The role of intelligence in phenylketonuria: A review of research and management

被引:28
作者
Brumm, V. L. [1 ]
Grant, M. L. [2 ,3 ]
机构
[1] Univ Utah, Sch Med, Dept Psychiat, Div Child & Adolescent Psychiat, Salt Lake City, UT 84112 USA
[2] Drexel Univ, Dept Psychiat, Coll Med, Philadelphia, PA 19134 USA
[3] Drexel Univ, Dept Pediat, Sect Child Neurol, St Christophers Hosp Children, Philadelphia, PA 19134 USA
关键词
Phenylketonuria; IQ; Blood phenylalanine; Neurocognitive function; EARLY-TREATED PHENYLKETONURIA; BLOOD-BRAIN-BARRIER; MATERNAL PHENYLKETONURIA; PREFRONTAL DYSFUNCTION; CHILDREN; PHENYLALANINE; PKU; DIET; AGE; DEFICITS;
D O I
10.1016/j.ymgme.2009.10.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Phenylketonuria (PKU) results in profound intellectual disability in untreated individuals and more subtle cognitive deficits in individuals treated early and continuously. The assessment of intellectual functioning has been an important outcome variable and the focus of extensive research. Since the implementation of neonatal PKU screening programs in the 1960s, research on intellectual functioning in individuals with PKU has played a significant and positive role in guiding therapy and improving results. This is a literature review examining the relationship between intellectual outcome and treatment parameters including initiation of treatment, duration of treatment, and blood phenylalanine (Phe) levels from infancy through adulthood. While current PKU treatment practices have eliminated severe neurological and cognitive impairment, evidence suggests that intellectual functioning, although typically within the average range when PKU is treated early and continuously, may not be maximized under the current definition of well-controlled PKU, which is based on blood Phe levels. Future research assessing intellectual and neurocognitive outcome in PKU will enhance the development of new treatment Strategies. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:S18 / S21
页数:4
相关论文
共 69 条
[1]  
*AFDPHE, 2005, ARCH PEDIATR, V12, P594
[2]   Stability of blood phenylalanine levels and IQ in children with phenylketonuria [J].
Anastasoaie, Vera ;
Kurzius, Laura ;
Forbes, Peter ;
Waisbren, Susan .
MOLECULAR GENETICS AND METABOLISM, 2008, 95 (1-2) :17-20
[3]   Are neuropsychological impairments in children with early-treated phenylketonuria (PKU) related to white matter abnormalities or elevated phenylalanine levels? [J].
Anderson, Peter J. ;
Wood, Stephen J. ;
Francis, Dorothy E. ;
Coleman, Lee ;
Anderson, Vicki ;
Boneh, Avihu .
DEVELOPMENTAL NEUROPSYCHOLOGY, 2007, 32 (02) :645-668
[4]  
[Anonymous], 1993, Arch Dis Child, V68, P426
[5]   Summary of findings from the United States Collaborative Study of children treated for phenylketonuria [J].
Azen, C ;
Koch, R ;
Friedman, E ;
Wenz, E ;
Fishler, K .
EUROPEAN JOURNAL OF PEDIATRICS, 1996, 155 :S29-S32
[6]   Plasma phenylalanine in patients with phenylketonuria self-managing their diet [J].
Bekhof, J ;
van Rijn, M ;
Sauer, PJJ ;
Ten Vergert, EM ;
Reijngoud, DJ ;
van Spronsen, FJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 2005, 90 (02) :163-164
[7]  
Bernheim MLC, 1944, J BIOL CHEM, V152, P481
[8]  
BERRY HK, 1958, PEDIATRICS, V21, P929
[9]   DISTURBED MYELINATION IN PATIENTS WITH TREATED HYPERPHENYLALANINEMIA - EVALUATION WITH MAGNETIC-RESONANCE-IMAGING [J].
BICK, U ;
FAHRENDORF, G ;
LUDOLPH, AC ;
VASSALLO, P ;
WEGLAGE, J ;
ULLRICH, K .
EUROPEAN JOURNAL OF PEDIATRICS, 1991, 150 (03) :185-189
[10]  
BICKEL H, 1954, Acta Paediatr, V43, P64, DOI 10.1111/j.1651-2227.1954.tb04000.x