American Journal of Medicine and Medical Sciences

p-ISSN: 2165-901X    e-ISSN: 2165-9036

2023;  13(5): 678-680

doi:10.5923/j.ajmms.20231305.28

Received: May 1, 2023; Accepted: May 15, 2023; Published: May 23, 2023

 

Efficiency of the Ursodeoxycholic Acid in Patients with Metabolic Syndrome

Avazova Takhmina Akhtamovna, Ziyadullaev Shukhrat Khudoyberdiyevich

Department of Internal Medicine No.1, Samarkand State Medical University, Uzbekistan

Correspondence to: Avazova Takhmina Akhtamovna, Department of Internal Medicine No.1, Samarkand State Medical University, Uzbekistan.

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Copyright © 2023 The Author(s). Published by Scientific & Academic Publishing.

This work is licensed under the Creative Commons Attribution International License (CC BY).
http://creativecommons.org/licenses/by/4.0/

Abstract

Metabolic syndrome is a cluster of factors associated with an increased risk of atherosclerotic cardiovascular disease and diabetes mellitus. In recent years, this syndrome has attracted close attention from cardiologists, endocrinologists and general practitioners. This is due to the widespread occurrence of this symptom complex in the population. Forty patients with MS were examined. All persons determined by the content IL-6, IL-17 in the blood serum before and after immune disorders correctiveby Ursosan forte. It is established that the MS increases the level of IL-6 and IL-17. The therapy had a positive impact on cytokine status. The activation of cytokine system occurs in metabolic syndrome and manifests as a significant in-crease of IL-6 and IL-17 in blood serum.

Keywords: Metabolic syndrome, Cytokines, IL-6, IL-17, Ursodeoxycholic acid

Cite this paper: Avazova Takhmina Akhtamovna, Ziyadullaev Shukhrat Khudoyberdiyevich, Efficiency of the Ursodeoxycholic Acid in Patients with Metabolic Syndrome, American Journal of Medicine and Medical Sciences, Vol. 13 No. 5, 2023, pp. 678-680. doi: 10.5923/j.ajmms.20231305.28.

1. Introduction

Metabolic syndrome is a cluster of factors associated with an increased risk of atherosclerotic car-diovascular disease and diabetes mellitus [4-17]. In recent years, this syndrome has attracted close attention from cardiologists, endocrinologists and general practitioners. This is due to the widespread occurrence of this symptom complex in the population.
Currently, one of the main factors in the development of cardiovascular vascular pathology is considered to be immune inflammation. Elevated inflammatory indicators such as interleukins (IL)-1, 6, tumor necrosis factor- (TNF-α) are associated with a high risk of complications in cardiac pathology and considered to be immunological markers of cardiovascular risk [2]. The main 'metabolic risk factors' are atherogenic dyslipidaemia, elevated blood pressure, elevated plasma glucose, prothrombotic state and pro-inflammatory state. The presence of this cluster of factors in a particular patient is referred to using the clinical concept of "metabolic syndrome" [18], and it is not necessary for all metabolic risk factors to be present in order to diagnose this phenomenon.
Interleukin-6 (IL-6) is synthesized by monocytes / macrophages, less by fibroblasts, endothe-lial cells during inflammation, trauma, hypoxia and exposure to bacterial endotoxins [1]. The bio-logical role of IL-6 lies primarily in the induction of repair mechanisms and activation of immune protection (activation and differentiation of T-cells, maturation of B-cells, synthesis of C-reactive protein in the liver, enhancement of hematopoiesis). In addition, IL-6 is also known to inhibit the inflammatory response by inhibiting the synthesis of a number of pro-inflammatory substances, including tumour necrosis factor a (TNFa) [1]. In the last decade, the role of IL-6 in the regulation of metabolism has been established. Interest in IL-6 has particularly increased with the discovery of the adipose tissue inflammation phenomenon in obesity and the search for its pathogenetic mechanisms. Besides the research interest in this side of cytokine action, the practical aspect is important due to the increase in metabolic diseases: obesity, metabolic syndrome (M.S.), type 2 diabetes mellitus (DM-2) and related atherosclerosis and its consequences.
Due to the range of inherent pleiotropic properties (choleretic, cytoprotective, immuno-modulatory, anti-apoptotic, hypocholesterolemic, and litholytic), Ursosan forte has a wide range of therapeutic effects.
The aim of our work was to study the content of interleukins 6 and 17 in patients with metabolic syndrome before and after therapy with Ursosan forte.

