Cytokines in Liver Cirrhosis (Their Importance in Assessing Activity and Decompensation)

G. K. Mirodzhov, S. D. Pulatova
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Abstract

Aim: studying the role of pro-inflammatory and anti-inflammatory cytokines in the pathogenesis of liver cirrhosis progression. Materials and methods. The material of the study was the data of clinical-instrumental, biochemical, virological studies of 109 patients with liver cirrhosis of various etiologty, who were hospitalized in the clinic of the Institute of Gastroenterology (Dushanbe, Republic of Tajikistan). The diagnosis of the underlying disease was established according to the clinical recommendations of the Russian Society for the Study of the Liver and the Russian Gastroenterological Association for the diagnosis and treatment of liver fibrosis and cirrhosis and their complications (2021); decompensated liver cirrhosis was established according to the 1996 Child — Pugh classification. The age of the patients ranged from 17 to 79 years (36.9 ± 0.8 years), there were 55 men and 54 women. Results. Among the examined patients, compensated liver cirrhosis (Class A) according to Child — Pugh was detected in 18 persons, subcompensated (Class B) — in 14, decompensated (Class C) — in 77. The study of the content of pro-inflammatory and anti-inflammatory cytokines in the blood serum of patients with Class A liver cirrhosis showed, that levels of tumour necrosis factor alpha (TNF-α), interleukin-2, interleukin-6 were statistically higher compared to healthy individuals, while the concentration of anti-inflammatory interleukin-10 was lower (30.7 ± 4.7 pg/mL) in comparison with the control group. In patients with Class B liver cirrhosis, the level of TNF-α increased to 75.0 ± 4.5 pg/mL ( p < 0.001), interleukin-2 — to 328.7 ± 23.9 pg/mL ( p < 0.05), and interleukin-6 — to 95.4 ± 7.7 pg/mL ( p < 0.001). Serum interleukin-10 decreased compared with the control group (23.1 ± 2.8 pg/mL; p > 0.05). At the decompensated stage of Class C cirrhosis, a huge release of pro-inflammatory cytokines occurs — the content of TNF-α increases by 80 times, of interleukin-2 — by more than 60 times, аs for interleukin-10, its content is progressively reduced. Conclusion. In liver cirrhosis, there is a significant disruption in the synthesis of pro-inflammatory cytokines, which is manifested by a sharp increase in the content of TNF-α, interleukin-2 and interleukin-6. High levels of proinflammatory cytokines in blood serum in liver cirrhosis correlate with the activity and degree of decompensation, which indicates their important role in the pathogenesis and progression of the pathological process.
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肝硬化中的细胞因子(在评估活动和失代偿中的重要性)
目的:探讨促炎和抗炎细胞因子在肝硬化发病机制中的作用。材料和方法。该研究的材料是109名不同病因的肝硬化患者的临床仪器、生化和病毒学研究数据,这些患者在塔吉克斯坦共和国杜尚别胃肠病学研究所的诊所住院。基础疾病的诊断是根据俄罗斯肝脏研究学会和俄罗斯胃肠病学协会关于肝纤维化和肝硬化及其并发症的诊断和治疗的临床建议确定的(2021年);失代偿性肝硬化是根据1996年Child - Pugh分类建立的。患者年龄17 ~ 79岁(36.9±0.8岁),男性55例,女性54例。结果。在检查的患者中,根据Child - Pugh, 18人发现代偿性肝硬化(A类),14人发现亚代偿性肝硬化(B类),77人发现失代偿性肝硬化(C类)。对A类肝硬化患者血清中促炎和抗炎细胞因子含量的研究表明,肿瘤坏死因子α (TNF-α)、白细胞介素-2、白细胞介素-6水平与健康人群相比均有统计学意义升高,而抗炎白细胞介素-10浓度与对照组相比有统计学意义降低(30.7±4.7 pg/mL)。B级肝硬化患者TNF-α水平升高至75.0±4.5 pg/mL (p <0.001),白细胞介素-2降至328.7±23.9 pg/mL (p <0.05),白细胞介素-6降至95.4±7.7 pg/mL (p <0.001)。血清白介素-10较对照组降低(23.1±2.8 pg/mL;p比;0.05)。在C类肝硬化失代偿期,促炎细胞因子大量释放,TNF-α含量增加80倍,白细胞介素-2含量增加60倍以上,白细胞介素-10含量逐渐降低。结论。在肝硬化中,促炎细胞因子的合成明显中断,表现为TNF-α、白细胞介素-2、白细胞介素-6含量急剧升高。肝硬化患者血清中促炎细胞因子的高水平与失代偿的活性和程度相关,提示其在肝硬化病理过程的发病和进展中起着重要作用。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
44
审稿时长
8 weeks
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