Disclaimer: CME certification for these activities has expired. All information is pertinent to the timeframe in which it was released.
Current Issues and Ongoing Challenges in MS: Neurodegeneration and Neuroprotection
To provide neurologists, multiple sclerosis (MS) specialists, and neuroscience nurses caring for patients with MS with up-to-date information on the treatment and management of patients with MS.
This activity is designed for neurologists, multiple sclerosis (MS) specialists, and neuroscience nurses caring for patients with MS. No prerequisites required.
At the conclusion of this activity, the participant should be able to:
- Differentiate the neuroprotective capabilities of current and future multiple sclerosis (MS) immunotherapies.
- Evaluate the relevance of neuroimaging techniques as they relate to the clinical and immunological effects of disease-modifying therapies and MS pathology.
- Identify 2 interventions to improve adherence and compliance with disease-modifying therapies in patients with MS.
The Johns Hopkins University School of Medicine and The Institute for Johns Hopkins Nursing take responsibility for the content, quality, and scientific integrity of this CE activity.
This activity has been planned and implemented in accordance with the Essential Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of The Johns Hopkins University School of Medicine and The Institute for Johns Hopkins Nursing.
The Johns Hopkins University School of Medicine is accredited by the ACCME to provide continuing medical education for physicians.
The Institute for Johns Hopkins Nursing is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center's Commission on Accreditation.
CREDIT DESIGNATION STATEMENT
The Johns Hopkins University School of Medicine designates this educational activity for a maximum of 2 AMA PRA Category 1 Credit(s)™. Physicians should only claim credit commensurate with the extent of their participation in the activity.
This 1.7 contact hour Educational Activity is provided by The Institute for Johns Hopkins Nursing. Claim only those contact hours actually spent in the activity.
The estimated time to complete this educational activity: 2 hours.
After reading this monograph, participants may receive credit by completing the CE test, evaluation, and receiving a score of 70% or higher.
Release date: July 15, 2009. Expiration date: July 15, 2011.
The opinions and recommendations expressed by faculty and other experts whose input is included in this program are their own. This enduring material is produced for educational purposes only. Use of The Johns Hopkins University School of Medicine and The Institute for Johns Hopkins Nursing names implies review of educational format, design, and approach. Please review the complete prescribing information of specific drugs or combinations of drugs, including indications, contraindications, warnings, and adverse effects, before administering pharmacologic therapy to patients.
This activity is supported by an educational grant from Teva Neuroscience.
Full Disclosure Policy Affecting CE Activities:
As a provider accredited by the Accreditation Council for Continuing Medical Education (ACCME), it is the policy of The Johns Hopkins University School of Medicine and The Institute for Johns Hopkins Nursing to require the disclosure of the existence of any relevant financial interest or any other relationship a faculty member or a sponsor has with the manufacturer(s) of any commercial product(s) discussed in an educational presentation. The Course Directors and Participating Faculty reported the following:
Arun Venkatesan, MD, PhD
Assistant Professor of Neurology
Department of Neurology
The Johns Hopkins Medical Institute
• Dr Venkatesan reports having no relevant financial or advisory relationships with corporate organizations related to this activity.
Michael K. Racke, MD
Professor and Chairman of Neurology
The Helen C. Kurtz Chair in Neurology
The Ohio State University Medical Center
• Dr Racke reports serving as a consultant for Bristol-Myers Squibb Company, Peptimmune, Inc, and Teva Neuroscience; and serving on the speakers' bureau for Genentech, Inc.
Peter A. Calabresi, MD
Professor of Neurology
Director, Multiple Sclerosis Center
The Johns Hopkins Hospital
• Dr Calabresi reports receiving grants/research support from Biogen Idec, Genentech, Inc, Serono, Teva Neuroscience, and Vertex Pharmaceuticals; and receiving honoraria from and serving as a consultant for Amplimmune, Inc, Biogen Idec, Centocor, Inc, Genentech, Inc, Novartis Pharmaceuticals Corporation, Serono, Teva Neuroscience, and Vertex Pharmaceutials.
Benjamin Greenberg, MD, MHS
Director, Transverse Myelitis and Neuromyelitis Optica Program
Deputy Director, Multiple Sclerosis Program
Cain Denius Scholar in Mobility Disorders
Department of Neurology
University of Texas Southwestern
• Dr Greenberg reports receiving grants/research support from Accelerated Cure Project, National Multiple Sclerosis Society, and Novartis Pharmaceuticals Corporation; serving as a consultant for and holding stock in DioGenix; and receiving honoraria from Biogen Idec and Teva Neuroscience.
