Multiple sclerosis
| Multiple sclerosis | |
|---|---|
| Other names | Multiple cerebral sclerosis, multiple cerebro-spinal sclerosis, disseminated sclerosis, encephalomyelitis disseminata |
| CD68-stained tissue shows several macrophages in the area of a demyelinated lesion caused by MS. | |
| Specialty | Neurology |
| Symptoms | Involving autonomic, visual, motor, and sensory systems, almost any central or peripheral neurological symptom.[1] |
| Usual onset | Age 20–50[2] |
| Duration | Long term[3] |
| Causes | Unknown[4] |
| Diagnostic method | Based on symptoms and medical tests[5] |
| Treatment | |
| Frequency | 0.032% (world) |
Multiple sclerosis (MS) is an autoimmune disease resulting in damage to myelin which is the insulating covers of nerve cells in the brain and spinal cord.[3] As a demyelinating disease, MS disrupts the nervous system's ability to transmit signals, resulting in a range of signs and symptoms, including physical, mental, and sometimes psychiatric problems.[1][8][9] Symptoms include double vision, vision loss, eye pain, muscle weakness, and loss of sensation or coordination.[3][10][11]
MS takes several forms of presentation:
- New symptoms can occur as an isolated attack; where the patient experiences neurological symptoms suddenly and then gets better (relapsing form) called relapsing- remitting MS which is seen in 85% of patients. [12]
- In other patients symptoms can slowly get worse over time (progressive form) called primarily progressive MS seen in 15% of patients. [13][14] [12]
- The patients with relapsing- remitting MS can experience gradual worsening of their symptoms following the attacks, this subtype is called secondary progressive MS.[12] In relapsing forms of MS, symptoms may disappear completely between attacks, although some permanent neurological problems often remain, especially as the disease advances.[14] In progressive forms of MS, the body's function slowly deteriorates once symptoms manifest and will steadily worsen if left untreated.[15]
- A patient might have a single attack and not meet the full criteria for being diagnosed with MS this is called a clinically isolated syndrome.[12]
While its cause is unclear, the underlying mechanism is thought to be due to either destruction by the immune system or inactivation of myelin-producing cells.[4] Proposed causes for this include immune dysregulation, genetics, and environmental factors, such as viral infections.[16][17][8][18] The McDonald criteria are a frequently updated set of guidelines used to establish an MS diagnosis.[19]
There is no cure for MS.[3] Current treatments aim to reduce inflammation and resulting symptoms from acute flares and prevent further attacks with disease-modifying medications, aiming at slowing prognosis and improving quality of life.[8][20] Physical therapy[7] and occupational therapy,[21] along with patient-centered symptom management, can help with people's ability to function. The long-term outcome is difficult to predict; better outcomes are more often seen in women, those who develop the disease early in life, those with a relapsing course, and those who initially experienced few attacks.[22]
New evidence suggests an important role of lifestyle factors in the prognosis of MS, where multiple lifestyle factors (including smoking, alcohol consumption, exercise, diet and vitamin D levels..) have been linked to affecting the EDSS score depending on patients' age, gender and disease duration. [23][24]
MS is the most common immune-mediated disorder affecting the central nervous system (CNS).[25] In 2020, about 2.8 million people were affected by MS globally, with rates varying widely in different regions and among different populations.[26] The disease usually begins between the ages of 20 and 50 [2]and is almost three times more common in females than in males (3:1 ratio).[27]
MS was first described in 1868 by French neurologist Jean-Martin Charcot.[28] The name "multiple sclerosis" is short for multiple cerebro-spinal sclerosis, which refers to the numerous glial scars (or sclerae – essentially plaques or lesions) that develop on the white matter of the brain and spinal cord.[28]
- ^ a b Compston A, Coles A (October 2008). "Multiple sclerosis". Lancet. 372 (9648): 1502–1517. doi:10.1016/S0140-6736(08)61620-7. PMID 18970977. S2CID 195686659.
- ^ a b Milo R, Kahana E (March 2010). "Multiple sclerosis: geoepidemiology, genetics and the environment". Autoimmunity Reviews. 9 (5): A387-94. doi:10.1016/j.autrev.2009.11.010. PMID 19932200.
- ^ a b c d "NINDS Multiple Sclerosis Information Page". National Institute of Neurological Disorders and Stroke. 30 June 2025. Archived from the original on 4 June 2025. Retrieved 30 June 2025.
- ^ a b Nakahara J, Maeda M, Aiso S, Suzuki N (February 2012). "Current concepts in multiple sclerosis: autoimmunity versus oligodendrogliopathy". Clinical Reviews in Allergy & Immunology. 42 (1): 26–34. doi:10.1007/s12016-011-8287-6. PMID 22189514. S2CID 21058811.
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- ^ a b c Alphonsus KB, Su Y, D'Arcy C (April 2019). "The effect of exercise, yoga and physiotherapy on the quality of life of people with multiple sclerosis: Systematic review and meta-analysis". Complementary Therapies in Medicine. 43: 188–195. doi:10.1016/j.ctim.2019.02.010. PMID 30935529. S2CID 86669723.
