COMPARATIVE EFFECTIVENESS OF PULSE THERAPY IN CHILDREN WITH SYSTEMIC LUPUS ERYTHEMATOSUS

Аннотация

The study included 18 patients with SLE, of which 9 were in the control group. A group of patients with ineffective standard therapy and high activity of the process was selected, i.e. the study included patients with a polysyndromic picture of systemic lupus erythematosus, all with more than 5-8 ARA criteria.

 

 

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Абдулкхакова R., Абдуракхмонов I., & Арифкхужаев A. (2025). COMPARATIVE EFFECTIVENESS OF PULSE THERAPY IN CHILDREN WITH SYSTEMIC LUPUS ERYTHEMATOSUS. Международный журнал медицинских наук, 1(5), 265–271. извлечено от https://www.inlibrary.uz/index.php/ijms/article/view/121075
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Аннотация

The study included 18 patients with SLE, of which 9 were in the control group. A group of patients with ineffective standard therapy and high activity of the process was selected, i.e. the study included patients with a polysyndromic picture of systemic lupus erythematosus, all with more than 5-8 ARA criteria.

 

 


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COMPARATIVE EFFECTIVENESS OF PULSE THERAPY IN CHILDREN WITH

SYSTEMIC LUPUS ERYTHEMATOSUS

Abdulxakova R.M., Abduraxmonov I.T., Arifxujayev A.T.

Andijan State Medical Institute

The study included 18 patients with SLE, of which 9 were in the control group. A group of

patients with ineffective standard therapy and high activity of the process was selected, i.e.

the study included patients with a polysyndromic picture of systemic lupus erythematosus,

all with more than 5-8 ARA criteria.

To standardize the assessment of the dynamics of clinical and laboratory parameters, we

used the results of clinical symptoms, clinical blood tests with the calculation of index

parameters of white blood cells, and the results of acute phase activity of the inflammatory

process.

In order to objectify the assessment of the effectiveness of combination therapy, we

compared the results of treatment with prednisolone alone and in combination with

cyclophosphamide (control group). The results of the dynamics of clinical manifestations of

SLE in patients receiving pulse therapy (Group 1) and standard therapy (Group II) are

presented in Table 1. Analysis of the obtained results showed that the use of combination

therapy was effective in relation to most extrarenal manifestations of the disease already in

the first days after the end of treatment. Almost complete disappearance of the joint

syndrome, significant reduction in skin and mucous membrane lesions, disappearance

Table 1.

Dynamics of clinical manifestations of SLE in patients receiving pulse therapy and standard

therapy

Clinical sign

Patient groups

I (n=9)

II (n=9)

Before

treatment

On the 7th

day of

therapy

Before

treatment

On the

7th day

of

therapy

Fever

8

-

7

6

Articular syndrome

9

1

6

8

Skin and mucous membrane lesions

6

-

4

6

Lupus nephritis

6

1

6

6

Nervous system lesions

6

1

8

8

Vasculitis

6

1

4

4

Serositis

7

2

7

7

Lymphadenopathy

8

2

7

6


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Thrombocytopenia

2

-

1

1

Anemia

9

9

9

9

Leukopenia

7

5

6

6

ESR>15 mm/hour

9

3

9

9

lymphadenopathy, a decrease in the manifestations of carditis and polyserositis were

observed in all patients. In 5 of 6 patients, we observed either a complete disappearance or a

significant decrease in Raynaud's syndrome. As for the manifestations of lupus nephritis, in

4 of 6 patients with nephrotic syndrome, a decrease in edema syndrome, a decrease and

stabilization of blood pressure were observed already on the 3rd day. During the days of

combined therapy, such patients showed a significant increase in diuresis. Hematuria and

proteinuria decreased in more than half of the patients.

In patients of the second group, who received standard therapy with the inclusion of

prednisolone orally at a dose of 1-3 mg / day, at the end of the first week of therapy, no clear

positive changes in clinical indicators were noted. Thus, fever and articular syndrome

continued to persist. Skin and mucous membrane lesions were noted in two more patients.

