Skip to main content
Top
Published in: Journal of Inherited Metabolic Disease 6/2017

01-11-2017 | Original Article

Predictability and inconsistencies in the cognitive outcome of early treated PKU patients

Authors: Filippo Manti, Francesca Nardecchia, Sabrina Paci, Flavia Chiarotti, Claudia Carducci, Carla Carducci, Silvia Dalmazzone, Graziella Cefalo, Elisabetta Salvatici, Giuseppe Banderali, Vincenzo Leuzzi

Published in: Journal of Inherited Metabolic Disease | Issue 6/2017

Login to get access

Abstract

Long-term cognitive outcome and treatment of adult early treated (ET)PKU patients is a main issue in PKU research. We questioned whether the intellectual development of ETPKU patients is stable and to what extent its variation may be predicted by the quality of metabolic control. The aims of the present longitudinal retrospective study were to assess in young adult ETPKU patients: i) the relationship between IQ and metabolic control during the first two decades of life; and ii) the intra- and interindividual variability in the developmental trajectory which cannot be predicted by the disease’s biomarkers. We collected biochemical data from 65 ETPKU patients (diagnostic blood Phe > 360 μmol/l) who were assessed twice for IQ (Wechsler Intelligence Scale) during their lifetime (mean age: 10.2 and 19.6 years, respectively). Results show that in ETPKU patients IQ over the second decade of life remained stable in about half of the patients (51%); while the rest experienced a gain (7 to 15 points) or loss (7 to 28 points) in IQ scores (23 and 26% respectively) whatever the quality of metabolic control was. The main factor affecting the second IQ was the value of the first IQ (p < 0.000) whose effect overruled that of the markers of metabolic control. Looking at the developmental trajectory of our ETPKU patients, the present study disclosed a remarkable interindividual variability in their cognitive outcome and also an inconsistent linkage between cognitive performances and biochemical control, thus supporting the hypothesis of an individual resilience or vulnerability to Phe in young adult ETPKU.
Appendix
Available only for authorised users
Footnotes
1
Critical difference (T2-T1) = zalpha*SDtest score*SQRT((1-rtt1) + (1-rtt2)); where: T1 and T2 = IQ total scores at time-point 1 and 2, respectively; zalpha = z-score (standard normal distribution) corresponding to alpha level (z0.05 = 1.96); SDtest score = standard deviation of the test score; rtt1 and rtt2 = test-retest reliability for T1 and T2, respectively.
 
