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Optimized loading test to evaluate responsiveness to tetrahydrobiopterin (BH4) in Brazilian patients with phenylalanine hydroxylase deficiency

机译:优化的负荷试验,以评估巴西苯丙氨酸羟化酶缺乏症患者对四氢生物蝶呤(BH4)的反应

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摘要

INTRODUCTION:\ud\udRecent studies showed that phenylalanine (Phe) plasma concentrations may decrease in some patients with hyperphenylalaninemia (HPA) due to phenylalanine hydroxylase (PAH) deficiency, after the administration of tetrahydrobiopterin (BH(4)).\udOBJECTIVE:\ud\udTo determine responsiveness to a single dose of BH(4) administered according to an innovative protocol using a combined Phe and BH(4) loading test in Brazilian phenylketonuria (PKU) patients.\udMETHODS:\ud\udPatient age should be ≥ 4 years, and median Phe plasma concentration ≤ 600 μmol/L when following dietary restrictions. Participants received a simple Phe loading test using 100mg/kg L-Phe (Test 1) and a combined Phe+BH(4) loading test using 100mg/kg L-Phe and 20mg/kg/BH(4) (Test 2). Blood samples were collected at baseline and 3, 11 and 27 h after Phe ingestion (T0, T1, T2 and T3). Responsiveness was defined as: criterion A: plasma Phe reduction of ≥ 30% at T1 and T2 for Tests 1 and 2; criterion B: plasma Phe reduction of ≥ 30% at T1 and T3 for Tests 1 and 2; and criterion C: at least 30% difference of the areas under the Phe curve for Tests 1 and 2.\udRESULTS:\ud\udEighteen patients (median age 12 yrs; 8 classical PKU; 10 mild PKU) participated in the study. Six patients (2 classical PKU; 4 mild PKU) were classified as responsive according to at least one of the criteria. Responsiveness was concordant when criteria A + B we compared with criterion C (kappa = 0.557; p = 0.017). Of the patients whose genotype was available (n = 16), six had data about BH(4)-responsiveness genotypes described in the literature, which were in agreement with our findings.\udCONCLUSION:\ud\udThe comparison of simple Phe loading and combined Phe + BH(4) loading seems to be an optimal method to evaluate responsiveness to BH(4) in patients with good metabolic control.\ud\udCopyright © 2011 Elsevier Inc. All rights reserved.
机译:简介:\ ud \ ud最近的研究表明,在服用四氢生物蝶呤(BH(4))后,由于苯丙氨酸羟化酶(PAH)缺乏,某些患有高苯丙氨酸血症(HPA)的患者的苯丙氨酸(Phe)血浆浓度可能会降低。 ud \ ud要确定对根据创新方案使用Phe和BH(4)联合负荷试验在巴西苯丙酮尿症(PKU)患者中服用单剂量BH(4)的反应。\ udMETHODS:\ ud \ ud患者年龄应≥ 4年,并且遵循饮食限制,Phe血浆中值浓度≤600μmol/ L。参与者接受了使用100mg / kg L-Phe的简单Phe负载测试(测试1)和使用100mg / kg L-Phe和20mg / kg / BH(4)的组合Phe + BH(4)负载测试(测试2)。在基线和苯丙氨酸摄入后3、11和27小时(T0,T1,T2和T3)采集血样。响应度定义为:标准A:测试1和2在T1和T2血浆Phe降低≥30%;标准B:在测试1和2的T1和T3时血浆Phe降低≥30%;标准C:测试1和测试2的Phe曲线下面积至少相差30%。\ ud结果:\ ud \ ud有18位患者(中位年龄12岁; 8位经典PKU; 10位轻度PKU)参加了研究。根据至少一项标准,将六名患者(2名经典PKU; 4名轻度PKU)归类为有反应。当我们将标准A + B与标准C进行比较时,响应能力是一致的(kappa = 0.557; p = 0.017)。在可获得基因型的患者中(n = 16),有六名文献中描述了有关BH(4)反应性基因型的数据,这与我们的发现相符。合并Phe + BH(4)的负载似乎是评估代谢控制良好的患者对BH(4)的反应性的最佳方法。\ ud \ ud版权所有©2011 Elsevier Inc.保留所有权利。

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