Department of Pediatrics, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Texas Pregnancy and Life-course Health Research Center, Department of Animal Science, University of Wyoming, Laramie, Wyoming, USA.
JPEN J Parenter Enteral Nutr. 2019 Nov;43(8):1053-1064. doi: 10.1002/jpen.1507. Epub 2019 Feb 7.
Parenteral amino acid (AA) nutrition administration after premature birth is necessary to ensure adequate growth and neurodevelopment. However, optimizing safety and efficacy remains a major challenge. This study investigated the effects of intravenous AA administration on plasma AA profiles in premature baboons and infants.
Premature baboons were delivered by cesarean section at 125 days (67% gestation) and chronically ventilated. At 24 hours of life, a parenteral AA protocol comparable to the early and high AA regimens used in premature infants was initiated. Serial plasma AA concentrations were obtained on days of life (DOLs) 1, 3, and 7 and compared with concentrations at similar DOLs from preterm infants. Fetal baboon (165 ± 2 days; 89% gestation) and term baboon plasma AA concentrations were obtained for comparison.
Premature baboons receiving early and high parenteral AA supplementation exhibited significant differences in plasma AA concentrations compared with fetuses. In particular, concentrations of leucine, isoleucine, valine, and ornithine were elevated (fold increase: 2.14, 2.03, 1.95, and 16.5, respectively; P < 0.001) on DOL 3 vs fetuses. These alterations mimicked those found in preterm infants.
Early and high AA supplementation in extremely premature baboons significantly disrupted plasma AA concentrations. Elevated concentrations of branched-chain AAs and ornithine raise concerns for adverse neurodevelopmental outcomes. These results are consistent with those found in premature human infants and emphasize the need to optimize parenteral AA solutions for the unique metabolic requirements of premature infants. Improved technologies for rapid monitoring of AA concentrations during treatment are essential.
早产儿出生后需要进行肠外氨基酸(AA)营养治疗,以确保其充分生长和神经发育。然而,如何优化安全性和疗效仍然是一个主要挑战。本研究旨在探讨静脉给予 AA 对早产狨猴和婴儿的血浆 AA 谱的影响。
通过剖宫产术于 125 日龄(67%孕龄)分娩早产狨猴,并进行慢性通气。出生后 24 小时,开始给予与早产儿早期和高 AA 方案相当的肠外 AA 方案。在出生后第 1、3 和 7 天,连续获取血浆 AA 浓度,并与早产儿相似日龄的浓度进行比较。同时,还获取了胎儿狨猴(165±2 日龄;89%孕龄)和足月产狨猴的血浆 AA 浓度,以作比较。
接受早期和高剂量肠外 AA 补充的早产狨猴与胎儿相比,血浆 AA 浓度存在显著差异。特别是亮氨酸、异亮氨酸、缬氨酸和鸟氨酸的浓度显著升高(倍数增加:2.14、2.03、1.95 和 16.5,均 P<0.001),在第 3 天达到峰值。这些改变与早产儿中的发现相似。
在极早产狨猴中进行早期和高剂量 AA 补充会显著破坏血浆 AA 浓度。支链氨基酸和鸟氨酸浓度的升高引起了对不良神经发育结局的担忧。这些结果与早产儿人类婴儿的结果一致,强调需要针对早产儿独特的代谢需求优化肠外 AA 溶液。在治疗期间,快速监测 AA 浓度的改进技术至关重要。