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Is the brain involved in patients with late‐onset Pompe disease?
Our objective was to investigate brain structure, cerebral vasculature, and cognitive function in a cohort of patients with late‐onset Pompe disease, with particular reference to the differences from those with the classic infantile phenotype, where extensive white‐matter abnormalities (WMA) and imp...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306606/ https://www.ncbi.nlm.nih.gov/pubmed/34927739 http://dx.doi.org/10.1002/jimd.12469 |
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author | van den Dorpel, Jan J. A. van der Vlugt, Willemijn M. C. Dremmen, Marjolein H. G. Muetzel, Ryan van den Berg, Esther Hest, Roos de Kriek, Joni Brusse, Esther van Doorn, Pieter A. van der Ploeg, Ans T. van den Hout, Johanna M. P. van der Beek, Nadine A. M. E. |
author_facet | van den Dorpel, Jan J. A. van der Vlugt, Willemijn M. C. Dremmen, Marjolein H. G. Muetzel, Ryan van den Berg, Esther Hest, Roos de Kriek, Joni Brusse, Esther van Doorn, Pieter A. van der Ploeg, Ans T. van den Hout, Johanna M. P. van der Beek, Nadine A. M. E. |
author_sort | van den Dorpel, Jan J. A. |
collection | PubMed |
description | Our objective was to investigate brain structure, cerebral vasculature, and cognitive function in a cohort of patients with late‐onset Pompe disease, with particular reference to the differences from those with the classic infantile phenotype, where extensive white‐matter abnormalities (WMA) and impaired cognition on long‐term enzyme treatment are reported in a subset of patients. Brain imaging (T1, T2, T2 fluid‐attenuated inversion recovery, susceptibility‐weighted images, and magnetic resonance angiography–time of flight) was combined with extensive cognitive testing of general intelligence (Wechsler IQ Test, Montreal Cognitive Assessment [MoCA]) and specific neuropsychological domains (verbal fluency, cognitive flexibility, attention, memory, and visuospatial abilities). We included 19 patients with late‐onset Pompe disease (age range 11‐56 years). Two patients showed mild punctate WMA within normal range for age, with a Fazekas score (FS) of 1 to 2. Magnetic resonance angiography revealed a slight vertebrobasilar dolichoectasia in two patients yet did not show any aneurysms or vascular dissections. Most patients had age‐adjusted scores within the normal range for the Wechsler index scores (verbal comprehension, perceptual reasoning, working memory, and processing speed) and combined total intelligence (IQ) score (median 101, interquartile range 91‐111; one patient had a below‐average score for total IQ) as well as for the specific domains verbal fluency, attention, and memory. A subset of patients performed suboptimally on the Rey Complex Figure Test (9/14 patients) or cube‐copying/clock‐drawing test of the MoCA (8/10 patients). We therefore concluded that our study showed no brain abnormalities, other than minor microvascular lesions considered within normal range for age, nor general cognitive impairment in late‐onset Pompe patients. These findings are in sharp contrast with the widespread WMA and cognitive problems found in some classic infantile patients. |
format | Online Article Text |
id | pubmed-9306606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93066062022-07-28 Is the brain involved in patients with late‐onset Pompe disease? van den Dorpel, Jan J. A. van der Vlugt, Willemijn M. C. Dremmen, Marjolein H. G. Muetzel, Ryan van den Berg, Esther Hest, Roos de Kriek, Joni Brusse, Esther van Doorn, Pieter A. van der Ploeg, Ans T. van den Hout, Johanna M. P. van der Beek, Nadine A. M. E. J Inherit Metab Dis Original Articles Our objective was to investigate brain structure, cerebral vasculature, and cognitive function in a cohort of patients with late‐onset Pompe disease, with particular reference to the differences from those with the classic infantile phenotype, where extensive white‐matter abnormalities (WMA) and impaired cognition on long‐term enzyme treatment are reported in a subset of patients. Brain imaging (T1, T2, T2 fluid‐attenuated inversion recovery, susceptibility‐weighted images, and magnetic resonance angiography–time of flight) was combined with extensive cognitive testing of general intelligence (Wechsler IQ Test, Montreal Cognitive Assessment [MoCA]) and specific neuropsychological domains (verbal fluency, cognitive flexibility, attention, memory, and visuospatial abilities). We included 19 patients with late‐onset Pompe disease (age range 11‐56 years). Two patients showed mild punctate WMA within normal range for age, with a Fazekas score (FS) of 1 to 2. Magnetic resonance angiography revealed a slight vertebrobasilar dolichoectasia in two patients yet did not show any aneurysms or vascular dissections. Most patients had age‐adjusted scores within the normal range for the Wechsler index scores (verbal comprehension, perceptual reasoning, working memory, and processing speed) and combined total intelligence (IQ) score (median 101, interquartile range 91‐111; one patient had a below‐average score for total IQ) as well as for the specific domains verbal fluency, attention, and memory. A subset of patients performed suboptimally on the Rey Complex Figure Test (9/14 patients) or cube‐copying/clock‐drawing test of the MoCA (8/10 patients). We therefore concluded that our study showed no brain abnormalities, other than minor microvascular lesions considered within normal range for age, nor general cognitive impairment in late‐onset Pompe patients. These findings are in sharp contrast with the widespread WMA and cognitive problems found in some classic infantile patients. John Wiley & Sons, Inc. 2022-01-25 2022-05 /pmc/articles/PMC9306606/ /pubmed/34927739 http://dx.doi.org/10.1002/jimd.12469 Text en © 2021 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles van den Dorpel, Jan J. A. van der Vlugt, Willemijn M. C. Dremmen, Marjolein H. G. Muetzel, Ryan van den Berg, Esther Hest, Roos de Kriek, Joni Brusse, Esther van Doorn, Pieter A. van der Ploeg, Ans T. van den Hout, Johanna M. P. van der Beek, Nadine A. M. E. Is the brain involved in patients with late‐onset Pompe disease? |
title | Is the brain involved in patients with late‐onset Pompe disease? |
title_full | Is the brain involved in patients with late‐onset Pompe disease? |
title_fullStr | Is the brain involved in patients with late‐onset Pompe disease? |
title_full_unstemmed | Is the brain involved in patients with late‐onset Pompe disease? |
title_short | Is the brain involved in patients with late‐onset Pompe disease? |
title_sort | is the brain involved in patients with late‐onset pompe disease? |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306606/ https://www.ncbi.nlm.nih.gov/pubmed/34927739 http://dx.doi.org/10.1002/jimd.12469 |
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