FREE ESSAY ON MULTIPLE SCLEROSIS A+ RESEARCH PAPER...

MULTIPLE SCLEROSIS A+ RESEARCH PAPER...

Introduction
Multiple Sclerosis
Stephanie ****
Multiple Sclerosis (MS) is a chronic, often disabling disease that randomly attacks the
central nervous system (brain and spinal cord). The progress, severity and specific
symptoms of
the disease can not be predicted; symptoms may range from tingling and numbness to
paralysis
and blindness. MS is a devastating disease because people live with its unpredictable
physical and
emotional effects for the rest of their lives.
MS is a well-known disease, but poorly understood. In the United States there are
approximately 200 new cases diagnosed each week; MS is a common disease and not always
caused by genetics. Therefore, I feel we all need to have a better understanding of this
disease that
has no cure yet. I hope to make MS more understanding in my paper.
In my paper I will explain what MS is, who gets MS, what MS has to do with the
metabolism, some new techniques being used to pinpoint genetic factors, what some of the
symptoms of MS is, and some treatments for MS. 
Multiple Sclerosis
Multiple sclerosis (MS) is a progressive disabling illness that affects nerve cells in
the brain and spinal
cord (Bernard). Under normal conditions these nerve cells are surrounded by an insulating
sheath made of fatty
myelin, which speeds the passage of nerve impulses. In MS, this myelin sheath is inflamed
or damaged,
disrupting nerve impulses and leaving areas of scarring (sclerosis). The disruption of
nerve signals within the
brain and spinal cord causes a variety of symptoms that may affect vision, sensation, and
body movements. "These
symptoms usually wax and wane through a series of relapses (episodes when symptoms
suddenly get worse)
alternating with remissions (periods of recovery, when symptoms improve)."
(Brunnscheiler) For many patients,
a long history of MS attacks over several decades leads to slowly progressing disability,
but for others the
disability is more rapid and severe.
MS is a life-long chronic disease diagnosed primarily in young adults who have a
virtually normal life
expectancy. Consequently, the economic, social, and medical costs associated with the
disease are significant.
Estimates place the annual costs of MS in the United States in excess of $2.5 billion.
(Melvin)
No one knows exactly how many people have MS. It is believed that, currently, there are
approximately
250,000 to 350,000 people in the United States with MS diagnosed by a physician. (Boyden)
This estimate
suggests that approximately 200 new cases are diagnosed each week. 
Also, MS is the most common nerve disease to develop in young persons after birth, and it
affects over 1
million young adults worldwide. "Close relatives of a person with MS are 8 times more
likely than average to
develop the disease themselves, and children of a person with MS run 30 to 50 times the
average risk."
(Waxman) 
Most people experience their first symptoms of MS between the ages of 20 and 40, but a
diagnosis is often
delayed. This is due to both the transitory nature of the disease and the lack of a
specific diagnostic test--specific 
symptoms and changes in the brain must develop before the diagnosis is confirmed. (Health
Central)
Although scientists have documented cases of MS in young children and elderly adults,
symptoms rarely
begin before age 15 or after age 60. Whites are more than twice as likely as other races
to develop MS. In general,
women are affected at almost twice the rate of men; however, among patients who develop
the symptoms of MS at
a later age, the gender ratio is more balanced. (Waxman)
To understand what is happening when a person has MS, it is first necessary to know a
little about how
the healthy immune system works. The immune system -- a complex network of specialized
cells and organs --
defends the body against attacks by foreign invaders such as bacteria, viruses, fungi,
and parasites. It does this
by seeking out and destroying the interlopers as they enter the body. Substances capable
of triggering an immune
response are called antigens. (Hofmann)
"The immune system displays both enormous diversity and extraordinary specificity."
(Hofmann) It can
recognize millions of distinctive foreign molecules and produce its own molecules and
cells to match up with and
counteract each of them. In order to have room for enough cells to match the millions of
possible foreign
invaders, the immune system stores just a few cells for each specific antigen. When an
antigen appears, those few
specifically matched cells are stimulated to multiply into a full-scale army. Later, to
prevent this army from
overexpanding, powerful mechanisms to suppress the immune response come into play. 
