Optical coherence tomography angiography analysis of retinal vascular plexuses and choriocapillaris in patients with type 1 diabetes without diabetic retinopathy
Aims To analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion cell layer (GCL) by structural optical coherence tomography (OCT) in patients with type 1 diabetes mellitus (T1DM) without diabetic retinopath...
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Published in | Acta diabetologica Vol. 54; no. 7; pp. 695 - 702 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Milan
Springer Milan
01.07.2017
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Abstract | Aims
To analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion cell layer (GCL) by structural optical coherence tomography (OCT) in patients with type 1 diabetes mellitus (T1DM) without diabetic retinopathy (DR).
Methods
A total of 25 eyes of 25 consecutive T1DM patients without signs of DR were prospectively recruited and compared to 25 healthy subjects (control eyes). All patients underwent OCT-A (CIRRUS HD-OCT model 5000, Carl Zeiss Meditec, Dublin, CA) and structural OCT. Qualitative and quantitative analyses with vessel density were performed on OCT-A images in the superficial capillary plexus (SCP), deep capillary plexus (DCP) and choriocapillaris for all patients.
Results
By means of OCT-A, a rarefaction of the perifoveal capillary network in SCP was detected in 7 out of 25 eyes. No significant difference was found in FAZ area of both SCP and DCP comparing diabetic and control groups. By analyzing the DCP, diabetic eyes revealed a significant decreased vessel density compared to control eyes [0.464 ± 0.016 and 0.477 ± 0.014, respectively (
p
= 0.005)]. Instead, no significant difference was found in the vessel density of all-retina plexus, SCP and choriocapillaris. By RFNL and GCL thickness analysis, no significant differences were disclosed between diabetics and healthy subjects.
Conclusions
We demonstrated the ability of OCT-A to disclose early vascular alterations in patients with T1DM diagnosed as without any signs of DR on the basis of fundus biomicroscopy. Our results also suggest that microvascular changes could precede detectable damage of diabetic neuroretinopathy. |
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AbstractList | Aims To analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion cell layer (GCL) by structural optical coherence tomography (OCT) in patients with type 1 diabetes mellitus (T1DM) without diabetic retinopathy (DR). Methods A total of 25 eyes of 25 consecutive T1DM patients without signs of DR were prospectively recruited and compared to 25 healthy subjects (control eyes). All patients underwent OCT-A (CIRRUS HD-OCT model 5000, Carl Zeiss Meditec, Dublin, CA) and structural OCT. Qualitative and quantitative analyses with vessel density were performed on OCT-A images in the superficial capillary plexus (SCP), deep capillary plexus (DCP) and choriocapillaris for all patients. Results By means of OCT-A, a rarefaction of the perifoveal capillary network in SCP was detected in 7 out of 25 eyes. No significant difference was found in FAZ area of both SCP and DCP comparing diabetic and control groups. By analyzing the DCP, diabetic eyes revealed a significant decreased vessel density compared to control eyes [0.464 ± 0.016 and 0.477 ± 0.014, respectively (p = 0.005)]. Instead, no significant difference was found in the vessel density of all-retina plexus, SCP and choriocapillaris. By RFNL and GCL thickness analysis, no significant differences were disclosed between diabetics and healthy subjects. Conclusions We demonstrated the ability of OCT-A to disclose early vascular alterations in patients with T1DM diagnosed as without any signs of DR on the basis of fundus biomicroscopy. Our results also suggest that microvascular changes could precede detectable damage of diabetic neuroretinopathy. Aims To analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion cell layer (GCL) by structural optical coherence tomography (OCT) in patients with type 1 diabetes mellitus (T1DM) without diabetic retinopathy (DR). Methods A total of 25 eyes of 25 consecutive T1DM patients without signs of DR were prospectively recruited and compared to 25 healthy subjects (control eyes). All patients underwent OCT-A (CIRRUS HD-OCT model 5000, Carl Zeiss Meditec, Dublin, CA) and structural OCT. Qualitative and quantitative analyses with vessel