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[Microangiopathy CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)
Insights
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a generalized small vessel disease. Early diagnosis through genetic testing and biopsy is crucial to avoid misdiagnosis of white matter changes.
Area of Science:
- Neurology
- Genetics
- Vascular Biology
Background:
- Small cerebral vessel diseases are increasingly diagnosed via neuroimaging.
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a prominent example, presenting with stroke, dementia, and migraines.
- Symptoms often appear in mid-adulthood, independent of typical vascular risk factors.
Purpose of the Study:
- To highlight the diagnostic challenges and importance of recognizing CADASIL.
- To differentiate CADASIL from other white matter lesions detected by neuroimaging.
Main Methods:
- Genetic testing for NOTCH3 gene mutations.
- Microscopic examination of blood vessels from skin or skin-muscle biopsy.
- Analysis of neuroimaging findings, including white matter hyperintensities and ischemic foci.
Main Results:
- CADASIL is caused by NOTCH3 gene mutations, leading to small artery degeneration.
- Neuroimaging reveals disseminated white matter changes, sometimes asymptomatic or misdiagnosed.
- Diagnosis relies on genetic and histopathological evidence.
Conclusions:
- Increased neuroimaging detection of white matter changes necessitates awareness of CADASIL.
- Knowledge of CADASIL and other microangiopathies is essential for accurate diagnosis.
- Avoiding diagnostic errors in small vessel diseases is critical for patient management.
Abstract:
Small cerebral vessel disease is a relatively new group of angiopathies diagnosed more frequently thanks to common availability of neuroimaging. The most frequent and the most known disease which belongs to this group is CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). Despite the name, it is a generalized small vessel disease, in which symptoms of brain damage dominate. The disease manifests as recurrent ischemic strokes, progressing dementia, migraine and mental disorders – symptoms which usually appear in 4-5 decade of life in patients without typical risk factors for vascular disease. In neuroimaging hyperintense changes and small ischemic foci disseminated in the cerebral white matter are seen. CADASIL is caused by mutations in the NOTCH 3 gene, which lead to the degeneration and loss of smooth muscle cells in small arteries. The disease is diagnosed on the basis of the result of the genetic test and microscopic examination of blood vessels in the material derived from a skin or skinmuscle biopsy. Since more and more frequently new techniques of neuroimaging reveal changes in the cerebral white matter - often asymptomatic or/ and mistakenly diagnosed as demyelinating lesions - only knowledge about CADASIL and other microangiopathies allows to avoid diagnostic errors.
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