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DIAGNOSING CADASIL

Magnetic Resonance Imaging (MRI)
Skin Biopsy
Genetic Testing

Magnetic Resonance Imaging (MRI)
Magnetic resonance imaging (MRI) is a method for making detailed images of the brain. In CADASIL, the MRI shows changes in the deep regions of the brain, particularly in the white matter. The white matter lies below the outer layers of the brain (the cortex or gray matter) and forms the connections among brain areas so that they work in a unified way. The blood supply to the white matter is provided by small blood vessels which make it especially vulnerable to CADASIL. Other disorders, such as multiple sclerosis, cause white matter changes that look similar on MRI, so CADASIL cannot be diagnosed from MRI alone. However, CADASIL might be suspected if the white matter changes are concentrated in certain brain areas (frontal lobes and/or temporal lobes).

MRI uses magnetic fields and radio waves to make its images and involves no x-rays or other forms of radiation. It is a safe and reliable test method with few health risks. However, it is not safe for people with pacemakers or certain other implanted medical devices or for people who may have small metal fragments or dust in their eyes. It is often helpful to have MRI scans repeated every few years to look for progression of the disease.

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Skin Biopsy
CADASIL causes characteristic changes in the blood vessels in almost all regions of the body. These vascular changes may be crucial in making a diagnosis but can only be seen under a powerful electron microscope. Since the blood vessels of the brain cannot be analyzed directly, microscopic examination is performed on the more readily accessible blood vessels in the skin. Under local anesthesia, a small piece of skin is taken from the upper arm or thigh and the resulting wound is closed with one or two sutures. The tissue sample is then sent to a facility that has an electron microscope. Under magnification, the changes typical of CADASIL can be seen in the vascular walls. One of these characteristics is called granular osmiophilic material, or GOM, which is thought to be made of clumps of excess protein. If such changes can be detected, the CADASIL diagnosis can be regarded as confirmed. The key limitation to skin biopsy is that there is a small chance that the disease could be missed if the skin specimen does not happen to contain any diseased blood vessels.

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Genetic Testing
CADASIL is caused by a mutation (mistake) in the structure of the NOTCH3 gene. It turns out, however, that the mutation can take different forms, and that not all people with CADASIL have the same precise mutation. Within a family, all those affected with the disease will have the same NOTCH3 mutation. Detection of a mutation is considered 100% proof of the existence of the disease. Since the NOTCH3 gene is very large, the search for mutations can be tedious, complex, and expensive. For this reason, many diagnostic laboratories test only the locations on the gene most likely to contain the CADASIL mutation. This makes the genetic test somewhat easier and less expensive, but some mutations may be missed. Therefore, in individual cases, it may be necessary to search the entire gene for a mutation.

Only a small amount of blood, which can be taken from a vein, is needed for genetic testing. In the United States, there is only one commercial laboratory that offers genetic testing for CADASIL. You and/or your physician can find more detailed information about the lab by visiting www.athenadiagnostics.com.

A decision to test for a genetic disorder is an important and sometimes difficult one. Learning that you have a genetic disorder can be psychologically distressing and can have an impact on health insurance. Some people with symptoms may want to know – others may not. The decision to have the test can be even more difficult for healthy members of a CADASIL family. You should discuss your concerns with your doctor before having the test. Genetic counselors have special expertise in working with people with genetic disorders and may provide helpful advice and guidance in making your decisions.


 

Memory and Aging Program
Butler Hospital
345 Blackstone Blvd.
Providence, RI 02906


401-455-6403
Fax: 401-455-6405
memorydisorder.org

 

 

Website: Thea Brennan-Krohn
email: theabk@yahoo.com