| Literature DB >> 33716917 |
Cindy W Yoon1, Young-Eun Kim2, Hee Jin Kim3, Chang-Seok Ki4, Hyejoo Lee3, Joung-Ho Rha1, Duk L Na3, Sang Won Seo3.
Abstract
No study yet has compared the longitudinal course and prognosis between subcortical vascular cognitive impairment patients with and without genetic component. In this study, we compared the longitudinal changes in cerebral small vessel disease markers and cognitive function between subcortical vascular mild cognitive impairment (svMCI) patients with and without NOTCH3 variant [NOTCH3(+) svMCI vs. NOTCH3(-) svMCI]. We prospectively recruited patients with svMCI and screened for NOTCH3 variants by sequence analysis for mutational hotspots in the NOTCH3 gene. Patients were annually followed-up for 5 years through clinical interviews, neuropsychological tests, and brain magnetic resonance imaging. Among 63 svMCI patients, 9 (14.3%) had either known mutations or possible pathogenic variants. The linear mixed effect models showed that the NOTCH3(+) svMCI group had much greater increases in the lacune and cerebral microbleed counts than the NOTCH3(-) svMCI group. However, there were no significant differences between the two groups regarding dementia conversion rate and neuropsychological score changes over 5 years.Entities:
Keywords: CADASIL; NOTCH3; cerebral microbleed; lacune; subcortical vascular cognitive impairment
Year: 2021 PMID: 33716917 PMCID: PMC7947323 DOI: 10.3389/fneur.2021.586366
Source DB: PubMed Journal: Front Neurol ISSN: 1664-2295 Impact factor: 4.003