaz-Perez S, DeLong J, Rivier C, Lee C, Askenase M, Zhu B bioRxiv. 2024; .

PMID: 39713290 PMC: 11661092. DOI: 10.1101/2024.12.06.627202.

References
1.
Munoz Maniega S, Meijboom R, Chappell F, Valdes Hernandez M, Starr J, Bastin M . Spatial Gradient of Microstructural Changes in Normal-Appearing White Matter in Tracts Affected by White Matter Hyperintensities in Older Age. Front Neurol. 2019; 10:784. PMC: 6673707. DOI: 10.3389/fneur.2019.00784. View

2.
Moeendarbary E, Weber I, Sheridan G, Koser D, Soleman S, Haenzi B . The soft mechanical signature of glial scars in the central nervous system. Nat Commun. 2017; 8:14787. PMC: 5364386. DOI: 10.1038/ncomms14787. View

3.
Alber J, Alladi S, Bae H, Barton D, Beckett L, Bell J . White matter hyperintensities in vascular contributions to cognitive impairment and dementia (VCID): Knowledge gaps and opportunities. Alzheimers Dement (N Y). 2019; 5:107-117. PMC: 6461571. DOI: 10.1016/j.trci.2019.02.001. View

4.
De Groot M, Verhaaren B, de Boer R, Klein S, Hofman A, van der Lugt A . Changes in normal-appearing white matter precede development of white matter lesions. Stroke. 2013; 44(4):1037-42. DOI: 10.1161/STROKEAHA.112.680223. View

5.
Nyquist P, Bilgel M, Gottesman R, Yanek L, Moy T, Becker L . Age differences in periventricular and deep white matter lesions. Neurobiol Aging. 2015; 36(4):1653-1658. PMC: 4380525. DOI: 10.1016/j.neurobiolaging.2015.01.005. View