39
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      What went wrong? The flawed concept of cerebrospinal venous insufficiency

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          In 2006, Zamboni reintroduced the concept that chronic impaired venous outflow of the central nervous system is associated with multiple sclerosis (MS), coining the term of chronic cerebrospinal venous insufficiency (‘CCSVI'). The diagnosis of ‘CCSVI' is based on sonographic criteria, which he found exclusively fulfilled in MS. The concept proposes that chronic venous outflow failure is associated with venous reflux and congestion and leads to iron deposition, thereby inducing neuroinflammation and degeneration. The revival of this concept has generated major interest in media and patient groups, mainly driven by the hope that endovascular treatment of ‘CCSVI' could alleviate MS. Many investigators tried to replicate Zamboni's results with duplex sonography, magnetic resonance imaging, and catheter angiography. The data obtained here do generally not support the ‘CCSVI' concept. Moreover, there are no methodologically adequate studies to prove or disprove beneficial effects of endovascular treatment in MS. This review not only gives a comprehensive overview of the methodological flaws and pathophysiologic implausibility of the ‘CCSVI' concept, but also summarizes the multimodality diagnostic validation studies and open-label trials of endovascular treatment. In our view, there is currently no basis to diagnose or treat ‘CCSVI' in the care of MS patients, outside of the setting of scientific research.

          Related collections

          Most cited references111

          • Record: found
          • Abstract: found
          • Article: not found

          Cortical demyelination and diffuse white matter injury in multiple sclerosis.

          Focal demyelinated plaques in white matter, which are the hallmark of multiple sclerosis pathology, only partially explain the patient's clinical deficits. We thus analysed global brain pathology in multiple sclerosis, focusing on the normal-appearing white matter (NAWM) and the cortex. Autopsy tissue from 52 multiple sclerosis patients (acute, relapsing-remitting, primary and secondary progressive multiple sclerosis) and from 30 controls was analysed using quantitative morphological techniques. New and active focal inflammatory demyelinating lesions in the white matter were mainly present in patients with acute and relapsing multiple sclerosis, while diffuse injury of the NAWM and cortical demyelination were characteristic hallmarks of primary and secondary progressive multiple sclerosis. Cortical demyelination and injury of the NAWM, reflected by diffuse axonal injury with profound microglia activation, occurred on the background of a global inflammatory response in the whole brain and meninges. There was only a marginal correlation between focal lesion load in the white matter and diffuse white matter injury, or cortical pathology, respectively. Our data suggest that multiple sclerosis starts as a focal inflammatory disease of the CNS, which gives rise to circumscribed demyelinated plaques in the white matter. With chronicity, diffuse inflammation accumulates throughout the whole brain, and is associated with slowly progressive axonal injury in the NAWM and cortical demyelination.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Environmental risk factors for multiple sclerosis. Part I: the role of infection.

            Although genetic susceptibility explains the clustering of multiple sclerosis (MS) cases within families and the sharp decline in risk with increasing genetic distance, it cannot fully explain the geographic variations in MS frequency and the changes in risk that occur with migration. Epidemiological data provide some support for the "hygiene hypothesis," but with the additional proviso for a key role of Epstein-Barr virus (EBV) in determining MS risk. We show that whereas EBV stands out as the only infectious agent that can explain many of the key features of MS epidemiology, by itself the link between EBV and MS cannot explain the decline in risk among migrants from high to low MS prevalence areas. This decline implies that either EBV strains in low-risk areas have less propensity to cause MS, or that other infectious or noninfectious factors modify the host response to EBV or otherwise contribute to determine MS risk. The role of infectious factors is discussed here; in a companion article, we will examine the possible role of noninfectious factors and provide evidence that high levels of vitamin D may have a protective role, particularly during adolescence. The primary purpose of these reviews is to identify clues to the causes of MS and to evaluate the possibility of primary prevention.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Multiple sclerosis: a complicated picture of autoimmunity.

              Understanding of autoimmune diseases, including multiple sclerosis, has expanded considerably in recent years. New insights have been provided by not only animal models but also studies of patients, often in conjunction with experimental therapies. It is accepted that autoimmune T cells mediate the early steps of new multiple sclerosis lesions, and although uncertainties remain about the specific targets of autoreactive T cells, several studies indicate myelin antigens. Recent findings obtained with both animal models and patients with multiple sclerosis indicate involvement of a T helper cell with a T(H)-17 phenotype, in contrast to previous data indicating that T helper type 1 cells are critical. Evidence has also been presented for CD8(+) and regulatory T cell populations, although their involvement remains to be established. Despite evidence supporting the idea that autoreactive T cells are involved in disease induction, cells of myeloid lineage, antibodies and complement as well as processes intrinsic to the central nervous system seem to determine the effector stages of tissue damage. Careful analysis of the alterations in immune processes should further advance knowledge of the relationship between the inflammatory component of this disease and the more diffuse degeneration of progressive multiple sclerosis.
                Bookmark

                Author and article information

                Journal
                J Cereb Blood Flow Metab
                J. Cereb. Blood Flow Metab
                Journal of Cerebral Blood Flow & Metabolism
                Nature Publishing Group
                0271-678X
                1559-7016
                May 2013
                27 February 2013
                1 May 2013
                : 33
                : 5
                : 657-668
                Affiliations
                [1 ]Neurological Center, Segeberger Kliniken , Bad Segeberg, Germany
                [2 ]Department of Neurology, Charité University Medicine Berlin , Berlin, Germany
                [3 ]Department of Neurology, MS Center Amsterdam, VU University Medical Center , Amsterdam, The Netherlands
                [4 ]Centre for Neuroscience and Trauma (Neuroimmunology Group), Barts and The London Queen Mary School of Medicine and Dentistry, Blizard Institute , London, UK
                [5 ]Neurocure Clinical Research Center and Experimental and Clinical Research Center, Charité University Medicine Berlin and Max Delbrueck Center for Molecular Medicine , Berlin, Germany
                [6 ]Department of Neurology, Clinical and Experimental Multiple Sclerosis Research Center, Charité University Medicine Berlin , Berlin, Germany
                [7 ]Deptartment of Radiology, MS Center Amsterdam, VU University Medical Center , Amsterdam, The Netherlands
                Author notes
                [* ]Neurological Center, Segeberger Kliniken , Hamdorfer Weg 3, Bad Segeberg 23795, Germany. E-mail: jose.valdueza@ 123456segebergerkliniken.de
                Article
                jcbfm201331
                10.1038/jcbfm.2013.31
                3652697
                23443168
                112292d8-d59d-4675-a66f-a22bb2111159
                Copyright © 2013 International Society for Cerebral Blood Flow & Metabolism, Inc.

                This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

                History
                : 13 November 2012
                : 01 February 2013
                : 08 February 2013
                Categories
                Review Article

                Neurosciences
                immunology,magnetic resonance,multiple sclerosis,neurosonology,ultrasound
                Neurosciences
                immunology, magnetic resonance, multiple sclerosis, neurosonology, ultrasound

                Comments

                Comment on this article