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Old Question Revisited: Are High-Protein Diets Safe in Pregnancy?

机译:重新审视的旧问题:怀孕的高蛋白质饮食安全吗?

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摘要

Background: 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. Methods: Individual participant data on singleton pregnancies from the Danish National Birth Cohort (DNBC) (n = 60,141) and the Norwegian Mother, Father and Child Cohort Study (MoBa) (n = 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. Results: 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)]. Conclusions: 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.
机译:背景技术:从20世纪70年代孕妇的先前随机饮食干预患者,哈林试验报告,胎儿生长和过度早期早产和新生儿死亡人员在接受高蛋白质补充剂的患者中。由于道德挑战,这些发现尚未在干预设置中得到解决。在观察环境中探索这些发现,由于这些结果的普及率低,因此需要大的统计力量。本研究的目的是通过组合来自两个大型出生队列的数据来调查高蛋白摄入量的调查结果。方法:在彻底协调过程中合并丹麦国家分娩队(DNBC)(DNBC)(N = 60,141)和挪威母亲,父亲队列(MOBA)(N = 66,302)的个人参与者数据。饮食被记录在中期怀孕中,并从国家出生登记处提取出生结果。结果:早产输送的患病率,低出生体重和胎儿和新生儿死亡分别为4.77%,2.93%,0.28%和0.17%。平均蛋白摄入(标准偏差)为89克/天(23)。总体高蛋白摄入量(> 100克/天)既不与低出生体重也没有胎儿或新生儿死亡。平均出生体重基本上在高蛋白质摄入量不变。与中度蛋白质摄入相比,观察到高(> 100克/天)观察到的早产递送的风险增加[差距(或):1.10(CI):1.01,19)](80-90g /日)。这种估计是由晚期早产的推动(第34周至<37),并且在更极端的摄入量下未观察到更大的风险。与中等蛋白质摄入相比,非常低(<60克/天)与具有低出生体重婴儿的风险较高有关[或:1.59(95%CI:1.25,2.03)]。结论:高蛋白质摄入弱与早产递送弱。与哈林试验的结果相反,未观察到对胎儿生长或围产期死亡率的有害影响的迹象。

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