CLINICAL AND NEUROLOGICAL FOR MULTIPLE SCLEROSIS
Karpov S.M., Pazhigova Z.B. Vyshlova I.A., Muravjev
K.A.
Stavropol State Medical University, Stavropol
Department of Neurology, Neurosurgery and Medical
Genetics
To this day, Multiple Sclerosis (MS) is still
recognized as an unsolved problem [2, 3, 6, 7, 9, 10, 11]. However, today, there is hope of a possible breakthrough in
the treatment and early diagnosis of the disease [5, 8, 9, 10, 12]. MS is very prevalent in today’s society [1,
4, 7]. The course of MS is, in most cases, the aggressive nature of the
disease, leading to varying degrees of disability. In this regard, early
diagnosis of the disease plays an important role.
Objective: to improve the diagnostic aspect of clinical and neurological
characteristics in patients with multiple sclerosis.
Materials and methods: A total of 79 patients (57 women and 22 men) with a
diagnosis of multiple sclerosis, a mean age of 34,31 ± 4,7 years, is in the
process of clinical examination and
under observation in the clinic of the Chechen Republic. Of the total
number of patients the following clinical forms of the disease have been
identified: remitting (RRMS) - 56.9%, secondary progressive (SPMS) - 18.9%, and
primary progressive (APP) to 24.2%. The age distribution of the types of MS are
presented in the table. The average duration of the disease, taking into
account the clinical form was: PPC - 3,3 ± 2,2 years, SPMS - 9,1 ± 4,2 years
PPRS - 2,7 ± 1,9 years.
Results and discussion: As a result of the clinical examination, 29 (36.7%)
patients had mild manifestations of MS (Group 1). In all cases, the patients in
this group was PPC. In 15 (51.7%) patients the severity of neurological
disorders on the EDSS scale score was 2.0, in 11 (37.9%) patients - 2.5 points,
3 (10.4%) patients - 3 points for scale EDSS. The neurological status of these
patients revealed a predominance of pyramidal insufficiency such as changes in
reflexes and the presence of paresis of varying severity, where the decline in
muscle strength varied from 1.5 to 3 points. In 26 (89.7%) cases, we recorded
anisoreflexsia along with loss of abdominal reflexes and pathological (jog,
Fist) reflexes. In 7 (24.1%) cases the motor disturbances had different
characteristics: monoparesis - in 2 (6.9%) patients, paraparesis - in 5
(17.2%). The total clinical score reflecting the severity of motor impairment
in the functional scale (FS 1), amounted to 1,4 ± 0,8. In 23 (79.3%) patients
cerebellar pathological changes were identified with light coordination
disorders such as mild ataxia, intention tremor and dysmetria when performing
the tests. The total clinical score reflecting the severity of violations on
the coordination functional scale (FS 2) was 1,41 ± 0,9. In 17 (58.6%) cases,
there has been a combination of pyramidal and cerebellar disorders, along with
hypoesthesia, the presence of paresthesia or numbness in one or both legs. An
objective examination revealed "mosaic" areas of infringement surface
sensitivity. Disturbances of proprioceptive sensitivity was observed in 5
(17.2%) patients. The total clinical score in this case, reflecting the
severity of sensory disorders in the functional scale (FS4), amounted to 1,1 ±
0,8. Violations of pelvic organs in the form of urgency combined with the
difficulty in emptying the bladder (detrusor-sphincter dyssynergia) was
observed in 6 (20.7%) patients, which were periodic. This corresponded to a
total clinical score on the scale (FS
5) 0,41 ± 0,9. In 13 (44.8%) patients abnormalities were identified in the
brainstem structures. For example, in 2 (6.9%) cases - violations of the
oculomotor nerve, in 5 (17.2%) cases - failure of the central facial nerve, in
4 (13.8%) patients - deviation of the tongue. The total clinical score on the
scale (FS 3), reflecting the degree of stem dysfunction was 1,68 ± 1,5.
It should be noted that in this group, symptoms
reported were associated with impaired phononastroeniya. So, in 16 (55.2%)
patients were noted fononastroeniya light violations, which could not affect
the EDSS scale score. In 12 (41.4%) cases, patients reported fatigue, loss of
memory, concentration, attention, rigid thinking. The total clinical score (FS
7), which reflects the degree of impairment of mnemonic functions, amounted to
1,11 ± 0,8. In 28 (63.3%) of people with MS medium severity was set (group 2).
