Professional Documents
Culture Documents
Multiple sclerosis (MS) is an autoimmune disease of the impaired in MS.5 Twelve weeks of body-weight supported
central nervous system that affects an estimated 400,000 peo- treadmill training at an exercise rehabilitation research center
ple in the United States and 2 million worldwide. Part 1 of this significantly improved QoL and somewhat reduced fatigue in
2-part article reviewed the epidemiology and pathogenesis of 6 patients with progressive MS.6
MS, usage of complementary and alternative medicine (CAM) A single-blinded, randomized clinical trial compared three
by patients, and evidence-based dietary interventions.1 This bicycling exercise intensities engaged in by three groups of
article reviews other CAM modalities for treating MS. patients for 20 minutes twice per week for 12 weeks as fol-
lows: continuous (n = 20); intermittent (n = 21); and combined
(n = 20). At 6 weeks, all participants improved in mobility as
Naturopathic Medicine assessed by 2-minute walk distance, compared with baseline.
Between 6 and 12 weeks, the highest number of adverse ef-
Naturopathic medicine, which encompasses a broad range of fects (primarily leg pain during cycling) and dropout rate were
CAM modalities, is used by many patients with MS. A study for the higher exercise intensity groups. The researchers con-
assessed quality of life (QoL) in 45 patients who were random- cluded that, while the greatest benefit may be associated with
ly assigned to receive usual care, naturopathic medicine plus higher-intensity exercise, this level may be less well-tolerated.7
usual care, or usual care plus MS education. Results favored the Evidence supports recommendations for participation in resis-
naturopathic-treated group with respect to measures of general tance, endurance, and combined exercise of low-to-moderate
health, neurologic impairment, and a timed walk.2 intensity for moderately impaired patients.8
The National Multiple Sclerosis Society (see Resources)
advises patients to consult with their physicians before ini-
Exercise and Physical Therapy tiating a new exercise program, and advises working with a
physical therapist experienced with MS and timing exercise
Aerobic Exercise to prevent excessive fatigue and overheating. The organization
In the past, there were concerns that patients might not be recommends yoga, adaptive t’ai chi chuan, and aquatics among
able to tolerate therapeutic exercise because of fatigue and exercises suitable for patients with MS.9 These three forms of
heat-related exacerbation of symptoms.3 In 1996, a land- exercise are discussed in the next sections.
mark study in which 54 patients with mild-to-moderate MS
were randomly assigned to either aerobic exercise or nonex- Yoga
ercise groups, provided the first scientific evidence that reg- In a survey of 1980 people with MS, 30% responded that
ular exercise could improve patients’ fitness and QoL. The they had participated in yoga classes. Of these patients, 57%
study looked at the effects of exercise training, consisting of reported that they had found yoga to be “very beneficial.” In
15 weeks of 40-minute sessions per week of combined arm addition to the demonstrated benefits of participation in any
and leg ergometry. The training produced significant im- physical activity, yoga may also be therapeutic by reducing
provements in measures of fitness (including maximal aero- stress and improving cognitive ability by focused attention on
bic capacity, upper- and lower-body muscle strength, body positioning and breathing techniques. Patients are advised to
composition, and serum lipid profile) and factors related opt for practices that incorporate props or supports rather than
to QoL (mood, social interaction, recreation, and home ones that make difficult demands on physical strength, heat
management ability).4 tolerance, balance, and flexibility.10
Physical activity and exercise training programs have been A trial examined the effects of yoga and aerobic exercise on
associated with improved walking function, which is often cognitive function, fatigue, mood, and QoL. Sixty-nine pa-
Cooling Therapy narcotic-containing drugs (as it will block their action) but is
considered safe in pregnancy.40
Cooling therapy has been described as a form of CAM A double-masked, placebo-controlled, crossover study evalu-
unique to treating MS. Because heat may produce an exacer- ated the efficacy of 8 weeks of treatment with 4.5 mg of LDN
bation of symptoms thought to result from adverse effects on nightly on the self-reported QoL of 60 patients with MS. LDN
neural transmission, treatments have long included exposure was well-tolerated and associated with some improvement on
to cool showers, fans, air-conditioning, and specialized cooling several QoL measures.42 Another randomized study of 96 pa-
garments.34 The use of cooling therapy is based on extensive tients validated the safety of LDN but did not result in signifi-
patient experience rather than clinical studies. cant differences in QoL.43
It has recently been hypothesized that LDN could enhance
the pain-relieving effect of acupuncture for chronic pain syn-
Patient Education/Support Programs dromes. This idea is based on the fact that both modalities act
on the opioid and cannabinoid receptors.44
Take Control, a program of the National Multiple Sclero-
sis Society, teaches patients to manage the fatigue common
