Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is a systemic genetic disorder affecting the cerebral small vessels, spine and hair follicles.
It should not be confused with its autosomal dominant counterpart, CADASIL. Autosomal recessive inherited diseases are usually more severe than autosomal dominant genetic disorders and CARASIL is no exception to this general rule.
CARASIL is a very rare disease with roughly 50 cases reported, mostly from inside Asia until recently, when the disease was also documented in a European family 1,2.
The true prevalence is unknown, and CARASIL is probably under-recognized since no founder haplotype has been identified, and the recently encountered European disease carriers support the theory of a wider distribution 1,2,4.
Typically patients present in young adulthood (twenties and thirties) with:
- premature alopecia (as early as teenage years; most common initial symptom)
- relapsing ischemic stroke-like episodes (typically in the 3rd decade) with gradually progressive vascular dementia
- not infrequently, symptomatic epilepsy (secondary to infarctions)
- relapsing severe low back pain and deforming spondylosis (present in roughly 80% of patients, notably early onset)
Shows cerebral arteriosclerotic changes, most intense in white matter and basal ganglia.
Intense arteriosclerosis is seen predominantly in the small penetrating arteries. Aids in differentiation from other entities are the lack of amyloid deposition and absence of the granular appearance characteristics of CADASIL.
Extraneural changes are less severe and although they include the cutis, skin biopsies are not helpful in establishing the diagnosis.
CARASIL is, after CADASIL, the second known genetic form of ischemic CNS disease caused by non-hypertensive microangiopathy in which the causative gene defect has been identified.
Mutations in HTRA1 gene on chromosome 10q (10q25.3-q26.2) are responsible for CARASIL. It codes for the ubiquitous HTRA1 enzyme, which regulates signaling by proteins in the transforming growth factor-beta (TGF-β) family, which again is essential for multiple critical cell functions including angiogenesis. The pivotal role of TGF-β in CARASIL is hypothesised, but not totally clarified.
- diffuse homogeneous leukoaraiosis
- ex-vacuo ventriculomegaly, predominantly affecting the lateral ventricles
- in ~25% of patients, small hypodense areas may be seen located in the pontine base (possibly presenting Wallerian degeneration of the corticospinal tract)
- absence of lacunes
- diffuse leukoencephalopathy
- multiple lacunar infarctions in the deep nuclei, most often
Changes may be appreciated by plain radiograph, CT or MRI, and are those of:
- deforming spondylosis with or without intervertebral space narrowing, located in the cervical and/or thoracolumbar spine
- typical location upper lumbar regions (which is in some contradiction to the sporadic spondylosis)
- elbow or knee osteoarthritis
Treatment and prognosis
As there are no causative treatment options, treatment focuses on the prevention of ischemic strokes. Interestingly, treatment with known antiplatelet agents and anticoagulant lacks evidence.
Another goal of management is to prevent the onset of dementia symptoms. Genetic counseling is also an important part of primary care.
History and etymology
It was first described by S Nemoto, a Japanese physician, in 1960 where it was initially described as part of the Binswanger spectrum 5,6. Nemoto went on to publish a seminal case series with S Maeda et al. in 1976 7. The disease is sometimes known as Nemoto disease or Maeda syndrome in recognition of their contributions.
- sporadic cerebral small vessel diseases (SVD)
- encephalitis subcorticalis chronica progressiva (Binswanger disease)
- primary angiitis of the CNS
progressive multiple sclerosis
- involvement of subcortical U-fibers is less pronounced in CARASIL
- symptom onset in CARASIL is 10-15 years earlier
- migraine and depression are not seen in CARASIL
- early white matter changes in CARASIL are homogenous rather than punctuate as seen in CADASIL
- 1. Fukutake T. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification. J Stroke Cerebrovasc Dis. 2011;20 (2): 85-93. doi:10.1016/j.jstrokecerebrovasdis.2010.11.008 - Pubmed citation
- 2. Bianchi S, Di Palma C, Gallus GN et-al. Two novel HTRA1 mutations in a European CARASIL patient. Neurology. 2014;82 (10): 898-900. doi:10.1212/WNL.0000000000000202 - Pubmed citation
- 3. Arima K, Yanagawa S, Ito N et-al. Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome). Neuropathology. 2004;23 (4): 327-34. Pubmed citation
- 4. Osamu O, Hiroaku N et-al. CARASIL. Gene Reviews. Last update Sep 11, 2014
- 5. Nemoto S. Einige beitrage zur Encephalitis subcorticalis chronica progressiva (Binswanger) [A note on chronic progressive subcortical encephalitis (Binswanger)]. In: Festschrift zum Rucktritt von Prof. Toshimi Ishibashi [Memorial for the retirement of Prof. Toshimi Ishibashi]. Sendai, Japan: Tohoku University, 1966:51-67
- 6. Fukutake T. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification. (2011) Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 20 (2): 85-93. doi:10.1016/j.jstrokecerebrovasdis.2010.11.008 - Pubmed
- 7. Maeda S, Nakayama H, Isaka K, Aihara Y, Nemoto S. Familial unusual encephalopathy of Binswanger's type without hypertension. (1976) Folia psychiatrica et neurologica japonica. 30 (2): 165-77. Pubmed
Related Radiopaedia articles
White matter disorders
- white matter
- normal myelination
white matter disorders
- anti-MOG associated encephalomyelitis
- Guillain-Barre Syndrome (GBS)
- chronic inflammatory demyelinating polyneuropathy (CIDP)
- transverse myelitis
- tumefactive demyelinating lesions
- acute disseminated encephalomyelitis (ADEM) and acute hemorrhagic encephalomyelitis (AHEM)
- neuromyelitis optica (NMO) (Devic disease)
multiple sclerosis (MS)
McDonald diagnostic criteria for MS (current 2017 revision)
- previous 2016 MAGNIMS consensus
- McDonald diagnostic criteria for MS (current 2017 revision)
- radiologically isolated syndrome (RIS)
- clinically isolated syndrome (CIS)
- early-onset neuronal degenerative disorders
- GM1 & GM2 gangliosidoses (e.g. Tay Sachs disease)
- giant axonal neuropathy
- hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC)
- hypomyelination with congenital cataract
- leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
- hypomyelination with brainstem and spinal cord involvement and leg spasticity
- Pol III-related leukodystrophies
- early-onset neuronal degenerative disorders
- myelin disorders
- myelin vacuolisation
- adult-onset autosomal dominant leukodystrophy
- cerebrotendinous xanthomathosis
- cystic leukoencephalopathy without megalencephaly
- L-2-hydroxyglutaric aciduria
- lysosomal storage diseases
- peroxisomal disorders
- Sjögren-Larsson syndrome