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Can untreated PKU patients escape from intellectual disability? A systematic review

BACKGROUND: Phenylketonuria (PKU) is often considered as the classical example of a genetic disorder in which severe symptoms can nowadays successfully be prevented by early diagnosis and treatment. In contrast, untreated or late-treated PKU is known to result in severe intellectual disability, seiz...

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Autores principales: van Vliet, Danique, van Wegberg, Annemiek M. J., Ahring, Kirsten, Bik-Multanowski, Miroslaw, Blau, Nenad, Bulut, Fatma D., Casas, Kari, Didycz, Bozena, Djordjevic, Maja, Federico, Antonio, Feillet, François, Gizewska, Maria, Gramer, Gwendolyn, Hertecant, Jozef L., Hollak, Carla E. M., Jørgensen, Jens V., Karall, Daniela, Landau, Yuval, Leuzzi, Vincenzo, Mathisen, Per, Moseley, Kathryn, Mungan, Neslihan Ö., Nardecchia, Francesca, Õunap, Katrin, Powell, Kimberly K., Ramachandran, Radha, Rutsch, Frank, Setoodeh, Aria, Stojiljkovic, Maja, Trefz, Fritz K., Usurelu, Natalia, Wilson, Callum, van Karnebeek, Clara D., Hanley, William B., van Spronsen, Francjan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116368/
https://www.ncbi.nlm.nih.gov/pubmed/30157945
http://dx.doi.org/10.1186/s13023-018-0890-7
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author van Vliet, Danique
van Wegberg, Annemiek M. J.
Ahring, Kirsten
Bik-Multanowski, Miroslaw
Blau, Nenad
Bulut, Fatma D.
Casas, Kari
Didycz, Bozena
Djordjevic, Maja
Federico, Antonio
Feillet, François
Gizewska, Maria
Gramer, Gwendolyn
Hertecant, Jozef L.
Hollak, Carla E. M.
Jørgensen, Jens V.
Karall, Daniela
Landau, Yuval
Leuzzi, Vincenzo
Mathisen, Per
Moseley, Kathryn
Mungan, Neslihan Ö.
Nardecchia, Francesca
Õunap, Katrin
Powell, Kimberly K.
Ramachandran, Radha
Rutsch, Frank
Setoodeh, Aria
Stojiljkovic, Maja
Trefz, Fritz K.
Usurelu, Natalia
Wilson, Callum
van Karnebeek, Clara D.
Hanley, William B.
van Spronsen, Francjan J.
author_facet van Vliet, Danique
van Wegberg, Annemiek M. J.
Ahring, Kirsten
Bik-Multanowski, Miroslaw
Blau, Nenad
Bulut, Fatma D.
Casas, Kari
Didycz, Bozena
Djordjevic, Maja
Federico, Antonio
Feillet, François
Gizewska, Maria
Gramer, Gwendolyn
Hertecant, Jozef L.
Hollak, Carla E. M.
Jørgensen, Jens V.
Karall, Daniela
Landau, Yuval
Leuzzi, Vincenzo
Mathisen, Per
Moseley, Kathryn
Mungan, Neslihan Ö.
Nardecchia, Francesca
Õunap, Katrin
Powell, Kimberly K.
Ramachandran, Radha
Rutsch, Frank
Setoodeh, Aria
Stojiljkovic, Maja
Trefz, Fritz K.
Usurelu, Natalia
Wilson, Callum
van Karnebeek, Clara D.
Hanley, William B.
van Spronsen, Francjan J.