T-cells, so named because they are processed in the thymus, appear to play a particularly
important role in
MS. They travel widely and continuously throughout the body patrolling for foreign
invaders. In order to
recognize and respond to each specific antigen, each T cell's surface carries special
receptor molecules for
particular antigens. 
T cells contribute to the body's defenses in two major ways. "Regulatory T cells help
orchestrate the
elaborate immune system. " ( Kaser) For instance, they assist other cells to make
antibodies, proteins programmed
to match one specific antigen much as a key matches a lock. Antibodies typically interact
with circulating 
antigens, such as bacteria, but are unable to penetrate living cells. Chief among the
regulatory T cells are those
known as helper (or inducer) cells. "Helper T cells are essential for activating the
body's defenses against foreign
substances. " (Kaser) Yet another subset of regulatory T cells acts to turn off, or
suppress, various immune
system cells when their job is done. 
Killer T cells, on the other hand, directly attack diseased or damaged body cells by
binding to them and
bombarding them with lethal chemicals called cytokines. ( Kaser) Since T cells can attack
cells directly, they
must be able to discriminate between self cells (those of the body) and nonself cells
(foreign invaders). To
enable the immune system to distinguish the self, each body cell carries identifying
molecules on its surface. T
cells likely to react against the self are usually eliminated before leaving the thymus;
the remaining T cells
recognize the molecular markers and coexist peaceably with body tissues in a state of
self-tolerance. 
"In autoimmune diseases such as MS, the detente between the immune system and the body is
disrupted
when the immune system seems to wrongly identify self as nonself and declares war on the
part of the body
(myelin) it no longer recognizes." (Hauser) Through intensive research efforts,
scientists are unraveling the 
complex secrets of the malfunctioning immune system of patients with MS. 
Components of myelin such as myelin basic protein have been the focus of much research
because, when
injected into laboratory animals, they can precipitate experimental allergic
encephalomyelitis (EAE), a chronic 
relapsing brain and spinal cord disease that resembles MS. The injected myelin probably
stimulates the immune
system to produce anti-myelin T cells that attack the animal's own myelin. (Leuven)
Investigators are also looking for abnormalities or malfunctions in the blood/brain
barrier, a protective
membrane that controls the passage of substances from the blood into the central nervous
system. It is possible
that, in MS, components of the immune system get through the barrier and cause nervous
system damage. 
"Scientists have studied a number of infectious agents (such as viruses) that have been
suspected of
causing MS, but have been unable to implicate any one particular agent." (Mayo Clinic)
Viral infections are
usually accompanied by inflammation and the production of gamma interferon, a naturally
occurring body
chemical that has been shown to worsen the clinical course of MS. It is possible that the
immune response to
viral infections may themselves precipitate an MS attack.
"The genes a person inherits may help determine whether that person is at increased risk
for developing
MS." ( Melvin) While there is evidence from studies that this genetic component exists,
it appears to be only one
factor among several. Most likely an individual's genetic blueprint ultimately determines
if that individual will be
susceptible to a triggering factor, which in turn initiates the autoimmune process that
leads to the development of
MS.
In the past few years, scientists have developed a set of tools that gives them the
ability to pinpoint the
genetic factors that make a person susceptible to MS. "These tools are the methods of
molecular
genetics-techniques used to isolate and determine the chemical structure of genes."
(Colin)
In the 1980s, scientists began to apply the tools of molecular genetics to human diseases
caused by defects
in single genes. This work led to major advances in understanding diseases such as
Duchenne muscular dystrophy
and cystic fibrosis. The situation for diseases such as multiple sclerosis is more
complicated. Scientists now believe
that a person is susceptible to multiple sclerosis only if he or she inherits an unlucky
combination of several genes.
(Colin)
Advances in molecular genetics and the identification of large families in which several
members have
MS-multiplex MS families-have made possible research to uncover MS susceptibility genes.
