Turki Abrar, Stockler-Ipsiroglu Sylvia, Sirrs Sandra, Branov Jennifer, Bosdet Taryn, Elango Rajavel
Clinical Nutrition Department, College of Applied Medical Sciences, University of Hafr Al Batin, Hafr Al Batin, Eastern Province, Saudi Arabia.
BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
J Inherit Metab Dis. 2025 Jan;48(1):e12806. doi: 10.1002/jimd.12806. Epub 2024 Oct 15.
Phenylketonuria (PKU) is caused by phenylalanine hydroxylase deficiency. Treatment is primarily a low-Phe diet combined with l-amino acid-based products (l-AA). Protein requirements in adults with PKU have not been directly determined. A formula with glycomacropeptide (GMP) and low phenylalanine is available, yet untested for optimal protein synthesis.
To determine the protein requirements in adults with PKU and the bioavailability of GMP-AA in the same patients using the indicator amino acid oxidation (IAAO) technique.
Each participant was allocated to 7 separate l-AA intakes (range: 0.1-1.8 g/kg/day) in Experiment 1. In Experiment 2, the same patients participated in 4 GMP-AA intakes (range: 0.1-0.9 g/kg/day). The IAAO method with l-[1-C]-lysine as the indicator amino acid and its oxidation to CO was used as the primary indicator of protein synthesis. Protein requirements were identified with a breakpoint, and bioavailability was determined by comparing CO slope from GMP-AA versus l-AA.
Six adults with PKU (4 M: 2F) completed a total of 54 study days over the 2 experiments. The estimated average requirement (EAR) for protein was determined to be 1.11 g/kg/day (R = 0.20). The bioavailability of protein from GMP-AA was determined to be 99.98%, which was high and near to 100% comparable to l-AA; although, the results apply only to the tested GMP-AA blend.
To our knowledge, this is the first study to directly define a quantitative protein requirement and indicates that current PKU protein recommendations for adults with PKU may be underestimated. The bioavailability of protein in the GMP-AA blend was high and optimal for protein synthesis in adults with PKU.
苯丙酮尿症(PKU)由苯丙氨酸羟化酶缺乏引起。治疗主要是低苯丙氨酸饮食并联合基于左旋氨基酸的产品(l-AA)。PKU成年患者的蛋白质需求量尚未直接确定。一种含有糖巨肽(GMP)和低苯丙氨酸的配方产品已存在,但尚未对其促进最佳蛋白质合成的效果进行测试。
使用指示氨基酸氧化(IAAO)技术确定PKU成年患者的蛋白质需求量以及同一患者中GMP-AA的生物利用度。
在实验1中,每位参与者被分配到7种不同的l-AA摄入量(范围:0.1 - 1.8克/千克/天)。在实验2中,相同的患者参与4种GMP-AA摄入量(范围:0.1 - 0.9克/千克/天)。以l-[1-C]-赖氨酸作为指示氨基酸并将其氧化为CO₂的IAAO方法被用作蛋白质合成的主要指标。通过转折点确定蛋白质需求量,并通过比较GMP-AA与l-AA的CO₂斜率来确定生物利用度。
6名PKU成年患者(4名男性:2名女性)在2个实验中总共完成了54个研究日。蛋白质的估计平均需求量(EAR)被确定为1.11克/千克/天(R = 0.20)。来自GMP-AA的蛋白质生物利用度被确定为99.98%,该数值很高,与l-AA相比接近100%;不过,结果仅适用于所测试的GMP-AA混合物。
据我们所知,这是第一项直接确定定量蛋白质需求量的研究,表明目前针对PKU成年患者的PKU蛋白质推荐量可能被低估。GMP-AA混合物中的蛋白质生物利用度很高,对PKU成年患者的蛋白质合成而言是最佳的。