density were performed on OCT-A images in the superficial capillary plexus (SCP), deep capillary plexus (DCP) and choriocapillaris for all patients. Results By means of OCT-A, a rarefaction of the perifoveal capillary network in SCP was detected in 7 out of 25 eyes. No significant difference was found in FAZ area of both SCP and DCP comparing diabetic and control groups. By analyzing the DCP, diabetic eyes revealed a significant decreased vessel density compared to control eyes [0.464 ± 0.016 and 0.477 ± 0.014, respectively ( p = 0.005)]. Instead, no significant difference was found in the vessel density of all-retina plexus, SCP and choriocapillaris. By RFNL and GCL thickness analysis, no significant differences were disclosed between diabetics and healthy subjects. Conclusions We demonstrated the ability of OCT-A to disclose early vascular alterations in patients with T1DM diagnosed as without any signs of DR on the basis of fundus biomicroscopy. Our results also suggest that microvascular changes could precede detectable damage of diabetic neuroretinopathy. To analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion cell layer (GCL) by structural optical coherence tomography (OCT) in patients with type 1 diabetes mellitus (T1DM) without diabetic retinopathy (DR). A total of 25 eyes of 25 consecutive T1DM patients without signs of DR were prospectively recruited and compared to 25 healthy subjects (control eyes). All patients underwent OCT-A (CIRRUS HD-OCT model 5000, Carl Zeiss Meditec, Dublin, CA) and structural OCT. Qualitative and quantitative analyses with vessel density were performed on OCT-A images in the superficial capillary plexus (SCP), deep capillary plexus (DCP) and choriocapillaris for all patients. By means of OCT-A, a rarefaction of the perifoveal capillary network in SCP was detected in 7 out of 25 eyes. No significant difference was found in FAZ area of both SCP and DCP comparing diabetic and control groups. By analyzing the DCP, diabetic eyes revealed a significant decreased vessel density compared to control eyes [0.464 ± 0.016 and 0.477 ± 0.014, respectively (p = 0.005)]. Instead, no significant difference was found in the vessel density of all-retina plexus, SCP and choriocapillaris. By RFNL and GCL thickness analysis, no significant differences were disclosed between diabetics and healthy subjects. We demonstrated the ability of OCT-A to disclose early vascular alterations in patients with T1DM diagnosed as without any signs of DR on the basis of fundus biomicroscopy. Our results also suggest that microvascular changes could precede detectable damage of diabetic neuroretinopathy. To analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion cell layer (GCL) by structural optical coherence tomography (OCT) in patients with type 1 diabetes mellitus (T1DM) without diabetic retinopathy (DR).AIMSTo analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion cell layer (GCL) by structural optical coherence tomography (OCT) in patients with type 1 diabetes mellitus (T1DM) without diabetic retinopathy (DR).A total of 25 eyes of 25 consecutive T1DM patients without signs of DR were prospectively recruited and compared to 25 healthy subjects (control eyes). All patients underwent OCT-A (CIRRUS HD-OCT model 5000, Carl Zeiss Meditec, Dublin, CA) and structural OCT. Qualitative and quantitative analyses with vessel density were performed on OCT-A images in the superficial capillary plexus (SCP), deep capillary plexus (DCP) and choriocapillaris for all patients.METHODSA total of 25 eyes of 25 consecutive T1DM patients without signs of DR were prospectively recruited and compared to 25 healthy subjects (control eyes). All patients underwent OCT-A (CIRRUS HD-OCT model 5000, Carl Zeiss Meditec, Dublin, CA) and structural OCT. Qualitative and quantitative analyses with vessel density were performed on OCT-A images in the superficial capillary plexus (SCP), deep capillary plexus (DCP) and choriocapillaris for all patients.By means of OCT-A, a rarefaction of the perifoveal capillary network in SCP was detected in 7 out of 25 eyes. No significant difference was found in FAZ area of both SCP and DCP comparing diabetic and control groups. By analyzing the DCP, diabetic eyes revealed a significant decreased vessel density compared to control eyes [0.464 ± 0.016 and 0.477 ± 0.014, respectively (p = 0.005)]. Instead, no significant difference was found in the vessel density of all-retina