"Since 1991, the
National MS Society has supported an international project searching for these genes." (
National Multiple
Sclerosis Society) 
However, even though genetic (inherited) factors seem to play a large role in the
development of MS, no
single MS gene has been identified so far. Instead, scientists suspect that MS develops
because of the influence of
several genes acting together. 
Many multiplex families from throughout the world have agreed to participate in these
studies. The
researchers are looking for patterns of genetic material that are consistently inherited
by people with MS. These
recognizable patterns are called DNA markers. (Melvin)
When one of these markers is identified, scientists focus on that area, seeking
additional markers closer
to that gene. Eventually the location of that gene can be identified. This process of
moving closer to the gene until
it is identified has to be repeated for each of the marker regions from the multiplex
families. (Melvin)
By 1996, as many as 20 locations that may contain genes contributing to MS were
identified, but no
single gene was shown to have a major influence on susceptibility to MS. (Melvin)
Research will likely find
that other, as yet unidentified, genes contribute to MS.
After the location of each susceptibility gene is identified, the role that the gene
plays in the immune
system and neuralgic aspects of people with MS will have to be determined. Because the
immune system is so
involved in MS, many scientists think at least some of the susceptibility genes are
related to the immune system.
Already there have been reports linking some immune system genes to MS.
Further indications that more than one gene is involved in MS susceptibility comes from
studies of
families in which more than one member has MS. Several research teams found that people
with MS inherit
certain regions on individual genes more frequently than people without MS. Of particular
interest is the human
leukocyte antigen (HLA) or major histocompatibility complex region on chromosome 6. HLAs
are genetically
determined proteins that influence the immune system. ( Kaser)
The HLA patterns of MS patients tend to be different from those of people without the
disease.
Investigations in northern Europe and America have detected three HLAs that are more
prevalent in people with
MS than in the general population. Studies of American MS patients have shown that people
with MS also tend
to exhibit these HLAs in combination--that is, they have more than one of the three
HLAs--more frequently than
the rest of the population. Furthermore, there is evidence that different combinations of
the HLAs may correspond
to variations in disease severity and progression. ( Kaser)
Studies of families with multiple cases of MS and research comparing genetic regions of
humans to those
of mice with EAE suggest that another area related to MS susceptibility may be located on
chromosome 5. Other
regions on chromosomes 2, 3, 7, 11, 17, 19, and X have also been identified as possibly
containing genes
involved in the development of MS. (Hauser)
These studies strengthen the theory that MS is the result of a number of factors rather
than a single gene
or other agent. Development of MS is likely to be influenced by the interactions of a
number of genes, each of
which (individually) has only a modest effect. Additional studies are needed to
specifically pinpoint which genes
are involved, determine their function, and learn how each gene's interactions with other
genes and with the
environment make an individual susceptible to MS. "In addition to leading to better ways
to diagnose MS, such 
studies should yield clues to the underlying causes of MS and, eventually, to better
treatments or a way to prevent
the disease." (Ronthal)
Finding the genes responsible for susceptibility to MS may lead to the development of
new
and more effective ways to treat the disease. Such research could also uncover the basic
cause of the disease and
help predict the course of the disease in an individual. This would make it easier for
physicians to tailor therapies
and provide information to help people make life decisions. 
Another possible benefit may be the early diagnosis of people in families where one or
more member
already has MS. Many physicians believe that the earlier MS is diagnosed and treatment
begun, the better the
outcome will be. 
Symptoms of MS may be mild or severe, of long duration or short, and may appear in
various
combinations, depending on the area of the nervous system affected. Complete or partial
remission of symptoms,
especially in the early stages of the disease, occurs in approximately 70 percent of MS
patients. 
"The initial symptom of MS is often blurred or double vision, red-green color distortion,
or even
blindness in one eye." (Brunnscheiler) Inexplicably, visual problems tend to clear up in
the later stages of MS.
