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Gravesteijn, G.; Hack, R.J.; Mulder, A.A.; Cerfontaine, M.N.; Doorn, R. van; Hegeman, I.M.; ... ; Oberstein, S.A.J.L. (2021)

NOTCH3 variant position is associated with NOTCH3 aggregation load in CADASIL vasculature

Article / Letter to editor
Aims CADASIL, the most prevalent hereditary cerebral small vessel disease, is caused by cysteine-altering NOTCH3 variants (NOTCH3(cys)) leading to vascular NOTCH3 protein aggregation. It has recently been shown that variants located in one of NOTCH3 protein epidermal growth-factor like repeat (EGFr) domains 1-6, are associated with a more severe phenotype than variants located in one of the EGFr domains 7-34. The underlying mechanism for this genotype-phenotype correlation is unknown. The aim of this study was to analyse whether NOTCH3(cys) variant position is associated with NOTCH3 protein aggregation load. Methods We quantified vascular NOTCH3 aggregation in skin biopsies (n = 25) and brain tissue (n = 7) of CADASIL patients with a NOTCH3(cys) EGFr 1-6 variant or a EGFr 7-34 variant, using NOTCH3 immunohistochemistry (NOTCH3 score) and ultrastructural analysis of granular osmiophilic material (GOM count). Disease severity was assessed by neuroimaging (lacune count and white matter...Show moreAims CADASIL, the most prevalent hereditary cerebral small vessel disease, is caused by cysteine-altering NOTCH3 variants (NOTCH3(cys)) leading to vascular NOTCH3 protein aggregation. It has recently been shown that variants located in one of NOTCH3 protein epidermal growth-factor like repeat (EGFr) domains 1-6, are associated with a more severe phenotype than variants located in one of the EGFr domains 7-34. The underlying mechanism for this genotype-phenotype correlation is unknown. The aim of this study was to analyse whether NOTCH3(cys) variant position is associated with NOTCH3 protein aggregation load. Methods We quantified vascular NOTCH3 aggregation in skin biopsies (n = 25) and brain tissue (n = 7) of CADASIL patients with a NOTCH3(cys) EGFr 1-6 variant or a EGFr 7-34 variant, using NOTCH3 immunohistochemistry (NOTCH3 score) and ultrastructural analysis of granular osmiophilic material (GOM count). Disease severity was assessed by neuroimaging (lacune count and white matter hyperintensity volume) and disability (modified Rankin scale). Results Patients with NOTCH3(cys) EGFr 7-34 variants had lower NOTCH3 scores (P = 1.3 center dot 10(-5)) and lower GOM counts (P = 8.2 center dot 10(-5)) than patients with NOTCH3(cys) EGFr 1-6 variants in skin vessels. A similar trend was observed in brain vasculature. In the EGFr 7-34 group, NOTCH3 aggregation levels were associated with lacune count (P = 0.03) and white matter hyperintensity volume (P = 0.02), but not with disability. Conclusions CADASIL patients with an EGFr 7-34 variant have significantly less vascular NOTCH3 aggregation than patients with an EGFr 1-6 variant. This may be one of the factors underlying the difference in disease severity between NOTCH3(cys) EGFr 7-34 and EGFr 1-6 variants.Show less
CADASIL
GOM deposit
NOTCH3 aggregation
NOTCH3 score
NOTCH3 variant position
All authors
Gravesteijn, G.; Hack, R.J.; Mulder, A.A.; Cerfontaine, M.N.; Doorn, R. van; Hegeman, I.M.; Jost, C.R.; Rutten, J.W.; Oberstein, S.A.J.L.
Date
2021-07-30
Journal
Neuropathology and Applied Neurobiology
Volume
48
Issue
1
DOI
doi:10.1111/nan.12751
Link
https://onlinelibrary.wiley.com/doi/10.1111/nan.12751