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四氢生物蝶呤负荷试验在高苯丙氨酸血症鉴别诊断中的价值
引用本文:张知新,叶军,邱文娟,韩连书,顾学范.四氢生物蝶呤负荷试验在高苯丙氨酸血症鉴别诊断中的价值[J].中华医学遗传学杂志,2005,22(4):438-440.
作者姓名:张知新  叶军  邱文娟  韩连书  顾学范
作者单位:1. 北京中日友好医院儿科
2. 200092,上海第二医科大学附属新华医院,上海市儿科医学研究所,小儿内分泌、遗传代谢病研究室
基金项目:上海市教委(03BK12)
摘    要:目的 对高苯丙氨酸血症患者进行口服四氢生物蝶呤(tetrahydrobiopterin,BH4)负荷试验,了解该方法在高苯丙氨酸血症中的鉴别诊断价值。方法 新生儿筛查阳性以及临床诊断的高苯丙氨酸血症患儿73例(男47例、女26例),中位数年龄1.93月,进行口服BH4负荷试验(20mg/kg)。对其中血苯丙氨酸(phenylalanine Phe)浓度〈600/μmol/L者给予口服Phe—BH4联合负荷试验,同时进行尿蝶呤谱分析,红细胞二氢生物蝶啶还原酶测定。结果 在BH4负荷试验或Phe-BH4联合负荷试验中,经典型苯丙酮尿症(phenylketonuria,PKU)的血Phe对BH4无反应;苯丙氨酸羟化酶缺乏引起的中度PKU的血Phe 24 h下降32.8%;BH4缺乏症患者服BH4后血Phe表现出特征性的快速下降,4 h降至正常水平,并且维持至24h。结合其他检测结果,22例诊断为经典型PKU,39例中度PKU,12例BH4缺乏症。结论 高苯丙氨酸血症是由苯丙氨酸羟化酶缺乏或者BH4缺乏所引起,早期鉴别诊断十分重要。BH4负荷试验是快速、简便的体内诊断试验,安全可靠,有较高的鉴别诊断价值。

关 键 词:四氢生物蝶呤  负荷试验  高苯丙氨酸血症  鉴别诊断  苯丙酮尿症
收稿时间:2004-11-25
修稿时间:2004年11月25

Tetrahydrobiopterin loading test in differential diagnosis among hyperphenylalaninemia patients
ZHANG Zhi-xin,YE Jun,QIU Wen-Juan,HAN Lian-shu,GU Xue-fan.Tetrahydrobiopterin loading test in differential diagnosis among hyperphenylalaninemia patients[J].Chinese Journal of Medical Genetics,2005,22(4):438-440.
Authors:ZHANG Zhi-xin  YE Jun  QIU Wen-Juan  HAN Lian-shu  GU Xue-fan
Institution:Department of Pediatric Endocrinology and Genetic Metabolism, Xinhua Hospital, Shanghai Second Medical University, Shanghai Institute for Pediatric Research, Shanghai, 200092 PR China.
Abstract:OBJECTIVE: To perform tetrahydrobiopterin (BH(4)) loading test and to further understand its usefulness in differential diagnosis among hyperphenylalaninemia(HPA) patients. METHODS: BH(4) loading test was carried out in 73 HPA patients, including the positive cases unveiled by neonatal screening and the clinically suspected cases. These patients, 47 males and 26 females, were at a mean age of 1.93 months. BH(4) (20 mg/kg) loading test was performed in all patients, and a combined phenylalanine (Phe)(100 mg/kg) and BH(4) loading test was performed among the patient who had a basic blood Phe concentration less than 600 micro mol/L. The urine pterine profile analysis and the dihydropteridine reductase activity in dry blood filter spot were tested simultaneously. RESULTS: During BH(4) loading test or combined Phe and BH(4) loading test, the patients with classic phenylketonuria showed no response to BH(4), the patients with moderate HPA caused by Phe hydroxylase deficiency decreased 32.8% of blood Phe level and the patients with BH(4) deficiency showed a prompt reduction in blood Phe level and it decreased to normal level at 4 h and lasted until 24 h. Twenty-two cases were diagnosed as classic phenylketonuria, 39 were moderate phenylketonuria and 12 were BH(4) deficiency. CONCLUSION: Hyperphenylalaninemia may be caused by deficiency of Phe hydroxylase or by deficiency of co-factor BH(4). Early diagnosis is important. BH(4) loading test is a safe and fast test in vivo. It is sensitive, easy-to-do, and is highly useful in differential diagnosis for suspected cases of HPA.
Keywords:tetrahydrobiopterin loading test  hyperphenylalaninemia  tetrahydrobiopterin deficiency  phenylketonuria
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