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Restorative Medicine Approach Multiple Sclerosis Michaёl Friedman, ND Financial Disclosure: Co- owner Restorative Formulations 1

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  • Restorative Medicine Approach Multiple Sclerosis

    Michaёl Friedman, NDFinancial Disclosure: Co- owner Restorative Formulations

    1

  • PATHOPHYSIOLOGY OF MS

    • Chronic Autoimmune,

    inflammatory

    neurological disease

    of the CNS.

    • Destroys myelin and

    axons to varying

    degree.

    2

    Calabresi PA . Diagnosis and management of multiple

    sclerosis. Am Fam Physician. 2004 Nov 15; 70(10):1935-

    44.

  • Demyelination

    • Demyelination leading

    to impaired saltatory

    conduction of action

    potentials.

    3

    Podbielska, Maria et al. “Myelin Recovery in Multiple Sclerosis:

    The Challenge of Remyelination.” Brain Sciences 3.3 (2013):

    1282–1324. PMC. Web. 4 Sept.2017.

  • SYMPTOMS OF MS

    4

    Goldenberg MM. Multiple Sclerosis Review. Pharmacy and Therapeutics. 2012;37(3):175-184.

  • MS LESIONS (MRI)

    5

    A

    B

    C

    D

  • Poor prognosis predictors

    • > 40 years of age at

    onset

    • Male sex

    • Non-Caucasian origin

    • Motor or polyregional

    symptoms in first year of

    attack.

    • Brain stem lesion.

    6

    Hunter SF. Overview and diagnosis of multiple sclerosis. Am J Manag Care. 2016 Jun; 22(6 Suppl):s141-50.

  • 7

  • 8

  • 9

    Cervical Lesion

  • 10

  • 11

  • 12

  • 13

  • 14

  • 15

  • 16

  • 17

  • 18

  • 19

  • 20

  • 21

  • Neurologist

    • what can account for

    your success as drug

    therapy alone can not

    explain your results of

    your MRI?

    22

  • Gut Bacteria Changes the

    Brain

    • Hepatic Encephalophy

    – Lactose & Lactulose

    protective

    Campollo O, Sprengers D, McIntyre N. The BCAA/AAA ratio of plasma amino acids in three different groups of cirrhotics. Rev Invest

    Clin. 1992 Oct-Dec;44(4):513-8.

  • Gut Bacteria Produces

    Neurotransmitters• Gut microbes like Bacillus

    spp. Account for almost half

    of the of body's DA

    production.1

    • Gut bacteria & Brain –

    Bidirectional signaling

    involving multiple

    neuroendocrine mechanisms.

    Eisenhofer, G., Aneman, A., Friberg, P., Hooper, D., Fandriks, L., Lonroth, H., Hunyady, B., and Mezey, E. Substantial production of

    dopamine in the human gastrointestinal tract. J. Clin. Endocrinol. Metabolism. 1997; 82: 3864–3871

  • 25

  • Microbiome and inflammatory

    demyelinating disease

    Ochoa-Repáraz J, Mielcarz DW, Haque-Begum S, Kasper LH. Induction of a regulatory B cell population in experimental allergic

    encephalomyelitis by alteration of the gut commensal microflora. Gut Microbes. 2010;1:103–8.

    Autoimmune

    Encephalomyelitis (EAE) is

    the most commonly used

    animal model for the human

    inflammatory demyelinating

    disease, multiple sclerosis

    (MS).

  • LPS & Intestinal Inflammation

    27LPS Inflamed intestines

  • Intestinal barrier and MS

    •Changes in intestinal tight junction

    permeability associated with industrial food

    additives explain the rising incidence of

    autoimmune disease.

    •Glucose, salt, emulsifiers, organic solvents,

    gluten, microbial transglutaminase, and

    nanoparticles are the culprits involved in the

    pathogenesis.