Inflammatory problems of the optic nerve may be diagnosed as retrobulbar or optic
neuritis. Fifty-five percent of
MS patients will have an attack of optic neuritis at some time or other and it will be
the first symptom of MS in
approximately 15 percent. This has led to general recognition of optic neuritis as an
early sign of MS, especially if
tests also reveal abnormalities in the patient's spinal fluid. (National Multiple
Sclerosis Society)
Most MS patients experience muscle weakness in their extremities and difficulty with
coordination and
balance at some time during the course of the disease. These symptoms may be severe
enough to impair walking or
even standing. In the worst cases, MS can produce partial or complete paralysis.
"Spasticity, the involuntary
increased tone of muscles leading to stiffness and spasms--is common, as is fatigue."
(Brunnscheiler) Fatigue may
be triggered by physical exertion and improve with rest, or it may take the form of a
constant and persistent
tiredness. 
Most people with MS also exhibit paresthesias, transitory abnormal sensory feelings such
as numbness,
prickling, or pins and needles sensations; uncommonly, some may also experience pain.
Loss of sensation
sometimes occurs. Speech impediments, tremors, and dizziness are other frequent
complaints. Occasionally, people
with MS have hearing loss. (Brunnscheiler ; National Multiple Sclerosis Society) 
Approximately half of all people with MS experience cognitive impairments such as
difficulties with
concentration, attention, memory, and poor judgment, but such symptoms are usually mild
and are frequently
overlooked. In fact, they are often detectable only through comprehensive testing.
Patients themselves may be
unaware of their cognitive loss; it is often a family member or friend who first notices
a deficit. Such impairments
are usually mild, rarely disabling, and intellectual and language abilities are generally
spared. (Brunnscheiler) 
"Cognitive symptoms occur when lesions develop in brain areas responsible for information
processing." 
(Brunnscheiler) These deficits tend to become more apparent as the information to be
processed becomes more
complex. Fatigue may also add to processing difficulties. Scientists do not yet know
whether altered cognition in 
MS reflects problems with information acquisition, retrieval, or a combination of both.
Types of memory problems
may differ depending on the individual's disease course (relapsing-remitting,
primary-progressive, etc.), but there
does not appear to be any direct correlation between duration of illness and severity of
cognitive dysfunction. 
(National Multiple Sclerosis Society)
"Depression, which is unrelated to cognitive problems, is another common feature of MS. 
(Brunnscheiler) In addition, about 10 percent of patients suffer from more severe
psychotic disorders such as
manic-depression and paranoia. Five percent may experience episodes of inappropriate
euphoria and
despair--unrelated to the patient's actual emotional state known as laughing/weeping
syndrome. This syndrome
is thought to be due to demyelination in the brainstem, the area of the brain that
controls facial expression and
emotions, and is usually seen only in severe cases. (National Multiple Sclerosis
Society)
As the disease progresses, sexual dysfunction may become a problem. Bowel and bladder
control may
also be lost. (Health Central)
In about 60 percent of MS patients, heat, whether generated by temperatures outside the
body or by
exercise may cause temporary worsening of many MS symptoms. In these cases, eradicating
the heat eliminates
the problem. Some temperature-sensitive patients find that a cold bath may temporarily
relieve their symptoms. For
the same reason, "swimming is often a good exercise choice for people with MS." (Wenzel)

The erratic symptoms of MS can affect the entire family as patients may become unable to
work at the
same time they are facing high medical bills and additional expenses for housekeeping
assistance and
modifications to homes and vehicles. The emotional drain on both patient and family is
immeasurable. Counseling
may help MS patients, their families, and friends find ways to cope with the many
problems the disease can cause. 
(Lambert)
"There is as yet no cure for MS. Many patients do well with no therapy at all, especially
since many
medications have serious side effects and some carry significant risks." (Health Central)
Naturally occurring or
spontaneous remissions make it difficult to determine therapeutic effects of experimental
treatments; however, the
emerging evidence that MRIs can chart the development of lesions is already helping
scientists evaluate new
therapies. 
