PHENYLKETONURIC PATIENTS DECADES AFTER DIET

被引:35
作者
FISCH, RO
CHANG, PN
WEISBERG, S
GULDBERG, P
GUTTLER, F
TSAI, MY
机构
[1] UNIV MINNESOTA, DEPT PSYCHOL, MINNEAPOLIS, MN 55455 USA
[2] UNIV MINNESOTA, DEPT APPL STAT, MINNEAPOLIS, MN 55455 USA
[3] JOHN F KENNEDY INST, DEPT BIOCHEM, DK-2600 GLOSTRUP, DENMARK
[4] UNIV MINNESOTA, DEPT LAB MED, MINNEAPOLIS, MN USA
关键词
D O I
10.1007/BF00710427
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nineteen early-treated phenylketonuric patients, whose diet was discontinued between 4.5 and 13 years of age, and who have been off the diet for 12-28 years, were reassessed in 1992-93. There was little change in mean IQ between end of diet and follow-up, less than one IQ point on the average, with no change for any individual exceeding 12 IQ points. Both prior and current IQ correlated slightly negatively with mean phenylalanine (Phe) concentration, and positively with parents' education. The phenylalanine level at follow-up was significantly lower on average by about 900 mu mol/L. Five of the subjects (26%) have evidence of mental disease. However, the data suggest that the discontinuation of the diet did not cause intellectual deterioration. Nonetheless, the patients' intellect cannot be the only consideration for maintenance of diet. The occurrence of psychopathology among phenylketonuric patients and the possible unknown effects of toxic elevation of phenylalanine during their lifetime suggest the need to maintain the diet. The use of DNA for diagnostic and prognostic purposes might assist in decisions about dietary quality and duration, and in anticipation of psychopathology.
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页码:347 / 353
页数:7
相关论文
共 30 条
[1]  
CHANG PN, 1983, J PSYCHIAT TREAT EV, V5, P157
[2]   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
[3]  
DOBSON JC, 1976, PEDIATRICS, V58, P53
[4]  
FISHLER K, 1989, J MENT DEFIC RES, V33, P493
[5]   MOLECULAR ANALYSIS OF PHENYLKETONURIA IN DENMARK - 99-PERCENT OF THE MUTATIONS DETECTED BY DENATURING GRADIENT GEL-ELECTROPHORESIS [J].
GULDBERG, P ;
HENRIKSEN, KF ;
GUTTLER, F .
GENOMICS, 1993, 17 (01) :141-146
[6]   MUTATIONAL SPECTRUM OF PHENYLALANINE-HYDROXYLASE DEFICIENCY IN SICILY - IMPLICATIONS FOR DIAGNOSIS OF HYPERPHENYL-ALANINEMIA IN SOUTHERN EUROPE [J].
GULDBERG, P ;
ROMANO, V ;
CERATTO, N ;
BOSCO, P ;
CIUNA, M ;
INDELICATO, A ;
MOLLICA, F ;
MELI, C ;
GIOVANNINI, M ;
RIVA, E ;
BIASUCCI, G ;
HENRIKSEN, KF ;
GUTTLER, F .
HUMAN MOLECULAR GENETICS, 1993, 2 (10) :1703-1707
[7]  
GUTTLER F, 1992, ENZYME, V46, P259
[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]   TERMINATION OF RESTRICTED DIET IN CHILDREN WITH PHENYLKETONURIA - RANDOMIZED CONTROLLED-STUDY [J].
HOLTZMAN, NA ;
WELCHER, DW ;
MELLITS, ED .
NEW ENGLAND JOURNAL OF MEDICINE, 1975, 293 (22) :1121-1124
[10]  
KANG ES, 1970, PEDIATRICS, V45, P83