to MS through six 2-hour group sessions of viewing a patient Bee Venom Therapy and Stinging Nettle
education digital video disc (DVD), discussion, homework,
and workbooks. In a clinical trial, 30 participants were ran- A systematic literature review found marginal support for
domly assigned to a group who immediately participated in bee venom therapy for MS, noting that its use is not wide-
the program or a wait-list group. The study demonstrated the spread because of the risk of an anaphylactic reaction.45 Sting-
program’s significant impact in reducing fatigue and bolstering ing nettle (Urtica dioica) is considered a safer anti-inflamma-
self-efficacy at all assessment points.35 tory alternative.46
In an analysis of its patient wellness management program,
the Can Do Multiple Sclerosis organization (see Resources)
found increased perceived well-being and self-efficacy irre- Treating Chronic Cerebral Venous Insufficiency
spective of disease severity in 119 patients.36
According to the Motivational Model of Pain Self-Manage- Preliminary findings suggest that chronic cerebral venous
ment, readiness to engage in pain self-management behaviors insufficiency (CCVI), anomalies in the extracranial blood ves-
is mediated by beliefs about the importance of the coping be- sels that drain blood from the brain and spinal cord, are more
havior and self-efficacy (ability to carry out the behavior). A prevalent in patients with MS than controls, may contribute to
study of a sample of 114 patients with MS and chronic pain CNS damage, and correlate with disease severity. Correction
provided support for the model.37 of this condition by blood-vessel dilatation via angioplasty and
stents could theoretically influence MS pathophysiology.47
Until further evidence for the benefits of treatment for
Low-Dose Naltrexone CCVI are evaluated, the Multiple Sclerosis International Fed-
eration (see Resources)48 and the United States Department
Clinical use of low-dose naltrexone (LDN) for treating im- of Veterans Affairs’ Multiple Sclerosis Center of Excellence in
mune-related diseases, including MS, is growing.38 Naltrexone Portland, Oregon,49 do not recommend this treatment outside
is an opiate antagonist, which, at a 50 mg dose, is approved of clinical trials.
by the Food and Drug Administration to treat addiction to
opioid drugs and alcohol. Much lower doses apparently work
by stimulating endogenous endorphins that regulate the body’s Hyperbaric Oxygen Therapy
immune system. In experimental autoimmune encephalomy-
elitis, an animal model of MS, LDN inhibited the onset and There are also debates over hyperbaric oxygen therapy
progression of the disease.39 (HBOT; oxygen administered under pressure) for treating
Available from compounding pharmacies, LDN can reduce MS. Based on extensive clinical experience, the late Rich-
pain, spasticity, fatigue, and other MS symptoms. Because of ard A. Neubauer, MD, who was a consultant in hyperbaric
unsubstantiated claims that LDN is incompatible with stan- medicine in Florida, concluded that, while HBOT is not a
dard interferon immunosuppressant drug therapy,40 patients cure for MS and intermittent long-term follow-up treatment
should consult their physicians before starting LDN and dis- was necessary, HBOT altered the course of the disease fa-
continuing usual care.41 vorably.50 In the United Kingdom, centers offer HBOT for
The recommended dose is 4.5 mg taken at bedtime, except MS.51 Based on a systematic review several years ago of nine
for patients with MS who have muscle spasms; these patients randomized controlled trials evaluating the efficacy and safe-
are advised to start treatment with 3 mg daily. Patients with ty for HBOT, reviewers did not recommend routine use of
sleep disturbance lasting longer than 2 weeks may decrease the this therapy.52 More-recent studies on HBOT for MS were
dose to 3 mg or 2 mg daily. LDN should not be taken with not found.
28. Bowling AC, Stewart JD. Pinning Your Hope on. . .Acupuncture. Online 43. Sharafaddinzadeh N, Moghtaderi A, Kashipazha D, et al. The effect of
document at: www.nationalmssociety.org/search-results/index.aspx?q=acupu low-dose naltrexone on quality of life in patients with multiple sclerosis: A
ncture&x=34&y=6&start=0&num=20 [click on article title in list] Accessed randomized placebo-controlled trial. Mult Scler 2010;16:964–969.
April 23, 2011. 44. Hesselink JM, Kopsy DJ. Enhancing acupuncture by low dose naltrexone.
29. Brunham S, Oger J, Watterson, Wang Y; UBC/Tzu/Chi Institute Acu- Acupunct Med 2011;29:127–130.
puncture Study Team. Acupuncture versus medical treatment for bladder dys- 45. Namaka M, Crook A, Doupe A, et al. Examining the evidence: Com-
function MS [poster]. In: The Spectrum of Multiple Sclerosis Care, p. 6. On- plementary adjunctive therapies for multiple sclerosis. Neurol Res 2008;
line document at: www.mscare.org/cmsc/images/pdf/CMSC2003Abstracts- 30:710–719.
Posters.pdf Accessed July 8, 2011.
46. Duke JA. The Green Pharmacy. Emmaus, PA: Rodale Press, 1997:334.
30. Tjon Eng Soe SH, Kopsky DJ, Jongen PJ, et al. Multiple sclerosis patients
with bladder dysfunction have decreased symptoms after electro-acupuncture. 47. Zamboni P, Menegatti E, Weinstock-Guttman B, et al. CSF dynamics and
Mult Scler 2009;15:1376–1377. brain volume in multiple sclerosis are associated with extracranial venous flow
anomalies: A pilot study. Int Angiol 2010;29:140–148.
