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Intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome
Symptoms of orthostatic intolerance (OI) are common in Chronic Fatigue Syndrome (CFS) and similar disorders. These symptoms may relate to individual differences in intracranial compliance and cerebral blood perfusion. The present study used phase-contrast, quantitative flow magnetic resonance imagin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029803/ https://www.ncbi.nlm.nih.gov/pubmed/29969498 http://dx.doi.org/10.1371/journal.pone.0200068 |
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author | Finkelmeyer, Andreas He, Jiabao Maclachlan, Laura Blamire, Andrew M. Newton, Julia L. |
author_facet | Finkelmeyer, Andreas He, Jiabao Maclachlan, Laura Blamire, Andrew M. Newton, Julia L. |
author_sort | Finkelmeyer, Andreas |
collection | PubMed |
description | Symptoms of orthostatic intolerance (OI) are common in Chronic Fatigue Syndrome (CFS) and similar disorders. These symptoms may relate to individual differences in intracranial compliance and cerebral blood perfusion. The present study used phase-contrast, quantitative flow magnetic resonance imaging (MRI) to determine intracranial compliance based on arterial inflow, venous outflow and cerebrospinal fluid flow along the spinal canal into and out of the cranial cavity. Flow-sensitive Alternating Inversion Recovery (FAIR) Arterial Spin Labelling was used to measure cerebral blood perfusion at rest. Forty patients with CFS and 10 age and gender matched controls were scanned. Severity of symptoms of OI was determined from self-report using the Autonomic Symptom Profile. CFS patients reported significantly higher levels of OI (p < .001). Within the patient group, higher severity of OI symptoms were associated with lower intracranial compliance (r = -.346, p = .033) and higher resting perfusion (r = .337, p = .038). In both groups intracranial compliance was negatively correlated with cerebral perfusion. There were no significant differences between the groups in intracranial compliance or perfusion. In patients with CFS, low intracranial compliance and high resting cerebral perfusion appear to be associated with an increased severity of symptoms of OI. This may signify alterations in the ability of the cerebral vasculature to cope with changes to systemic blood pressure due to orthostatic stress, but this may not be specific to CFS. |
format | Online Article Text |
id | pubmed-6029803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60298032018-07-19 Intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome Finkelmeyer, Andreas He, Jiabao Maclachlan, Laura Blamire, Andrew M. Newton, Julia L. PLoS One Research Article Symptoms of orthostatic intolerance (OI) are common in Chronic Fatigue Syndrome (CFS) and similar disorders. These symptoms may relate to individual differences in intracranial compliance and cerebral blood perfusion. The present study used phase-contrast, quantitative flow magnetic resonance imaging (MRI) to determine intracranial compliance based on arterial inflow, venous outflow and cerebrospinal fluid flow along the spinal canal into and out of the cranial cavity. Flow-sensitive Alternating Inversion Recovery (FAIR) Arterial Spin Labelling was used to measure cerebral blood perfusion at rest. Forty patients with CFS and 10 age and gender matched controls were scanned. Severity of symptoms of OI was determined from self-report using the Autonomic Symptom Profile. CFS patients reported significantly higher levels of OI (p < .001). Within the patient group, higher severity of OI symptoms were associated with lower intracranial compliance (r = -.346, p = .033) and higher resting perfusion (r = .337, p = .038). In both groups intracranial compliance was negatively correlated with cerebral perfusion. There were no significant differences between the groups in intracranial compliance or perfusion. In patients with CFS, low intracranial compliance and high resting cerebral perfusion appear to be associated with an increased severity of symptoms of OI. This may signify alterations in the ability of the cerebral vasculature to cope with changes to systemic blood pressure due to orthostatic stress, but this may not be specific to CFS. Public Library of Science 2018-07-03 /pmc/articles/PMC6029803/ /pubmed/29969498 http://dx.doi.org/10.1371/journal.pone.0200068 Text en © 2018 Finkelmeyer et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Finkelmeyer, Andreas He, Jiabao Maclachlan, Laura Blamire, Andrew M. Newton, Julia L. Intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome |
title | Intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome |
title_full | Intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome |
title_fullStr | Intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome |
title_full_unstemmed | Intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome |
title_short | Intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome |
title_sort | intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029803/ https://www.ncbi.nlm.nih.gov/pubmed/29969498 http://dx.doi.org/10.1371/journal.pone.0200068 |
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