    28

    Autoimmunity ReviewsVolume 14, Issue 6, June 2015, Pages 479-489

    Review

    Fasano, Alessio. “Zonulin, Regulation of Tight Junctions, and Autoimmune Diseases.” Annals of the New York Academy of

    Sciences 1258.1 (2012): 25–33. PMC. Web. 4 Sept. 2017.

    http://www.sciencedirect.com/science/journal/15689972/14/6http://www.sciencedirect.com/science/journal/15689972http://www.sciencedirect.com/science/journal/15689972/14/6http://www.sciencedirect.com/science/journal/15689972/14/6

  • Nuro-Endotoxins Up-Regulate

    Inflammation

    29

    http://medical-dictionary.thefreedictionary.com/endotoxin

    Lee, Jae Woong et al. “Neuro-Inflammation Induced by Lipopolysaccharide Causes Cognitive Impairment through Enhancement of

    Beta-Amyloid Generation.” Journal of Neuroinflammation 5 (2008): 37. PMC. Web. 4 Sept. 2017.

  • All seven patients with MS

    had elevated Candida tests

  • Good News

    • Dysbiois can be

    changed and alter

    progression and

    symptomology of MS

    with Fecal Microbial

    Transplant (FMT).

    Wei, Yanling et al. “Successful Treatment with Fecal Microbiota Transplantation in Patients with Multiple Organ Dysfunction

    Syndrome and Diarrhea Following Severe Sepsis.” Critical Care 20 (2016): 332. PMC. Web. 4 Sept. 2017.

  • Fecal Microbiota

    transplantation

    Fecal Microbiota

    transplantation• What is it?• Administration of fecal material containing distal gut microbiota

    from a healthy person to a patient with a disease or condition related to dysbiosis.

    • Why do it?• Restore phylogenetic diversity and therefore microbiome

    physiological functions.

    • Replace and or inhibit pathogenic species.

    • Does it work?• For recurrent C. difficile infections the efficacy of FMT is now

    undisputed, with cure rates of 85-90% in case series.

    1. Van Nood et al. Duodenal Infusion of Donor Feces for Recurrent Clostridium difficile NEJM 368;5

    2. Kelly et al. Update on Fecal Microbiota Transplantation 2015: Indications, Methodologies, Mechanisms and Outlook.

    Gastroenterology 2015; 149: 223-237

  • FMT and MS

    • Reported three wheelchair-bound patients with MS treated with FMT for constipation.

    • Bowel symptoms resolved following FMT.

    • Two of the patients with prior indwelling urinary catheters experienced restoration of urinary function.

    Borody TJ, Leis S, Campbell J, et al. Fecal microbiota transplantation (FMT) in multiple sclerosis (MS). Am J

    Gastroenterol 2011; 106:S352ssion and ‘no evidence of active disease

  • • all three patients regaining the ability to

    walk unassisted.

    • In one patient of the three, follow-up MRI

    15 years after FMT showed a halting of

    disease progression

    34Borody TJ, Leis S, Campbell J, et al. Fecal microbiota transplantation (FMT) in multiple sclerosis (MS) [abstract].Am J

    Gastroenterol 2011; 106:S352ssion and ‘no evidence of active disease.

  • Carlos walks after FMT

    35

  • 36

  • Microbial diversity

    • How to Grow Your Microbiome

    37

  • CNS Lymphatics

    38

    Louveau A, Smirnov I, Keyes TJ, Eccles JD, Rouhani SJ, Peske JD, Derecki NC, Castle D, Mandell JW, Lee KS, Harris TH, Kipnis J.

    Corrigendum: Structural and functional features of central nervous system lymphatic vessels. Nature. 2016 May 12;533(7602):278.

  • Vitamin-D in MS

    • High-dose vitamin D (∼10,000 IU/day) in

    multiple sclerosis is safe, with evidence of

    immunomodulatory effects.

    • Patients had fewer relapses.

    • Low Vit-D levels – Risk for MS development.

