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GABA deficiency in NF1: A multimodal [(11)C]-flumazenil and spectroscopy study
OBJECTIVE: To provide a comprehensive investigation of the γ-aminobutyric acid (GABA) system in patients with neurofibromatosis type 1 (NF1) that allows understanding the nature of the GABA imbalance in humans at pre- and postsynaptic levels. METHODS: In this cross-sectional study, we employed multi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035153/ https://www.ncbi.nlm.nih.gov/pubmed/27473134 http://dx.doi.org/10.1212/WNL.0000000000003044 |
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author | Violante, Inês R. Patricio, Miguel Bernardino, Inês Rebola, José Abrunhosa, Antero J. Ferreira, Nuno Castelo-Branco, Miguel |
author_facet | Violante, Inês R. Patricio, Miguel Bernardino, Inês Rebola, José Abrunhosa, Antero J. Ferreira, Nuno Castelo-Branco, Miguel |
author_sort | Violante, Inês R. |
collection | PubMed |
description | OBJECTIVE: To provide a comprehensive investigation of the γ-aminobutyric acid (GABA) system in patients with neurofibromatosis type 1 (NF1) that allows understanding the nature of the GABA imbalance in humans at pre- and postsynaptic levels. METHODS: In this cross-sectional study, we employed multimodal imaging and spectroscopy measures to investigate GABA type A (GABA(A)) receptor binding, using [(11)C]-flumazenil PET, and GABA concentration, using magnetic resonance spectroscopy (MRS). Fourteen adult patients with NF1 and 13 matched controls were included in the study. MRS was performed in the occipital cortex and in a frontal region centered in the functionally localized frontal eye fields. PET and MRS acquisitions were performed in the same day. RESULTS: Patients with NF1 have reduced concentration of GABA+ in the occipital cortex (p = 0.004) and frontal eye fields (p = 0.026). PET results showed decreased binding of GABA(A) receptors in patients in the parieto-occipital cortex, midbrain, and thalamus, which are not explained by decreased gray matter levels. CONCLUSIONS: Abnormalities in the GABA system in NF1 involve both GABA concentration and GABA(A) receptor density suggestive of neurodevelopmental synaptopathy with both pre- and postsynaptic involvement. |
format | Online Article Text |
id | pubmed-5035153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-50351532016-10-13 GABA deficiency in NF1: A multimodal [(11)C]-flumazenil and spectroscopy study Violante, Inês R. Patricio, Miguel Bernardino, Inês Rebola, José Abrunhosa, Antero J. Ferreira, Nuno Castelo-Branco, Miguel Neurology Article OBJECTIVE: To provide a comprehensive investigation of the γ-aminobutyric acid (GABA) system in patients with neurofibromatosis type 1 (NF1) that allows understanding the nature of the GABA imbalance in humans at pre- and postsynaptic levels. METHODS: In this cross-sectional study, we employed multimodal imaging and spectroscopy measures to investigate GABA type A (GABA(A)) receptor binding, using [(11)C]-flumazenil PET, and GABA concentration, using magnetic resonance spectroscopy (MRS). Fourteen adult patients with NF1 and 13 matched controls were included in the study. MRS was performed in the occipital cortex and in a frontal region centered in the functionally localized frontal eye fields. PET and MRS acquisitions were performed in the same day. RESULTS: Patients with NF1 have reduced concentration of GABA+ in the occipital cortex (p = 0.004) and frontal eye fields (p = 0.026). PET results showed decreased binding of GABA(A) receptors in patients in the parieto-occipital cortex, midbrain, and thalamus, which are not explained by decreased gray matter levels. CONCLUSIONS: Abnormalities in the GABA system in NF1 involve both GABA concentration and GABA(A) receptor density suggestive of neurodevelopmental synaptopathy with both pre- and postsynaptic involvement. Lippincott Williams & Wilkins 2016-08-30 /pmc/articles/PMC5035153/ /pubmed/27473134 http://dx.doi.org/10.1212/WNL.0000000000003044 Text en © 2016 American Academy of Neurology https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Violante, Inês R. Patricio, Miguel Bernardino, Inês Rebola, José Abrunhosa, Antero J. Ferreira, Nuno Castelo-Branco, Miguel GABA deficiency in NF1: A multimodal [(11)C]-flumazenil and spectroscopy study |
title | GABA deficiency in NF1: A multimodal [(11)C]-flumazenil and spectroscopy study |
title_full | GABA deficiency in NF1: A multimodal [(11)C]-flumazenil and spectroscopy study |
title_fullStr | GABA deficiency in NF1: A multimodal [(11)C]-flumazenil and spectroscopy study |
title_full_unstemmed | GABA deficiency in NF1: A multimodal [(11)C]-flumazenil and spectroscopy study |
title_short | GABA deficiency in NF1: A multimodal [(11)C]-flumazenil and spectroscopy study |
title_sort | gaba deficiency in nf1: a multimodal [(11)c]-flumazenil and spectroscopy study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035153/ https://www.ncbi.nlm.nih.gov/pubmed/27473134 http://dx.doi.org/10.1212/WNL.0000000000003044 |
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