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Demyelinating disease

(Redirected from Demyelinating disorder)

A demyelinating disease refers to any disease affecting the nervous system where the myelin sheath surrounding neurons is damaged.[1] This damage disrupts the transmission of signals through the affected nerves, resulting in a decrease in their conduction ability. Consequently, this reduction in conduction can lead to deficiencies in sensation, movement, cognition, or other functions depending on the nerves affected.

Demyelinating disease
Photomicrograph of a demyelinating MS-lesion: Immunohistochemical staining for CD68 highlights numerous macrophages (brown). Original magnification 10×.
SpecialtyNeurology Edit this on Wikidata

Various factors can contribute to the development of demyelinating diseases, including genetic predisposition, infectious agents, autoimmune reactions, and other unknown factors. Proposed causes of demyelination include genetic predisposition, environmental factors such as viral infections or exposure to certain chemicals. Additionally, exposure to commercial insecticides like sheep dip, weed killers, and flea treatment preparations for pets, which contain organophosphates, can also lead to nerve demyelination.[2] Chronic exposure to neuroleptic medications may also cause demyelination.[3] Furthermore, deficiencies in vitamin B12 can result in dysmyelination.[4][5]

Demyelinating diseases are traditionally classified into two types: demyelinating myelinoclastic diseases and demyelinating leukodystrophic diseases. In the first group, a healthy and normal myelin is destroyed by toxic substances, chemicals, or autoimmune reactions. In the second group, the myelin is inherently abnormal and undergoes degeneration.[6] The Poser criteria named this second group dysmyelinating diseases.[7]

In the most well-known demyelinating disease, multiple sclerosis, evidence suggests that the body's immune system plays a significant role. Acquired immune system cells, specifically T-cells, are found at the site of lesions. Other immune system cells, such as macrophages (and possibly mast cells), also contribute to the damage.[8]

Signs and symptoms

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Symptoms and signs that present in demyelinating diseases are different for each condition. These symptoms and signs can present in a person with a demyelinating disease:[9]

Evolutionary considerations

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The role of prolonged cortical myelination in human evolution has been implicated as a contributing factor in some cases of demyelinating disease. Unlike other primates, humans exhibit a unique pattern of postpubertal myelination, which may contribute to the development of psychiatric disorders and neurodegenerative diseases that present in early adulthood and beyond. The extended period of cortical myelination in humans may allow greater opportunities for disruption in myelination, resulting in the onset of demyelinating disease.[10] Furthermore, humans have significantly greater prefrontal white matter volume than other primate species, which implies greater myelin density.[11] Increased myelin density in humans as a result of a prolonged myelination may, therefore, structure risk for myelin degeneration and dysfunction. Evolutionary considerations for the role of prolonged cortical myelination as a risk factor for demyelinating disease are particularly pertinent given that genetics and autoimmune deficiency hypotheses fail to explain many cases of demyelinating disease. As has been argued, diseases such as multiple sclerosis cannot be accounted for by autoimmune deficiency alone, but strongly imply the influence of flawed developmental processes in disease pathogenesis.[12] Therefore, the role of the human-specific prolonged period of cortical myelination is an important evolutionary consideration in the pathogenesis of demyelinating disease.[citation needed]

Diagnosis

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Various methods/techniques are used to diagnose demyelinating diseases:

Types

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Demyelinating diseases can be divided in those affecting the central nervous system (CNS) and those affecting the peripheral nervous system (PNS). They can also be classified by the presence or absence of inflammation. Finally, a division may be made based on the underlying cause of demyelination: the disease process can be demyelinating myelinoclastic, wherein myelin is destroyed; or dysmyelinating leukodystrophic, wherein myelin is abnormal and degenerative.

CNS

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The demyelinating disorders of the central nervous system include:[citation needed]

The myelinoclastic disorders are typically associated with symptoms such as optic neuritis and transverse myelitis, because the demyelinating inflammation can affect the optic nerve or spinal cord. Many are idiopathic. Both myelinoclastic and leukodystrophic modes of disease may result in lesional demyelinations of the central nervous system.