    39

    •J.M. Burton, MD, MSc, FRCPC, S. Kimball, MSc, MLT, R. Vieth, PhD, A. Bar-Or, MD, MSc, FRCPC, H.-M. Dosch, MD, PhD, R.

    Cheung, MSc, D. Gagne, C. D'Souza, PhD, M. Ursell, MS, MSc, FRCPC, and P. O'Connor, MS, MSc, FRCPC. A phase I/II dose-

    escalation trial of vitamin D3 and calcium in multiple sclerosis. Neurology. 2010 Jun 8; 74(23): 1852–1859.

    •Alharbi, Fatimah M. “Update in Vitamin D and Multiple Sclerosis.” Neurosciences 20.4 (2015): 329–335.

  • Vit B12

    ❖Easily passes Blood Brain Barrier.

    ❖Neuroprotective & anti-oxidant agent

    involved in the synthesis of

    phospholipids and myelin.

    40Moosavirad, Saeedeh Alsadat et al. “Protective Effect of Vitamin C, Vitamin B12 and Omega-3 on Lead-Induced Memory Impairment

    in Rat.” Research in Pharmaceutical Sciences 11.5 (2016): 390–396. PMC. Web. 3 Feb. 2017.

  • Testosterone

    41Pakpoor J, Wotton CJ, Schmierer K, Giovannoni G, Goldacre MJ. Gender identity disorders and multiple sclerosis risk: A

    national record-linkage study. Mult Scler. 2016 Nov;22(13):1759-1762. Epub 2016 Feb 8.

    ➢ Low testosterone in males –

    Increased risk of MS.

    ➢Testosterone – converted to

    estrogen (estradiol) in brain.

    ➢Anti-inflammatory,

    neuroprotective.

  • Modafinil and Neuroprotection

    • Modafinil (50 and 100 mg/kg) - Prevented against

    decrease of DA, 5-HT, and NA in the striatum and

    GSH, GABA in the SN induced by MPTP in PD

    models.

    • This was due to antioxidant effects

    42

    Xiao YL, Fu JM, Dong Z, Yang JQ, Zeng FX, Zhu LX, He BC. Neuroprotective mechanism of modafinil on Parkinson disease

    induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine.Acta Pharmacol Sin. 2004 Mar;25(3):301-5.

  • Polyphenols

    • Polyphenols - potential to block neural inflammation

    and damage by modulation of inflammatory

    cytokines.

    • limiting demyelination in MS

    43Bhullar KS, Rupasinghe HPV. Polyphenols: Multipotent Therapeutic Agents in Neurodegenerative Diseases. Oxidative

    Medicine and Cellular Longevity. 2013;2013:891748.

  • Neurotrophins

    44

    Neurotrophins -

    Neural survival,

    development,

    function, plasticity

    BDNF

    Considerably low in

    Alzheimer’s &

    cognitive impairment

    Administration of S.

    miltiorrhiza reduced

    Aβ-induced

    reductions in BDNF

    in pre-clinical

    models

    Rosmarinic acid –

    Increased BDNF

    and restored

    hippocampal BDNF

    - Protective against

    memory deficits

    Lopresti, Adrian L. “Salvia (Sage): A Review of Its Potential Cognitive-Enhancing and Protective Effects.” Drugs in R&D 17.1 (2017):

    53–64. PMC. Web. 7 Sept. 2017.

  • Fulgenzi A.et al A case of multiple sclerosis improvement following removal of heavy metal intoxication: lessons learnt from Matteo's

    case. Biometals 2012 Jun;25(3):569-76.

    • The Clinical data correlated with the

    reduction of heavy metal levels in the urine to

    normal range values.

    • Case reports suggest that levels of toxic

    metals can be tested in patients affected by

    neurodegenerative diseases as MS.

    Heavy Metals

    MS

  • Dietary considerations

    • The human brain is nearly 60 percent fat.

    • Omega-3 fatty acids reduces the level of matrix

    metalloproteinase (MMP) which plays an

    important role in the migration of inflammatory

    cells in the CNS fluid, which breaks down blood–

    brain barriers.

