Cargando…

Evaluation of Cerebral Microvascular Regulatory Mechanisms with Transcranial Doppler in Fabry Disease

Background: Fabry disease (FD) causes cerebrovascular disease (CVD) even if asymptomatic, and this is why it is important to identify non-invasive methods to monitor the disease. We evaluated the usefulness of the cerebral autoregulation, vasoreactivity, and neurovascular coupling assessed by transc...

Descripción completa

Detalles Bibliográficos
Autores principales: Castro, Pedro, Gutierres, Mariana, Pereira, Gilberto, Ferreira, Susana, Oliveira, João Paulo, Azevedo, Elsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464258/
https://www.ncbi.nlm.nih.gov/pubmed/32784589
http://dx.doi.org/10.3390/brainsci10080528
_version_ 1783577323203723264
author Castro, Pedro
Gutierres, Mariana
Pereira, Gilberto
Ferreira, Susana
Oliveira, João Paulo
Azevedo, Elsa
author_facet Castro, Pedro
Gutierres, Mariana
Pereira, Gilberto
Ferreira, Susana
Oliveira, João Paulo
Azevedo, Elsa
author_sort Castro, Pedro
collection PubMed
description Background: Fabry disease (FD) causes cerebrovascular disease (CVD) even if asymptomatic, and this is why it is important to identify non-invasive methods to monitor the disease. We evaluated the usefulness of the cerebral autoregulation, vasoreactivity, and neurovascular coupling assessed by transcranial Doppler (TCD) in FD. Methods: Ten adult patients with classic phenotype FD, without clinical expression of CVD, and ten healthy controls, were included. We monitored cerebral blood flow velocity with TCD in the middle and posterior cerebral arteries, blood pressure, heart rate, and non-invasive expired carbon dioxide (CO(2)). Cerebral autoregulation was calculated from the spontaneous oscillations of blood pressure, cerebral vasoreactivity through CO(2) inhalation and hyperventilation and neurovascular coupling by the flow velocity change to visual stimulation. Results: FD male patients showed blunted vasoreactivity in posterior circulation (0.70 ± 0.36%/mmHg vs. 1.09 ± 0.18%/mmHg CO(2), p = 0.01) and impaired neurovascular coupling (overshoot 15 ± 2.9% vs. 28 ± 6.1%, p < 0.01). Cerebral autoregulation was similar to controls. Conclusion: Male patients with FD classic phenotype and hitherto clinical expression of CVD already show impairment of cerebral vasoreactivity and neurovascular coupling. It supports the notion of an early dysfunction of cerebral microvascular in a presymptomatic stage of CVD in FD and that TCD could be useful in its assessment.
format Online
Article
Text
id pubmed-7464258
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-74642582020-09-04 Evaluation of Cerebral Microvascular Regulatory Mechanisms with Transcranial Doppler in Fabry Disease Castro, Pedro Gutierres, Mariana Pereira, Gilberto Ferreira, Susana Oliveira, João Paulo Azevedo, Elsa Brain Sci Article Background: Fabry disease (FD) causes cerebrovascular disease (CVD) even if asymptomatic, and this is why it is important to identify non-invasive methods to monitor the disease. We evaluated the usefulness of the cerebral autoregulation, vasoreactivity, and neurovascular coupling assessed by transcranial Doppler (TCD) in FD. Methods: Ten adult patients with classic phenotype FD, without clinical expression of CVD, and ten healthy controls, were included. We monitored cerebral blood flow velocity with TCD in the middle and posterior cerebral arteries, blood pressure, heart rate, and non-invasive expired carbon dioxide (CO(2)). Cerebral autoregulation was calculated from the spontaneous oscillations of blood pressure, cerebral vasoreactivity through CO(2) inhalation and hyperventilation and neurovascular coupling by the flow velocity change to visual stimulation. Results: FD male patients showed blunted vasoreactivity in posterior circulation (0.70 ± 0.36%/mmHg vs. 1.09 ± 0.18%/mmHg CO(2), p = 0.01) and impaired neurovascular coupling (overshoot 15 ± 2.9% vs. 28 ± 6.1%, p < 0.01). Cerebral autoregulation was similar to controls. Conclusion: Male patients with FD classic phenotype and hitherto clinical expression of CVD already show impairment of cerebral vasoreactivity and neurovascular coupling. It supports the notion of an early dysfunction of cerebral microvascular in a presymptomatic stage of CVD in FD and that TCD could be useful in its assessment. MDPI 2020-08-07 /pmc/articles/PMC7464258/ /pubmed/32784589 http://dx.doi.org/10.3390/brainsci10080528 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Castro, Pedro
Gutierres, Mariana
Pereira, Gilberto
Ferreira, Susana
Oliveira, João Paulo
Azevedo, Elsa
Evaluation of Cerebral Microvascular Regulatory Mechanisms with Transcranial Doppler in Fabry Disease
title Evaluation of Cerebral Microvascular Regulatory Mechanisms with Transcranial Doppler in Fabry Disease
title_full Evaluation of Cerebral Microvascular Regulatory Mechanisms with Transcranial Doppler in Fabry Disease
title_fullStr Evaluation of Cerebral Microvascular Regulatory Mechanisms with Transcranial Doppler in Fabry Disease
title_full_unstemmed Evaluation of Cerebral Microvascular Regulatory Mechanisms with Transcranial Doppler in Fabry Disease
title_short Evaluation of Cerebral Microvascular Regulatory Mechanisms with Transcranial Doppler in Fabry Disease
title_sort evaluation of cerebral microvascular regulatory mechanisms with transcranial doppler in fabry disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464258/
https://www.ncbi.nlm.nih.gov/pubmed/32784589
http://dx.doi.org/10.3390/brainsci10080528
work_keys_str_mv AT castropedro evaluationofcerebralmicrovascularregulatorymechanismswithtranscranialdopplerinfabrydisease
AT gutierresmariana evaluationofcerebralmicrovascularregulatorymechanismswithtranscranialdopplerinfabrydisease
AT pereiragilberto evaluationofcerebralmicrovascularregulatorymechanismswithtranscranialdopplerinfabrydisease
AT ferreirasusana evaluationofcerebralmicrovascularregulatorymechanismswithtranscranialdopplerinfabrydisease
AT oliveirajoaopaulo evaluationofcerebralmicrovascularregulatorymechanismswithtranscranialdopplerinfabrydisease
AT azevedoelsa evaluationofcerebralmicrovascularregulatorymechanismswithtranscranialdopplerinfabrydisease