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Галина Северьевна Суржикова
Сатеник Аршавиловна Клочкова-Абельянц
Сергей Николаевич Филимонов

Abstract

Objective – to study the cytokine status of blood serum in hypochromic anemias of various origins.

Methods. The studies were carried out in 396 women aged 16 to 60 years. 79 of them were practically healthy and constituted a control group. 317 had anemic syndrome, 103 of them suffered from iron deficiency anemia, 214 – from chronic diseases.

Results. The study of the level of proinflammatory cytokines in persons with ACD revealed an increase in the level of IL-6, TNF-α and interferon-γ, and a pronounced correlation was established between the level of pro-inflammatory cytokines and the content of hepcidin.

Conclusions. In hypochromic anemias, a significant increase in proinflammatory cytokines was revealed in persons with anemia of chronic diseases, which leads to a decrease in the availability of iron for erythropoiesis and the formation of functional iron deficiency, in contrast to true iron deficiency in iron deficiency anemias. The approaches to the treatment of these anemias (ACD and IDA) are fundamentally different and this explains the importance of the differential diagnosis of these anemias.

Keywords

iron deficiency anemia, anemia of chronic diseases, gepcidin, cytokines

Author Biographies

Галина Северьевна Суржикова,
candidate of medical sciences, docent, head department of clinical laboratory diagnostics
Сатеник Аршавиловна Клочкова-Абельянц,
candidate of medical sciences, docent
Сергей Николаевич Филимонов,
doctor of medical sciences, professor, director

Article Details

Information about financing and conflict of interests

The study had no sponsorship.
The authors declare that they have no apparent or potential conflicts of interest related to the publication of this article.

How to Cite

Суржикова, Г. С., Клочкова-Абельянц, С. А., & Филимонов, С. Н. (2020). CYTOKINE STATUS IN HYPOCHROMIC ANEMIAS OF DIFFERENT GENESIS. Medicine in Kuzbass, 19(4), 59-63. https://doi.org/10.24411/2687-0053-2020-10040

References

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