    46Jahromi SR, Toghae M, Jahromi MJR, Aloosh M. Dietary pattern and risk of multiple sclerosis. Iranian Journal of Neurology.

    2012;11(2):47-53.

  • Dietary considerations

    • Omega-3 fatty acids as immune system

    regulators which act by reducing the levels

    of inflammatory cytokines such as TNF-α,

    IL-1, IL-2, and vascular cell adhesion

    molecule (VCAM1).

    • Shinto L, Marracci G, Baldauf-Wagner S, et al. Omega-3 fatty acid supplementation decreases matrix

    metalloproteinase-9 production in relapsing-remitting multiple sclerosis. Prostaglandins, leukotrienes, and essential

    fatty acids. 2009;80(2-3):131-136.47

  • ❖n-3 PUFAs possibly have a role in promotion of

    remyelination after toxic injury to CNS

    oligodendrocytes via modulation of the immune

    system or a direct effect on oligodendrocytes through

    EPA-derived lipid metabolites as demonstrated in pre-

    clinical studies.

    n-3 PUFAs and Remyelination

    Siegert E, Paul F, Rothe M, Weylandt KH. The effect of omega-3 fatty acids on central nervous system remyelination in fat-1 mice.

    BMC Neuroscience. 2017;18:19. doi:10.1186/s12868-016-0312-5.

  • Brain needs oxygen

    49

    • Lipopolyscharide induced

    demylination prevents and

    decreases with oxygen and

    thymoquinone found in Black

    Cumin Seed Extracts.

    •Noor NA, Fahmy HM, Mohammed FF, Elsayed AA, Radwan NM. Nigella sativa amliorates inflammation and demyelination in the

    experimental autoimmune encephalomyelitis-induced Wistar rats. International Journal of Clinical and Experimental Pathology.

    2015;8(6):6269-6286.

    •Desai RA, Davies AL, Tachrount M, Kasti M, Laulund F, Golay X, Smith KJ.Cause and prevention of demyelination in a model

    multiple sclerosis lesion. Ann Neurol. 2016 Apr;79(4):591-604.

  • Chronic Cerebrospinal Venous

    Insufficiency (CCSVI) & MS

    • Veins in the head and neck are narrowed resulting

    in inefficient blood drain from the CNS.

    • Reflux of blood back to the CNS due to pressure

    caused by build-up of blood.

    • Compensatory blood vessels developed lack the

    same structural integrity and are leaky.

    • Leaked blood with iron deposits in the CNS

    triggering immune response and MS.

    50Costello F et al. Validity of the diagnostic criteria for chronic cerebrospinal venous insufficiency and association with

    multiple sclerosis. Canadian Medical Association Journal 2014 June 2

  • Exercise/ Physical activity

    ✓ Exercise - Shown to increase synaptic density and growth in

    the hippocampus in the animal model of MS.

    ✓ Physical activity Increases levels of neurotrophic factors,

    elevates expression of anti-inflammatory cytokines, and

    reduces levels of pro-inflammatory cytokines and activates

    microglia and is thus neuroprotective.

    • Rossi S., Furlan R., De Chiara V., Musella A., Lo Guidice T., Mataluni G. (2009) Exercise attenuates the clinical, synaptic

    and dendritic abnormalities of EAE. Neurobiol Dis 36: 51–59.

    • Svensson M, Lexell J, Deierborg T.Neurorehabil Neural Repair. Effects of Physical Exercise on Neuroinflammation,

    Neuroplasticity, Neurodegeneration, and Behavior: What We Can Learn From Animal Models in Clinical Settings. 2015

    Jul;29(6):577-89. 51

  • Seasonality of MS – Role of

    Melatonin

    52

    Seasonal

    changes (length

    of day and night)

    Melatonin levels

    Negatively

    correlate

    with MS

    Melatonin

    treatment

    ameliorates MS

    Induces expression

    of transcription factor

    Nfil3, promotes

    generation of

    protective Tr1 cells

    Influence

    differentiation

    of T cells

    Farez, Mauricio F. et al. “Melatonin Contributes To The Seasonality Of Multiple Sclerosis Relapses.” Cell 162.6 (2015):

    1338–1352. PMC. Web. 7 Sept. 2017.