plexus, SCP and choriocapillaris. By RFNL and GCL thickness analysis, no significant differences were disclosed between diabetics and healthy subjects.RESULTSBy means of OCT-A, a rarefaction of the perifoveal capillary network in SCP was detected in 7 out of 25 eyes. No significant difference was found in FAZ area of both SCP and DCP comparing diabetic and control groups. By analyzing the DCP, diabetic eyes revealed a significant decreased vessel density compared to control eyes [0.464 ± 0.016 and 0.477 ± 0.014, respectively (p = 0.005)]. Instead, no significant difference was found in the vessel density of all-retina plexus, SCP and choriocapillaris. By RFNL and GCL thickness analysis, no significant differences were disclosed between diabetics and healthy subjects.We demonstrated the ability of OCT-A to disclose early vascular alterations in patients with T1DM diagnosed as without any signs of DR on the basis of fundus biomicroscopy. Our results also suggest that microvascular changes could precede detectable damage of diabetic neuroretinopathy.CONCLUSIONSWe demonstrated the ability of OCT-A to disclose early vascular alterations in patients with T1DM diagnosed as without any signs of DR on the basis of fundus biomicroscopy. Our results also suggest that microvascular changes could precede detectable damage of diabetic neuroretinopathy. |
Author | Carnevali, Adriano Tomasso, Livia Querques, Lea Sacconi, Riccardo Querques, Giuseppe Scorcia, Vincenzo Bandello, Francesco Zerbini, Gianpaolo Corbelli, Eleonora |
Author_xml | – sequence: 1 givenname: Adriano surname: Carnevali fullname: Carnevali, Adriano organization: Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele, Department of Ophthalmology, University of “Magna Graecia” – sequence: 2 givenname: Riccardo surname: Sacconi fullname: Sacconi, Riccardo organization: Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele, Department of Ophthalmology, University of Verona, University Hospital of Verona – sequence: 3 givenname: Eleonora surname: Corbelli fullname: Corbelli, Eleonora organization: Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele – sequence: 4 givenname: Livia surname: Tomasso fullname: Tomasso, Livia organization: Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele – sequence: 5 givenname: Lea surname: Querques fullname: Querques, Lea organization: Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele – sequence: 6 givenname: Gianpaolo surname: Zerbini fullname: Zerbini, Gianpaolo organization: Complications of Diabetes Unit, Division of Metabolic and Cardiovascular Sciences, San Raffaele Scientific Institute – sequence: 7 givenname: Vincenzo surname: Scorcia fullname: Scorcia, Vincenzo organization: Department of Ophthalmology, University of “Magna Graecia” – sequence: 8 givenname: Francesco surname: Bandello fullname: Bandello, Francesco organization: Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele – sequence: 9 givenname: Giuseppe surname: Querques fullname: Querques, Giuseppe email: giuseppe.querques@hotmail.it organization: Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28474119$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | Springer-Verlag Italia 2017 Acta Diabetologica is a copyright of Springer, 2017. |
Copyright_xml | – notice: Springer-Verlag Italia 2017 – notice: Acta Diabetologica is a copyright of Springer, 2017. |
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DOI | 10.1007/s00592-017-0996-8 |
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Keywords | Diabetic retinopathy Retinal nerve fiber layer Optical coherence tomography angiography Ganglion cell layer Retinal imaging |
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retinopathy publication-title: Dev Ophthalmol doi: 10.1159/000442801 – volume: 58 start-page: 190 year: 2017 end-page: 196 ident: CR22 article-title: Quantitative retinal optical coherence tomography angiography in patients with diabetes without diabetic retinopathy publication-title: Invest Ophthalmol Vis Sci doi: 10.1167/iovs.16-20531 – volume: 63 start-page: 3926 year: 2014 end-page: 3937 ident: CR39 article-title: Neuroretinal dysfunction with intact blood-retinal barrier and absent vasculopathy in diabetes type 1 publication-title: Diabetes doi: 10.2337/db13-1673 – volume: 7 start-page: 227 year: 1993 end-page: 229 ident: CR7 article-title: Microvascular haemodynamics in diabetes publication-title: Eye doi: 10.1038/eye.1993.54 – volume: 26 