Lupus nephritis, vasculitis, serositis, leukopenia did not have positive changes in any patient.

Analysis of the results of the peripheral blood picture showed (Table 2) that in patients of

the first group, who received pulse therapy, at the end of the 7th day there was

Table 2.

Dynamics of peripheral blood parameters in patients with SLE who received pulse therapy

and standard therapy

Indicators

In healthy people

Group I (n=9)

II group (n=9)

Erythrocytes

3,78±0,03

3,17±0,46

3,06±0,54

3,33±0,43

3,02±0,62

Hemoglobin, g/l

123,20±0,10

67,61±2,47

71,39±2,31

82,41±3,19

68,88±3,12

Color index

0,95±0,01

0,77±0,01

0,79±0,86

0,81±0,01

0,76±0,01

SHE, (in pg)

30,21±0,14

28,48±0,18

28,59±0,15

30,40±0,19

29,04±0,17

SSHE, (in %)

31,90±0,18

27,92±0,26

28,90±0,19

31,54±0,35

28,73±0,23


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ESR, (µm3)

94,59±0,27

101,49±0,82

102,69±0,59

95,80±0,76

100,62±0,47

Leukocytes

6,72±0,17

4,95±0,87

4,88±0,76

6,74±1,09

5,01±0,61

Band

3,02±0,20

4,93±0,26

4,78±0,20

2,12±0,14

4,41±0,09

Segmented

54,35±1,18

63,51±0,90

62,93±0,73

53,06±1,49

60,34±0,78

Lymphocytes

35,29±1,00

26,56±0,69

25,81±0,61

37,96±1,30

30,49±0,65

Monocytes

5,03±0,30

3,16±0,17

4,40±0,19

4,65±0,28

4,59±0,18

Eosinophils

2,31±0,20

1,84±0,09

2,15±0,08

2,20±0,19

2,17±0,14

ESR mm/h

7.50±0,06

43,56±2,33

39,23±3,11

24,91±3,12

40,51±4,08

Note: MCH - mean corpuscular hemoglobin; MCH - mean corpuscular hemoglobin

concentration; ESR - mean corpuscular volume.

The numerator shows the values ​ ​ before treatment. The denominator shows the

normalization of erythrocyte balance values ​ ​ 7 days after the start of therapy: the

erythrocyte content significantly increased, although it still remained lower than in healthy

children. The hemoglobin concentration increased significantly (severe anemia became

moderate), and the color index returned to normal. MCH, MCH, and ESR values ​ ​ did

not differ from those in healthy children. In terms of leukocyte content and leukocyte

formula values, patients in Group 1 did not differ from healthy children in the second period

of the study. The erythrocyte sedimentation rate in patients in this group significantly

decreased compared to the value upon admission. This indicates the onset of the stage of

attenuation of the immune-inflammatory process and the favorability of pulse therapy.

Unfavorable results were obtained in patients of group II in the second period of the study.

Thus, none of their indicators returned to normal in the second period of the study. Moderate

hypochromic anemia became severe, the indicators of SSGE, SGE and ESR were still

abnormal, which indicates the onset of severe anemia. Leukopenia, neutrophilia with a shift

to the left, relative and absolute lymphopenia, persistent acceleration of the erythrocyte

sedimentation rate still persisted. These general clinical laboratory data indicate the

continued activity of the inflammatory process and its unfavorable course.


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A comparative assessment of the treatment results showed that in patients of group II, the

overall clinical effect was worse than in patients of group I, which is confirmed by persistent

fever, articular syndrome, an increase in the frequency of lesions of the skin and mucous

membranes, lupus nephritis, vasculitis, serositis, leukopenia and negative indicators of white

blood. The results of the study of white blood index indicators are presented in Table 3.

Table 3.

