补充维生素A和铁对喀麦隆学龄前儿童疟疾治疗的影响

C. T. Mofor, Denis Zofou, P. Zollo
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引用次数: 2

摘要

这项研究调查了维生素A和铁作为被感染的学龄前儿童的补充剂对疟疾治疗的影响。在一项安慰剂对照补充试验中,招募了132名年龄在6至60个月之间的儿童,并将其分为4组:第一组每天服用68mg(6-30个月)或102mg(30-60个月)的铁,第二组在治疗开始时单剂量服用30mg(6-12个月)或60mg(12-60个月)的维生素a。第三组同时服用维生素A和铁,而安慰剂组没有补充。采用世界卫生组织(1982年)的方法获得了寄生虫病、临床(体重、活力)和血液学参数(红细胞、白细胞和血红蛋白)的完整数据,并分别采用荧光光谱法和原子吸收分光光度法获得了微量营养素状况(血清维生素A和铁)的完整数据。本研究发现,约40.15%的疟疾患儿患有贫血(40.15%的患儿血红蛋白水平在9.02±1.60 ~ 10.72±1.21 g/dl之间,红细胞水平低于3500000/ mm3)。血清维生素A在0.53±0.14 ~ 0.66±0.24μmol/l之间,存在中度至重度维生素A缺乏。与安慰剂组相比,接受补充剂的婴儿在临床和亚临床参数(体重从0.49±1.48 kg增加到0.64±1.97Kg,而安慰剂组为- 0.76±2.17Kg)、铁状态(血红蛋白水平从0.63±1.33 g/dl变化到0.94±1.2.10 g/dl,而安慰剂组为- 0.68±0.98 g/l)方面有了显著改善。维生素A补充组血清维生素A水平显著提高(0.08±0.20 ~ 0.11±0.17μmol/l),而未补充组血清维生素A水平显著降低(铁组为- 0.04±0.05μmol/l,安慰剂组为- 0.07±0.13μmol/l)。与只服用铁或维生素A的组相比,服用维生素A或铁补充剂的组的改善最为显著。这项研究表明,如果给感染疟疾的儿童补充维生素A和铁,可以显著改善疟疾的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects Of Vitamin A And Iron Supplementation On The Treatment Of Malaria In Cameroonian Preschool Children
This study investigated the effect of vitamin A and iron on the treatment of malaria, when they are given as supplements to infected preschool children. In a placebo-controlled supplementation trial, 132 children aged between 6 and 60 months were recruited and divided into 4 groups: the first group received 68mg (6-30 months) or 102mg (30-60 months) iron daily and the second, 30mg (6-12 months) or 60mg (12-60 months) of vitamin A in single dose at the beginning of the treatment. The third group received both vitamin A and iron while the placebo received no supplement. Completed data was obtained on parasitaemia, clinical (weight, vitality) and haematological parameters ( red blood cells, white blood cells and haemoglobin) using WHO (1982) methods, and micronutrients status (serum vitamin A and iron) respectively by spectrofluorimetry and atomic absorption spectrophotometry. From this study, it was observed that about 40.15% of the children suffering of malaria were anaemic (haemoglobin level from 9.02 ± 1.60 to 10.72 ± 1.21 g/dl and red blood cells level less than 3500000/ mm3 among 40.15% of infants recruited). They also had moderate to severe vitamin A deficiency (serum vitamin A between 0.53 ± 0.14 and 0.66 ± 0.24μmol/l). Compared with placebo group, infants receiving supplements improved considerably, for clinical and sub clinical parameters (weight gain from 0.49 ± 1.48 to 0.64 ± 1.97Kg, as against – 0.76 ± 2.17Kg in placebo group), iron status (haemoglobin level varied from 0.63 ± 1.33 to 0.94 ± 1.2.10 g/dl as against – 0.68 ± 0.98 g/l). A significant improvement of vitamin A status was observed within groups receiving vitamin A supplementation (serum level 0.08 ± 0.20 to 0.11 ± 0.17μmol/l), while there was a notable decrease in the non supplemented group (– 0.04 ± 0.05μmol/l within the group that received iron, and – 0.07 ± 0.13μmol/l in the placebo group). The improvement was most important in the group receiving either vitamin A or iron supplements than those who received iron or vitamin A alone. This study showed that vitamin A and iron could remarkably improve the treatment of malaria when they are given as supplements to infected children.
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