El-khayat Hamed, Shaaban Sanaa, Emam Ehab Khairy, Elwakkad Amany
National Research Center, Dokki, Cario, Egypt.
Pak J Biol Sci. 2007 Jun 1;10(11):1773-81. doi: 10.3923/pjbs.2007.1773.1781.
Aiming to find out a correlation between plasma LC-PUFA levels and neurodevelopmental status of malnourished infants, the present study was conducted on 42 infants suffering from PEM, with a mean age of 11.28 +/- 4.59 months. They were divided clinically into edematous and non-edematous groups. Fifteen age and sex matched well nourished apparently healthy infants were chosen to serve as controls. All patients were subjected to a 3-phase workup, while controls were subjected only to phase 1. Phase I: includes clinical assessment, laboratory investigations including plasma LC-PUFA levels and Neurodevelopmental assessment. In Phase II: An interventional program of 8 weeks duration; where all patients were receiving an initial supportive treatment followed by nutritional rehabilitation according to WHO guidelines, 1999 as well as developmental stimulation. According to the formula supplied to patients, they were randomly divided into either PUFA supplemented (+ve group) or nonBsupplemented (-ve group). In Phase III: All patients were re-assessed clinically and neurodevelopmentaly as well as re-evaluation for plasma LC-PUFA levels. The study revealed that, the mean plasma AA and DHA levels as well as the mean MDI and PDI scores of BSID-II were significantly lower in PEM patients compared to those levels after nutritional rehabilitation and to controls. Moreover, the mean MDI score was significantly lower in edematous subgroup compared to non-edematous one. Meanwhile, the mean rate of change in plasma DHA level was significantly higher in edematous subgroup compared to non-edematous one. However, there was no significant difference in the mean of rate of change in AA level or MDI and PDI scores between the 2 subgroups. Further, the mean rate of change in plasma AA and DHA levels as well as MDI score were significantly higher in PUFA +ve patients compared to PUFA Bve ones after nutritional rehabilitation. Finally, the study showed significant positive correlations between plasma AA and DHA levels and both MDI and PDI scores. From the course of this study we concluded that malnourished infants had impaired neurodevelopmental functions that could be related to the poor status of plasma LC-PUF. Thus, we recommend early intervention including nutritional rehabilitation and LC-PUFA supplementation as well as stimulation program, so as to have a better effect on future cognitive abilities of these infants.
为了找出血浆长链多不饱和脂肪酸(LC-PUFA)水平与营养不良婴儿神经发育状况之间的相关性,本研究对42例患有蛋白质-能量营养不良(PEM)的婴儿进行了研究,其平均年龄为11.28±4.59个月。临床上将他们分为水肿组和非水肿组。选择15例年龄和性别匹配的营养良好、明显健康的婴儿作为对照。所有患者均接受三个阶段的检查,而对照组仅接受第一阶段检查。第一阶段:包括临床评估、实验室检查(包括血浆LC-PUFA水平)和神经发育评估。第二阶段:为期8周的干预计划;所有患者均接受初始支持治疗,然后根据1999年世界卫生组织指南进行营养康复以及发育刺激。根据提供给患者的配方,将他们随机分为补充多不饱和脂肪酸(PUFA)组(阳性组)或未补充组(阴性组)。第三阶段:对所有患者进行临床和神经发育重新评估以及血浆LC-PUFA水平的重新评估。研究表明,与营养康复后的水平以及对照组相比,PEM患者的血浆花生四烯酸(AA)和二十二碳六烯酸(DHA)平均水平以及贝利婴幼儿发展量表第二版(BSID-II)的平均心理发展指数(MDI)和精神运动发育指数(PDI)得分显著更低。此外,水肿亚组的平均MDI得分显著低于非水肿亚组。同时,水肿亚组的血浆DHA水平平均变化率显著高于非水肿亚组。然而,两个亚组之间的AA水平、MDI和PDI得分的平均变化率没有显著差异。此外,营养康复后,PUFA阳性患者的血浆AA和DHA水平以及MDI得分的平均变化率显著高于PUFA阴性患者。最后,研究表明血浆AA和DHA水平与MDI和PDI得分之间存在显著正相关。从本研究过程中我们得出结论,营养不良的婴儿神经发育功能受损,这可能与血浆LC-PUF的不良状态有关。因此,我们建议进行早期干预,包括营养康复、补充LC-PUFA以及刺激计划,以便对这些婴儿未来的认知能力产生更好的影响。