足月和早产儿在生命第一年的血清促红细胞生成素水平。

H Yamashita, J Kukita, S Ohga, H Nakayama, K Akazawa, K Ueda
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引用次数: 19

摘要

目的:为了评估促红细胞生成素(EPO)产生的动力学和解决早产儿贫血的发病机制,我们测量了出生后第一年婴儿的促红细胞生成素水平。患者和方法:采用放射免疫法测定97例婴儿血清EPO水平,按体重分为3组:a组,n = 40, < 1,500 g;B组,n = 19, 1500 ~ 2499 g;C组,n = 38, >或= 2500 g。结果:新生儿早期第0 ~ 6天血清EPO水平变化较大(A组< 5 ~ 307 mU/ml;B组10 ~ 340 mU/ml;C组9 ~ 108 mU/ml)。EPO在第7 ~ 50天达到最低水平(< 20 mU/ml)。各组血红蛋白浓度在第51天至第150天达到最低点,低出生体重儿的血红蛋白浓度最低。相比之下,贫血期EPO水平约为20 mU/ml,与出生体重无关。血清EPO水平与血红蛋白浓度仅在C组呈负相关(r = -0.54, p < 0.05)。C组回归方程负斜率大于A、B组(p < 0.05)。当分别在7-50天、51-100天和> 101天期间评估EPO和Hb之间的关系时,我们注意到a组在第7天和第50天(r = -0.53, p < 0.05)和B组在第51天和第100天(r = -0.76, p < 0.05)之间的值具有显著相关性。结论:这些数据表明,早产儿中EPO的产生是明显的,但其对血红蛋白水平降低的反应不足,这意味着需要对早产儿贫血给予外源性EPO。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum erythropoietin levels in term and preterm infants during the first year of life.

Purpose: To evaluate the kinetics of erythropoietin (EPO) production and address the pathogenesis of anemia of prematurity, we measured EPO levels in infants during the first year of life.

Patients and methods: Using a radioimmunoassay, serum EPO levels were measured in 97 infants classified into three groups according to weight: group A, n = 40, < 1,500 g; group B, n = 19, 1,500-2,499 g; and group C, n = 38, > or = 2,500 g.

Results: The serum EPO level ranged widely during the early neonatal period from days 0 to 6 (group A, < 5 to 307 mU/ml; group B, 10-340 mU/ml; and group C, 9-108 mU/ml). EPO reached its lowest level (< 20 mU/ml) between days 7 and 50 in all groups. The hemoglobin concentration reached its nadir between days 51 and 150 in all groups, with the lowest concentration observed in low birth weight infants. In contrast, the EPO level during the anemic phase was approximately 20 mU/ml and was independent of birth weight. A negative correlation between serum EPO level and hemoglobin concentration was observed only in group C (r = -0.54, p < 0.05). The negative slope of the regression equation in group C exceeded that of groups A and B (p < 0.05). When the relationship between EPO and Hb was evaluated over periods of 7-50 days, 51-100 days, and > 101 days, respectively, we noted a significant correlation between values on days 7 and 50 in group A (r = -0.53, p < 0.05) and between days 51 and 100 in group B (r = -0.76, p < 0.05).

Conclusions: These data suggest the appreciable EPO production in premature infants, but its insufficient response to the depressed hemoglobin level, implying the need to administer exogenous EPO to infants with anemia of prematurity.

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