2. Materials and Methods

We examined the clinical and immunological parameters of 40 subjects, including 18 females and 22 males aged 25-55, with a body mass index of 25.0-32.2 kg/m2 and 30 healthy controls.
Metabolic syndrome was identified based on the International Diabetes Federation criteria (IDF, 2007). All subjects were measured for interleukin IL-6 and IL-17 in blood serum by ELISA test using the Vector-Best test system, Russia, and a set of anthropometric data (height, weight, body mass index, waist circumference and hip circumference).
All patients have prescribed Ursosan forte 500 mg at night for 30 days on a hypocaloric diet.
All patients were informed about the forthcoming treatment, and their written consent was taken.
The patients were divided into groups according to their B.P. and BMI.
Depending on blood pressure level, patients were divided into 2 groups: those whose blood pressure did not exceed 140/80 mmHg (19 people) and those with blood pressure higher than 140/80 mmHg (21 people).
Depending on BMI, Group 1 included 20 patients with BMI less than 30 kg/m2 and Group 2 included 20 patients with type I obesity (BMI greater than 30 kg/m2).
The data were statistically processed using a R-studio version 3.6.2. as well as using the programs developed in the EXCEL package with the library of statistical functions.

3. Results

Table 1 presents data on IL-6 and IL-17 content in blood serum in MS depending on B.P. level before and after monotherapy with ursosan forte.
Table 1. IL-6 and IL-17 in MS depending on B.P.
     
As it can be seen from the table, IL-6 level before treatment in patients with MS without A.H. is 2.8 times higher than in healthy persons, and IL-17 content is more than 6 times higher (p<0.001). Similar changes were revealed in MS patients with A.H. Thus, the IL-6 content was 5.3 ± 0.5, and IL-17 - 2.8 ± 0.23 (more than 3 and 6 times the control values, respectively). After the conducted treatment, only a tendency to a decrease of IL-6 and IL-17 levels was registered in both groups, but their content was still high and significantly differed from the control values (p<0,001).
The examination of group 1 patients depending on BMI revealed that IL-6 and IL-17 serum levels significantly exceeded the normative values. Thus, at control values of IL-6 -1,55±0,25 its values were increased up to 3,01±0,18 (p<0,001), and IL-17 content increased 6-fold and amount-ed to 2,7±0,15 against 0,45±0,22 in group of healthy patients.
In blood of the 2nd group patients with M.S., the IL-6 content sharply increased and was 6,94±0,34, which was 4,5 times higher than in healthy persons (p<0,001) and more than 2 times higher than in the 1st group patients.
Table 2. IL-6 and IL-17 content in MS depending on BMI before and after treatment
     
IL-17 content in blood serum of patients with obesity exceeded the control values more than 6 times (p<0,001), but no difference with the indices of the 1st and 2nd groups patients was found (p>0,05).
After application of Ursosan forte, the levels of IL-6 and IL-17 in the blood serum of the 1st group of examinees slightly decreased, the 2nd group patients showed a reliable decrease of IL-6 after treatment (p<0,001), but its values remained high and reliably differed from the levels of healthy patients (p<0,001).
Thus, our investigations show, that metabolic syndrome is associated with activation of cytokine system, expressed in manifold increase of IL-6 and IL-17 in blood serum. It should be noted, that in patients with MS without A.H. and with AH, the contents of the studied cytokines were practically identical. The conducted therapy had a positive effect on cytokine status.
The levels of IL-6 and IL-17 in patients with BMI over 30 kg/m2 were significantly higher than those in patients with BMI under 30 kg/m2. Therapy resulted in a decrease in IL-6 and had no significant effect on IL-17.

4. Conclusions

The activation of the cytokine system occurs in metabolic syndrome and manifests as a significant increase of IL-6 and IL-17 in blood serum. IL-6 and IL-17 levels are significantly higher in obese and overweight patients. Therapy with ursosan forte showed a positive effect on cytokine status.

ACKNOWLEDGEMENTS

We acknowledge the support of Khasan IBRAGIMOV on preparation of this manuscript.

