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Imaging Characteristics of Neovascular and Atrophic Pachychoroidal Spectrum Diseases

BACKGROUND: This study qualitatively and quantitatively compared imaging characteristics between neovascular and atrophic pachychoroid spectrum disease (PSD) by optical coherence tomography (OCT), and OCT angiography (OCTA). METHODS: The subtypes of PSD were identified by multi-modality imaging appr...

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Autores principales: Hua, Rui, Zhang, Meixia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289118/
https://www.ncbi.nlm.nih.gov/pubmed/35860744
http://dx.doi.org/10.3389/fmed.2022.891397
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author Hua, Rui
Zhang, Meixia
author_facet Hua, Rui
Zhang, Meixia
author_sort Hua, Rui
collection PubMed
description BACKGROUND: This study qualitatively and quantitatively compared imaging characteristics between neovascular and atrophic pachychoroid spectrum disease (PSD) by optical coherence tomography (OCT), and OCT angiography (OCTA). METHODS: The subtypes of PSD were identified by multi-modality imaging approaches. Subfoveal choroidal thickness (SFCT), choroidal vascular index (CVI), and vascular density of choroidal neovascularization (CNV) were measured. RESULTS: The CVI and SFCT of 174 PSD eyes were 67.6% ± 5.48% and 362.2 ± 131.88 μm, respectively. After adjustment for age, linear regression indicated that SFCT was positively associated with CVI (p < 0.001), and patched hyper-reflective lesions in choriocapillaris layers (p = 0.009). Compared with neovascular PSD eyes, atrophic PSD eyes had similar patient age (57.1 ± 16.72 years, p = 0.639), SFCT (332.0 ± 111.00 μm, p = 0.51), and CVI (67.6% ± 3.94%, p = 0.527). There were no differences between polypoidal choroidal vasculopathy (PCV) eyes with aneurysmal polypoidal lesions and PCV eyes with tangled polypoidal lesions in terms of age, CVI, SFCT, vascular density, or the occurrence of double layer signs (DLSs, all p > 0.05). Logistic regression indicated that age (p = 0.003), SFCT (p = 0.003), patched hyper-reflective lesions in choriocapillaris layers (p = 0.009), and DLSs (p < 0.001) were predictive factors for CNV progression in PSD eyes (all p < 0.05). CONCLUSIONS: Our study highlighted the similarities in SFCT and CVI between neovascular and atrophic PSD, both of which were late stage lesions. Besides, age, SFCT, patched hyper-reflective lesions in choriocapillaris layers, and DLSs were risk factors for CNV in PSD. Our results showed that atrophic PSD is an important change in the late stage of PSD disease, which is helpful for in-depth understanding of the pathological mechanism of PSD and corresponding intervention.
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spelling pubmed-92891182022-07-19 Imaging Characteristics of Neovascular and Atrophic Pachychoroidal Spectrum Diseases Hua, Rui Zhang, Meixia Front Med (Lausanne) Medicine BACKGROUND: This study qualitatively and quantitatively compared imaging characteristics between neovascular and atrophic pachychoroid spectrum disease (PSD) by optical coherence tomography (OCT), and OCT angiography (OCTA). METHODS: The subtypes of PSD were identified by multi-modality imaging approaches. Subfoveal choroidal thickness (SFCT), choroidal vascular index (CVI), and vascular density of choroidal neovascularization (CNV) were measured. RESULTS: The CVI and SFCT of 174 PSD eyes were 67.6% ± 5.48% and 362.2 ± 131.88 μm, respectively. After adjustment for age, linear regression indicated that SFCT was positively associated with CVI (p < 0.001), and patched hyper-reflective lesions in choriocapillaris layers (p = 0.009). Compared with neovascular PSD eyes, atrophic PSD eyes had similar patient age (57.1 ± 16.72 years, p = 0.639), SFCT (332.0 ± 111.00 μm, p = 0.51), and CVI (67.6% ± 3.94%, p = 0.527). There were no differences between polypoidal choroidal vasculopathy (PCV) eyes with aneurysmal polypoidal lesions and PCV eyes with tangled polypoidal lesions in terms of age, CVI, SFCT, vascular density, or the occurrence of double layer signs (DLSs, all p > 0.05). Logistic regression indicated that age (p = 0.003), SFCT (p = 0.003), patched hyper-reflective lesions in choriocapillaris layers (p = 0.009), and DLSs (p < 0.001) were predictive factors for CNV progression in PSD eyes (all p < 0.05). CONCLUSIONS: Our study highlighted the similarities in SFCT and CVI between neovascular and atrophic PSD, both of which were late stage lesions. Besides, age, SFCT, patched hyper-reflective lesions in choriocapillaris layers, and DLSs were risk factors for CNV in PSD. Our results showed that atrophic PSD is an important change in the late stage of PSD disease, which is helpful for in-depth understanding of the pathological mechanism of PSD and corresponding intervention. Frontiers Media S.A. 2022-07-04 /pmc/articles/PMC9289118/ /pubmed/35860744 http://dx.doi.org/10.3389/fmed.2022.891397 Text en Copyright © 2022 Hua and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Hua, Rui
Zhang, Meixia
Imaging Characteristics of Neovascular and Atrophic Pachychoroidal Spectrum Diseases
title Imaging Characteristics of Neovascular and Atrophic Pachychoroidal Spectrum Diseases
title_full Imaging Characteristics of Neovascular and Atrophic Pachychoroidal Spectrum Diseases
title_fullStr Imaging Characteristics of Neovascular and Atrophic Pachychoroidal Spectrum Diseases
title_full_unstemmed Imaging Characteristics of Neovascular and Atrophic Pachychoroidal Spectrum Diseases
title_short Imaging Characteristics of Neovascular and Atrophic Pachychoroidal Spectrum Diseases
title_sort imaging characteristics of neovascular and atrophic pachychoroidal spectrum diseases
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289118/
https://www.ncbi.nlm.nih.gov/pubmed/35860744
http://dx.doi.org/10.3389/fmed.2022.891397
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