Association of <i>NOTCH3</i> Variant Risk Category With 2-Year Clinical and Radiologic Small Vessel Disease Progression in Patients With CADASIL.

Abstract

Pathogenic variants in <i>NOTCH3</i> are the main cause of hereditary cerebral small vessel disease (SVD). SVD-associated <i>NOTCH3</i> variants have recently been categorized into high risk (HR), moderate risk (MR), or low risk (LR) for developing early-onset severe SVD. The most severe NOTCH3-associated SVD phenotype is also known as cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). We aimed to investigate whether <i>NOTCH3</i> variant risk category is associated with 2-year progression rate of SVD clinical and neuroimaging outcomes in CADASIL. A single-center prospective 2-year follow-up study was performed of patients with CADASIL. Clinical outcomes were incident stroke, disability (modified Rankin Scale), and executive function (Trail Making Test B given A <i>t</i>-scores). Neuroimaging outcomes were mean skeletonized mean diffusivity (MSMD), normalized white matter hyperintensity volume (nWMHv), normalized lacune volume (nLV), and brain parenchymal fraction (BPF). Cox regression and mixed-effect models, adjusted for age, sex, and cardiovascular risk factors, were used to study 2-year changes in outcomes and differences in disease progression between patients with HR-<i>NOTCH3</i> and MR-<i>NOTCH3</i> variants. One hundred sixty-two patients with HR (n = 90), MR (n = 67), and LR (n = 5) <i>NOTCH3</i> variants were included. For the entire cohort, there was 2-year mean progression for MSMD (β = 0.20, 95% CI 0.17-0.23, <i>p</i> = 7.0 × 10^-24), nLV (β = 0.13, 95% CI 0.080-0.19, <i>p</i> = 2.1 × 10^-6), nWMHv (β = 0.092, 95% CI 0.075-0.11, <i>p</i> = 8.8 × 10^-20), and BPF (β = -0.22, 95% CI -0.26 to -0.19, <i>p</i> = 3.2 × 10^-22), as well as an increase in disability (<i>p</i> = 0.002) and decline of executive function (β = -0.15, 95% CI -0.30 to -3.4 × 10^-5, <i>p</i> = 0.05). The HR-NOTCH3 group had a higher probability of 2-year incident stroke (hazard ratio 4.3, 95% CI 1.4-13.5, <i>p</i> = 0.011), and a higher increase in MSMD (β = 0.074, 95% CI 0.013-0.14, <i>p</i> = 0.017) and nLV (β = 0.14, 95% CI 0.034-0.24, <i>p</i> = 0.0089) than the MR-NOTCH3 group. Subgroup analyses showed significant 2-year progression of MSMD in young (n = 17, β = 0.014, 95% CI 0.0093-0.019, <i>p</i> = 1.4 × 10^-5) and premanifest (n = 24, β = 0.012, 95% CI 0.0082-0.016, <i>p</i> = 1.1 × 10^-6) individuals. In a trial-sensitive time span of 2 years, we found that patients with HR-<i>NOTCH3</i> variants have a significantly faster progression of major clinical and neuroimaging outcomes, compared with patients with MR-<i>NOTCH3</i> variants. This has important implications for clinical trial design and disease prediction and monitoring in the clinic. Moreover, we show that MSMD is a promising outcome measure for trials enrolling premanifest individuals.