Dynamics of white blood cell index values ​ ​ in patients with SLE who received pulse

therapy and standard therapy

Indicators

In healthy

people

In patients

Group I

Group II

Leukocyte intoxication index

(LII)

0,57±0,02

1,16±0,08

0,94±0,07

0,49±0,06

0,69±0,05

Left shift index (LSI)

5,67±0,08

7,76±0,19

7,59±0,17

4,10±0,59

4,03±0,14

Granulocyte-agronulocyte index

(GAI)

1,52±0,02

2,48±0,10

2,48±0,08

1,38±0,09

1,91±0,04

General intoxication index (GII)

7,77±0,14

11,38±0,26

11,01±0,21

5,98±0,14

6,64±0,14

Neutrophil-lymphocyte ratio

index (NLR)

1,67±0,02

2,75±0,23

2,83±0,18

1,49±0,10

2,14±0,10

Neutrophil-monocyte ratio index

(NMR)

12,44±0,31

31,95±0,64

20,52±0,35

14,67±0,42

18,76±0,84

Lymphocyte-monocyte ratio

index (LMR)

7,53±0,27

12,60±0,38

7,94±0,24

10,03±0,76

6,64±0,89

Lymphocyte-eosinophil ratio

index (LER)

15,79±0,76

10,88±1,04

10,44±0,76

23,35±1,00

18,26±0,68

Note: the numerator shows the values ​ ​ before treatment, the denominator shows the

values ​ ​ on the 7th day of therapy.


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Among the index indicators in patients of the 1st group, complete normalization occurred for

LII due to a significant decrease in band neutrophils, GAI due to a decrease in the absolute

and relative number of neutrophils, and ISNL due to a decrease in the number of neutrophils

in peripheral blood. Normalization has not yet been noted for the ISI, OII, ISLM and ISLE

indicators. It should be noted that the ISLE indicator in patients of this group has

significantly increased due to an increase in the relative number of lymphocytes compared to

the data upon admission. In our opinion, this additionally indicates the onset of the stage of

attenuation of the immune-inflammatory process.

It should be emphasized that in most cases, patients of the 1st group showed a clear

correlation between the positive dynamics of index indicators and clinical manifestations of

SLE. In patients of the second group who received standard therapy, none of the studied

index parameters normalized, with the exception of ISLM, which was restored due to a

slight decrease in the number of lymphocytes and an increase in the number of monocytes.

Here, correlative connections were also noted between the index parameters of white blood

cells and the clinical manifestations of SLE.

The dynamics of biochemical parameters in the observed patients with SLE are presented in

Table 4.

The data in the table indicate that complex therapy led to a significant normalization of

biochemical parameters in the observed patients, but the degree of their normalization was

different in the studied groups (Table 4). Thus, the concentration of sialic acids was

completely normalized only in patients of group I, while in patients of group II, despite their

significant decrease in comparison with the results upon admission (P < 0.001), complete

normalization did not occur (P < 0.001). According to the concentration of diphenylamino

acid, significant normalization occurred in patients of the first group. However, this

indicator remained reliably high in patients of both groups. The latter indicator, in our

opinion, is the most reliable among the indicators of acute-phase inflammation activity.

Malen's test, detected in all patients, by the end of the observation was the most positive in

patients of group II (P<0.001) and the least positive in patients of group I (P<0.001).

Interesting results were obtained when setting up the Veltman test. Thus, in patients of

group II at the last stage of observation, a shift of the test to the right was noted (P<0.01),

indicating the chronicity of the inflammatory process, and in patients of group I, statistical

differences were not found compared with the control group.

Table 4.

