TY - JOUR T1 - Prominent juxtacortical white matter lesion hallmarks <em>NOTCH3</em>-related intracerebral haemorrhage JF - Stroke and Vascular Neurology JO - Stroke Vasc Neurol SP - 38 LP - 46 DO - 10.1136/svn-2021-001020 VL - 7 IS - 1 AU - Chih-Hao Chen AU - Hao-Chia Hsu AU - Yu-Wen Cheng AU - Ya-Fang Chen AU - Sung-Chun Tang AU - Jiann-Shing Jeng Y1 - 2022/02/01 UR - http://svn.bmj.com/content/7/1/38.abstract N2 - Background and purpose NOTCH3 p.R544C mutation accounts for 5% of spontaneous intracerebral haemorrhage (ICH) in East Asian patients. We investigated whether certain CT features are associated with NOTCH3-related ICH.Methods Patients with spontaneous ICH from a prospective stroke registry were screened for NOTCH3 p.R544C mutation. The neuroimaging features on the initial non-contrast CT scans selected to predict NOTCH3 p.R544C mutation, including burden of white matter lesion (WML), degree of brain atrophy, number of lacunes, prominent juxtacortical WML and prominent lobar lacunes, were analysed by neuroradiologists blinded to the mutation status.Results Of 299 patients with spontaneous ICH (mean age, 61 years; male, 68%; ICH volumes, 14.1±17.8 mL), 13 patients (4.3%) carried NOTCH3 p.R544C mutation. The clinical features, haematoma size and location were similar between NOTCH3 p.R544C mutation carriers and non-carriers. The CT scan revealed that patients with NOTCH3 p.R544C mutation had more severe WML and more frequently had prominent juxtacortical WML (69.2% vs 17.8%, p&lt;0.001), and the effects were not driven by ageing as seen in patients without mutation. Prominent juxtacortical WML (area under receiver operating characteristic curve=0.76) outperformed the total WML score and prominent lobar lacunes and significantly predicted NOTCH3 p.R544C mutation in a multivariable-adjusted model (OR, 20.9; 95% CI 4.94 to 88.6).Conclusion In patients with spontaneous ICH, the severity and topographic distribution of WML can help in identifying potential NOTCH3 mutation-related ICH.Data are available upon reasonable request. ER -