Clyde E. Markowitz, MD
Associate Professor of Neurology
Director, Multiple Sclerosis Center
The Hospital of the University of Pennsylvania
University of Pennsylvania School of Medicine
• Dr Markowitz reports receiving grants/research support from Bayer, Biogen Idec, BioMS, EMD Serono, Inc, Genentech, Inc, Novartis Pharmaceuticals Corporation, and Teva; serving as a consultant for Bayer, Biogen Idec, BioMS, EMD Serono, Inc, Genentech, Inc, and Novartis Pharmaceuticals Corporation; receiving honoraria from Bayer, Biogen Idec, EMD Serono, Inc, and Teva; and serving on the speakers' bureau for Bayer, Biogen Idec, and EMD Serono, Inc.
Bruce D. Trapp, PhD
Chairman, Department of Neurosciences
Lerner Research Institute
• Dr Trapp reports having no relevant financial or advisory relationships with corporate organizations related to this activity.
This activity was reviewed by Faith H. Howarth, MSN, EdM, CRNP, CS, LNC, for the American Nurses Credentialing Center's accreditation purposes.
Notice: The audience is advised that articles in this CE activity may contain reference(s) to unlabeled or unapproved uses of drugs or devices.
Dr Greenberg—alemtuzumab, BG-12, cladribine, cyclophosphamide, daclizumab, fingolimod, laquinomod, rituximab, and teriflunomide.
Dr Racke—rituximab and other agents for treatment of neuromyelitis optica.
All other faculty have indicated that they have not referenced unlabeled or unapproved uses of drugs or devices.
Johns Hopkins Advanced Studies in Medicine provides disclosure information from contributing authors, lead presenters, and participating faculty. Johns Hopkins Advanced Studies in Medicine does not provide disclosure information from authors of abstracts and poster presentations. The reader shall be advised that these contributors may or may not maintain financial relationships with pharmaceutical companies.
Current Issues and Ongoing Challenges in MS: Neurodegeneration and Neuroprotection
Arun Venkatesan, MD, PhD,* and Michael K. Racke, MD †
Multiple sclerosis (MS) is a chronic, progressive, disabling condition that is characterized by inflammation and demyelination of central nervous system (CNS) axons. Individuals with MS typically begin to exhibit significant impairment in the ability to walk without aid approximately 10 to 12 years after diagnosis, and many are essentially confined to a wheelchair within 25 to 30 years.1 Due to the relatively young age at the time of diagnosis (typically between the ages of 20 and 50) and the potential for permanent neurologic impairment, MS is a major cause of disability in developed nations. Disability associated with MS also creates a significant economic burden for most patients, who often experience sustained loss of income and unreimbursed expenses associated with medical or nursing care.2
Most patients with MS initially experience discrete episodes of CNS inflammation and a return to normal or near-normal function between episodes. Inflammatory lesions occur throughout the brain and spinal cord, and the disease therefore produces a variety of non-specific signs and symptoms that may include pain, muscle weakness, spasticity, visual disturbances, paresthesia, sexual dysfunction, or cognitive impairment. Disease-modifying therapies that suppress CNS inflammation have been shown to significantly reduce relapse rates, disease progression, and magnetic resonance imaging (MRI) evidence of disease activity in patients with MS, and 4 immunomodulators are considered first-line treatment options (2 formulations of interferon β-1a, interferon β-1b, and glatiramer acetate).3 Although these agents are effective for individuals with relapsing forms of MS, many patients continue to exhibit significant disease activity despite first-line therapy. In addition, most patients with MS eventually develop irreversible and progressive neurologic impairment that is less responsive to treatment with the approved MS therapies.3
Although MS has traditionally been viewed as a disorder of CNS inflammation and demyelination, a growing body of evidence has demonstrated that axonal damage and progressive neurodegeneration are also important in the pathogenesis of MS. Neurodegeneration has been identified at even the earliest stages of MS, and is thought by many experts to be an important contributor to the long-term progression of disability.4,5 Several mechanisms have been hypothesized to account for axon loss in MS, including increased vulnerability to the effects of inflammatory mediators following demyelination, the loss of myelin-derived substances that support neuronal survival, and neuronal toxicity due to intracellular calcium overload. These observations suggest that treatment strategies that are designed to prevent neurodegeneration may provide entirely new approaches to the treatment of MS. Several recent studies have examined the potential neuroprotective effects of current MS therapies and have explored novel approaches to reduce neurologic injury. In addition, conventional imaging technologies may not be sensitive to neurodegeneration, and new imaging techniques may be required to identify and quantify neurodegeneration in clinical practice and in clinical trials of potential neuroprotective therapies.6