Until recently, the principal medications physicians used to treat MS were steroids
possessing
anti-inflammatory properties; these include adrenocorticotropic hormone (better known as
ACTH), prednisone, 
prednisolone, methylprednisolone, betamethasone, and dexamethasone. Studies suggest that
intravenous
methylprednisolone may be superior to the more traditional intravenous ACTH for patients
experiencing acute
relapses; no strong evidence exists to support the use of these drugs to treat
progressive forms of MS. Also, there is
some indication that steroids may be more appropriate for people with movement, rather
than sensory, symptoms. 
(Mayo Clinic)
While steroids do not affect the course of MS over time, they can reduce the duration and
severity of
attacks in some patients. The mechanism behind this effect is not known; one study
suggests the medications work
by restoring the effectiveness of the blood/brain barrier. "Because steroids can produce
numerous adverse side
effects (acne, weight gain, seizures, psychosis), they are not recommended for long-term
use." (Bernard)
One of the most promising MS research areas involves naturally occurring antiviral
proteins known as
interferons. Two forms of beta interferon (Avonex and Betaseron) have now been approved
by the Food and Drug 
Administration for treatment of relapsing-remitting MS. A third form (Rebif) is marketed
in Europe. Beta
interferon has been shown to reduce the number of exacerbation's and may slow the
progression of physical
disability. When attacks do occur, they tend to be shorter and less severe. In addition,
MRI scans suggest that beta
interferon can decrease myelin destruction. (Mayo Clinic)
Investigators speculate that the effects of beta interferon may be due to the drug's
ability to correct an
MS-related deficiency of certain white blood cells that suppress the immune system and/or
its ability to inhibit
gamma interferon, a substance believed to be involved in MS attacks. Alpha interferon is
also being studied as a
possible treatment for MS. (Mayo Clinic) "Common side effects of interferons include
fever, chills, sweating,
muscle aches, fatigue, depression, and injection site reactions." (Health Central)
Scientists continue their extensive efforts to create new and better therapies for MS.
Goals of therapy are
threefold: to improve recovery from attacks, to prevent or lessen the number of relapses,
and to halt disease
progression.
In conclusion, MS is a disease that is well known but poorly understood by the medical
and nursing
community as well as the general public. It has no known cure and the genes that are
accountable for it have yet
been pin pointed. The United States is capable of finding a cure for this disease; over
the years, medical researchers
have found cures for many diseases that were thought incurable. Not only time and money
are needed to find a cure
for this disease, but faith and heart are needed to realize the importance 
Glossary
antibodies -- proteins made by the immune system that bind to structures
(antigens) they recognize as foreign to the body. 
antigen -- a structure foreign to the body, such as a virus. The body usually
responds to antigens by producing antibodies. 
ataxia -- a condition in which the muscles fail to function in a coordinated
manner. 
autoimmune disease -- a disease in which the body's defense system
malfunctions and attacks a part of the body itself rather than foreign matter. 
blood/brain barrier -- a membrane that controls the passage of substances
from the blood into the central nervous system. 
cerebrospinal fluid -- the colorless liquid, consisting partially of substances
filtered from blood and partially by secretions released by brain cells, that
circulates around and through the cavities of the brain and spinal cord.
Physicians use a variety of tests--electrophoresis, isoelectric focusing, capillary
isotachophoresis, and radioimmunoassay--to study cerebrospinal fluid for
abnormalities often associated with MS. 
cytokines -- powerful chemical substances secreted by T cells. Cytokines are
an important factor in the production of inflammation and show promise as
treatments for MS. 
demyelination -- damage caused to myelin by recurrent attacks of
inflammation. Demyelination ultimately results in nervous system scars, called
plaques, which interrupt communications between the nerves and the rest of the
body. 
experimental allergic encephalomyelitis (EAE) -- a chronic brain and
spinal cord disease similar to MS which is induced by injecting myelin basic
protein into laboratory animals. 
fatigue -- tiredness that may accompany activity or may persist even without
exertion. 
