细胞因子在孕妇慢性缺铁性贫血子痫前期发病中的作用

K. DzhabbarovaYu, T. IsmoilovaSh, Musakhodzhayeva Da
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引用次数: 3

摘要

IDA患者出现高血压状态的频率达32-45%。妊娠合并贫血和子痫前期并发症的发病机制,包括免疫学方面的研究很少。目的:阐明贫血孕妇总体和局部细胞因子状态异常在子痫前期发生中的作用,并证明免疫抑制剂用于预防和治疗子痫前期的必要性。材料与方法:采用ELISA法检测96例妊娠晚期缺铁性贫血(IDA)合并子痫前期孕妇外周血及胎盘蜕膜组织提取物中IL-1β、IL-6、IL-8、TNFα、乳铁蛋白等细胞因子水平。将孕妇分为4组:轻度贫血24例,中度贫血18例,子痫前期伴轻度贫血26例,子痫前期伴中度贫血28例。结果:在中度贫血背景下的子痫前期发展中,IDA背景下的子痫前期伴炎性细胞因子水平(p< 0.05)和急性期蛋白乳铁蛋白(p< 0.05)在全身水平显著升高,在更大程度上局部水平升高(p< 0.05)。讨论:所得数据证实免疫系统参与子痫前期发病,其触发机制之一是缺铁性贫血免疫失衡。给出了联合病理使用免疫抑制治疗的病理原理。结论:应用胎盘激素-孕酮作为免疫抑制药物,为预防子痫前期提供新的免疫治疗策略,是产科实践的热点趋势。
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Role of cytokines in pregnant women with chronic iron deficiency anemia in preeclampsia pathogenesis
The frequency of development of hypertensive states in IDA reaches 32-45%. The pathogenesis of the combined complications of pregnancy with anemia and preeclampsia, including immunological aspects has been little studied. Purpose: to clarify the role of violations general and local cytokine status in pregnant women with anemia in the genesis of preeclampsia and justify the need to include immuno suppressants for the prevention and treatment of preeclampsia. Materials and methods: In 96 pregnant women with iron deficiency anemia (IDA) and preeclampsia in the third trimester of gestation the cytokine status of IL-1β, IL-6, IL-8, TNFα and lactoferrin in the serum of peripheral blood and in extracts of the placenta decidual tissue was examined by ELISA. Pregnant women were divided into 4 groups: 24-with mild anemia, 18-with moderate anemia, 26-with preeclampsia and with mild anemia and 28 pregnant women with preeclampsia and with moderate anemia. Results: It has been established that preeclampsia on the background of IDA is accompanied by a significant increase in the level of pro-inflammatory cytokines (p<0,05) and the acute phase protein lactoferrin (p<0,05) on the systemic and to a greater extent on the local level in the development of preeclampsia on the background of anemia of moderate severity (p<0,05). Discussion: The data obtained confirm the involvement of the immune system in the pathogenesis of preeclampsia, one of the trigger mechanisms of which is the immune imbalance in iron deficiency anemia. A pathogenetic rationale for the use of immunosuppressive therapy for combined pathology is given. Conclusion: The use of placental hormone - progesterone as an immunosuppressive drug in terms of substantiating new immunotherapy strategies for the prevention of preeclampsia is a topical trend in obstetric practice.
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