Depressive symptoms in adolescents with early and continuously treated phenylketonuria: Associations with phenylalanine and tyrosine levels

被引:22
|
作者
Sharman, Rachael [1 ,2 ]
Sullivan, Karen [2 ,3 ]
Young, Ross McD [3 ]
McGill, Jim [4 ]
机构
[1] Univ Sunshine Coast, Sch Social Sci, Maroochydore, Qld 4558, Australia
[2] Queensland Univ Technol, Sch Psychol & Counselling, Brisbane, Qld 4001, Australia
[3] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld 4001, Australia
[4] Royal Childrens Hosp, Dept Metab Med, Brisbane, Qld, Australia
关键词
Phenylketonuria; PKU; Phenylalanine; Tyrosine; Depression; BEHAVIOR RATING INVENTORY; EXECUTIVE FUNCTION; CHILDREN; VALIDITY; DEFICITS; PKU;
D O I
10.1016/j.gene.2012.05.007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Previous research has suggested an increased risk for individuals with phenylketonuria (PKU) of developing depression and other mood disorders. As PKU can disrupt neurotransmitter synthesis via biochemical mechanisms, depressive symptoms are hypothesised to result from neurotransmitter dysregulation. Whilst adherence (or return) to the phenylalanine-restricted diet may resolve or improve symptoms of depression, data to demonstrate a direct relationship between biochemistry and mood in this population are lacking. Methods: Thirteen adolescents with early and continuously treated PKU and eight sibling controls were compared in their total reported depressive symptoms. A general executive function assessment was also undertaken in the PKU group. Correlations between depressive symptoms and biochemical markers were examined within the PKU group only. Results: Correlational analyses within the PKU group demonstrated strong and significant associations between depressive symptoms and long term exposure to either a high phenylalanine:tyrosine ratio, or low tyrosine. Increasing symptoms of depression were also found to be associated with poorer executive function in the PKU sample. However, both groups of adolescents scored within the normal range in symptoms of depression (p > 0.05). Conclusions: Significant associations were observed between biochemical markers indicating poorer dietary control and increasing depressive symptoms in a sample of adolescents with early and continuously treated PKU, although symptoms of depression remained within the normal range. An association between depressive symptoms and poorer EF was also demonstrated. Further research is needed to establish whether the depressive symptoms observed in this young population represent an emerging (subclinical) risk for major depressive disorder as they age. Crown Copyright (c) 2012 Published by Elsevier By. All rights reserved.
引用
收藏
页码:288 / 291
页数:4
相关论文
共 50 条
  • [1] Associations between phenylalanine-to-tyrosine ratios and performance on tests of neuropsychological function in adolescents treated early and continuously for phenylketonuria
    Luciana, M
    Sullivan, J
    Nelson, CA
    [J]. CHILD DEVELOPMENT, 2001, 72 (06) : 1637 - 1652
  • [2] BIOCHEMICAL MARKERS ASSOCIATED WITH DEPRESSIVE SYMPTOMS IN A SAMPLE OF ADOLESCENTS WITH EARLY AND CONTINUOUSLY TREATED PHENYLKETONURIA
    Sharman, R.
    Sullivan, K. A.
    Young, R. Mc D.
    McGill, J. J.
    [J]. MOLECULAR GENETICS AND METABOLISM, 2009, 98 (1-2) : 32 - 32
  • [3] AN INTERNATIONAL PRACTICE SURVEY OF THE MEASUREMENT AND MANAGEMENT OF TYROSINE LEVELS IN CHILDREN WITH EARLY AND CONTINUOUSLY TREATED PHENYLKETONURIA
    Sharman, R.
    Sullivan, K. A.
    Young, R. McD
    McGill, J. J.
    [J]. MOLECULAR GENETICS AND METABOLISM, 2009, 98 (1-2) : 33 - 33
  • [4] Emotional outcome of adolescents and young adults with early and continuously treated phenylketonuria
    Sullivan, JE
    [J]. JOURNAL OF PEDIATRIC PSYCHOLOGY, 2001, 26 (08) : 477 - 484
  • [5] Biochemical markers associated with executive function in adolescents with early and continuously treated phenylketonuria
    Sharman, R.
    Sullivan, K.
    Young, R.
    McGill, J.
    [J]. CLINICAL GENETICS, 2009, 75 (02) : 169 - 174
  • [6] Tyrosine monitoring in children with early and continuously treated phenylketonuria: results of an international practice survey
    Sharman, Rachael
    Sullivan, Karen A.
    Young, Ross McD
    McGill, James J.
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2010, 33 : S417 - S420
  • [7] A Preliminary Investigation of the Role of the Phenylalynine: Tyrosine Ratio in Children With Early and Continuously Treated Phenylketonuria: Toward Identification of "Safe" Levels
    Sharman, Rachael
    Sullivan, Karen
    Young, Ross
    McGill, Jim
    [J]. DEVELOPMENTAL NEUROPSYCHOLOGY, 2010, 35 (01) : 57 - 65
  • [8] VARIATIONS WITH AGE IN PLASMA PHENYLALANINE AND TYROSINE LEVELS IN PHENYLKETONURIA
    PARTINGTON, MW
    LEWIS, EJM
    [J]. JOURNAL OF PEDIATRICS, 1963, 2 (03): : 348 - +
  • [9] TREATED PHENYLKETONURIA - INTELLIGENCE AND BLOOD PHENYLALANINE LEVELS
    FULLER, R
    SHUMAN, J
    [J]. AMERICAN JOURNAL OF MENTAL DEFICIENCY, 1971, 75 (05): : 539 - &
  • [10] Prefrontal dysfunction in early and continuously treated phenylketonuria
    Stemerdink, NBA
    van der Molen, MW
    Kalverboer, AF
    van der Meere, JJ
    Huisman, J
    de Jong, LW
    Slijper, FME
    Verkerk, PH
    van Spronsen, FJ
    [J]. DEVELOPMENTAL NEUROPSYCHOLOGY, 1999, 16 (01) : 29 - 57