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Microvascular and Morphologic Changes of the Macula over Lifetime

In ocular, neurologic, and cardiovascular diseases, macular segmentation data from spectral-domain optical coherence tomography (SD-OCT) provide morphologic, and OCT-angiography (OCTA) results give microvascular information about the macula. Age was shown to influence both methods’ measurements. To...

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Autores principales: Lever, Mael, Chen, Ying, Glaser, Moritz, Unterlauft, Jan Darius, Lommatzsch, Claudia, Bechrakis, Nikolaos E., Böhm, Michael R. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024868/
https://www.ncbi.nlm.nih.gov/pubmed/35455059
http://dx.doi.org/10.3390/life12040568
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author Lever, Mael
Chen, Ying
Glaser, Moritz
Unterlauft, Jan Darius
Lommatzsch, Claudia
Bechrakis, Nikolaos E.
Böhm, Michael R. R.
author_facet Lever, Mael
Chen, Ying
Glaser, Moritz
Unterlauft, Jan Darius
Lommatzsch, Claudia
Bechrakis, Nikolaos E.
Böhm, Michael R. R.
author_sort Lever, Mael
collection PubMed
description In ocular, neurologic, and cardiovascular diseases, macular segmentation data from spectral-domain optical coherence tomography (SD-OCT) provide morphologic, and OCT-angiography (OCTA) results give microvascular information about the macula. Age was shown to influence both methods’ measurements. To further characterize this association, macular SD-OCT and OCTA changes were investigated in a population of juvenile, adult, and older individuals. Macular segment thickness and superficial (SCP) and deep plexus (DCP) vascular density (VD) of 157 healthy individuals aged 10–79 years were analyzed retrospectively. One-way analysis of variance (ANOVA) was used to compare age groups. The association between macular segmentation and OCTA parameters and between these and age was evaluated using linear regression. ANOVA and linear regression analysis showed a thickness decrease in the whole macular and in the ganglion cell and inner plexiform layers with age. While the foveal avascular zone area remained constant between age groups, VD of the SCP and DCP also decreased with age. In multiple linear regression, SCP and DCP VD were associated with inner macular segment thickness in an age-independent way. To conclude, the age-related microvascular and morphological changes in the macula described in this study can contribute to improving the understanding of macular aging processes and better interpreting OCT(A) results in healthy individuals and patients suffering from various retinal diseases.
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spelling pubmed-90248682022-04-23 Microvascular and Morphologic Changes of the Macula over Lifetime Lever, Mael Chen, Ying Glaser, Moritz Unterlauft, Jan Darius Lommatzsch, Claudia Bechrakis, Nikolaos E. Böhm, Michael R. R. Life (Basel) Article In ocular, neurologic, and cardiovascular diseases, macular segmentation data from spectral-domain optical coherence tomography (SD-OCT) provide morphologic, and OCT-angiography (OCTA) results give microvascular information about the macula. Age was shown to influence both methods’ measurements. To further characterize this association, macular SD-OCT and OCTA changes were investigated in a population of juvenile, adult, and older individuals. Macular segment thickness and superficial (SCP) and deep plexus (DCP) vascular density (VD) of 157 healthy individuals aged 10–79 years were analyzed retrospectively. One-way analysis of variance (ANOVA) was used to compare age groups. The association between macular segmentation and OCTA parameters and between these and age was evaluated using linear regression. ANOVA and linear regression analysis showed a thickness decrease in the whole macular and in the ganglion cell and inner plexiform layers with age. While the foveal avascular zone area remained constant between age groups, VD of the SCP and DCP also decreased with age. In multiple linear regression, SCP and DCP VD were associated with inner macular segment thickness in an age-independent way. To conclude, the age-related microvascular and morphological changes in the macula described in this study can contribute to improving the understanding of macular aging processes and better interpreting OCT(A) results in healthy individuals and patients suffering from various retinal diseases. MDPI 2022-04-11 /pmc/articles/PMC9024868/ /pubmed/35455059 http://dx.doi.org/10.3390/life12040568 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lever, Mael
Chen, Ying
Glaser, Moritz
Unterlauft, Jan Darius
Lommatzsch, Claudia
Bechrakis, Nikolaos E.
Böhm, Michael R. R.
Microvascular and Morphologic Changes of the Macula over Lifetime
title Microvascular and Morphologic Changes of the Macula over Lifetime
title_full Microvascular and Morphologic Changes of the Macula over Lifetime
title_fullStr Microvascular and Morphologic Changes of the Macula over Lifetime
title_full_unstemmed Microvascular and Morphologic Changes of the Macula over Lifetime
title_short Microvascular and Morphologic Changes of the Macula over Lifetime
title_sort microvascular and morphologic changes of the macula over lifetime
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024868/
https://www.ncbi.nlm.nih.gov/pubmed/35455059
http://dx.doi.org/10.3390/life12040568
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