Long-term follow up of patients with classical phenylketonuria after diet relaxation at 5 years of age - The Paris study

被引:24
作者
Rey, F [1 ]
Abadie, V [1 ]
Plainguet, F [1 ]
Rey, J [1 ]
机构
[1] HOP NECKER ENFANTS MALAD, F-75743 PARIS 15, FRANCE
关键词
D O I
10.1007/PL00014246
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
The age for discontinuing dietary treatment of phenylketonuria (PKU) has been a worldwide source of controversy for many years. It is the reason we report here the results of a prospective, controlled study in which the diet was relaxed at 5 years of age in 31 so far well-treated children with classical PKU. The increase of phenylalanine (Phe) plasma levels to about 1500 mu mol/l (25 mg/dl) after relaxing the diet was not associated with any significant decline of intellectual performance as measured by the Wechsler scores. Paired comparisons at 7-8 years and 11-13 years of age (n = 12) have shown WISC scores of 102.6 +/- 16.2 and 104.8 +/- 16, respectively, which were not significantly different. Similarly, paired comparisons at 9-10 years and 14-16 years (n = 6) did not demonstrate a significant loss of IQ points (107.7 +/- 13 vs 104.8 +/- 18). Of course, it is possible to argue that we should have observed an increase in IQ with increasing age in our patients and that the absence of deterioration cannot be considered by itself as a good result. Nevertheless, it cannot be excluded that the subtle but global intellectual impairments that have been documented in early-treated subjects are, to a very substantial degree, determined in the pre-school years, long before there is any question of stopping or relaxing the diet.
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页码:S39 / S44
页数:6
相关论文
共 31 条
[1]
ABADIE V, 1992, ARCH FR PEDIATR, V49, P773
[2]
INTELLECTUAL-DEVELOPMENT IN 12-YEAR-OLD CHILDREN TREATED FOR PHENYLKETONURIA [J].
AZEN, CG ;
KOCH, R ;
FRIEDMAN, EG ;
BERLOW, S ;
COLDWELL, J ;
KRAUSE, W ;
MATALON, R ;
MCCABE, E ;
OFLYNN, M ;
PETERSON, R ;
ROUSE, B ;
SCOTT, CR ;
SIGMAN, B ;
VALLE, D ;
WARNER, R .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1991, 145 (01) :35-39
[3]
BARABAS G, 1986, PEDIATRICS, V77, P434
[4]
THE HISTORY OF ENTHUSIASM FOR PROTEIN [J].
CARPENTER, KJ .
JOURNAL OF NUTRITION, 1986, 116 (07) :1364-1370
[5]
MAGNETIC-RESONANCE-IMAGING OF THE BRAIN IN PHENYLKETONURIA [J].
CLEARY, MA ;
WALTER, JH ;
WRAITH, JE ;
JENKINS, JPR ;
ALANI, SM ;
TYLER, K ;
WHITTLE, D .
LANCET, 1994, 344 (8915) :87-90
[6]
CORRELATION BETWEEN POLYMORPHIC DNA HAPLOTYPES AT PHENYLALANINE-HYDROXYLASE LOCUS AND CLINICAL PHENOTYPES OF PHENYLKETONURIA [J].
GUTTLER, F ;
LEDLEY, FD ;
LIDSKY, AS ;
DILELLA, AG ;
SULLIVAN, SE ;
WOO, SLC .
JOURNAL OF PEDIATRICS, 1987, 110 (01) :68-71
[7]
HENDRIKX MMT, 1994, EUR J PEDIATR, V153, P832
[8]
EFFECT OF AGE AT LOSS OF DIETARY CONTROL ON INTELLECTUAL-PERFORMANCE AND BEHAVIOR OF CHILDREN WITH PHENYLKETONURIA [J].
HOLTZMAN, NA ;
KRONMAL, RA ;
VANDOORNINCK, W ;
AZEN, C ;
KOCH, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (10) :593-598
[9]
THE EFFECTS OF DIET DISCONTINUATION IN CHILDREN WITH PHENYLKETONURIA [J].
KOCH, R ;
AZEN, CG ;
HURST, N ;
FRIEDMAN, EG ;
FISHLER, K .
EUROPEAN JOURNAL OF PEDIATRICS, 1987, 146 :A12-A16
[10]
PKU IN ADOLESCENTS - RATIONALE AND PSYCHOSOCIAL FACTORS IN DIET CONTINUATION [J].
LEVY, HL ;
WAISBREN, SE .
ACTA PAEDIATRICA, 1994, 83 :92-97