Literature
go back to reference Beasley MG, Costello PM, Smith I (1994) Outcome of treatment in young adults with phenylketonuria detected by routine neonatal screening between 1964 and 1971. Q J Med 87:155–160PubMed Beasley MG, Costello PM, Smith I (1994) Outcome of treatment in young adults with phenylketonuria detected by routine neonatal screening between 1964 and 1971. Q J Med 87:155–160PubMed
go back to reference Bilder DA, Burton BK, Coon H et al (2013) Psychiatric symptoms in adults with phenylketonuria. Mol Genet Metab 108:155–160CrossRefPubMed Bilder DA, Burton BK, Coon H et al (2013) Psychiatric symptoms in adults with phenylketonuria. Mol Genet Metab 108:155–160CrossRefPubMed
go back to reference Crone MR, van Spronsen FJ, Oudshoorn K et al (2005) Behavioural factors related to metabolic control in patients with phenylketonuria. J Inherit Metab Dis 28:627–637CrossRefPubMed Crone MR, van Spronsen FJ, Oudshoorn K et al (2005) Behavioural factors related to metabolic control in patients with phenylketonuria. J Inherit Metab Dis 28:627–637CrossRefPubMed
go back to reference Hindley CB, Owen CF (1978) The extent of individual changes in I.Q. For ages between 6 months and 17 years, in a British longitudinal sample. J Child Psychol Psychiatry 19(4):329–350CrossRefPubMed Hindley CB, Owen CF (1978) The extent of individual changes in I.Q. For ages between 6 months and 17 years, in a British longitudinal sample. J Child Psychol Psychiatry 19(4):329–350CrossRefPubMed
go back to reference Hindley CB, Owen CF (1979) An analysis of individual patterns of DQ and IQ curves from 6 months to 17 years. Br J Psychol 70:273–293CrossRef Hindley CB, Owen CF (1979) An analysis of individual patterns of DQ and IQ curves from 6 months to 17 years. Br J Psychol 70:273–293CrossRef
go back to reference Holtzman NA, Kronmal RA, van Doorninck W, Azen C, Koch R (1986) Effect of age at loss of dietary control on intellectual performance and behavior of children with phenylketonuria. N Engl J Med 314(10):593–8 Holtzman NA, Kronmal RA, van Doorninck W, Azen C, Koch R (1986) Effect of age at loss of dietary control on intellectual performance and behavior of children with phenylketonuria. N Engl J Med 314(10):593–8
go back to reference Hujibregts SC, de Sonneville LM, Licht R, van Spronsen FJ, Sergeant JA (2002) Short-term dietary interventions in children and adolescents with treated phenylketonuria: effects on neuropsychological outcome of a well-controlled population. J Inherit Metab Dis 25:419–430CrossRef Hujibregts SC, de Sonneville LM, Licht R, van Spronsen FJ, Sergeant JA (2002) Short-term dietary interventions in children and adolescents with treated phenylketonuria: effects on neuropsychological outcome of a well-controlled population. J Inherit Metab Dis 25:419–430CrossRef
go back to reference Koch R, Azen CG, Friedman EG, Williamson ML (1982) Preliminary report on the effects of diet discontinuation in PKU. J Pediatr 100(6):870–875CrossRefPubMed Koch R, Azen CG, Friedman EG, Williamson ML (1982) Preliminary report on the effects of diet discontinuation in PKU. J Pediatr 100(6):870–875CrossRefPubMed
go back to reference Koch R, Burton B, Hoganson G et al (2002) Phenylketonuria in adulthood: a collaborative study. J Inherit Metab Dis 25:333–346CrossRefPubMed Koch R, Burton B, Hoganson G et al (2002) Phenylketonuria in adulthood: a collaborative study. J Inherit Metab Dis 25:333–346CrossRefPubMed
go back to reference Menard S (1995) Applied logistic regression analysis: Sage University series on quantitative applications in the social sciences. Sage, Thousand Oaks Menard S (1995) Applied logistic regression analysis: Sage University series on quantitative applications in the social sciences. Sage, Thousand Oaks
go back to reference Moyle JJ, Fox AM, Arthur M, Bynevelt M, Burnett JR (2007) Meta-analysis of neuropsychological symptoms of adolescents and adults with PKU. Neuropsychol Rev 17:91–101CrossRefPubMed Moyle JJ, Fox AM, Arthur M, Bynevelt M, Burnett JR (2007) Meta-analysis of neuropsychological symptoms of adolescents and adults with PKU. Neuropsychol Rev 17:91–101CrossRefPubMed
go back to reference Nardecchia F, Manti F, Chiarotti F, Carducci C, Carducci C, Leuzzi V (2015) Neurocognitive and neuroimaging outcome of early treated young adult PKU patients: a longitudinal study. Mol Genet Metab 115(2–3):84–90CrossRefPubMed Nardecchia F, Manti F, Chiarotti F, Carducci C, Carducci C, Leuzzi V (2015) Neurocognitive and neuroimaging outcome of early treated young adult PKU patients: a longitudinal study. Mol Genet Metab 115(2–3):84–90CrossRefPubMed
