Haiden Nadja, Klebermass Katrin, Cardona Francesco, Schwindt Jens, Berger Angelika, Kohlhauser-Vollmuth Christina, Jilma Bernd, Pollak Arnold
Department of Pediatrics, Division of Neonatology, Inborn Errors, and Pediatric Intensive Care, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Pediatrics. 2006 Jul;118(1):180-8. doi: 10.1542/peds.2005-2475.
Premature infants, especially those with birth weights of <1500 g, often suffer from anemia of prematurity and associated problems. Erythropoietin therapy is a safe effective way to prevent and to treat anemia of prematurity. We hypothesized that combined administration of vitamin B12 and folate with erythropoietin and iron would enhance erythropoietin-induced erythropoiesis.
In a randomized, controlled trial, 64 premature infants (birth weight: 801-1300 g) receiving erythropoietin and iron supplementation were assigned randomly to receive either vitamin B12 (3 microg/kg per day) and folate (100 microg/kg per day) (treatment group) or a lower dose of folate (60 microg/kg per day) (control group).
During the 4-week observation period, vitamin B12 and folate enhanced erythropoietin-induced erythropoiesis significantly, as indicated by a 10% increase in red blood cell counts, compared with folate alone. Hemoglobin and hematocrit levels remained stable in the treatment group, whereas they decreased in the control group. Vitamin B12 levels in the treatment group increased over baseline and control values, whereas red blood cell folate levels were comparable between the groups. Subsequent analysis showed slight nonsignificant differences in baseline red blood cell count, hemoglobin level, hematocrit level, and mean corpuscular volume values, which must be addressed as a limitation.
With the limitation of a slight imbalance in baseline data between the study groups, combined therapy with vitamin B12, folate, erythropoietin, and orally and intravenously administered iron seemed more effective in stimulating erythropoiesis among premature infants, compared with erythropoietin, iron, and low-dose folate alone. Additional trials are necessary to confirm these data.
早产儿,尤其是出生体重<1500g的早产儿,常患有早产儿贫血及相关问题。促红细胞生成素治疗是预防和治疗早产儿贫血的一种安全有效的方法。我们假设维生素B12和叶酸与促红细胞生成素及铁联合使用会增强促红细胞生成素诱导的红细胞生成。
在一项随机对照试验中,将64名接受促红细胞生成素和铁补充剂的早产儿(出生体重:801-1300g)随机分为两组,一组接受维生素B12(每日3μg/kg)和叶酸(每日100μg/kg)(治疗组),另一组接受低剂量叶酸(每日60μg/kg)(对照组)。
在4周的观察期内,与单独使用叶酸相比,维生素B12和叶酸显著增强了促红细胞生成素诱导的红细胞生成,红细胞计数增加了10%。治疗组血红蛋白和血细胞比容水平保持稳定,而对照组则下降。治疗组维生素B12水平高于基线和对照组值,而两组间红细胞叶酸水平相当。后续分析显示,基线红细胞计数、血红蛋白水平、血细胞比容水平和平均红细胞体积值存在轻微的非显著性差异,这必须作为一个局限性加以说明。
尽管研究组间基线数据存在轻微不平衡这一局限性,但与单独使用促红细胞生成素、铁和低剂量叶酸相比,维生素B12、叶酸、促红细胞生成素与口服及静脉注射铁联合治疗在刺激早产儿红细胞生成方面似乎更有效。需要更多试验来证实这些数据。