Department of Dietetics, National Taiwan University Hospital, Taipei, Taiwan.
School of Nursing, College of Nursing, National Taipei University of Nursing and Health Sciences, Taipei, Taiwan.
Sci Rep. 2020 Sep 3;10(1):14537. doi: 10.1038/s41598-020-71361-8.
Phenylalanine hydroxylase (PAH) deficiency leads to phenylalanine accumulation and results in phenylketonuria (PKU). Phenylketonuria can contribute to severe inability such as mental impairment. Early diagnosis and dietary intervention can have beneficial effects on maintaining normal neural and cognitive function in patients with PKU. However, a long-term low phenylalanine diet may put children at risk of malnutrition. A food supplement was therefore used for children with PKU under dietician supervision according to dietary reference intakes (DRIs). In this cross-sectional study, we enrolled patients with PKU and age-matched controls to compare their anthropometry data [weight, height, body mass index (BMI), and body composition using bioelectrical impedance analysis (BIA)], and correlated it with their dietary intake based on 24-h dietary recall. For continuous parameters, the data were expressed as median ± standard deviation (SD), and the Mann-Whitney U test was used to test the difference among the groups. Correlation by natural proteins, body fat, and fat-free mass were evaluated using the Pearson correlation coefficient. Twenty-two participants diagnosed with PKU (ages 8-27 years; mean 15.23 ± 5.23) and a control group of 22 non-PKU participants (ages 8-39 years; mean 19.73 ± 10.6) were recruited for this study. Between the two groups of participants, no significant difference was found in height, weight, BMI, muscle mass, or fat mass. The percentage of natural protein has no effect on body composition. We found a significant positive correlation between the total protein intake percentage of DRIs and muscle mass (r = 0.491, p = 0.020) and a significant negative correlation in the total protein intake percentage of DRIs and fat mass (r = -0.475, p = 0.025) in participants with PKU. There were no significant differences in body composition and nutrition intake between patients with PKU (under metabolic control) and healthy subjects. Thus, giving proper nutrition treatment may have beneficial effects on body growth and nutrition status in patients with PKU in Taiwan.
苯丙氨酸羟化酶(PAH)缺乏导致苯丙氨酸积累,从而导致苯丙酮尿症(PKU)。PKU 可导致严重的残疾,如智力障碍。早期诊断和饮食干预可以对维持 PKU 患者的正常神经和认知功能产生有益影响。然而,长期的低苯丙氨酸饮食可能会使儿童面临营养不良的风险。因此,在营养师的监督下,为 PKU 儿童使用饮食补充剂,以满足饮食参考摄入量(DRIs)。在这项横断面研究中,我们招募了 PKU 患者和年龄匹配的对照组,比较他们的人体测量数据[体重、身高、体重指数(BMI)和生物电阻抗分析(BIA)测量的身体成分],并根据 24 小时饮食回忆来比较他们的饮食摄入。对于连续参数,数据表示为中位数±标准差(SD),并使用曼-惠特尼 U 检验检验组间差异。用皮尔逊相关系数评估天然蛋白质、体脂肪和去脂体重的相关性。本研究共纳入 22 名确诊为 PKU 的患者(年龄 8-27 岁;平均 15.23±5.23 岁)和 22 名非 PKU 对照组参与者(年龄 8-39 岁;平均 19.73±10.6 岁)。在两组参与者中,身高、体重、BMI、肌肉量或脂肪量无显著差异。天然蛋白质的百分比对身体成分没有影响。我们发现,DRIs 总蛋白摄入量百分比与肌肉量呈显著正相关(r=0.491,p=0.020),与脂肪量呈显著负相关(r=-0.475,p=0.025)。PKU 患者中 DRIs 总蛋白摄入量百分比与肌肉量呈显著正相关(r=0.491,p=0.020),与脂肪量呈显著负相关(r=-0.475,p=0.025)。在代谢控制良好的 PKU 患者和健康受试者之间,身体成分和营养摄入没有显著差异。因此,在台湾,给予适当的营养治疗可能对 PKU 患者的身体生长和营养状况有有益的影响。