Dynamics of biochemical blood parameters in patients with SLE who received pulse therapy

and standard therapy


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Indicators

In healthy people

In patients

Group I

Group II

Sialic acids, units of optical density

187,73

1,64

326,1±6,87

311,7±3,01

189,8±4,26*

264,1±2,24*

Diphenylamine acid, units of

optical density

0,160

0,01

0,343±0,04

0,335±0,02

0,204±0,03*

0,257±0,02*

Malena test

Отр

Положительная у 100% больных

22,2%*

77,7%*

Veltman test

0,36

0,01

0,20±0,01

0,20±0,01

0,34±0,01*

0,40±0,01*

C-reactive protein, mm.:

Отр

3,30±0,06

3,24±0,05

0,59±0,14*

1,91±0,07*

Blood protein, g/l

70,76

0,50

68,32±0,80

68,60±0,81

69,21±0,28

65,53±0,23*

Albumins, in %:

59,19

0,41

48,10±0,41

48,01±0,43

54,37±0,56*

52,18±0,23*

α-globulins

13,31

0,66

21,37±0,40

20,69±0,45

15,02±0,33*

17,13±0,14*

β-globulins

11,97

0,35

14,21±0,31

14,56±0,29

12,28±0,33

8,93±0,20*

-globulins

15,53

0,37

16,32±0,36

16,74±0,32

18,33±0,46*

21,76±0,32*

Despite the therapy, CRP was detected in all the studied groups, with its highest content

noted in patients of group II, and the lowest - in patients of group I (P < 0.01-0.001). This

indicator most fully determines the degree of activity of the inflammatory process. In

patients of group I, pulse therapy did not have a significant effect on total blood protein, and

in patients of group II, hypoproteinemia occurred against the background of treatment (P <

0.001). Blood albumins still remained low in all compared groups (P < 0.001). Serum α-

globulins, characterizing the severity of the inflammatory process, still remained high in all

patients, with the highest in patients of group II (P < 0.001), and relatively low in patients of

group I (P < 0.01). β-globulins were elevated in all groups of patients, and by the end of the

observation - in patients of group II (P < 0.05) they significantly decreased, while in patients

of group I at this time of the study no reliable differences were found. Serum γ-globulins in


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all patients at the last observation period significantly increased (P < 0.001), which indicated

the chronicity of the inflammatory process, or indirectly one can assume the suppression of

antidiv formation or hyperimmunoglobulinemia. At the same time, the highest

concentration of gamma globulins was recorded in patients of group II, rather than in

patients of group I (P < 0.05). In general, in patients in this study, pulse therapy with

methylprednisolone was effective in 77.7% of patients with SLE, persistent remission was

noted in 66.6% of patients. In 22.2% of patients, despite the therapy, no noticeable clinical

and laboratory effect was observed. As for standard therapy, for patients with high activity

of the inflammatory process, with persistent vasculitis, visceritis, this method is ineffective

and requires further improvement in relation to the use of pulse therapy.

References:

1. Иванова М.М. Эволюция методов лечения системной красной волчанки. Избранные

лекции по клинической ревматологии. Под ред. В.А. Насоновой, Н.В. Бунчука. М.:

Медицина, 2001: 91-100.

2. Клюквина Н.Г., Насонов Е.Л. Фармакотерапия системной красной волчанки:

современные рекомендации. РМЖ, 2010, 18(382): 1108-113.

3. Клинические рекомендации по ревматологии. 2-е изд., испр. и доп. Под ред. акад.

РАМН Е.Л. Насонова, М.: ГЭОТАР-Медиа, 2010: 429-481.

4. Клюквина Н.Г., Насонов Е.Л. Особенности клинических и лабораторных

проявлений системной красной волчанки. Современная ревматология, 2012, 4: 40-48.

5. Насонов Е.Л., Александрова Е.Н., Новиков А.А. Аутоиммунные ревматические

заболевания - проблемы иммунопатологии и персо-ниицированной терапии. Вестник

РАМН. 2015, 2: 169-182.

6. Соловьев С.К., Асеева Е.А., Торгашина А.В. Интенсифицированная терапия

аутоиммунных ревматических заболеваний. РМЖ, 2010, 11(375), 18: 748-751.

7. Лечение ревматических заболеваний ударными дозами метилпреднизолона.

Пособие для врачей. Под ред. акад. РАМН, проф. В.А. Насоновой. Киев, 2006.

