Faculty of Food Science and Nutrition, School of Health Sciences, University of Iceland, 101 Reykjavik, Iceland.
Centre for Foetal Programming, Department of Epidemiology Research, Statens Serum Institut, 2300 Copenhagen, Denmark.
Nutrients. 2021 Jan 29;13(2):440. doi: 10.3390/nu13020440.
A previous randomized dietary intervention in pregnant women from the 1970s, the Harlem Trial, reported retarded fetal growth and excesses of very early preterm births and neonatal deaths among those receiving high-protein supplementation. Due to ethical challenges, these findings have not been addressed in intervention settings. Exploring these findings in an observational setting requires large statistical power due to the low prevalence of these outcomes. The aim of this study was to investigate if the findings on high protein intake could be replicated in an observational setting by combining data from two large birth cohorts.
Individual participant data on singleton pregnancies from the Danish National Birth Cohort (DNBC) ( = 60,141) and the Norwegian Mother, Father and Child Cohort Study (MoBa) ( = 66,302) were merged after a thorough harmonization process. Diet was recorded in mid-pregnancy and information on birth outcomes was extracted from national birth registries.
The prevalence of preterm delivery, low birth weight and fetal and neonatal deaths was 4.77%, 2.93%, 0.28% and 0.17%, respectively. Mean protein intake (standard deviation) was 89 g/day (23). Overall high protein intake (>100 g/day) was neither associated with low birth weight nor fetal or neonatal death. Mean birth weight was essentially unchanged at high protein intakes. A modest increased risk of preterm delivery [odds ratio (OR): 1.10 (95% confidence interval (CI): 1.01, 1.19)] was observed for high (>100 g/day) compared to moderate protein intake (80-90 g/day). This estimate was driven by late preterm deliveries (weeks 34 to <37) and greater risk was not observed at more extreme intakes. Very low (<60 g/day) compared to moderate protein intake was associated with higher risk of having low-birth weight infants [OR: 1.59 (95%CI: 1.25, 2.03)].
High protein intake was weakly associated with preterm delivery. Contrary to the results from the Harlem Trial, no indications of deleterious effects on fetal growth or perinatal mortality were observed.
20 世纪 70 年代的一项针对孕妇的随机饮食干预试验——哈莱姆试验报告称,高蛋白补充组的胎儿生长迟缓、极早产和新生儿死亡的发生率过高。由于伦理方面的挑战,这些发现并未在干预环境中得到解决。在观察性环境中探索这些发现需要大量的统计能力,因为这些结果的发生率较低。本研究旨在通过合并来自两个大型出生队列的数据,在观察性环境中验证高蛋白摄入的发现是否可以复制。
丹麦国家出生队列(DNBC)(=60141)和挪威母亲、父亲和儿童队列研究(MoBa)(=66302)的单胎妊娠个体参与者数据在经过彻底的协调过程后合并。在妊娠中期记录饮食,从国家出生登记处提取出生结局信息。
早产、低出生体重和胎儿及新生儿死亡的发生率分别为 4.77%、2.93%、0.28%和 0.17%。平均蛋白质摄入量(标准差)为 89 克/天(23)。总体而言,高蛋白摄入(>100 克/天)与低出生体重或胎儿或新生儿死亡均无关。高蛋白质摄入时的平均出生体重基本不变。与中等蛋白质摄入量(80-90 克/天)相比,高(>100 克/天)蛋白质摄入与早产风险略有增加[比值比(OR):1.10(95%置信区间(CI):1.01,1.19)]。这一估计受晚期早产(34 至<37 周)的驱动,而在更极端的摄入量下并未观察到更高的风险。与中等蛋白质摄入量相比,极低(<60 克/天)与低出生体重儿的风险增加相关[比值比(OR):1.59(95%置信区间(CI):1.25,2.03)]。
高蛋白摄入与早产有弱相关性。与哈莱姆试验的结果相反,没有迹象表明对胎儿生长或围产儿死亡率有不良影响。