Clinical and imaging features of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and cysteine-sparing NOTCH3 mutations

PLoS One. 2020 Jun 18;15(6):e0234797. doi: 10.1371/journal.pone.0234797. eCollection 2020.

Abstract

Background: Characteristics of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and cysteine-sparing NOTCH3 mutations are relatively unknown. This study compared clinical and imaging characteristics between patients with CADASIL and cysteine-sparing NOTCH3 mutations and those with CADASIL and cysteine-involving NOTCH3 mutations.

Methods: We retrospectively reviewed medical records of patients with CADASIL admitted to the Asan Medical Center between September 1999 and September 2017. We compared clinical and brain magnetic resonance imaging (MRI) characteristics based on the presence or absence of cysteine-involving NOTCH3 gene mutations. We compared white matter change frequencies and grades in specific spatial regions between the groups according to age-related white matter change (ARWMC) scores. We evaluated the presence, number, and anatomical distributions of cerebral microbleeds according to the microbleed anatomical rating scale.

Results: We reviewed data from 79 patients (55 cysteine-involving, 24 cysteine-sparing NOTCH3 mutations). Clinical symptoms and signs did not differ significantly between the groups. The white matter change frequency and ARWMC scores (adjusted for age and stroke risk factors) in the anterior temporal lobes were lower in cysteine-sparing patients than in cysteine-involving patients. Frequencies and grades of the other brain region's white matter changes and cerebral microbleeds were similar between the groups.

Conclusions: Patients with CADASIL and cysteine-sparing NOTCH3 mutations showed less involvement of the anterior temporal lobes in brain MRI than those with CADASIL and cysteine-involving NOTCH3 mutations, although both groups showed similar clinical characteristics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Brain / diagnostic imaging
  • CADASIL / complications
  • CADASIL / genetics
  • CADASIL / pathology*
  • Cysteine / genetics*
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Mutation, Missense
  • Polymorphism, Single Nucleotide
  • Receptor, Notch3 / genetics*
  • Retrospective Studies
  • Risk Factors
  • Sex Factors
  • Stroke / etiology
  • Temporal Lobe / metabolism
  • Temporal Lobe / pathology

Substances

  • NOTCH3 protein, human
  • Receptor, Notch3
  • Cysteine

Grants and funding

This study was supported by grants from the Ministry of Science and ICT, South Korea (NRF-2018R1C1B6008884, NRF-2018M3A9E8066249) and Ministry of Health & Welfare, South Korea (HI18C2383). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.