The clinical manifestations of MS medium severity are characterized by the
presence of persistent focal neurologic deficit. In this group, 16 (57.1%) patients
had remission, in 8 (28.6%) - secondary progressive, in 4 (14.3%) - primary
progressive process. In all cases, in the 2nd group of patients, pyramidal
and cerebellar syndromes of varying
severity were identified in contrast to the 1st group, where defect of
pyramidal and cerebellar systems reported in 24.1%, 79.3% respectively. Pyramid
violations were detected in 19 (67.9%) patients in the form of paresis,
moderate or elevated. Monoparesis was detected in 4 (14.3%) patients,
paraparesis - in 6 (21.4%), hemiparesis - in 4 (14.3%), tetraparesis - in 5
(17.9%) patients. The total clinical score reflecting the severity of motor
impairment in the functional scale (FS 1), amounted to 3,7 ± 0,5, in 2.64 times
greater relative to the 1st group. The degree of Staten coordination violations
in the functional scale (FS 2), the total clinical score was 1,99 ± 0,9, which
is 1.38 times more than in the 1st group. In 15 (53.6%) patients had sensory
disorders manifested as a reduction in deep sensitivity, which clinically
manifested in the form of sensory ataxia, which is 36.4% more than in the 1st
group. The total clinical score reflecting the severity of sensory disorders in
the functional scale (FS 4) was 2,4 ± 0,7, which exceeds the total clinical
score in the 1st group in 2 times. Violations of the pelvic organs were
observed in 12 (42.9%) patients, which is 22.2% more relative to the 1st group.
The total clinical score scale (FS 5) was 1.05 ± 1.3, 2.56 times greater in
comparison to the 1st group. In 8 (28.6%) cases oculomotor disturbances were
recognized. Nystagmus was detected in 15 (53.6%) cases, which is almost 2 times
the display data on the 1st group. The total clinical score on this scale (FS
3) violations stem functions amounted to 2,2 ± 0,8 a 76% increase in Group 1.
Psychopathological changes were detected in 18 (64.3%) cases, which were
manifested in the form of mood lability,
in 8 patients (28.6%) there was a reduction of cognitive and mnemonic
processes, and reduced concentration. The total clinical score reflecting the
degree of impairment of cerebral functions (FS 7) was 1.41 ± 0.7, which is 1.41
times greater relative to the 1st group. In 22 (27.8%) cases of severe forms of
MS (group 3) , 7 (31.8%) - secondary progressive, 15 (68.2%) - primary progressive
type flow. The clinical picture of severe MS included the presence of coarse,
and significant focal neurologic deficit. The neurological movement disorder
prevailed, which is based on the defect of the pyramidal and cerebellar
connections and structures that have been identified in all cases (100%).
Impaired function of the pyramidal system manifested in the form of hypertonia,
hyperreflexia, pathological reflexes.
Tetraparesis, paraplegia or hemiplegia of varying severity, usually
combined with a stop or clonus patella. The total clinical score reflecting the
severity of motor impairment in the functional scale (FS 1) was 4,4 ± 0,8, 3.14
times greater relative to group 1, and 1.19 more than in the 2nd group. In 6
(27.3%) patients coordination symptoms was presented in the form of expressed
intention tremor, and discoordination impairments that significantly reduces
the quality of life of the patient. In 4 (18.2%) patients, getting out of bed
they experienced head tremor. In seven (31.8%) cases tremor was experienced
along with postural. Dysfunction in the cerebellar system is manifested in the
form hypermetric, adiadochokinesia, symptom Homs, chanting speech. The total
clinical score on the functional scale (FS 2) amounted to 2,4 ± 1,2, which is 1.7
times more relative to group 1, and 1.21 times greater relative to the 2nd
group. It should be noted that an objective assessment of cerebellar
dysfunction was significantly complicated due to the presence of a number of
patients with extremity paresis of more than 3 points. This fact explains why
patients of group 3 have been identified as not having a significant increase
in clinical score assessment of cerebellar function. The total clinical score
reflecting the degree of impairment of stem functions (FS 3) amounted to 2,4 ±
0,6 and has reliably been a similar indicator of the 2nd group. Sensitive areas
presented loss of proprioception, which was observed in 7 (31.8%) patients.
That percentage had no significant difference from patients in group 2. The total
clinical score reflecting the severity of sensory disorders by (FS 4) amounted
to 2,4 ± 0,6 and had no significant difference from that of group 2. Impaired
function of pelvic organs were detected in 17 (77.3%) cases, which is 34.4%
more in comparison to the 2nd group. The total clinical score was (FS 5) 1,6 ±
0,7, 3.9 times more relative to group 1, 1.5 more than the 2nd group.
Psychopathological changes were noted in 19 (86.4%) patients and were
characterized by euphoric, reducing criticism to his condition, apathy or
depression of varying degrees. The total clinical score reflecting the degree
of impairment of higher cortical functions (FS 7) amounted to 1,7 ± 0,9, which
is more than 1.53 relative to group 1, and 1.21 more than the 2nd group.
Conclusion. The study revealed that in the test groups, patients with remitting MS
were dominant, where their clinical score, according to the EDSS scale
corresponded to a mild disability. The number of patients with moderate
severity prevailed at SPMS, 3 times greater, and with severe, 5.5 times. All
groups had coordination and motor disturbances. However, patients with the
severe form of the disease had maximum expression of the clinical symptoms and
the greatest occurrence of neurological symptoms. As the conditions worsened,
the occurrence of pelvic disorders also increased with the greatest dysfunction
in patients having the severe form of the disease.
Bibliography
1. Алифирова В.М.,
Титова М.А. Клиническая характеристика рассеянного склероза в Томской области
// Неврология, нейропсихиатрия, психосоматика. – 2012. – №2. – С. 50-51.
2. Бурнусус Н.И., Карпов
С.М., Шевченко П.П. Нейротрансмиттеры в патогенезе рассеянного склероза //
Международный журнал прикладных и фундаментальных исследований. – 2012. – № 1.
– С. 20-21.
3. Барабаш И.А. Влияние
психологических факторов на качество жизни при рассеянном склерозе //
Нейроиммунология. – 2007. – Т. V. – № 2. – С. 9.
4. Зихова А.Р.,
Березгова Л.М., Тлапшокова Л.Б., Бойко А.Н. Эпидемиологические характеристики
рассеянного склероза в Кабардино-Балкарской республике // Журнал неврологии и
психиатрии им. С.С. Корсакова. – 2013. – Т. 113. – №10. – С. 5-7.
5. Карпов С.М., Батурин
В.А., Тельбух В.П., Францева А.П., Белякова Н.А., Чичановская Л.В. Аутоантитела
к основному белку миелина и их роль при демиелинизирующих процессах //
Клиническая неврология. – 2013. – № 3. – С. 16-19.
6. Лукина Е.В.,
Кузнецова Д.Е. Оценка уровня тревожности и депрессии у больных рассеянным
склерозом. Саратовский научно-медицинский журнал. – 2012. – Т. 8. – № 2. – С.
484–488.
7. Пажигова З.Б., Карпов
С.М., Шевченко П.П., Бурнусус Н.И. Распространенность рассеянного склероза в
мире (обзорная статья) // Международный журнал экспериментального образования.
– 2014. – № 1(2). – С. 78-82.
8. Столяров И.Д.
Современные методы диагностики и лечения рассеянного склероза // Вестник
Росздравнадзора. – 2010. – № 4. – С. 64-67.
9. Hamdard A.A., Mamedova A.E., Shevchenko P.P., Karpov S.M. Hyperthermia-syndrome as the debut
of the development of multiple sclerosis. European
Journal of Biomedical and Life Sciences. 2015. № 1. С. 10-11.
11. O’Connor P., Confavreux C., Comi G., et al. Oral
terifl unomide in patients with relapsing MS: baseline clinical features of
patients in the TEMSO phase III trial. Multiple sclerosis. – 2008. – suppl.1. –
S. 85.
12. Karpov S.M., Padgigova Z.B., Karpov A.S., Vishlova
I.A. Invoked visual potentials in the
study of the visual analyzer in patients with diffuse sclerosis. Медицинский
вестник Северного Кавказа. 2015. № 2 (38). С. 155-159.