author_sort van Vliet, Danique
collection PubMed
description BACKGROUND: Phenylketonuria (PKU) is often considered as the classical example of a genetic disorder in which severe symptoms can nowadays successfully be prevented by early diagnosis and treatment. In contrast, untreated or late-treated PKU is known to result in severe intellectual disability, seizures, and behavioral disturbances. Rarely, however, untreated or late-diagnosed PKU patients with high plasma phenylalanine concentrations have been reported to escape from intellectual disability. The present study aimed to review published cases of such PKU patients. METHODS: To this purpose, we conducted a literature search in PubMed and EMBASE up to 8th of September 2017 to identify cases with 1) PKU diagnosis and start of treatment after 7 years of age; 2) untreated plasma phenylalanine concentrations ≥1200 μmol/l; and 3) IQ ≥80. Literature search, checking reference lists, selection of articles, and extraction of data were performed by two independent researchers. RESULTS: In total, we identified 59 published cases of patients with late-diagnosed PKU and unexpected favorable outcome who met the inclusion criteria. Although all investigated patients had intellectual functioning within the normal range, at least 19 showed other neurological, psychological, and/or behavioral symptoms. CONCLUSIONS: Based on the present findings, the classical symptomatology of untreated or late-treated PKU may need to be rewritten, not only in the sense that intellectual dysfunction is not obligatory, but also in the sense that intellectual functioning does not (re)present the full picture of brain damage due to high plasma phenylalanine concentrations. Further identification of such patients and additional analyses are necessary to better understand these differences between PKU patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-018-0890-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-61163682018-09-04 Can untreated PKU patients escape from intellectual disability? A systematic review van Vliet, Danique van Wegberg, Annemiek M. J. Ahring, Kirsten Bik-Multanowski, Miroslaw Blau, Nenad Bulut, Fatma D. Casas, Kari Didycz, Bozena Djordjevic, Maja Federico, Antonio Feillet, François Gizewska, Maria Gramer, Gwendolyn Hertecant, Jozef L. Hollak, Carla E. M. Jørgensen, Jens V. Karall, Daniela Landau, Yuval Leuzzi, Vincenzo Mathisen, Per Moseley, Kathryn Mungan, Neslihan Ö. Nardecchia, Francesca Õunap, Katrin Powell, Kimberly K. Ramachandran, Radha Rutsch, Frank Setoodeh, Aria Stojiljkovic, Maja Trefz, Fritz K. Usurelu, Natalia Wilson, Callum van Karnebeek, Clara D. Hanley, William B. van Spronsen, Francjan J. Orphanet J Rare Dis Review BACKGROUND: Phenylketonuria (PKU) is often considered as the classical example of a genetic disorder in which severe symptoms can nowadays successfully be prevented by early diagnosis and treatment. In contrast, untreated or late-treated PKU is known to result in severe intellectual disability, seizures, and behavioral disturbances. Rarely, however, untreated or late-diagnosed PKU patients with high plasma phenylalanine concentrations have been reported to escape from intellectual disability. The present study aimed to review published cases of such PKU patients. METHODS: To this purpose, we conducted a literature search in PubMed and EMBASE up to 8th of September 2017 to identify cases with 1) PKU diagnosis and start of treatment after 7 years of age; 2) untreated plasma phenylalanine concentrations ≥1200 μmol/l; and 3) IQ ≥80. Literature search, checking reference lists, selection of articles, and extraction of data were performed by two independent researchers. RESULTS: In total, we identified 59 published cases of patients with late-diagnosed PKU and unexpected favorable outcome who met the inclusion criteria. Although all investigated patients had intellectual functioning within the normal range, at least 19 showed other neurological, psychological, and/or behavioral symptoms. CONCLUSIONS: Based on the present findings, the classical symptomatology of untreated or late-treated PKU may need to be rewritten, not only in the sense that intellectual dysfunction is not obligatory, but also in the sense that intellectual functioning does not (re)present the full picture of brain damage due to high plasma phenylalanine concentrations. Further identification of such patients and additional analyses are necessary to better understand these differences between PKU patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-018-0890-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-29 /pmc/articles/PMC6116368/ /pubmed/30157945 http://dx.doi.org/10.1186/s13023-018-0890-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
van Vliet, Danique
van Wegberg, Annemiek M. J.
Ahring, Kirsten
Bik-Multanowski, Miroslaw
Blau, Nenad
Bulut, Fatma D.
Casas, Kari
Didycz, Bozena
Djordjevic, Maja
Federico, Antonio
Feillet, François
Gizewska, Maria
Gramer, Gwendolyn
Hertecant, Jozef L.
Hollak, Carla E. M.
Jørgensen, Jens V.
Karall, Daniela
Landau, Yuval
Leuzzi, Vincenzo
Mathisen, Per
Moseley, Kathryn
Mungan, Neslihan Ö.
Nardecchia, Francesca
Õunap, Katrin
Powell, Kimberly K.
Ramachandran, Radha
Rutsch, Frank
Setoodeh, Aria
Stojiljkovic, Maja
Trefz, Fritz K.
Usurelu, Natalia
Wilson, Callum
van Karnebeek, Clara D.
Hanley, William B.
van Spronsen, Francjan J.
Can untreated PKU patients escape from intellectual disability? A systematic review
title Can untreated PKU patients escape from intellectual disability? A systematic review
title_full Can untreated PKU patients escape from intellectual disability? A systematic review
title_fullStr Can untreated PKU patients escape from intellectual disability? A systematic review
title_full_unstemmed Can untreated PKU patients escape from intellectual disability? A systematic review
title_short Can untreated PKU patients escape from intellectual disability? A systematic review
title_sort can untreated pku patients escape from intellectual disability? a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116368/
https://www.ncbi.nlm.nih.gov/pubmed/30157945
http://dx.doi.org/10.1186/s13023-018-0890-7
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