Cavernous angioma risk factors: Difference between revisions
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(/* Genetic Testing and Counseling Recommendations: {{cite journal| author=Akers A, Al-Shahi Salman R, A Awad I, Dahlem K, Flemming K, Hart B | display-authors=etal| title=Synopsis of Guidelines for the Clinical Management of Cerebral Cavernous Malformations: Consensus Recommendations Based on Systematic Literature Review by the Angioma Alliance Scientific Advisory Board Clinical Experts Panel. | journal=Neurosurgery | year= 2017 | volume= 80 | issue= 5 | pages= 665-680 | pmid=28387823 | doi=1...) |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Edzel Lorraine Co, D.M.D., M.D.
Overview
Family history increases the risk of having cavernous angioma. Genetic testing is recommended for the pathogenic variants of cavernous angioma (KRIT1, MGC4607, and PDCD10'').
Risk Factors
- There are three known genetic loci for cavernous angioma. These are CCM1, CCM2, and CCM3.
- CCM1 encodes for krev interaction trapped 1 (KRIT1) which binds to integrin cytoplasmic domain associated protein alpha (ICAP1-alpha), a beta-1 integrin associated protein. [1]
- CCM2 encodes for MGC4607. [1] The exact nature of CCM2 is still unclear. However, it been proven that there is a macromolecularcomplex formed by CCM1 and CCM2 proteins and ICAP1 alpha inside the cell. Also, CCM2 protein can serve as a scaffolding protein for enzymes like MAP kinases which is essential in p38 activation responsible for regulation of osmotic stress including MEKK3 and MKK3. It also attaches to Rac and actin. Because of these, CCM2 protein is oftentimes called osmo-sensing scaffold (OSM) for MEKK3.
- CCM3 gene is the most recently identified CCM gene. It was originally known as programmed cell death 10 (PDCD10) , which was thought to be responsible for upregulation of apoptosis (cell death) in TF-1, a human myeloid cell line. As of now, the specific role of the PDCD10 protein and its association with CCM3 gene is not yet established.[1]
- The mutations in CCM1, CCM2, and CCM3 genes account for almost 70 to 80 percent of all cases of cerebral cavernous malformations. The rest has yet to be identified.
Genetic Testing
Genetic Testing and Counseling Recommendations: [1]
- A three-generation family history should be obtained at the time of diagnosis. More focus should be given to symptoms such as headache, stroke, any abnormal magnetic resonance (MRI) scan findings, or other neurological findings.
- In the setting of cavernous angioma without an association of developmental venous anomalies, brain radiation history, or a family history of cavernous angioma, CCM 1-3 genes by Sanger or NextGen sequencing followed by duplication/ deletion analysis should be considered.
- Counseling the patient and whole family about autosomal dominant inheritance should be done when there is a positive proband.
References
- ↑ 1.0 1.1 1.2 1.3 Akers A, Al-Shahi Salman R, A Awad I, Dahlem K, Flemming K, Hart B; et al. (2017). "Synopsis of Guidelines for the Clinical Management of Cerebral Cavernous Malformations: Consensus Recommendations Based on Systematic Literature Review by the Angioma Alliance Scientific Advisory Board Clinical Experts Panel". Neurosurgery. 80 (5): 665–680. doi:10.1093/neuros/nyx091. PMC 5808153. PMID 28387823.