- ^ a b c Compston A, Coles A (April 2002). "Multiple sclerosis". Lancet. 359 (9313): 1221–1231. doi:10.1016/S0140-6736(02)08220-X. PMID 11955556. S2CID 14207583.
- ^ Murray ED, Buttner EA, Price BH (2012). "Depression and Psychosis in Neurological Practice". In Daroff R, Fenichel G, Jankovic J, Mazziotta J (eds.). Bradley's neurology in clinical practice (6th ed.). Philadelphia, PA: Elsevier/Saunders. ISBN 978-1-4377-0434-1.
- ^ Piryonesi SM, Rostampour S, Piryonesi SA (April 2021). "Predicting falls and injuries in people with multiple sclerosis using machine learning algorithms". Multiple Sclerosis and Related Disorders. 49 102740. doi:10.1016/j.msard.2021.102740. PMID 33450500. S2CID 231624230.
- ^ Mazumder R, Murchison C, Bourdette D, Cameron M (25 September 2014). "Falls in people with multiple sclerosis compared with falls in healthy controls". PLOS ONE. 9 (9): e107620. Bibcode:2014PLoSO...9j7620M. doi:10.1371/journal.pone.0107620. PMC 4177842. PMID 25254633.
{{cite journal}}: CS1 maint: article number as page number (link) - ^ a b c d Ford H (July 2020). "Clinical presentation and diagnosis of multiple sclerosis". Clinical Medicine. 20 (4). London, England: 380–383. doi:10.7861/clinmed.2020-0292. ISSN 1473-4893. PMC 7385797. PMID 32675142.
- ^ Baecher-Allan C, Kaskow BJ, Weiner HL (February 2018). "Multiple Sclerosis: Mechanisms and Immunotherapy". Neuron. 97 (4): 742–768. doi:10.1016/j.neuron.2018.01.021. PMID 29470968. S2CID 3499974.
- ^ a b Lublin FD, Reingold SC (April 1996). "Defining the clinical course of multiple sclerosis: results of an international survey. National Multiple Sclerosis Society (USA) Advisory Committee on Clinical Trials of New Agents in Multiple Sclerosis". Neurology. 46 (4): 907–911. doi:10.1212/WNL.46.4.907. PMID 8780061. S2CID 40213123.
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- ^ Ward M, Goldman MD (August 2022). "Epidemiology and Pathophysiology of Multiple Sclerosis". Continuum. 28 (4): 988–1005. doi:10.1212/CON.0000000000001136. PMID 35938654. S2CID 251375096.
- ^ Aloisi F, Cross AH (October 2022). "MINI-review of Epstein-Barr virus involvement in multiple sclerosis etiology and pathogenesis". Journal of Neuroimmunology. 371 577935. doi:10.1016/j.jneuroim.2022.577935. PMID 35931008. S2CID 251152784.
- ^ Ascherio A, Munger KL (April 2007). "Environmental risk factors for multiple sclerosis. Part I: the role of infection". Annals of Neurology. 61 (4): 288–299. doi:10.1002/ana.21117. PMID 17444504. S2CID 7682774.
- ^ "The McDonald criteria". MS Society UK. 31 May 2023. Archived from the original on 2 December 2024. Retrieved 26 November 2024.
- ^ McGinley MP, Goldschmidt CH, Rae-Grant AD (February 2021). "Diagnosis and Treatment of Multiple Sclerosis: A Review". JAMA. 325 (8): 765–779. doi:10.1001/jama.2020.26858. PMID 33620411. S2CID 232019589.
- ^ Quinn É, Hynes SM (July 2021). "Occupational therapy interventions for multiple sclerosis: A scoping review". Scandinavian Journal of Occupational Therapy. 28 (5): 399–414. doi:10.1080/11038128.2020.1786160. hdl:10379/16066. PMID 32643486. S2CID 220436640.
- ^ Weinshenker BG (1994). "Natural history of multiple sclerosis". Annals of Neurology. 36 (Suppl): S6-11. doi:10.1002/ana.410360704. PMID 8017890. S2CID 7140070.
- ^ Wecker S, Freudenstein D, Ganser I, Angstwurm K, Lee DH, Linker RA (2024). "The impact of different lifestyle factors on disability in multiple sclerosis at older ages: a monocentric retrospective study". Therapeutic Advances in Neurological Disorders. 17 17562864241284166. doi:10.1177/17562864241284166. ISSN 1756-2856. PMC 11528639. PMID 39494114.
- ^ Dobson R, Giovannoni G (2019). "Multiple sclerosis – a review". European Journal of Neurology. 26 (1): 27–40. doi:10.1111/ene.13819. ISSN 1468-1331. PMID 30300457.
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- ^ a b Clanet M (June 2008). "Jean-Martin Charcot. 1825 to 1893". International MS Journal. 15 (2): 59–61. PMID 18782501.
* Charcot J (1868). "Histologie de la sclerose en plaques". Gazette des Hopitaux, Paris. 41: 554–5.