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The Association of Type 2 Diabetes Mellitus with Cerebral Gray Matter Volume Is Independent of Retinal Vascular Architecture and Retinopathy

It is uncertain whether small vessel disease underlies the relationship between Type 2 Diabetes Mellitus (T2DM) and brain atrophy. We aimed to study whether retinal vascular architecture, as a proxy for cerebral small vessel disease, may modify or mediate the associations of T2DM with brain volumes....

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Autores principales: Moran, C., Tapp, R. J., Hughes, A. D., Magnussen, C. G., Blizzard, L., Phan, T. G., Beare, R., Witt, N., Venn, A., Münch, G., Amaratunge, B. C., Srikanth, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897713/
https://www.ncbi.nlm.nih.gov/pubmed/27314049
http://dx.doi.org/10.1155/2016/6328953
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author Moran, C.
Tapp, R. J.
Hughes, A. D.
Magnussen, C. G.
Blizzard, L.
Phan, T. G.
Beare, R.
Witt, N.
Venn, A.
Münch, G.
Amaratunge, B. C.
Srikanth, V.
author_facet Moran, C.
Tapp, R. J.
Hughes, A. D.
Magnussen, C. G.
Blizzard, L.
Phan, T. G.
Beare, R.
Witt, N.
Venn, A.
Münch, G.
Amaratunge, B. C.
Srikanth, V.
author_sort Moran, C.
collection PubMed
description It is uncertain whether small vessel disease underlies the relationship between Type 2 Diabetes Mellitus (T2DM) and brain atrophy. We aimed to study whether retinal vascular architecture, as a proxy for cerebral small vessel disease, may modify or mediate the associations of T2DM with brain volumes. In this cross-sectional study using Magnetic Resonance Imaging (MRI) scans and retinal photographs in 451 people with and without T2DM, we measured brain volumes, geometric measures of retinal vascular architecture, clinical retinopathy, and MRI cerebrovascular lesions. There were 270 people with (mean age 67.3 years) and 181 without T2DM (mean age 72.9 years). T2DM was associated with lower gray matter volume (p = 0.008). T2DM was associated with greater arteriolar diameter (p = 0.03) and optimality ratio (p = 0.04), but these associations were attenuated by adjustments for age and sex. Only optimality ratio was associated with lower gray matter volume (p = 0.03). The inclusion of retinal measures in regression models did not attenuate the association of T2DM with gray matter volume. The association of T2DM with lower gray matter volume was independent of retinal vascular architecture and clinical retinopathy. Retinal vascular measures or retinopathy may not be sufficiently sensitive to confirm a microvascular basis for T2DM-related brain atrophy.
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spelling pubmed-48977132016-06-16 The Association of Type 2 Diabetes Mellitus with Cerebral Gray Matter Volume Is Independent of Retinal Vascular Architecture and Retinopathy Moran, C. Tapp, R. J. Hughes, A. D. Magnussen, C. G. Blizzard, L. Phan, T. G. Beare, R. Witt, N. Venn, A. Münch, G. Amaratunge, B. C. Srikanth, V. J Diabetes Res Research Article It is uncertain whether small vessel disease underlies the relationship between Type 2 Diabetes Mellitus (T2DM) and brain atrophy. We aimed to study whether retinal vascular architecture, as a proxy for cerebral small vessel disease, may modify or mediate the associations of T2DM with brain volumes. In this cross-sectional study using Magnetic Resonance Imaging (MRI) scans and retinal photographs in 451 people with and without T2DM, we measured brain volumes, geometric measures of retinal vascular architecture, clinical retinopathy, and MRI cerebrovascular lesions. There were 270 people with (mean age 67.3 years) and 181 without T2DM (mean age 72.9 years). T2DM was associated with lower gray matter volume (p = 0.008). T2DM was associated with greater arteriolar diameter (p = 0.03) and optimality ratio (p = 0.04), but these associations were attenuated by adjustments for age and sex. Only optimality ratio was associated with lower gray matter volume (p = 0.03). The inclusion of retinal measures in regression models did not attenuate the association of T2DM with gray matter volume. The association of T2DM with lower gray matter volume was independent of retinal vascular architecture and clinical retinopathy. Retinal vascular measures or retinopathy may not be sufficiently sensitive to confirm a microvascular basis for T2DM-related brain atrophy. Hindawi Publishing Corporation 2016 2016-05-25 /pmc/articles/PMC4897713/ /pubmed/27314049 http://dx.doi.org/10.1155/2016/6328953 Text en Copyright © 2016 C. Moran et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Moran, C.
Tapp, R. J.
Hughes, A. D.
Magnussen, C. G.
Blizzard, L.
Phan, T. G.
Beare, R.
Witt, N.
Venn, A.
Münch, G.
Amaratunge, B. C.
Srikanth, V.
The Association of Type 2 Diabetes Mellitus with Cerebral Gray Matter Volume Is Independent of Retinal Vascular Architecture and Retinopathy
title The Association of Type 2 Diabetes Mellitus with Cerebral Gray Matter Volume Is Independent of Retinal Vascular Architecture and Retinopathy
title_full The Association of Type 2 Diabetes Mellitus with Cerebral Gray Matter Volume Is Independent of Retinal Vascular Architecture and Retinopathy
title_fullStr The Association of Type 2 Diabetes Mellitus with Cerebral Gray Matter Volume Is Independent of Retinal Vascular Architecture and Retinopathy
title_full_unstemmed The Association of Type 2 Diabetes Mellitus with Cerebral Gray Matter Volume Is Independent of Retinal Vascular Architecture and Retinopathy
title_short The Association of Type 2 Diabetes Mellitus with Cerebral Gray Matter Volume Is Independent of Retinal Vascular Architecture and Retinopathy
title_sort association of type 2 diabetes mellitus with cerebral gray matter volume is independent of retinal vascular architecture and retinopathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897713/
https://www.ncbi.nlm.nih.gov/pubmed/27314049
http://dx.doi.org/10.1155/2016/6328953
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