There are so many things in the world
that are out of our hands. The first thing that comes to my mind is
neurological diseases because in most cases these are genetic so it is not much
you can do to prevent them. For example, Multiple sclerosis is partially
genetic, however, there are risk factors that could increase one's risk of
developing this disease (Lassmann). Multiple sclerosis (MS) is a chronic
inflammatory demyelinating disease, meaning it is because of focal lesions in
the white and gray matter that diffuse neurodegenerative neurons in the brain
(Lassmann). In the brain, lesions trick the human immune system to attack the
protective sheath that covers nerve fibers. Once the brain when the myelin
sheath reaches a point where there is no protection, permanent damage begins,
meaning the deterioration of the nerves cannot grow back (Patsopoulos).
When it comes to treatments there are
different ways to approach it, many researchers focus on disease-modifying
therapies. As more disease-modifying therapies (DMT) are developed it continues
to reduce the frequency of relapses of MS making it easier for people living
with this disease. The main goal of this therapy is to reduce the early
clinical disease activity that is known to contribute to long-term disabilities
(Hart).
A trial with Alemtuzumab (which is a
DMT), “given 3 times weekly, and showed superior efficacy in both trials…
annualized relapse rate was 52%, then patients receiving Alemtuzumab had a 26%
relapse rate” (Hart). They observed that they had more successful results when
the treatment was initiated early during MS (Noyes).
A common type of drug that is given to
MS patients is corticosteroids, which increase the hormone cortisol in your
body (Negaresh). Cortisol helps your body manage blood glucose levels as well
as the metabolism of proteins and carbohydrates (Negaresh). Another common
treatment is plasma exchange, which means taking the plasma out of your blood
and mixing it with a high protein solution then returning it back into the
body, this is used for decreasing symptoms that are severe and do not respond
to steroids (Negaresh). Both treatments are used to slow the development of
symptoms, not necessarily stop all the symptoms.
Overall, there is no cure for MS, however,
research has been done to prove that there are treatments to help improve the
quality of life of MS patients. These treatments include corticosteroids, plasma
exchange, physical therapy, muscle relaxants, yoga and aquatics, coordination
therapy, and of course medications to lessen specific symptoms. Researchers
have made a lot of progress with treatments, however much more is needed to
make real improvements within the MS community. With the correct treatment and
therapy, MS patients can very much so live a somewhat normal life, many even
continue to work their jobs years after being diagnosed (Kleinman).
Hart FM, Bainbridge J. Current, and emerging treatment of
multiple sclerosis. Am J Manag Care. 2016 Jun;22(6 Suppl): s159-70. PMID:
27356025.
Kleinman NL, Beren IA, Rajagopalan K, Brook RA. Medication
adherence with disease-modifying treatments for multiple sclerosis among US
employees. J Med Econ. 2010;13(4):633-40. doi: 10.3111/13696998.2010.527588.
Epub 2010 Oct 19. PMID: 20958113.
Lassmann H. Multiple Sclerosis Pathology. Cold Spring Harb
Perspect Med. 2018 Mar 1;8(3): a028936. doi: 10.1101/cshperspect. a028936.
PMID: 29358320; PMCID: PMC5830904.
Negaresh R, Motl R, Mokhtarzade M,
Ranjbar R, Majdinasab N, Khodadoost M, Zimmer P, Baker JS, Patel D. Effect of
Short-Term Interval Exercise Training on Fatigue, Depression, and Fitness in
Normal Weight vs. Overweight Person with Multiple Sclerosis. Explore (NY). 2019
Mar-Apr;15(2):134-141. doi: 10.1016/j.explore.2018.07.007. Epub 2018 Jul 20.
PMID: 30122328.
Noyes K, Weinstock-Guttman B. Impact of diagnosis and early
treatment on the course of multiple sclerosis. Am J Manag Care. 2013 Nov;19(17
Suppl): s321-31. PMID: 24494633.
Patsopoulos NA. Genetics of Multiple Sclerosis: An Overview
and New Directions. Cold Spring Harb Perspect Med. 2018 Jul 2;8(7): a028951.
doi: 10.1101/cshperspect. a028951. PMID: 29440325; PMCID: PMC6027932
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