Glycomacropeptide for nutritional management of phenylketonuria: a randomized, controlled, crossover trial

被引:61
作者
Ney, Denise M. [1 ]
Stroup, Bridget M. [1 ]
Clayton, Murray K. [2 ,3 ]
Murali, Sangita G. [1 ]
Rice, Gregory M. [4 ,5 ]
Rohr, Frances [6 ]
Levy, Harvey L. [6 ]
机构
[1] Univ Wisconsin, Dept Nutr Sci, 1415 Linden Dr, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Stat, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Plant Pathol, Madison, WI 53706 USA
[4] Univ Wisconsin, Waisman Ctr, Sch Med & Publ Hlth, Madison, WI 53705 USA
[5] Univ Wisconsin, Dept Pediat, Sch Med & Publ Hlth, Madison, WI USA
[6] Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA USA
关键词
inborn errors of amino acid metabolism; phenylalanine; tyrosine; threonine; medical food; sapropterin dihydrochloride; executive function; PHENYLALANINE-HYDROXYLASE DEFICIENCY; BONE-MINERAL DENSITY; AMINO-ACIDS; CHEESE WHEY; SUPPORTS GROWTH; MURINE MODEL; YOUNG MEN; DIETARY; PROTEIN; INDIVIDUALS;
D O I
10.3945/ajcn.116.135293
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: To prevent cognitive impairment, phenylketonuria requires lifelong management of blood phenylalanine (Phe) concentration with a low-Phe diet. The diet restricts intake of Phe from natural proteins in combination with traditional amino acid medical foods (AA-MFs) or glycomacropeptide medical foods (GMP-MFs) that contain primarily intact protein and a small amount of Phe. Objective: We investigated the efficacy and safety of a low-Phe diet combined with GMP-MFs or AA-MFs providing the same quantity of protein equivalents in free-living subjects with phenylketonuria. Design: This 2-stage, randomized crossover trial included 30 early-treated phenylketonuria subjects (aged 15-49 y), 20 with classical and 10 with variant phenylketonuria. Subjects consumed, in random order for 3 wk each, their usual low-Phe diet combined with AA-MFs or GMP-MFs. The treatments were separated by a 3-wk washout with AA-MFs. Fasting plasma amino acid profiles, blood Phe concentrations, food records, and neuropsychological tests were obtained. Results: The frequency of medical food intake was higher with GMP-MFs than with AA-MFs. Subjects rated GMP-MFs as more acceptable than AA-MFs and noted improved gastrointestinal symptoms and less hunger with GMP-MFs. ANCOVA indicated no significant mean +/- SE increase in plasma Phe (62 +/- 40 mu mol/L, P = 0.136), despite a significant increase in Phe intake from GMP-MFs (88 +/- 6 mg Phe/d, P = 0.026). AA-MFs decreased plasma Phe (285 +/- 40 mu mol/L, P = 0.044) with stable Phe intake. Blood concentrations of Phe across time were not significantly different (AA-MFs = 444 +/- 34 mu mol/L, GMP-MFs = 497 +/- 34 mu mol/L), suggesting similar Phe control. Results of the Behavior Rating Inventory of Executive Function were not significantly different. Conclusions: GMP-MFs provide a safe and acceptable option for the nutritional management of phenylketonuria. The greater acceptability and fewer side effects noted with GMP-MFs than with AA-MFs may enhance dietary adherence for individuals with phenylketonuria.
引用
收藏
页码:334 / 345
页数:12
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