Multiple sclerosis: blood flow insufficiency not found to contribute to development of disease


Two important new studies challenge the controversial hypothesis that venous congestion, chronic cerebrospinal venous insufficiency ( CCSVI ), contributes to the development of multiple sclerosis. This theory has resulted in many multiple sclerosis patients receiving experimental endovascular angioplasty, a treatment for multiple sclerosis unproven by clinical trials.

For nearly 150 years it has been known that focal multiple sclerosis lesions tend to develop around cerebral veins that are thought to the portal by which inflammatory cells targeting myelin enter the brain. However, a 2009 study by Zamboni et al offered an alternative theory suggesting that chronically impaired venous drainage from the central nervous system - a term that he labeled Chronic Cerebrospinal Venous Insufficiency or CCSVI - leads to multiple sclerosis development.
Zamboni et al. also claimed that endovascular angioplasty was markedly effective in multiple sclerosis patients.

According Stephen L Hauser, at the University of California, San Francisco, and editor-in-chief of the Annals of Neurology, these two papers should add a note of caution for multiple sclerosis patients and physicians who are contemplating interventions for possible venous abnormalities based on the findings of Zamboni. At this time, the theory must be considered unconfirmed and unproven. Such interventions carry risk, and several people have already been harmed by the inappropriate application of venous angioplasty and stenting for multiple sclerosis. A previously published review of the evidence in the Annals by Khan et al noted that treatment procedures, based upon these findings, have included placing stents in the jugular veins of multiple sclerosis patients which led to serious injury in some cases.

Florian Doepp and colleagues in Germany performed an extended extra- and trans-cranial color-coded sonography study on 56 multiple sclerosis patients ( 36 female; 20 male ) and 20 control subjects ( 12 female; 8 male ). The analysis included extra-cranial venous blood volume flow ( BVF ), internal jugular vein ( IJV ) flow analysis during Valsalva maneuver, as well as tests included in the CCSVI criteria.

Results showed that blood flow direction was normal in all participants, excluding one subject with relapsing-remitting multiple sclerosis. Furthermore, the research team noted that blood volume flow in both groups were equal in the supine body position. In summary, the researchers determined that none of the study participants fulfilled more than one criterion for CCSVI.
Researchers did not find supporting evidence that cerebral venous congestion plays a significant role in the development of multiple sclerosis.

A second study by researchers at Umeå University in Sweden also concluded that CCSVI does not contribute to the development of multiple sclerosis. The Swedish research team led by Peter Sundström, tested the vital component of the CCSVI theory - the obstructed IJV flow- in 21 multiple sclerosis patients and 20 healthy controls using magnetic resonance imaging with phase contrast ( PC-MRI ).
Using PC-MRI, investigators were not able to reproduce the findings by Zamboni et al which suggest CCSVI contributes to the development of multiple sclerosis. The researchers found no significant differences between the multiple sclerosis group and control group relating to total IJV blood flow.

Multiple sclerosis is an inflammatory disease of the central nervous system in which lesions ( plaques ) form in the white matter of the brain and destroy the myelin sheath around nerve fibers. Initial symptoms of multiple sclerosis - typically blurred or double vision, muscle weakness, sensory changes, or difficulty with balance -usually appear between the ages of 20 and 40. The course can be relapsing-remitting or relentlessly progressive, and if untreated results in permanent neurologic disability in most affected individuals.
Multiple sclerosis affects 2.5 million individuals worldwide, making it one of the most common neurological disorders and causes of disability in young adults.

Source: Annals of Neurology, 2010

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