References

[1]  В. Шварц. Регуляция метаболических процессов интерлейкина 6. Журнал «Цитокины и воспаление», №3, 2009, с. 3-10.
[2]  И.Ю. Пирогова, С.В. Яковлева, Т.В. Неуймина и др. Плейотропные эффекты урсодезоксихолевой кислоты при неалкогольной жировой болезни печени и метаболическом синдроме. Consilium Medicum. 2019; 21 (8): 65–70. DOI: 10.26442/20751753.2019.8.190365.
[3]  О.А. Танченко, С.В. Нарышкины, О.Н.Сивякова Урсодезоксихолевая кислота в комплексном лечении больных с метаболическим синдромом. Российский журнал гастроэнтерологии, гепатологии, колопроктологии, 2012 22(1) 82-86 ISSN: 1382-4376e ISSN: 2658-6673.
[4]  BE. Wisse The inflammatory syndrome: the role of adipose tissue cytokines in metabolic disorders linked to obesity /// J Am SocNephrol – 2014 – 15: 2792–80.
[5]  Х.М. Халимова, Ф.Ю. Меметов, М.М. Раимова. Динамика показателей клетлчного т гуморального иммунитета у больных с ишемическим инсультом на фоне лечения «TAF» Лактофлором. / Вестник Казахского национального медицинского университета, №4, 2015, с. 232-233.
[6]  Third report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III). Final Report. Circulation 106, 3143-3421 (2012). The 2001 NCEP report sparked in-creased interest of the medical community in the metabolic syndrome. It led to new re-search as well as controversy about the clinical utility of the syndrome.
[7]  S.M. Grundy, et al. Definition of metabolic syndrome: report of the National Heart, Lung, and Blood Insti-tute/American Heart Association conference on scientific issues related to definition. Circulation 109, 433-438 (2014).
[8]  S.M Grundy. et al. Clinical management of metabolic syndrome: report of the American Heart Association / Na-tional Heart, Lung, and Blood Institute / American Diabetes Associa-tion conference on scientific issues related to management. Circulation 109, 551-556 (2014).
[9]  R.H. Eckel, S.M. Grundy, P.Z. Zimmet, The metabolic syndrome: epidemiology, mechanisms, and therapy. Lancet 365, 1415-1428 (2015). Reviews the worldwide epidemi-ology, pathophysiology and manage-ment of the metabolic syndrome.
[10]  B. Isomaa, et al. Cardiovascular morbidity and mor-tality associated with the metabolic syndrome. Diabe-tesCare 24, 683-689 (2011).
[11]  HM. Lakka, et al. 2012. The metabolic syndrome and total and cardiovascular disease mortality in middleaged men. JAMA 288, 2709-2716.
[12]  N. Sattar, et al. Metabolic syndrome with and without C-reactive protein as a predictor of coronary heart disease and diabetes in the West of Scotland Coronary Prevention Study. Circulation 108, 414- 419 (2013).
[13]  C.J. Girman, et al. The metabolic syndrome and risk of major coronary events in the Scan-dinavian Simvastatin Survival Study (4S) and the Air Force/Texas Coronary Atherosclero-sis Prevention Study (AFCAPS/Tex- CAPS). Am. J. Cardiol. 93, 136-141 (2014).
[14]  S. Malik et al. Impact of the metabolic syndrome on mortality from coronary heart disease, cardiovascular dis-ease, and all causes in United States adults. Circulation 110, 1245–1250 (2014).
[15]  J.K. Olijhoek et al. The metabolic syndrome is asso-ciated with advanced vascular damage in patients with coronary heart disease, stroke, peripheral arterial disease or abdominal aor-tic aneurysm. Eur. Heart J. 25, 342–348 (2014).
[16]  C.M. Alexander et al. NCEP-defined metabolic syndrome, diabetes, and prevalence of coronary heart disease among NHANES III participants age 50 years and older. Diabetes 52, 1210-1214 (2013). Shows that most patients with type 2 diabetes have the metabolic syndrome, and the syndrome accounts for most of the increased risk for coro-nary heart dis-ease resulting from diabetes.
[17]  J.K. Ninomiya et al. Association of the metabolic syndrome with history of myocardial in-farction and stroke in the Third National Health and Nutrition Examination Survey. Circulation 109, 42-46 (2014).
[18]  A.M. McNeill et al. The metabolic syndrome and 11-year risk of incident cardiovascular disease in the ath-erosclerosis risk in communities study. DiabetesCare 28, 385-390 (2015).
[19]  B.C. Solymoss et al. Incidence and clinical charac-teristics of the metabolic syndrome in patients with coro-nary artery disease. Coron. ArteryDis. 14, 207-212 (2013).
[20]  S.M. Grundy, et al. Diagnosis and management of the metabolic syndrome. An American Heart Association / Na-tional Heart, Lung, and Blood Institute Scientific Statement. Circulation 112, 2735–2752 (2015).