PNS

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Guillain–Barré syndrome – demyelination

The demyelinating diseases of the peripheral nervous system include:[citation needed]

Treatment

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See also: Multiple sclerosis § Medications, and Management of multiple sclerosis

Treatments are patient-specific and depend on the symptoms that present with the disorder, as well as the progression of the condition. Improvements to the patient's life may be accomplished through the management of symptoms or slowing of the rate of demyelination. Treatment can include medication, lifestyle changes (i.e. smoking cessation, increased rest, and dietary changes), counselling, relaxation, physical exercise, patient education, and in some cases, deep brain thalamic stimulation (to ameliorate tremors).[13]: 227–248 

Prognosis

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Prognosis depends on the condition itself. Some conditions such as MS depend on the subtype of the disease and various attributes of the patient such as age, sex, initial symptoms, and the degree of disability the patient experiences.[14] Life expectancy in MS patients is 5 to 10 years lower than unaffected people.[15] MS is an inflammatory demyelinating disease of the central nervous system (CNS) that develops in genetically susceptible individuals after exposure to unknown environmental trigger(s). The bases for MS are unknown but are strongly suspected to involve immune reactions against autoantigens, particularly myelin proteins. The most accepted hypothesis is that dialogue between T-cell receptors and myelin antigens leads to an immune attack on the myelin-oligodendrocyte complex. These interactions between active T cells and myelin antigens provoke a massive destructive inflammatory response and promote continuing proliferation of T and B cells and macrophage activation, which sustains secretion of inflammatory mediators.[16] Other conditions such as central pontine myelinolysis have about a third of patients recover and the other two-thirds experience varying degrees of disability.[17] In some cases, such as transverse myelitis, the patient can begin recovery as early as 2 to 12 weeks after the onset of the condition.[citation needed]

Epidemiology

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Incidence of demyelinating diseases varies by disorder. Some conditions, such as tabes dorsalis appear predominantly in males and begin in midlife. Optic neuritis, though, occurs preferentially in females typically between the ages of 30 and 35.[18] Other conditions such as multiple sclerosis vary in prevalence depending on the country and population.[19] This condition can appear in children and adults.[15]

Research

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Much of the research conducted on demyelinating diseases is targeted towards discovering the mechanisms by which these disorders function in an attempt to develop therapies and treatments for individuals affected by these conditions. For example, proteomics has revealed several proteins which contribute to the pathophysiology of demyelinating diseases.[20] For example, COX-2 has been implicated in oligodendrocyte death in animal models of demyelination.[21] The presence of myelin debris has been correlated with damaging inflammation as well as poor regeneration, due to the presence of inhibitory myelin components.[22][23]

N-cadherin is expressed in regions of active remyelination and may play an important role in generating a local environment conducive to remyelination.[24] N-cadherin agonists have been identified and observed to stimulate neurite growth and cell migration, key aspects of promoting axon growth and remyelination after injury or disease.[25]

Immunomodulatory drugs such as fingolimod have been shown to reduce immune-mediated damage to the CNS, preventing further damage in patients with MS. The drug targets the role of macrophages in disease progression.[26][27]

Manipulating thyroid hormone levels may become a viable strategy to promote remyelination and prevent irreversible damage in MS patients.[28] It has also been shown that intranasal administration of apotransferrin (aTf) can protect myelin and induce remyelination.[29] Finally, electrical stimulation which activates neural stem cells may provide a method by which regions of demyelination can be repaired.[30]

In other animals

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Demyelinating diseases/disorders have been found worldwide in various animals. Some of these animals include mice, pigs, cattle, hamsters, rats, sheep, Siamese kittens, and a number of dog breeds (including Chow Chow, Springer Spaniel, Dalmatian, Samoyed, Golden Retriever, Lurcher, Bernese Mountain Dog, Vizsla, Weimaraner, Australian Silky Terrier, and mixed breeds).[31][32]

