Dominant CST3 variants cause adult onset leukodystrophy without amyloid angiopathy
© The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For commercial re-use, please contact reprintsoup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com..
Leukodystrophies are rare genetic white matter disorders that have been regarded as mainly occurring in childhood. Recent years altered this perception, as a growing number of leukodystrophies was described to have an onset at adult ages. Still, many adult patients presenting with white matter changes remain without a specific molecular diagnosis. We describe a novel adult onset leukodystrophy in 16 patients from eight families carrying one of four different stop-gain or frameshift dominant variants in the CST3 gene. Clinical and radiological features differ markedly from the previously described Icelandic Cerebral Amyloid Angiopathy that was found in patients carrying p.Leu68Asn substitution in CST3. The clinical phenotype consists of recurrent episodes of hemiplegic migraine associated with transient unilateral focal deficits and slowly progressing motor symptoms and cognitive decline in mid-old adult ages. In addition, in some cases acute onset clinical deterioration led to a prolonged episode with reduced consciousness and even early death. Radiologically, pathognomonic changes are found at typical predilection sites involving the deep cerebral white matter sparing a periventricular and directly subcortical rim, the middle blade of corpus callosum, posterior limb of the internal capsule, middle cerebellar peduncles, cerebral peduncles, and specifically the globus pallidus. Histopathologic characterization in two autopsy cases did not reveal angiopathy, but instead micro- to macrocystic degeneration of the white matter. Astrocytes were activated at early stages and later on displayed severe degeneration and loss. In addition, despite loss of myelin, elevated numbers of partly apoptotic oligodendrocytes were observed. A structural comparison of the variants in CST3 suggests that specific truncations of Cystatin C result in an abnormal function, possibly by rendering the protein more prone to aggregation. Future studies are required to confirm the assumed effect on the protein and to determine pathophysiologic downstream events at the cellular level.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
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| Enthalten in: |
Brain : a journal of neurology - (2024) vom: 15. März |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Bergner, Caroline G [VerfasserIn] |
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| Links: |
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| Themen: |
Adulthood leukodystrophy |
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| Anmerkungen: |
Date Revised 15.03.2024 published: Print-Electronic Citation Status Publisher |
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| doi: |
10.1093/brain/awae085 |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM36979267X |
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| 100 | 1 | |a Bergner, Caroline G |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Dominant CST3 variants cause adult onset leukodystrophy without amyloid angiopathy |
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| 520 | |a © The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For commercial re-use, please contact reprintsoup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com. | ||
| 520 | |a Leukodystrophies are rare genetic white matter disorders that have been regarded as mainly occurring in childhood. Recent years altered this perception, as a growing number of leukodystrophies was described to have an onset at adult ages. Still, many adult patients presenting with white matter changes remain without a specific molecular diagnosis. We describe a novel adult onset leukodystrophy in 16 patients from eight families carrying one of four different stop-gain or frameshift dominant variants in the CST3 gene. Clinical and radiological features differ markedly from the previously described Icelandic Cerebral Amyloid Angiopathy that was found in patients carrying p.Leu68Asn substitution in CST3. The clinical phenotype consists of recurrent episodes of hemiplegic migraine associated with transient unilateral focal deficits and slowly progressing motor symptoms and cognitive decline in mid-old adult ages. In addition, in some cases acute onset clinical deterioration led to a prolonged episode with reduced consciousness and even early death. Radiologically, pathognomonic changes are found at typical predilection sites involving the deep cerebral white matter sparing a periventricular and directly subcortical rim, the middle blade of corpus callosum, posterior limb of the internal capsule, middle cerebellar peduncles, cerebral peduncles, and specifically the globus pallidus. Histopathologic characterization in two autopsy cases did not reveal angiopathy, but instead micro- to macrocystic degeneration of the white matter. Astrocytes were activated at early stages and later on displayed severe degeneration and loss. In addition, despite loss of myelin, elevated numbers of partly apoptotic oligodendrocytes were observed. A structural comparison of the variants in CST3 suggests that specific truncations of Cystatin C result in an abnormal function, possibly by rendering the protein more prone to aggregation. Future studies are required to confirm the assumed effect on the protein and to determine pathophysiologic downstream events at the cellular level | ||
| 650 | 4 | |a Journal Article | |
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| 650 | 4 | |a adulthood leukodystrophy | |
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| 650 | 4 | |a cystatin C | |
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| 700 | 1 | |a Soto-Bernardini, M Clara |e verfasserin |4 aut | |
| 700 | 1 | |a Schäfer, Lisa |e verfasserin |4 aut | |
| 700 | 1 | |a Lier, Julia |e verfasserin |4 aut | |
| 700 | 1 | |a Le Duc, Diana |e verfasserin |4 aut | |
| 700 | 1 | |a Bundalian, Linnaeus |e verfasserin |4 aut | |
| 700 | 1 | |a Schubert, Susanna |e verfasserin |4 aut | |
| 700 | 1 | |a Brenner, David |e verfasserin |4 aut | |
| 700 | 1 | |a Kreuz, Friedmar R |e verfasserin |4 aut | |
| 700 | 1 | |a Schulte, Björn |e verfasserin |4 aut | |
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| 700 | 1 | |a Köhler, Wolfgang |e verfasserin |4 aut | |
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| 700 | 1 | |a Abou Jamra, Rami |e verfasserin |4 aut | |
| 700 | 1 | |a van der Knaap, Marjo S |e verfasserin |4 aut | |
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