Cargando…

White matter is increased in the brains of adults with neurofibromatosis 1

BACKGROUND: Neurofibromatosis 1 (NF1) is a rare autosomal dominant disease characterized by increased Schwann cell proliferation in peripheral nerves. Several small studies of brain morphology in children with NF1 have found increased total brain volume, total white matter volume and/or corpus callo...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Su, Friedman, Jan M., Suppa, Per, Buchert, Ralph, Mautner, Victor-Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898512/
https://www.ncbi.nlm.nih.gov/pubmed/35248131
http://dx.doi.org/10.1186/s13023-022-02273-1
_version_ 1784663665737203712
author Wang, Su
Friedman, Jan M.
Suppa, Per
Buchert, Ralph
Mautner, Victor-Felix
author_facet Wang, Su
Friedman, Jan M.
Suppa, Per
Buchert, Ralph
Mautner, Victor-Felix
author_sort Wang, Su
collection PubMed
description BACKGROUND: Neurofibromatosis 1 (NF1) is a rare autosomal dominant disease characterized by increased Schwann cell proliferation in peripheral nerves. Several small studies of brain morphology in children with NF1 have found increased total brain volume, total white matter volume and/or corpus callosum area. Some studies (mostly in children with NF1) also attempted to correlate changes in brain morphology and volume with cognitive or behavioural abnormalities, although the findings were inconsistent. We aimed to characterize alterations in brain volumes by three-dimensional (3D) MRI in adults with NF1 in major intracranial sub-regions. We also aimed to assess the effect of age on these volumes and correlated brain white matter and grey matter volumes with neuropsychometric findings in adults with NF1. METHODS: We obtained brain volume measurements using 3D magnetic resonance imaging for 351 adults with NF1 and, as a comparison group, 43 adults with neurofibromatosis 2 (NF2) or Schwannomatosis. We assessed a subset of 19 adults with NF1 for clinical severity of NF1 features and neurological problems and conducted psychometric testing for attention deficiencies and intelligence quotient. We compared brain volumes between NF1 patients and controls and correlated volumetric measurements to clinical and psychometric features in the NF1 patients. RESULTS: Total brain volume and total and regional white matter volumes were all significantly increased in adults with NF1. Grey matter volume decreased faster with age in adults with NF1 than in controls. Greater total brain volume and white matter volume were correlated with lower attention deficits and higher intelligence quotients in adults with NF1. CONCLUSION: Our findings are consistent with the hypothesis that dysregulation of brain myelin production is a cardinal manifestation of NF1 and that these white matter changes may be functionally important in affected adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02273-1.
format Online
Article
Text
id pubmed-8898512
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-88985122022-03-17 White matter is increased in the brains of adults with neurofibromatosis 1 Wang, Su Friedman, Jan M. Suppa, Per Buchert, Ralph Mautner, Victor-Felix Orphanet J Rare Dis Research BACKGROUND: Neurofibromatosis 1 (NF1) is a rare autosomal dominant disease characterized by increased Schwann cell proliferation in peripheral nerves. Several small studies of brain morphology in children with NF1 have found increased total brain volume, total white matter volume and/or corpus callosum area. Some studies (mostly in children with NF1) also attempted to correlate changes in brain morphology and volume with cognitive or behavioural abnormalities, although the findings were inconsistent. We aimed to characterize alterations in brain volumes by three-dimensional (3D) MRI in adults with NF1 in major intracranial sub-regions. We also aimed to assess the effect of age on these volumes and correlated brain white matter and grey matter volumes with neuropsychometric findings in adults with NF1. METHODS: We obtained brain volume measurements using 3D magnetic resonance imaging for 351 adults with NF1 and, as a comparison group, 43 adults with neurofibromatosis 2 (NF2) or Schwannomatosis. We assessed a subset of 19 adults with NF1 for clinical severity of NF1 features and neurological problems and conducted psychometric testing for attention deficiencies and intelligence quotient. We compared brain volumes between NF1 patients and controls and correlated volumetric measurements to clinical and psychometric features in the NF1 patients. RESULTS: Total brain volume and total and regional white matter volumes were all significantly increased in adults with NF1. Grey matter volume decreased faster with age in adults with NF1 than in controls. Greater total brain volume and white matter volume were correlated with lower attention deficits and higher intelligence quotients in adults with NF1. CONCLUSION: Our findings are consistent with the hypothesis that dysregulation of brain myelin production is a cardinal manifestation of NF1 and that these white matter changes may be functionally important in affected adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02273-1. BioMed Central 2022-03-05 /pmc/articles/PMC8898512/ /pubmed/35248131 http://dx.doi.org/10.1186/s13023-022-02273-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wang, Su
Friedman, Jan M.
Suppa, Per
Buchert, Ralph
Mautner, Victor-Felix
White matter is increased in the brains of adults with neurofibromatosis 1
title White matter is increased in the brains of adults with neurofibromatosis 1
title_full White matter is increased in the brains of adults with neurofibromatosis 1
title_fullStr White matter is increased in the brains of adults with neurofibromatosis 1
title_full_unstemmed White matter is increased in the brains of adults with neurofibromatosis 1
title_short White matter is increased in the brains of adults with neurofibromatosis 1
title_sort white matter is increased in the brains of adults with neurofibromatosis 1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898512/
https://www.ncbi.nlm.nih.gov/pubmed/35248131
http://dx.doi.org/10.1186/s13023-022-02273-1
work_keys_str_mv AT wangsu whitematterisincreasedinthebrainsofadultswithneurofibromatosis1
AT friedmanjanm whitematterisincreasedinthebrainsofadultswithneurofibromatosis1
AT suppaper whitematterisincreasedinthebrainsofadultswithneurofibromatosis1
AT buchertralph whitematterisincreasedinthebrainsofadultswithneurofibromatosis1
AT mautnervictorfelix whitematterisincreasedinthebrainsofadultswithneurofibromatosis1