gadolinium -- a chemical compound given during MRI scans that helps
distinguish new lesions from old. 
human leukocyte antigens (HLAs) -- antigens, tolerated by the body, that
correspond to genes that govern immune responses. Also known as major
histocompatibility complex. 
immunoglobulin G (IgG) -- an antibody-containing substance produced by
human plasma cells in diseased central nervous system plaques. Levels of IgG
are increased in the cerebrospinal fluid of most MS patients. 
immunosuppression -- suppression of immune system functions. Many
medications under investigation for the treatment of MS are
immunosuppressants. 
interferons -- cytokines belonging to a family of antiviral proteins that occur
naturally in the body. Gamma interferon is produced by immune system cells,
enhances T-cell recognition of antigens, and causes worsening of MS
symptoms. Alpha and beta interferon probably exert a suppressive effect on
the immune system and may be beneficial in the treatment of MS. 
lesion -- an abnormal change in the structure of an organ due to disease or
injury. 
magnetic resonance imaging (MRI) -- a non-invasive scanning technique
that enables investigators to see and track MS lesions as they evolve. 
myelin -- a fatty covering insulating nerve cell fibers in the brain and spinal
cord, myelin facilitates the smooth, high-speed transmission of electrochemical
messages between these components of the central nervous system and the
rest of the body. In MS, myelin is damaged through a process known as
demyelination, which results in distorted or blocked signals. 
myelin basic protein (MBP) -- a major component of myelin. When myelin
breakdown occurs (as in MS), MBP can often be found in abnormally high
levels in the patient's cerebrospinal fluid. When injected into laboratory animals,
MBP induces experimental allergic encephalomyelitis, a chronic brain and
spinal cord disease similar to MS. 
oligodendrocytes -- cells that make and maintain myelin. 
optic neuritis -- an inflammatory disorder of the optic nerve that usually
occurs in only one eye and causes visual loss and sometimes blindness. It is
generally temporary. 
paresthesias -- abnormal sensations such as numbness, prickling, or pins and
needles. 
plaques -- patchy areas of inflammation and demyelination typical of MS,
plaques disrupt or block nerve signals that would normally pass through the
regions affected by the plaques. 
receptor -- a protein on a cell's surface that allows the cell to identify antigens. 
retrobulbar neuritis -- an inflammatory disorder of the optic nerve that is
usually temporary. It causes rapid loss of vision and may cause pain upon
moving the eye. 
spasticity -- involuntary muscle contractions leading to spasms and stiffness or
rigidity. In MS, this condition primarily affects the lower limbs. 
T cells -- immune system cells that develop in the thymus gland. Findings
suggest that T cells are implicated in myelin destruction. 
transverse myelitis -- an acute spinal cord disorder causing sudden low back
pain and muscle weakness and abnormal sensory sensations in the lower
extremities. Transverse myelitis often remits spontaneously; however, severe or
long-lasting cases may lead to permanent disability. 
white matter -- nerve fibers that are the site of MS lesions and underlie the
gray matter of the brain and spinal cord. 
Bibliography
Bibliography
Bernard, Bobby. "Multiple Sclerosis Continues to Puzzle Scientists." The Vermillion
March 1998.
Brunnscheiler, H. "Problems Associated with MS"
(July 28, 1999)
"Inteli Health" http://www.intelihealth.com/ (28 July 1999).
Boyden, Kathleen M. "Compolmer-1 in the Treatment of Multiple Sclerosis."
Journal of Neuroscience Nursing 5 October 1998.
Waxman, Stephen. "Demyelinating Diseases -- New Pathological Insights, New Therapeutic
Targets."
New England Journal of Medicine 29 Jan. 1998, Vol. 338, No. 5, 323-327.
Health Central "General Information about Multiple Sclerosis" 
(July 16, 1999)
Hofmann, Robert. " Multiple Sclerosis" American Journal of Human Genetics June 1998, 
62:492-495
Kaser, Arthur. "Inter