Vazenmiller Dmitriy, Ponamaryova Olga, Muravlyova Larisa, Molotov-Luchanskiy Vilen, Klyuyev Dmitriy, Bakirova Riszhan, Amirbekova Zhanna
Karaganda State Medical University, Karaganda, Kazakhstan.
Open Access Maced J Med Sci. 2018 Nov 23;6(11):2111-2114. doi: 10.3889/oamjms.2018.471. eCollection 2018 Nov 25.
The purpose of the present research was to study the content of erythropoietin and hepcidin in serum in pregnant women with iron deficiency anaemia and anaemia of chronic inflammation.
The authors examined 98 pregnant women who were observed in LLP (Regional obstetric-gynaecological centre) in Karaganda. The including criteria for pregnant women in the study was the informed consent of the woman to participate in the study. Exclusion criteria were oncological diseases, HIV-infection, tuberculosis, severe somatic pathology, mental illness, drug addiction. The design of the study was by the legislation of the Republic of Kazakhstan, international ethical norms and normative documents of research organisations, approved by the ethics committee of the Karaganda State Medical University.
As a result of the study, it was determined that the content of erythropoietin and hepcidin in pregnant women with anemias of different genesis varies ambiguously. In the main group of pregnant women with IDA, the erythropoietin content rises, and the hepcidin level decreases. In pregnant women with ACI, on the contrary, the level of hepcidin increases, and in one subgroup it is significant. However, in pregnant women and with IDA and anemia of chronic inflammation, there is a subgroup of women in whom erythropoietin is either comparable with hepcidin, or their changes are of opposite nature.
The authors concluded that the obtained data indicate ambiguous changes in the level of erythropoietin and hepcidin in pregnant women with anaemias of various origins. In all likelihood, there are still unaccounted factors affecting the content of these protein-regulators of iron metabolism, which require further definition and interpretation in anaemia of pregnant women.
本研究旨在探讨缺铁性贫血和慢性炎症性贫血孕妇血清中促红细胞生成素和铁调素的含量。
作者对在卡拉干达市有限责任合伙公司(地区妇产科中心)接受观察的98名孕妇进行了检查。本研究纳入孕妇的标准是其自愿参与研究的知情同意书。排除标准为肿瘤疾病、艾滋病毒感染、结核病、严重躯体疾病、精神疾病、药物成瘾。本研究的设计符合哈萨克斯坦共和国法律、国际伦理规范以及研究机构的规范性文件,并经卡拉干达国立医科大学伦理委员会批准。
研究结果表明,不同病因贫血孕妇血清中促红细胞生成素和铁调素的含量变化不明确。在缺铁性贫血孕妇的主要研究组中,促红细胞生成素含量升高,而铁调素水平降低。相反,在慢性炎症性贫血孕妇中,铁调素水平升高,且在一个亚组中升高显著。然而,在缺铁性贫血和慢性炎症性贫血孕妇中,有一个亚组的女性促红细胞生成素水平与铁调素相当,或者其变化性质相反。
作者得出结论,所获得的数据表明不同病因贫血孕妇促红细胞生成素和铁调素水平变化不明确。很可能仍有未被考虑的因素影响这些铁代谢蛋白调节剂的含量,这需要在孕妇贫血中进一步明确和解释。