go back to reference National Institutes of Health Consensus Development Panel (2001 Oct) National Institutes of Health consensus development conference statement: phenylketonuria: screening and management, October 16-18, 2000. Pediatrics 108(4):972–982CrossRef National Institutes of Health Consensus Development Panel (2001 Oct) National Institutes of Health consensus development conference statement: phenylketonuria: screening and management, October 16-18, 2000. Pediatrics 108(4):972–982CrossRef
go back to reference Palermo L, Geberhiwot T, MacDonald A, Limback E, Hall SK, Romani C (2017) Cognitive outcomes in early-treated adults with phenylketonuria (PKU): a comprehensive picture across domains. Neuropsychology 31:255–267CrossRefPubMedPubMedCentral Palermo L, Geberhiwot T, MacDonald A, Limback E, Hall SK, Romani C (2017) Cognitive outcomes in early-treated adults with phenylketonuria (PKU): a comprehensive picture across domains. Neuropsychology 31:255–267CrossRefPubMedPubMedCentral
go back to reference Ramus SJ, Forrest SM, Pitt DD, Cotton RG (1999) Genotype and intellectual phenotype in untreated phenylketonuria patients. Pediatr Res 45(4 Pt 1):474–481CrossRefPubMed Ramus SJ, Forrest SM, Pitt DD, Cotton RG (1999) Genotype and intellectual phenotype in untreated phenylketonuria patients. Pediatr Res 45(4 Pt 1):474–481CrossRefPubMed
go back to reference Romano C, Balsamo A, Burroni M, Cardillo A, Carnevale F, Caruso U, Cerone R, Ciatti R, Cioni M, Corbetta C, Dotti L, Impellizzeri A, Lelli A, Leuzzi V, Lilliu F, Pagliardini S, Piazzi S, Principi R, Salardi S, Schiaffino MC (1997) Diagnosis, classification, basis of treatment of hyperphenylalaninemias. Riv Ital Ped 23:1040–1044 Romano C, Balsamo A, Burroni M, Cardillo A, Carnevale F, Caruso U, Cerone R, Ciatti R, Cioni M, Corbetta C, Dotti L, Impellizzeri A, Lelli A, Leuzzi V, Lilliu F, Pagliardini S, Piazzi S, Principi R, Salardi S, Schiaffino MC (1997) Diagnosis, classification, basis of treatment of hyperphenylalaninemias. Riv Ital Ped 23:1040–1044
go back to reference Romani C, Palermo L, MacDonald A, Limback E, Hall SK, Geberhiwot T (2017) The impact of phenylalanine levels on cognitive outcomes in adults with phenylketonuria: effects across tasks and developmental stages. Neuropsychology 31:242–254CrossRefPubMedPubMedCentral Romani C, Palermo L, MacDonald A, Limback E, Hall SK, Geberhiwot T (2017) The impact of phenylalanine levels on cognitive outcomes in adults with phenylketonuria: effects across tasks and developmental stages. Neuropsychology 31:242–254CrossRefPubMedPubMedCentral
go back to reference Smith I, Beasley MG, Ades AE (1990) Intelligence and quality of dietary treatment in phenylketonuria. Arch Dis Child 65:311–316CrossRef Smith I, Beasley MG, Ades AE (1990) Intelligence and quality of dietary treatment in phenylketonuria. Arch Dis Child 65:311–316CrossRef
go back to reference Smith I, Wolff OH (1974) Natural history of phenylketonuria and influence of early treatment. Lancet 2(7880):540–544CrossRefPubMed Smith I, Wolff OH (1974) Natural history of phenylketonuria and influence of early treatment. Lancet 2(7880):540–544CrossRefPubMed
go back to reference Sullivan JE (2001) Emotional outcome of adolescents and young adults with early and continuously treated phenylketonuria. J Pediatr Psychol 26:477–484CrossRefPubMed Sullivan JE (2001) Emotional outcome of adolescents and young adults with early and continuously treated phenylketonuria. J Pediatr Psychol 26:477–484CrossRefPubMed
go back to reference Trefz FK, Cipcic-Schmidt S, Koch R (2000) Final intelligence in late treated patients with phenylketonuria. Eur J Pediatr 159(Suppl 2):S145–S148CrossRefPubMed Trefz FK, Cipcic-Schmidt S, Koch R (2000) Final intelligence in late treated patients with phenylketonuria. Eur J Pediatr 159(Suppl 2):S145–S148CrossRefPubMed
go back to reference van Spronsen FJ, Huijbregts SC, Bosch AM, Leuzzi V (2011) Cognitive, neurophysiological, neurological and psychosocial outcomes in early-treated PKU-patients: a start toward standardized outcome measurement across development. Mol Genet Metab 104:S45–S51. https://doi.org/10.1016/j.ymgme van Spronsen FJ, Huijbregts SC, Bosch AM, Leuzzi V (2011) Cognitive, neurophysiological, neurological and psychosocial outcomes in early-treated PKU-patients: a start toward standardized outcome measurement across development. Mol Genet Metab 104:S45–S51. https://​doi.​org/​10.​1016/​j.​ymgme