8. Andersen L.S., Petersen J., Bendtzen K. Production of interleukin (IL)-1beta, IL-1

receptor antagonist and IL-10 by blood mononuclear cells in chronic arthritis. //Cytokine

-2000. -N1. -P.62-68.

9. Arguedas O., Fasth A., Anderson-Gare B., Porras O. Juvenile chronic arthritis in urban

San Jose, Costa Rica: a 2 year prospective study. //J. Rheumatol. -1998. -N9. -P.1844-

1850.

10. Gillis J, Yazdany J, Trupin I, Julian L. Et al. Medicaid and access to care among persons

with systemic lupus erythematosus. Arthr. Rheum., 2007, 57: 601-607.

11. Petri M. Epidemiology of systemic lupus erythematosus. Best Pract Res Clin Rheumatol.

2002, 16 (5): 847-858.

12. Bertsias GK, Salmon JE, Boumpas DT. Therapeutic opportunities in systemic lupus

erythematosus: state of the art and prospects for the new decade. Ann Rheum Dis, 2010, 69:

1603-1611.

13. Haubitz M. Exploring new territory: the move towards individualized treatment. Lupus,

2007, 16: 227-231.

14. Mehmedbasic A. Algorithms in the diagnosis and treatment of systemic lupus

erythemato-sus. Interna Med, 2010, 18(3): 157-161.

Библиографические ссылки

Иванова М.М. Эволюция методов лечения системной красной волчанки. Избранные лекции по клинической ревматологии. Под ред. В.А. Насоновой, Н.В. Бунчука. М.: Медицина, 2001: 91-100.

Клюквина Н.Г., Насонов Е.Л. Фармакотерапия системной красной волчанки: современные рекомендации. РМЖ, 2010, 18(382): 1108-113.

Клинические рекомендации по ревматологии. 2-е изд., испр. и доп. Под ред. акад. РАМН Е.Л. Насонова, М.: ГЭОТАР-Медиа, 2010: 429-481.

Клюквина Н.Г., Насонов Е.Л. Особенности клинических и лабораторных проявлений системной красной волчанки. Современная ревматология, 2012, 4: 40-48.

Насонов Е.Л., Александрова Е.Н., Новиков А.А. Аутоиммунные ревматические заболевания - проблемы иммунопатологии и персо-ниицированной терапии. Вестник РАМН. 2015, 2: 169-182.

Соловьев С.К., Асеева Е.А., Торгашина А.В. Интенсифицированная терапия аутоиммунных ревматических заболеваний. РМЖ, 2010, 11(375), 18: 748-751.

Лечение ревматических заболеваний ударными дозами метилпреднизолона. Пособие для врачей. Под ред. акад. РАМН, проф. В.А. Насоновой. Киев, 2006.

Andersen L.S., Petersen J., Bendtzen K. Production of interleukin (IL)-1beta, IL-1 receptor antagonist and IL-10 by blood mononuclear cells in chronic arthritis. //Cytokine -2000. -N1. -P.62-68.

Arguedas O., Fasth A., Anderson-Gare B., Porras O. Juvenile chronic arthritis in urban San Jose, Costa Rica: a 2 year prospective study. //J. Rheumatol. -1998. -N9. -P.1844-1850.

Gillis J, Yazdany J, Trupin I, Julian L. Et al. Medicaid and access to care among persons with systemic lupus erythematosus. Arthr. Rheum., 2007, 57: 601-607.

Petri M. Epidemiology of systemic lupus erythematosus. Best Pract Res Clin Rheumatol. 2002, 16 (5): 847-858.

Bertsias GK, Salmon JE, Boumpas DT. Therapeutic opportunities in systemic lupus erythematosus: state of the art and prospects for the new decade. Ann Rheum Dis, 2010, 69: 1603-1611.

Haubitz M. Exploring new territory: the move towards individualized treatment. Lupus, 2007, 16: 227-231.

Mehmedbasic A. Algorithms in the diagnosis and treatment of systemic lupus erythemato-sus. Interna Med, 2010, 18(3): 157-161.