This issue of Johns Hopkins Advanced Studies in Medicine includes proceedings from The 6th Annual Johns Hopkins MS Symposium, and will provide an overview of the opportunities and challenges of neuroprotective strategies in MS therapy. In the first article, Bruce D. Trapp, PhD, discusses some of the pathologic evidence that neurodegeneration is an important contributor to the pathogenesis of MS and examines the relationship between chronic axonal demyelination and neurodegeneration. Benjamin Greenberg, MD, MHS, describes research supporting a role for neurodegeneration that is independent of inflammation and reviews findings suggesting that current MS therapies may produce direct or indirect neuroprotective effects. Peter A. Calabresi, MD, discusses the limitations of current MRI techniques for the assessment of neurodegeneration and describes newer imaging technologies to quantify neuronal and axonal loss. Clyde E. Markowitz, MD, examines important issues in the management of breakthrough disease and reviews the importance of identifying and overcoming barriers to treatment adherence. Dr Markowitz also summarizes recent research regarding the use of several medication strategies for patients with continued MS activity despite disease-modifying therapy. Michael K. Racke, MD, presents an excerpt from a case-based clinical decision-making exercise on the use of MRI that was conducted with clinicians who treat MS. This issue concludes with highlights from the question and answer sessions that took place at the meeting.
This educational activity is designed to provide neurologists, MS specialists, neuroscience nurses, and other clinicians who care for patients with MS with an update on the role of neurodegeneration in the pathophysiology and treatment of MS. Participants who complete this educational activity will be better able to describe the significance of neurodegeneration for the long-term course of MS, identify and overcome barriers to treatment adherence, and manage patients with continued disease activity despite therapy with first-line agents. In addition, participants will be prepared to interpret the results of new CNS imaging techniques that are designed to assess neurodegeneration and neuroprotection, and to incorporate the results of clinical trial data from neuroprotection studies into clinical practice.
1. Confavreux C, Vukusic S, Moreau T, Adeleine P. Relapses and progression of disability in multiple sclerosis. N Engl J Med. 2000;343:1430-1438.
2. Whetten-Goldstein K, Sloan FA, Goldstein LB, Kulas ED. A comprehensive assessment of the cost of multiple sclerosis in the United States. Mult Scler. 1998;4:419-425.
3. Goodin DS, Frohman EM, Garmany GP Jr, et al. Disease modifying therapies in multiple sclerosis: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology and the MS Council for Clinical Practice Guidelines. Neurology. 2002;58:169-178.
4. De Stefano N, Narayanan S, Francis GS, et al. Evidence of axonal damage in the early stages of multiple sclerosis and its relevance to disability. Arch Neurol. 2001;58:65-70.
5. Bjartmar C, Wujek JR, Trapp BD. Axonal loss in the pathology of MS: consequences for understanding the progressive phase of the disease. J Neurol Sci. 2003;206:165-171.
6. Meier DS, Weiner HL, Khoury SJ, Guttmann CR. Magnetic resonance imaging surrogates of multiple sclerosis pathology and their relationship to central nervous system atrophy. J Neuroimaging. 2004;14(3 suppl):46S-53S.
*Assistant Professor of Neurology, Department of Neurology, The Johns Hopkins Medical Institute, Baltimore, Maryland.
†Professor and Chairman of Neurology, The Helen C. Kurtz Chair in Neurology, The Ohio State University Medical Center, Columbus, Ohio.
Address correspondence to: Arun Venkatesan, MD, PhD, Assistant Professor of Neurology, The Johns Hopkins University School of Medicine, Department of Neurology, 600 North Wolfe Street, Pathology 509, Baltimore, MD 21287. E-mail: email@example.com.
The content in this monograph was developed with the assistance of a medical writer. Each author had final approval of his article and all its contents.