Yacoub Maha F, Ferwiz Hala Fouad, Said Fadwa
Internal Medicine and Clinical Hematology, Faculty of Medicine, Cairo University, Giza, Egypt.
El-Sahel Teaching Hospital, General Organization of Teaching Hospital, Cairo, Egypt.
Anemia. 2020 Feb 7;2020:3041738. doi: 10.1155/2020/3041738. eCollection 2020.
Anemia of chronic disease (ACD) also termed as the anemia of inflammation has been found to be associated with inflammations, chronic infections, and cancers, particularly in old age. Recent studies revealed that interleukin-6 (IL-6), a proinflammatory cytokine, and hepcidin, an antimicrobial hepatic peptide, play a key role in ACD pathogenesis. The study included 40 subjects with chronic diseases and 40 normal subjects of the same age group. Red cell indices, levels of IL-6 and hepcidin, and iron profile were measured in all participants using Bayer ADVIA 120, VITROS 5600, Integrated System/2008, and ELISA assay, respectively.
The level of hemoglobin was considerably less in patients of chronic diseases referred to as "cases" than the normal subjects or "controls" (8.7 ± 1.5 vs. 13.2 ± 0.9). Red blood corpuscle (RBC) count, hematocrit (HCT) level, serum iron, mean corpuscular hemoglobin concentration (MCHC), and serum total iron-binding capacity (TIBC) were found to be significantly lower in the cases as compared to controls ( < 0.001). Serum IL-6 and hepcidin levels were substantially higher in the cases than in the controls ( < 0.001). Serum IL-6 and hepcidin levels were substantially higher in the cases than in the controls ( < 0.001). Serum IL-6 and hepcidin levels were substantially higher in the cases than in the controls (.
This study detected a significant increase in serum IL-6 and hepcidin levels in patients with ACD than the controls. These findings offer an insight into the role played by both cytokine and peptide in the pathogenesis of ACD and thus provide a rationale for future use of novel drugs inhibiting their effects on iron metabolism.
慢性病贫血(ACD)也被称为炎症性贫血,已发现其与炎症、慢性感染和癌症有关,尤其是在老年人群中。最近的研究表明,促炎细胞因子白细胞介素-6(IL-6)和抗菌性肝脏肽铁调素在ACD发病机制中起关键作用。该研究纳入了40名患有慢性病的受试者和40名同年龄组的正常受试者。分别使用拜耳ADVIA 120、VITROS 5600、Integrated System/2008和ELISA检测法对所有参与者的红细胞指数、IL-6和铁调素水平以及铁参数进行了测量。
被称为“病例”的慢性病患者的血红蛋白水平明显低于正常受试者或“对照”(8.7±1.5对13.2±0.9)。与对照组相比,病例组的红细胞(RBC)计数、血细胞比容(HCT)水平、血清铁、平均红细胞血红蛋白浓度(MCHC)和血清总铁结合力(TIBC)显著降低(<0.001)。病例组的血清IL-6和铁调素水平显著高于对照组(<0.001)。病例组的血清IL-6和铁调素水平显著高于对照组(<0.001)。病例组的血清IL-6和铁调素水平显著高于对照组(。
本研究发现,与对照组相比,ACD患者血清IL-6和铁调素水平显著升高。这些发现深入了解了细胞因子和肽在ACD发病机制中的作用,从而为未来使用抑制它们对铁代谢影响的新型药物提供了理论依据。