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Increased risk for cerebral small vessel disease is associated with quantitative susceptibility mapping in HIV infected and uninfected individuals

The aim of this study was to assess, in the context of cerebral small vessel disease (CSVD), whether cardiovascular risk factors and white matter hyperintensities (WMHs) were associated with brain tissue susceptibility as measured by quantitative susceptibility mapping (QSM). Given that CSVD is diag...

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Autores principales: Murray, Kyle D., Uddin, Md Nasir, Tivarus, Madalina E., Sahin, Bogachan, Wang, Henry Z., Singh, Meera V., Qiu, Xing, Wang, Lu, Spincemaille, Pascal, Wang, Yi, Maggirwar, Sanjay B., Zhong, Jianhui, Schifitto, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429957/
https://www.ncbi.nlm.nih.gov/pubmed/34500428
http://dx.doi.org/10.1016/j.nicl.2021.102786
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author Murray, Kyle D.
Uddin, Md Nasir
Tivarus, Madalina E.
Sahin, Bogachan
Wang, Henry Z.
Singh, Meera V.
Qiu, Xing
Wang, Lu
Spincemaille, Pascal
Wang, Yi
Maggirwar, Sanjay B.
Zhong, Jianhui
Schifitto, Giovanni
author_facet Murray, Kyle D.
Uddin, Md Nasir
Tivarus, Madalina E.
Sahin, Bogachan
Wang, Henry Z.
Singh, Meera V.
Qiu, Xing
Wang, Lu
Spincemaille, Pascal
Wang, Yi
Maggirwar, Sanjay B.
Zhong, Jianhui
Schifitto, Giovanni
author_sort Murray, Kyle D.
collection PubMed
description The aim of this study was to assess, in the context of cerebral small vessel disease (CSVD), whether cardiovascular risk factors and white matter hyperintensities (WMHs) were associated with brain tissue susceptibility as measured by quantitative susceptibility mapping (QSM). Given that CSVD is diagnosed by the presence of lacunar strokes, periventricular and deep WMHs, increased perivascular spaces, and microbleeds, we expected that QSM could capture changes in brain tissue due to underlying CSVD pathology. We compared a cohort of 101 HIV-infected individuals (mean age ± SD = 53.2 ± 10.9 years) with mild to moderate cardiovascular risk scores, as measured by the Reynolds risk score, to 102 age-matched controls (mean age (SD) = 50.3 (15.7) years) with similar Reynolds scores. We performed brain MRI to assess CSVD burden by acquiring 3D T1-MPRAGE, 3D FLAIR, 2D T2-TSE, and mGRE for QSM. We found that signs of CSVD are significantly higher in individuals with HIV-infection compared to controls and that WMH volumes are significantly correlated with age and cardiovascular risk scores. Regional QSM was associated with cardiovascular risk factors, age, sex, and WMH volumes but not HIV status. These results suggest that QSM may be an early imaging marker reflective of alterations in brain microcirculation.
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spelling pubmed-84299572021-09-14 Increased risk for cerebral small vessel disease is associated with quantitative susceptibility mapping in HIV infected and uninfected individuals Murray, Kyle D. Uddin, Md Nasir Tivarus, Madalina E. Sahin, Bogachan Wang, Henry Z. Singh, Meera V. Qiu, Xing Wang, Lu Spincemaille, Pascal Wang, Yi Maggirwar, Sanjay B. Zhong, Jianhui Schifitto, Giovanni Neuroimage Clin Regular Article The aim of this study was to assess, in the context of cerebral small vessel disease (CSVD), whether cardiovascular risk factors and white matter hyperintensities (WMHs) were associated with brain tissue susceptibility as measured by quantitative susceptibility mapping (QSM). Given that CSVD is diagnosed by the presence of lacunar strokes, periventricular and deep WMHs, increased perivascular spaces, and microbleeds, we expected that QSM could capture changes in brain tissue due to underlying CSVD pathology. We compared a cohort of 101 HIV-infected individuals (mean age ± SD = 53.2 ± 10.9 years) with mild to moderate cardiovascular risk scores, as measured by the Reynolds risk score, to 102 age-matched controls (mean age (SD) = 50.3 (15.7) years) with similar Reynolds scores. We performed brain MRI to assess CSVD burden by acquiring 3D T1-MPRAGE, 3D FLAIR, 2D T2-TSE, and mGRE for QSM. We found that signs of CSVD are significantly higher in individuals with HIV-infection compared to controls and that WMH volumes are significantly correlated with age and cardiovascular risk scores. Regional QSM was associated with cardiovascular risk factors, age, sex, and WMH volumes but not HIV status. These results suggest that QSM may be an early imaging marker reflective of alterations in brain microcirculation. Elsevier 2021-08-28 /pmc/articles/PMC8429957/ /pubmed/34500428 http://dx.doi.org/10.1016/j.nicl.2021.102786 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Murray, Kyle D.
Uddin, Md Nasir
Tivarus, Madalina E.
Sahin, Bogachan
Wang, Henry Z.
Singh, Meera V.
Qiu, Xing
Wang, Lu
Spincemaille, Pascal
Wang, Yi
Maggirwar, Sanjay B.
Zhong, Jianhui
Schifitto, Giovanni
Increased risk for cerebral small vessel disease is associated with quantitative susceptibility mapping in HIV infected and uninfected individuals
title Increased risk for cerebral small vessel disease is associated with quantitative susceptibility mapping in HIV infected and uninfected individuals
title_full Increased risk for cerebral small vessel disease is associated with quantitative susceptibility mapping in HIV infected and uninfected individuals
title_fullStr Increased risk for cerebral small vessel disease is associated with quantitative susceptibility mapping in HIV infected and uninfected individuals
title_full_unstemmed Increased risk for cerebral small vessel disease is associated with quantitative susceptibility mapping in HIV infected and uninfected individuals
title_short Increased risk for cerebral small vessel disease is associated with quantitative susceptibility mapping in HIV infected and uninfected individuals
title_sort increased risk for cerebral small vessel disease is associated with quantitative susceptibility mapping in hiv infected and uninfected individuals
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429957/
https://www.ncbi.nlm.nih.gov/pubmed/34500428
http://dx.doi.org/10.1016/j.nicl.2021.102786
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