Neurovascular imaging with QUTE-CE MRI in APOE4 rats reveals early vascular abnormalities.

Cerebrovascular abnormality is linked to Alzheimer's disease and related dementias (ADRDs). ApoE-Ɛ4 (APOE4) is known to play a critical role in neurovascular dysfunction, however current medical imaging technologies are limited in quantification. This cross-sectional study tested the feasibilit...

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Autores principales: Joshua Leaston, Craig F Ferris, Praveen Kulkarni, Dharshan Chandramohan, Anne L van de Ven, Ju Qiao, Liam Timms, Jorge Sepulcre, Georges El Fakhri, Chao Ma, Marc D Normandin, Codi Gharagouzloo
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:6fd6878838654be6add5ef9afa96e68c2021-12-02T20:19:24ZNeurovascular imaging with QUTE-CE MRI in APOE4 rats reveals early vascular abnormalities.1932-620310.1371/journal.pone.0256749https://doaj.org/article/6fd6878838654be6add5ef9afa96e68c2021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0256749https://doaj.org/toc/1932-6203Cerebrovascular abnormality is linked to Alzheimer's disease and related dementias (ADRDs). ApoE-Ɛ4 (APOE4) is known to play a critical role in neurovascular dysfunction, however current medical imaging technologies are limited in quantification. This cross-sectional study tested the feasibility of a recently established imaging modality, quantitative ultra-short time-to-echo contrast-enhanced magnetic resonance imaging (QUTE-CE MRI), to identify small vessel abnormality early in development of human APOE4 knock-in female rat (TGRA8960) animal model. At 8 months, 48.3% of the brain volume was found to have significant signal increase (75/173 anatomically segmented regions; q<0.05 for multiple comparisons). Notably, vascular abnormality was detected in the tri-synaptic circuit, cerebellum, and amygdala, all of which are known to functionally decline throughout AD pathology and have implications in learning and memory. The detected abnormality quantified with QUTE-CE MRI is likely a result of hyper-vascularization, but may also be partly, or wholly, due to contributions from blood-brain-barrier leakage. Further exploration with histological validation is warranted to verify the pathological cause. Regardless, these results indicate that QUTE-CE MRI can detect neurovascular dysfunction with high sensitivity with APOE4 and may be helpful to provide new insights into health and disease.Joshua LeastonCraig F FerrisPraveen KulkarniDharshan ChandramohanAnne L van de VenJu QiaoLiam TimmsJorge SepulcreGeorges El FakhriChao MaMarc D NormandinCodi GharagouzlooPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 8, p e0256749 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Joshua Leaston
Craig F Ferris
Praveen Kulkarni
Dharshan Chandramohan
Anne L van de Ven
Ju Qiao
Liam Timms
Jorge Sepulcre
Georges El Fakhri
Chao Ma
Marc D Normandin
Codi Gharagouzloo
Neurovascular imaging with QUTE-CE MRI in APOE4 rats reveals early vascular abnormalities.
description Cerebrovascular abnormality is linked to Alzheimer's disease and related dementias (ADRDs). ApoE-Ɛ4 (APOE4) is known to play a critical role in neurovascular dysfunction, however current medical imaging technologies are limited in quantification. This cross-sectional study tested the feasibility of a recently established imaging modality, quantitative ultra-short time-to-echo contrast-enhanced magnetic resonance imaging (QUTE-CE MRI), to identify small vessel abnormality early in development of human APOE4 knock-in female rat (TGRA8960) animal model. At 8 months, 48.3% of the brain volume was found to have significant signal increase (75/173 anatomically segmented regions; q<0.05 for multiple comparisons). Notably, vascular abnormality was detected in the tri-synaptic circuit, cerebellum, and amygdala, all of which are known to functionally decline throughout AD pathology and have implications in learning and memory. The detected abnormality quantified with QUTE-CE MRI is likely a result of hyper-vascularization, but may also be partly, or wholly, due to contributions from blood-brain-barrier leakage. Further exploration with histological validation is warranted to verify the pathological cause. Regardless, these results indicate that QUTE-CE MRI can detect neurovascular dysfunction with high sensitivity with APOE4 and may be helpful to provide new insights into health and disease.
format article
author Joshua Leaston
Craig F Ferris
Praveen Kulkarni
Dharshan Chandramohan
Anne L van de Ven
Ju Qiao
Liam Timms
Jorge Sepulcre
Georges El Fakhri
Chao Ma
Marc D Normandin
Codi Gharagouzloo
author_facet Joshua Leaston
Craig F Ferris
Praveen Kulkarni
Dharshan Chandramohan
Anne L van de Ven
Ju Qiao
Liam Timms
Jorge Sepulcre
Georges El Fakhri
Chao Ma
Marc D Normandin
Codi Gharagouzloo
author_sort Joshua Leaston
title Neurovascular imaging with QUTE-CE MRI in APOE4 rats reveals early vascular abnormalities.
title_short Neurovascular imaging with QUTE-CE MRI in APOE4 rats reveals early vascular abnormalities.
title_full Neurovascular imaging with QUTE-CE MRI in APOE4 rats reveals early vascular abnormalities.
title_fullStr Neurovascular imaging with QUTE-CE MRI in APOE4 rats reveals early vascular abnormalities.
title_full_unstemmed Neurovascular imaging with QUTE-CE MRI in APOE4 rats reveals early vascular abnormalities.
title_sort neurovascular imaging with qute-ce mri in apoe4 rats reveals early vascular abnormalities.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/6fd6878838654be6add5ef9afa96e68c
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