See also

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References

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  1. ^ "demyelinating disease" at Dorland's Medical Dictionary
  2. ^ Lotti M, Moretto A (2005). "Organophosphate-induced delayed polyneuropathy". Toxicol Rev. 24 (1): 37–49. doi:10.2165/00139709-200524010-00003. PMID 16042503. S2CID 29313644.
  3. ^ Konopaske GT, Dorph-Petersen KA, Sweet RA, Pierri JN, Zhang W, Sampson AR, Lewis DA (April 2008). "Effect of chronic antipsychotic exposure on astrocyte and oligodendrocyte numbers in macaque monkeys". Biol Psychiatry. 63 (8): 759–65. doi:10.1016/j.biopsych.2007.08.018. PMC 2386415. PMID 17945195.
  4. ^ Agadi S, Quach MM, Haneef Z (2013). "Vitamin-responsive epileptic encephalopathies in children". Epilepsy Res Treat. 2013: 510529. doi:10.1155/2013/510529. PMC 3745849. PMID 23984056.
  5. ^ Yoganathan S, Varman M, Oommen SP, Thomas M (2017). "A Tale of Treatable Infantile Neuroregression and Diagnostic Dilemma with Glutaric Aciduria Type I". J Pediatr Neurosci. 12 (4): 356–359. doi:10.4103/jpn.JPN_35_17. PMC 5890558. PMID 29675077.
  6. ^ Fernández O, Fernández VE, Guerrero M (2015). "Demyelinating diseases of the central nervous system". Medicine. 11 (77): 4601–4609. doi:10.1016/j.med.2015.04.001.
  7. ^ POSER CM (March 1961). "Leukodystrophy and the concept of dysmyelination". Arch Neurol. 4 (3): 323–32. doi:10.1001/archneur.1961.00450090089013. PMID 13737358.
  8. ^ Laetoli (January 2008). "Demyelination". Archived from the original on 2012-07-28.
  9. ^ "Symptoms of Demyelinating Disorders - Right Diagnosis." Right Diagnosis. Right Diagnosis, 01 Feb 2012. Web. 24 Sep 2012
  10. ^ Miller DJ, Duka T, Stimpson CD, Schapiro SJ, Baze WB, McArthur MJ, Fobbs AJ, Sousa AM, Sestan N, Wildman DE, Lipovich L, Kuzawa CW, Hof PR, Sherwood CC (October 2012). "Prolonged myelination in human neocortical evolution". Proc Natl Acad Sci U S A. 109 (41): 16480–5. Bibcode:2012PNAS..10916480M. doi:10.1073/pnas.1117943109. PMC 3478650. PMID 23012402.
  11. ^ Schoenemann PT, Sheehan MJ, Glotzer LD (February 2005). "Prefrontal white matter volume is disproportionately larger in humans than in other primates". Nat Neurosci. 8 (2): 242–52. doi:10.1038/nn1394. PMID 15665874. S2CID 205430527.
  12. ^ Chaudhuri A (October 2013). "Multiple sclerosis is primarily a neurodegenerative disease". J Neural Transm (Vienna). 120 (10): 1463–6. doi:10.1007/s00702-013-1080-3. PMID 23982272. S2CID 8575687.
  13. ^ a b c d e f g Freedman MS (2005). Advances in Neurology Volume 98: Multiple Sclerosis and Demyelinating Diseases. Philadelphia: Lippincott Williams & Wilkins. p. 112. ISBN 0781751705.
  14. ^ Weinshenker BG (1994). "Natural history of multiple sclerosis". Ann Neurol. 36 Suppl: S6–11. doi:10.1002/ana.410360704. PMID 8017890. S2CID 7140070.
  15. ^ a b Compston A, Coles A (October 2008). "Multiple sclerosis". Lancet. 372 (9648): 1502–17. doi:10.1016/S0140-6736(08)61620-7. PMID 18970977. S2CID 195686659.
  16. ^ Minagar A, Alexander JS (December 2003). "Blood-brain barrier disruption in multiple sclerosis". Mult Scler. 9 (6): 540–9. doi:10.1191/1352458503ms965oa. PMID 14664465. S2CID 10189144.
  17. ^ Abbott R, Silber E, Felber J, Ekpo E (October 2005). "Osmotic demyelination syndrome". BMJ. 331 (7520): 829–30. doi:10.1136/bmj.331.7520.829. PMC 1246086. PMID 16210283.
  18. ^ Rodriguez M, Siva A, Cross SA, O'Brien PC, Kurland LT (February 1995). "Optic neuritis: a population-based study in Olmsted County, Minnesota". Neurology. 45 (2): 244–50. doi:10.1212/wnl.45.2.244. PMID 7854520. S2CID 25800388.
  19. ^ Rosati G (April 2001). "The prevalence of multiple sclerosis in the world: an update". Neurol Sci. 22 (2): 117–39. doi:10.1007/s100720170011. PMID 11603614. S2CID 207051545.