31. Carson EA, Swait G, Johnson IP, Cunliffe C. Chiropractic care among
people with multiple sclerosis: A survey of MS therapy centres in the UK. Clin 48. Multiple Sclerosis International Federation. MSIF Statement on CCSVI.
Chiropract 2009;12:23–27. Online document at: www.msif.org/en/news/msif_news/msif_statement_o
.html Accessed April 5, 2011.
32. Dougherty P, Lawrence D. Chiropractic management of musculoskeletal
pain in the multiple sclerosis patient. Clin Chiropractic 2005;8:57–65. 49. Bourdette D. CCSVI and the “Liberation” Treatment. Portland, OR: MS
Veteran Newsletter, Spring 2010. Online document at: www.va.gov/MS/ar
33. Elster EL. Eighty-One Patients with Multiple Sclerosis and Parkinson’s
ticles/CCSCI.asp Accessed April 12, 2011.
Disease Undergoing Upper Cervical Chiropractic Care to Correct Vertebral
Subluxation: A Retrospective Analysis. Online document at: www.chiro.org/re 50. Neubauer RA, Neubauer V, Gottlieb SF. The controversy over hyperbaric
search/ABSTRACTS/Eighty-One_Patients_With_MS.shtml Accessed April oxygenation therapy for multiple sclerosis. J Am Phys Surg 2005;10:112–115.
19, 2011. 51. Multiple Sclerosis Resource Center. Hyperbaric Oxygen Therapy. Online
34. Bowling AC. Complementary and Alternative Medicine and Multiple document at: www.msrc.co.uk/index.cfm/fuseaction/show/pageid/779 Ac-
Sclerosis, 2nd ed. New York: Demos Medical Publishing, 2007. cessed April 16, 2011.
35. Hugos CL, Copperman LF, Fuller BE, et al. Clinical trial of a formal group 52. Bennett M, Heard R. Hyperbaric oxygen therapy for multiple sclerosis.
fatigue program in multiple sclerosis. Mult Scler 2010;16:724–732. Cochrane Database Syst Rev 2004;1:CD003057.
36. Can Do Multiple Sclerosis. Can Do Research: The Impact of Empower- 53. Baker D, Jackson SJ, Pryce G. Cannabinoid control of neuroinflammation
ment. Online document at: www.mscando.org/can-do-ms-research/ Accessed related to MS. Br J Pharmacol 2007;152:649–654.
April 12, 2011. 54. Smith PF. New approaches in the management of spasticity in multiple scle-
37. Kratz AL, Molton IR, Jensen MP, et al. Further evaluation of the Motiva- rosis patients: Role of cannabinoids. Ther Clin Risk Manage 2010;6:59–63.
tional Model of Pain Self-Management: Coping with chronic pain in multiple 55. Ruggieri MR Sr. Cannabinoids: Potential targets for bladder dysfunction.
sclerosis. Ann Behav Med 2011;41:391–400. Handb Exp Pharmacol 2011;202:425–451.
38. LDN and Multiple Sclerosis (MS). Online document at: www.lowdosen 56. Health Canada. Fact Sheet—SATIVEX. Online document at: www.hc-sc.
altrexone.org/ldn_and_ms.htm Accessed March 15, 2011. gc.ca/dhp-mps/prodpharma/notices-avis/conditions/sativex_fs_fd_091289-
39. Rahn KA, McLaughlin PJ, Zagon IS. Prevention and diminished eng.php Accessed March 25, 2011.
expression of experimental autoimmune encephalomyelitis by low dose 57. NORML. United Kingdom approves marijuana spray as medicine-pre-
naltrexone (LDN) or opioid growth factor (OGF) for an extended period: scription oral spray Sativex, now available to patients. Online document at:
Therapeutic implications for multiple sclerosis. Brain Res 2011;1381: http://norml.org/index.cfm?Group_ID=8232 Accessed March 25, 2011.
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58. National Multiple Sclerosis Society. Cannabis (Marijuana). Online
40. Further Questions and Answers About LDN. Online document at: www. document at: www.nationalmssociety.org/about-multiple-sclerosis/what-we-
lowdosenaltrexone.org/further_q_and_a.htm Accessed March 24, 2011. know-about-ms/treatments/complementary--alternative-medicine/marijua
41. Bourdette D. Spotlight on Low Dose Naltrexone (LDN). Online docu- na/index.aspx Accessed April 21, 2011.
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42. Cree BA, Kornyeyeva E, Goodin DS. Pilot trial of low-dose naltrexone To order reprints of this article, e-mail Karen Ballen at: Kballen@liebertpub.com
and quality of life in multiple sclerosis. Ann Neurol 2010;68:145–150. or call (914) 740-2100.