    Variation in

  • Serum Glutamate and MS

    • Neurotransmitter Glutamate –

    Implicated in autoimmune

    demyelination in MS.

    MS Control

    Serum

    Glutnmol/ml

    1.318 ±

    0.543

    0.873 ±

    0.341 

    53

    The mean

    serum glutamate levels

    determmined by ELISA

    Al Gawwam G, Sharquie IK. Serum Glutamate Is a

    Predictor for the Diagnosis of Multiple Sclerosis.

    ScientificWorldJournal. 2017;2017:9320802.

  • Cholinergic signaling in

    remyelination

    54Fields RD, Dutta DJ, Belgrad J, Robnett M. Cholinergic signaling in myelination. Glia. 2017 May;65(5):687-698.

    • Cholinesterase inhibitors - Shown to

    improve remyelination in animal models

    of MS.

    • Cholinergic signalling in oligodendroglial

    development and myelination seems

    possible

  • Progesterone and

    Remyelination• Progesterone and synthetic progestins

    • modulate inflammatory responses and partially

    reverse the age-dependent decline

    in remyelination.

    • Progesterone and Nestorone promoted repair of

    severe chronic demyelinating lesions induced by

    feeding cuprizone to female mice for up to 12

    weeks,

    55

    El-Etr M, Rame M, Boucher C, Ghoumari AM, Kumar N, Liere P, Pianos A, Schumacher M, Sitruk-Ware R. Progesterone and

    nestorone promote myelin regeneration in chronic demyelinating lesions of corpus callosum and cerebral cortex. Glia. 2015

    Jan;63(1):104-17.

  • T3 and Remyelination

    • Thyroid hormone (T3) promotes remyelination.

    • T3 promotes Kruppel-like factor 9 (KLF9)

    transcription factor a novel integral component of

    signaling cascade that promotes the regeneration

    of lost myelin.

    56Dugas, Jason C., Adiljan Ibrahim, and Ben A. Barres. “The T3-Induced Gene KLF9 Regulates Oligodendrocyte Differentiation and

    Myelin Regeneration.” Molecular and cellular neurosciences 50.1 (2012): 45–57. PMC. Web. 7 Sept. 2017.

  • 57

    Treating the Terrain

    Healthy

    Microbiome

    Acetylcholine

    Epinephrine

    GABA

    Serotonin

    Dopamine

  • 58

    Treating the Terrain

    Sick

    MicrobiomeBlood Brain

    PermeabilityNeuroinflammation

    Gut Permeability

  • 59

    Treating the Apparent Mechanism

    Neuroinflamation

    Polyphenols

    Exercise

    Omega 3

    Microbiome

    Diterpenes

    Cortisol

  • 60

    Treating the Apparent Mechanism

    Oxidation

    Microbiome

    Melatonin

    Glutathione

    Detoxification

    Monoclonal Antibodies

    Modafinil

    Dimethyl fumarate

    Antioxidants

  • 61

    Treating the Apparent Mechanism

    GlutamateKava

    Neurosteroids

    GABA

    Green Tea

    (Theanine)

  • 62

    Treating the Apparent Mechanism

    Demylination

    Oxygen Omega 3

    Neuroprotecants

  • 63

    Treating the Apparent Mechanism

    Monoclonal

    Antibodies

    Phytollaca

    (Poke)

    Dimethyl

    Fumarate

    Interferon

    Glatiramer

    Acetate

    Immunomodulation

  • 64

    Treating the Apparent Mechanism

    Remylination

    T3

    Microbiome

    Turmerones

    Lion’s Mane

    Mushroom

    Exercise

    Deiodinase