  20. ^ Newcombe J, Eriksson B, Ottervald J, Yang Y, Franzén B (February 2005). "Extraction and proteomic analysis of proteins from normal and multiple sclerosis postmortem brain". J Chromatogr B. 815 (1–2): 191–202. doi:10.1016/j.jchromb.2004.10.073. PMID 15652809.
  21. ^ Palumbo S, Toscano CD, Parente L, Weigert R, Bosetti F (May 2012). "The cyclooxygenase-2 pathway via the PGE₂ EP2 receptor contributes to oligodendrocytes apoptosis in cuprizone-induced demyelination". J Neurochem. 121 (3): 418–27. doi:10.1111/j.1471-4159.2011.07363.x. PMC 3220805. PMID 21699540.
  22. ^ Clarner T, Diederichs F, Berger K, Denecke B, Gan L, van der Valk P, Beyer C, Amor S, Kipp M (October 2012). "Myelin debris regulates inflammatory responses in an experimental demyelination animal model and multiple sclerosis lesions". Glia. 60 (10): 1468–80. doi:10.1002/glia.22367. PMID 22689449. S2CID 205834726.
  23. ^ Podbielska M, Banik NL, Kurowska E, Hogan EL (August 2013). "Myelin recovery in multiple sclerosis: the challenge of remyelination". Brain Sci. 3 (4): 1282–324. doi:10.3390/brainsci3031282. PMC 4061877. PMID 24961530.
  24. ^ Hochmeister S, Romauch M, Bauer J, Seifert-Held T, Weissert R, Linington C, Hartung HP, Fazekas F, Storch MK (September 2012). "Re-expression of N-cadherin in remyelinating lesions of experimental inflammatory demyelination". Exp Neurol. 237 (1): 70–7. doi:10.1016/j.expneurol.2012.06.010. PMID 22735489. S2CID 33883037.
  25. ^ Burden-Gulley SM, Gates TJ, Craig SE, Gupta M, Brady-Kalnay SM (May 2010). "Stimulation of N-cadherin-dependent neurite outgrowth by small molecule peptide mimetic agonists of the N-cadherin HAV motif". Peptides. 31 (5): 842–9. doi:10.1016/j.peptides.2010.02.002. PMID 20153391. S2CID 207357858.
  26. ^ Gasperini C, Ruggieri S (2012). "Development of oral agent in the treatment of multiple sclerosis: how the first available oral therapy, fingolimod will change therapeutic paradigm approach". Drug Des Devel Ther. 6: 175–86. doi:10.2147/DDDT.S8927. PMC 3414371. PMID 22888218.
  27. ^ Ransohoff RM, Howe CL, Rodriguez M (November 2002). "Growth factor treatment of demyelinating disease: at last, a leap into the light". Trends Immunol. 23 (11): 512–6. doi:10.1016/s1471-4906(02)02321-9. PMID 12401395.
  28. ^ Silvestroff L, Bartucci S, Pasquini J, Franco P (May 2012). "Cuprizone-induced demyelination in the rat cerebral cortex and thyroid hormone effects on cortical remyelination". Exp Neurol. 235 (1): 357–67. doi:10.1016/j.expneurol.2012.02.018. PMID 22421533. S2CID 1534460.
  29. ^ Guardia Clausi M, Paez PM, Campagnoni AT, Pasquini LA, Pasquini JM (October 2012). "Intranasal administration of aTf protects and repairs the neonatal white matter after a cerebral hypoxic-ischemic event". Glia. 60 (10): 1540–54. doi:10.1002/glia.22374. hdl:11336/67318. PMID 22736466. S2CID 28658807.
  30. ^ Sherafat MA, Heibatollahi M, Mongabadi S, Moradi F, Javan M, Ahmadiani A (September 2012). "Electromagnetic field stimulation potentiates endogenous myelin repair by recruiting subventricular neural stem cells in an experimental model of white matter demyelination". J Mol Neurosci. 48 (1): 144–53. doi:10.1007/s12031-012-9791-8. PMID 22588976. S2CID 15779187.
  31. ^ "Merck Veterinary Manual – Demyelinating Disorders: Introduction". Archived from the original on 2010-12-19. Retrieved 2012-10-30.
  32. ^ Johnson RT (2004). "Demyelinating Diseases". The Infectious Etiology of Chronic Diseases: Defining the Relationship, Enhancing the Research, and Mitigating the Effects: Workshop Summary. NIH.
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