血清转铁蛋白受体浓度表明肯尼亚无症状疟疾儿童红细胞生成量增加。

H. Verhoef, C. West, P. Ndeto, J. Burema, Y. Beguin, F. Kok
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引用次数: 138

摘要

背景:血清转铁蛋白受体浓度表明红细胞生成活性和红细胞中功能性铁的缺失。与血清铁蛋白浓度相反,血清转铁蛋白受体浓度不受或仅受感染炎症反应的轻微影响。目的评估2-36月龄无疟疾症状儿童铁状态,并探讨血清转铁蛋白受体浓度与疟疾的关系。这是一项以社区为基础的整群调查(n = 318)。结果疟疾、贫血(血红蛋白浓度<110 g/L)、缺铁(血清铁蛋白浓度<12微克/L)和缺铁性贫血的患病率分别为18%、69%、53%和46%。疟疾与较低的平均血红蛋白浓度相关(92.7比104.1 g/L;P = 0.0001)和更高的几何平均血清转铁蛋白受体浓度(11.4比7.8 mg/L;P = 0.005),铁蛋白(21.6比11.9 μ g/L;P = 0.05), c反应蛋白(12.5比6.8 mg/L;P = 0.004)。没有证据表明血清c反应蛋白浓度与转铁蛋白受体之间存在关联。疟疾患儿的血清转铁蛋白受体浓度高于贫血程度的预期,即使在调整了血清c反应蛋白浓度四分位数所指示的炎症后也是如此(P = 0.02)。结论本研究结果与疟疾引起的溶血伴随红细胞生成增加的观点一致。血清转铁蛋白受体浓度对检测疟疾患者缺铁没有帮助。如果使用血清铁蛋白浓度<12微克/升来测量疟疾流行地区的缺铁情况,则应排除血清c反应蛋白或类似急性期反应物浓度较高的个体。
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Serum transferrin receptor concentration indicates increased erythropoiesis in Kenyan children with asymptomatic malaria.
BACKGROUND Serum transferrin receptor concentrations indicate both erythropoietic activity and the deficit of functional iron in the erythron. In contrast with serum ferritin concentrations, serum transferrin receptor concentrations are not or are only marginally influenced by the inflammatory response to infection. OBJECTIVE We assessed iron status and examined the relation between serum transferrin receptor concentrations and malaria in children aged 2-36 mo who were asymptomatic for malaria. DESIGN This was a community-based cluster survey (n = 318). RESULTS Prevalences of malaria, anemia (hemoglobin concentration <110 g/L), iron deficiency (serum ferritin concentration <12 microg/L), and iron deficiency anemia were 18%, 69%, 53%, and 46%, respectively. Malaria was associated with lower mean hemoglobin concentrations (92.7 compared with 104.1 g/L; P = 0.0001) and higher geometric mean serum concentrations of transferrin receptor (11.4 compared with 7.8 mg/L; P = 0.005), ferritin (21.6 compared with 11.9 microg/L; P = 0.05), and C-reactive protein (12.5 compared with 6.8 mg/L; P = 0.004). There was no evidence for an association between serum concentrations of C-reactive protein and transferrin receptor. Children with malaria had higher serum transferrin receptor concentrations than expected for the degree of anemia, even after adjustment for inflammation indicated by serum C-reactive protein concentration quartiles (P = 0.02). CONCLUSIONS Our findings are consistent with the notion that malaria-induced hemolysis is accompanied by increased erythropoiesis. Serum transferrin receptor concentration is not useful for detecting iron deficiency in individuals with malaria. Individuals with high concentrations of serum C-reactive protein or similar acute phase reactants should be excluded from analysis if serum ferritin concentrations <12 microg/L are to be used to measure iron deficiency in malaria-endemic areas.
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