Kasvosve Ishmael, Gomo Zvenyika A R, Nathoo Kusum J, Matibe Petronella, Mudenge Boniface, Loyevsky Mark, Nekhai Sergei, Gordeuk Victor R
Department of Chemical Pathology, University of Zimbabwe College of Health Sciences, Harare, Zimbabwe.
Clin Chim Acta. 2006 Sep;371(1-2):130-6. doi: 10.1016/j.cca.2006.02.034. Epub 2006 Apr 17.
Clinical studies have shown that degree of erythropoiesis, the hypoxic response, and iron status each independently influences transferrin receptor concentration, but there is conflicting information regarding the effect of inflammation on transferrin receptor expression.
Levels of hemoglobin, reticulocytes, serum ferritin, transferrin receptors and inflammatory markers (C-reactive protein, interleukin-6 and neutrophils) were determined in 208 Zimbabwean children <or=5 years attending well-child clinics in a non-malaria transmission, non-hookworm area.
In linear regression models among 147 children with ferritin >10 ng/mL that adjusted for erythropoiesis with log(10) reticulocyte count, the hypoxic response with hemoglobin concentration and iron status with log(10) ferritin concentration, positive correlations were found between log(10) transferrin receptor concentration and log(10) C-reactive protein concentration (P=0.012), log(10) interleukin-6 concentration (P=0.011) and log(10) neutrophil count (P=0.013). These models predict that, with a baseline transferrin receptor concentration in the upper normal range of 8.0 mg/L and holding hemoglobin concentration and reticulocyte count constant, an increase from 1 to 10 mg/L in C-reactive protein is associated with a rise of 1.6 mg/L in transferrin receptor (95% C.I. 0.3-3.0 mg/L), an increase from 0.5-to-5.0 pg/mL in interleukin-6 with a rise of 1.9 mg/L (0.4-3.7 mg/L), and an increase from 2000 to 20,000/microL in neutrophil count with a rise of 3.6 mg/L (0.7-7.5 mg/L).
Our results suggest that inflammation leads to an increase in circulating transferrin receptor concentration that is independent of the degree of erythropoiesis, the hypoxic response and iron status.
临床研究表明,红细胞生成程度、低氧反应和铁状态各自独立影响转铁蛋白受体浓度,但关于炎症对转铁蛋白受体表达的影响存在相互矛盾的信息。
对208名年龄≤5岁、在非疟疾传播、非钩虫感染地区的儿童保健门诊就诊的津巴布韦儿童,测定其血红蛋白、网织红细胞、血清铁蛋白、转铁蛋白受体及炎症标志物(C反应蛋白、白细胞介素-6和中性粒细胞)水平。
在147名铁蛋白>10 ng/mL的儿童中,采用线性回归模型,校正了用对数(10)网织红细胞计数表示的红细胞生成、用血红蛋白浓度表示的低氧反应以及用对数(10)铁蛋白浓度表示的铁状态,发现对数(10)转铁蛋白受体浓度与对数(10)C反应蛋白浓度(P = 0.012)、对数(10)白细胞介素-6浓度(P = 0.011)和对数(10)中性粒细胞计数(P = 0.013)之间呈正相关。这些模型预测,在转铁蛋白受体浓度处于正常上限8.0 mg/L的基线水平且血红蛋白浓度和网织红细胞计数保持不变的情况下,C反应蛋白从1 mg/L增加到10 mg/L与转铁蛋白受体升高1.6 mg/L相关(95%可信区间0.3 - 3.0 mg/L),白细胞介素-6从0.5 pg/mL增加到5.0 pg/mL与升高1.9 mg/L(0.4 - 3.7 mg/L)相关,中性粒细胞计数从2000/μL增加到20,000/μL与升高3.6 mg/L(0.7 - 7.5 mg/L)相关。
我们的结果表明,炎症导致循环转铁蛋白受体浓度升高,且该升高独立于红细胞生成程度、低氧反应和铁状态。