Evaluation of microvascular changes in the perifoveal vascular network using optical coherence tomography angiography (OCTA) in type I diabetes mellitus: a large scale prospective trial

dc.contributor.authorZarranz Ventura, Javier
dc.contributor.authorBarraso, Marina
dc.contributor.authorAlé Chilet, Aníbal Raimundo
dc.contributor.authorHernandez, Teresa
dc.contributor.authorOliva, Cristian
dc.contributor.authorGascon, Jesus
dc.contributor.authorSala Puigdollers, Anna
dc.contributor.authorFigueras Roca, Marc
dc.contributor.authorVinagre, Irene
dc.contributor.authorOrtega Martínez de Victoria, Emilio
dc.contributor.authorEsmatjes Mompó, Enric
dc.contributor.authorAdán Civera, Alfredo
dc.date.accessioned2020-05-29T14:27:08Z
dc.date.available2020-05-29T14:27:08Z
dc.date.issued2019-11-21
dc.date.updated2020-05-29T14:27:08Z
dc.description.abstractBackground: Diabetic retinopathy (DR) is the leading cause of blindness in type 1 Diabetes Mellitus (DM) patients, as a consequence of impaired blood flow in the retina. Optical coherence tomography angiography (OCTA) is a newly developed, non-invasive, retinal imaging technique that permits adequate delineation of the perifoveal vascular network. It allows the detection of paramacular areas of capillary non perfusion and/or enlargement of the foveal avascular zone (FAZ), representing an excellent tool for assessment of DR. The relationship of these microvascular changes with systemic factors such as metabolic control or duration of the disease still needs to be elucidated. Methods: Prospective, consecutive, large-scale OCTA study. A complete ocular examination including a comprehensive series of OCTA images of different scan sizes captured with 2 OCT devices (Cirrus HD-OCT, Carl Zeiss Meditec, Dublin, CA, USA, and Triton Deep Range Imaging OCT, Topcon Corp, Topcon, Japan) will be obtained as part of the yearly routine follow up visits in type 1 DM patients seen in the Diabetes Unit of the Endocrinology department which give written informed consent to participate in the project. The aim of this study is to investigate the relationship between OCTA-derived parameters and systemic factors, as metabolic control (Hb1Ac, lipid profile, cholesterol, etc), and other relevant clinical factors as demographics or duration of the disease. Discussion: This study is directed to investigate the relationship between the status of the perifoveal vascular network and systemic markers of the disease, and in particular to study whether these changes reflect those occurring elsewhere in the body affected by diabetic microvascular disease, as the kidneys or the brain. If these relationships were demonstrated, early detection of these microvascular changes by OCTA could lead to modifications in the pharmacological management of type 1 diabetic patients, as a way to reduce the risk of future complications in both the eye and other organs.
dc.format.extent6 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec695067
dc.identifier.issn1471-2342
dc.identifier.pmid31752726
dc.identifier.urihttps://hdl.handle.net/2445/163125
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1186/s12880-019-0391-8
dc.relation.ispartofBMC Medical Imaging, 2019, vol. 19, p. 91
dc.relation.urihttps://doi.org/10.1186/s12880-019-0391-8
dc.rightscc-by (c) Zarranz Ventura, Javier et al., 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationRetinopatia diabètica
dc.subject.classificationCeguesa
dc.subject.classificationDiabetis
dc.subject.classificationAngiografia
dc.subject.otherDiabetic retinopathy
dc.subject.otherBlindness
dc.subject.otherDiabetes
dc.subject.otherAngiography
dc.titleEvaluation of microvascular changes in the perifoveal vascular network using optical coherence tomography angiography (OCTA) in type I diabetes mellitus: a large scale prospective trial
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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