4.7 Article

Cerebrovascular Disease Progression in Patients With ACTA2 Arg179 Pathogenic Variants

Journal

NEUROLOGY
Volume 96, Issue 4, Pages E538-E552

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000011210

Keywords

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Funding

  1. NIH [R01 HL109942]
  2. American Heart Association Merit Award
  3. Temerty Family Foundation
  4. NINDS [K08 NS094683-01]

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Patients with ACTA2 Arg179 pathogenic variants exhibit characteristic patterns of acute white matter ischemic injury and progressive internal carotid artery stenosis. Longitudinal analysis shows stable white matter hyperintensities but increasing cystic-like lesions in patients older than 1.2 years. 80% of patients experience progressive narrowing of the terminal internal carotid artery, which correlates with the number of critical stenoses in cerebral arteries and arterial ischemic infarctions.
Objective To establish progression of imaging biomarkers of stroke, arterial steno-occlusive disease, and white matter injury in patients with smooth muscle dysfunction syndrome caused by mutations in the ACTA2 gene, we analyzed 113 cerebral MRI scans from a retrospective cohort of 27 patients with ACTA2 Arg179 pathogenic variants. Methods Systematic quantifications of arterial ischemic strokes and white matter lesions were performed on baseline and follow-up scans using planimetric methods. Critical stenosis and arterial vessel diameters were quantified applying manual and semiautomated methods to cerebral magnetic resonance angiograms. We then assessed correlations between arterial abnormalities and parenchymal injury. Results We found characteristic patterns of acute white matter ischemic injury and progressive internal carotid artery stenosis during infancy. Longitudinal analysis of patients older than 1.2 years showed stable white matter hyperintensities but increased number of cystic-like lesions over time. Progressive narrowing of the terminal internal carotid artery occurred in 80% of patients and correlated with the number of critical stenoses in cerebral arteries and arterial ischemic infarctions. Arterial ischemic strokes occurred in same territories affected by critical stenosis. Conclusions We found characteristic, early, and progressive cerebrovascular abnormalities in patients with ACTA2 Arg179 pathogenic variants. Our longitudinal data suggest that while steno-occlusive disease progresses over time and is associated with arterial ischemic infarctions and cystic-like white matter lesions, white matter hyperintensities can remain stable over long periods. The evaluated metrics will enable diagnosis in early infancy and be used to monitor disease progression, guide timing of stroke preventive interventions, and assess response to current and future therapies.

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