go back to reference Vockley J, Andersson HC, Antshel KM et al (2014) Phenylalanine hydroxylase deficiency: diagnosis and management guideline. Genet Med 16:188–200CrossRefPubMed Vockley J, Andersson HC, Antshel KM et al (2014) Phenylalanine hydroxylase deficiency: diagnosis and management guideline. Genet Med 16:188–200CrossRefPubMed
go back to reference Waisbren SE, Noel K, Fahrbach K et al (2007) Phenylalanine blood levels and clinical outcomes in phenylketonuria: a systematic literature review and meta-analysis. Mol Genet Metab 92:63–70CrossRefPubMed Waisbren SE, Noel K, Fahrbach K et al (2007) Phenylalanine blood levels and clinical outcomes in phenylketonuria: a systematic literature review and meta-analysis. Mol Genet Metab 92:63–70CrossRefPubMed
go back to reference Walter JH, White FJ, Hall SK et al (2002) How practical are recommendations for dietary control in phenylketonuria? Lancet 360:55–57CrossRefPubMed Walter JH, White FJ, Hall SK et al (2002) How practical are recommendations for dietary control in phenylketonuria? Lancet 360:55–57CrossRefPubMed
go back to reference Wechsler D (1997) Wechsler adult intelligence scale- revised (WAIS-R), New York, The Psychological Corporation, 1981. Italian version, C. Laicardi, A. Orsini, Scala di intelligenza Wechsler per adulti, Organizzazioni Speciali, Firenze Wechsler D (1997) Wechsler adult intelligence scale- revised (WAIS-R), New York, The Psychological Corporation, 1981. Italian version, C. Laicardi, A. Orsini, Scala di intelligenza Wechsler per adulti, Organizzazioni Speciali, Firenze
go back to reference Wechsler D (2006) Wechsler intelligence scale for children III (WISC-III), New York, The Psychological Corporation, 1991. Italian version, A. Orsini, L. Picone, Scala di intelligenza Wechsler per bambini- terza edizione, Organizzazioni Speciali, Firenze Wechsler D (2006) Wechsler intelligence scale for children III (WISC-III), New York, The Psychological Corporation, 1991. Italian version, A. Orsini, L. Picone, Scala di intelligenza Wechsler per bambini- terza edizione, Organizzazioni Speciali, Firenze
go back to reference Wechsler D (1986) Wechsler intelligence scale for children Revived (WISC-R), New York, The Psychological Corporation, 1974. Italian version, V. Rubini, F. Padovani, Scala di intelligenza Wechsler per bambini- riveduta, Organizzazioni Speciali, Firenze Wechsler D (1986) Wechsler intelligence scale for children Revived (WISC-R), New York, The Psychological Corporation, 1974. Italian version, V. Rubini, F. Padovani, Scala di intelligenza Wechsler per bambini- riveduta, Organizzazioni Speciali, Firenze
go back to reference Weglage J, Fromm J, van Teeffelen-Heithoff A et al (2013) Neurocognitive functioning in adults with phenylketonuria: results of a long term study. Mol Genet Metab 110:S44–S48CrossRefPubMed Weglage J, Fromm J, van Teeffelen-Heithoff A et al (2013) Neurocognitive functioning in adults with phenylketonuria: results of a long term study. Mol Genet Metab 110:S44–S48CrossRefPubMed
go back to reference Weglage J, Pietsch M, Denecke J, Sprinz A, Feldmann R, Grenzebach M, Ullrich K (1999) Regression of neuropsychological deficits in early-treated phenylketonurics during adolescence. J Inherit Metab Dis 22(6):693–705 Weglage J, Pietsch M, Denecke J, Sprinz A, Feldmann R, Grenzebach M, Ullrich K (1999) Regression of neuropsychological deficits in early-treated phenylketonurics during adolescence. J Inherit Metab Dis 22(6):693–705
go back to reference Weglage J, Ullrich K, Pietsch M, Fünders B, Zass R, Koch HG (1996) Untreated non-phenylketonuric-hyperphenylalaninaemia: intellectual and neurological outcome. Eur J Pediatr 155(Suppl 1):S26–S28CrossRefPubMed Weglage J, Ullrich K, Pietsch M, Fünders B, Zass R, Koch HG (1996) Untreated non-phenylketonuric-hyperphenylalaninaemia: intellectual and neurological outcome. Eur J Pediatr 155(Suppl 1):S26–S28CrossRefPubMed
Metadata
Title
Predictability and inconsistencies in the cognitive outcome of early treated PKU patients
Authors
Filippo Manti
Francesca Nardecchia
Sabrina Paci
Flavia Chiarotti
Claudia Carducci
Carla Carducci
Silvia Dalmazzone
Graziella Cefalo
Elisabetta Salvatici
Giuseppe Banderali
Vincenzo Leuzzi
Publication date
01-11-2017
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 6/2017
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-017-0082-y

Other articles of this Issue 6/2017

Journal of Inherited Metabolic Disease 6/2017 Go to the issue

Highlights

News and views

Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine