To assess the alteration in the macular microvascular in type 2 diabetic patients with peripheral neuropathy (DPN) and without peripheral neuropathy (NDPN) by optical coherence tomography angiography (OCTA) and explore the correlation between retinal microvascular abnormalities and DPN disease. Twenty-seven healthy controls (42 eyes), 36 NDPN patients (62 eyes), and 27 DPN patients (40 eyes) were included. OCTA was used to image the macula in the superficial vascular complex (SVC) and deep vascular complex (DVC). In addition, a state-of-the-art deep learning method was employed to quantify the microvasculature of the two capillary plexuses in all participants using vascular length density (VLD). Compared with the healthy control group, the average VLD values of patients with DPN in SVC ( = 0.010) and DVC ( = 0.011) were significantly lower. Compared with NDPN, DPN patients showed significantly reduced VLD values in the SVC ( = 0.006) and DVC ( = 0.001). Also, DPN patients showed lower VLD values ( < 0.05) in the nasal, superior, temporal and inferior sectors of the inner ring of the SVC when compared with controls; VLD values in NDPN patients were lower in the nasal section of the inner ring of SVC (p < 0.05) compared with healthy controls. VLD values in the DVC (AUC = 0.736, < 0.001) of the DPN group showed a higher ability to discriminate microvascular damage when compared with NDPN. OCTA based on deep learning could be potentially used in clinical practice as a new indicator in the early diagnosis of DM with and without DPN.
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http://dx.doi.org/10.3389/fcell.2022.1081285 | DOI Listing |
Int J Retina Vitreous
December 2024
Department of Biomedicine - Unit of Anatomy, Faculty of Medicine, University of Porto, Porto, Portugal.
Purpose: To assess the retinal microvasculature of Systemic Lupus Erythematosus (SLE) patients using Optical Coherence Tomography Angiography (OCTA).
Methods: Twenty adult SLE patients without disease activity and no ocular manifestations were recruited and cross-sectionally assessed. A demographically similar cohort of healthy subjects was used for comparison.
Int J Retina Vitreous
November 2024
Department of Ophthalmology, University Hospital Mannheim & Medical Faculty Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, Mannheim, 68167, Germany.
Background: Diabetes mellitus (DM) causes microvascular damage due to long-term hyperglycemia, even before the onset of retinal changes. We aimed to investigate the association between optical coherence tomography angiography (OCTA) metrics and disease duration in type 2 diabetic patients without retinopathy.
Methods: Eighty-two eyes of 82 type 2 diabetic patients without diabetic retinopathy (DR) were included.
Sci Rep
November 2024
Department of Ophthalmology, University Hospital Mannheim & Medical Faculty of Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany.
Optical coherence tomography angiography (OCTA) offers the possibility of obtaining objective quantification of retinal vasculature, with increasing utility as biomarkers for both systemic and ocular diseases. However, the differences between different manufacturers and scan settings are still an important limitation, as many parameters could affect vessel quantification. Here we aim to study the influence of scan speed on quantitative vascular parameters using OCTA.
View Article and Find Full Text PDFMicrovasc Res
January 2025
Department of Ophthalmology, Farabi Eye Hospital, School of medicine, Tehran University of Medical Sciences, Tehran, Iran. Electronic address:
Purpose: To investigate the healing process of conjunctival autografts (CAG) following pterygium surgery using optical coherence tomography angiography (OCTA).
Methods: Twenty-one eyes of 21 patients diagnosed with pterygium underwent pterygium excision with CAG without using Mitomycin-C. Over a 12-week follow-up period, changes in vascular density (VD), vascular density index (VDI), and vascular length density (VLD) were assessed at two distinct depths: superficial (<200 μm) and deep (>200 μm) using OCTA.
Cureus
April 2024
Department of Pathology and Laboratory Medicine/Oncology, Aga Khan University Hospital, Karachi, PAK.
Introduction Multiple myeloma (MM) is a hematological disorder characterized by aberrant multiplication of malignant plasma cells in the bone marrow. The current mainstay of treatment for patients with newly diagnosed MM (NDMM) is a triplet regimen with a proteasome inhibitor, immunomodulatory imide, and dexamethasone. The two most common of these triplet regimens are VLD (bortezomib/lenalidomide/dexamethasone) and VCD (bortezomib/cyclophosphamide/dexamethasone).
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