start-page: 226 year: 2003 end-page: 229 ident: CR5 article-title: Diabetic Retinopathy publication-title: Diabetes Care doi: 10.2337/diacare.26.1.226 – volume: 52 start-page: 73 year: 2015 end-page: 80 ident: CR12 article-title: Body mass index and retinopathy in Asian populations with diabetes mellitus publication-title: Acta Diabetol doi: 10.1007/s00592-014-0602-2 – volume: 57 start-page: 5355 year: 2016 end-page: 5360 ident: CR15 article-title: Retinal nerve fiber layer and ganglion cell complex thicknesses are reduced in children with type 1 diabetes with no evidence of vascular retinopathy publication-title: Invest Ophthalmol Vis Sci doi: 10.1167/iovs.16-19988 – volume: 75 start-page: 514 year: 1991 end-page: 518 ident: CR36 article-title: Retinal microcirculation in patients with diabetes mellitus: dynamic and morphological analysis of perifoveal capillary network publication-title: Br J Ophthalmol doi: 10.1136/bjo.75.9.514 – volume: 52 start-page: 1113 year: 2015 end-page: 1119 ident: CR11 article-title: Molecular mechanisms of extracellular vesicle-induced vessel destabilization in diabetic retinopathy publication-title: Acta Diabetol doi: 10.1007/s00592-015-0798-9 – volume: 35 start-page: 2364 year: 2015 end-page: 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publication-title: Pediatrics doi: 10.1542/peds.2005-0875 – volume: 35 start-page: 2384 year: 2015 end-page: 2391 ident: CR33 article-title: Capillary plexus anomalies in diabetic retinopathy on optical coherence tomography angiography publication-title: Retina doi: 10.1097/IAE.0000000000000859 – volume: 67 start-page: 21 year: 1969 end-page: 38 ident: CR6 article-title: Ocular pathology of diabetes mellitus publication-title: Am J Ophthalmol doi: 10.1016/0002-9394(69)90004-X – year: 2017 ident: CR18 article-title: Retina and choroid of diabetic patients without observed retinal vascular changes: a longitudinal study publication-title: Am J Ophthalmol – year: 2016 ident: CR38 article-title: Reproducibility and reliability of optical coherence tomography angiography for foveal avascular zone evaluation and measurement in different settings publication-title: Retina – volume: 98 start-page: 1266 year: 1991 end-page: 1271 ident: CR40 article-title: Oscillatory potentials and permeability of the blood-retinal barrier in noninsulin-dependent diabetic patients without retinopathy publication-title: Ophthalmology doi: 10.1016/S0161-6420(91)32144-4 – volume: 90 start-page: 50 year: 2013 end-page: 58 ident: CR17 article-title: Retinal layers changes in human preclinical and early clinical diabetic retinopathy support early retinal neuronal and Müller cells alterations publication-title: J Diabetes Res – volume: 25 start-page: 333 issue: 7 year: 2016 end-page: 341 ident: CR2 article-title: Treatment of diabetic retinopathy: recent advances and unresolved challenges publication-title: World J Diabetes doi: 10.4239/wjd.v7.i16.333 – volume: 35 start-page: 2188 year: 2015 end-page: 2195 ident: CR28 article-title: Correlation of foveal avascular zone size with foveal morphology in normal eyes using optical coherence tomography angiography publication-title: Retina doi: 10.1097/IAE.0000000000000847 – volume: 47 start-page: 171 year: 2012 end-page: 188 ident: CR1 article-title: 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macrovascular diseases in the physical therapy setting publication-title: Phys Ther doi: 10.2522/ptj.20080008 – volume: 161 start-page: e51 issue: 50–55 year: 2016 ident: CR29 article-title: Measurement of foveal avascular zone dimensions and its reliability in healthy eyes using optical coherence tomography angiography publication-title: Am J Ophthalmol – volume: 168 start-page: 129 year: 2016 end-page: 138 ident: CR32 article-title: Deep retinal capillary nonperfusion is associated with photoreceptor disruption in diabetic macular ischemia publication-title: Am J Ophthalmol doi: 10.1016/j.ajo.2016.05.002 – volume: 57 start-page: 362 year: 2016 end-page: 370 ident: CR21 article-title: Quantifying microvascular density and morphology in diabetic retinopathy using spectral-domain optical coherence tomography angiography publication-title: Invest Ophthalmol Vis Sci doi: 10.1167/iovs.15-18904 – volume: 11 start-page: 243 year: 2016 end-page: 245 ident: CR42 article-title: Optical coherence tomography angiography: Evolution or revolution? expert publication-title: Rev of Ophthalmol doi: 10.1080/17469899.2016.1209409 – volume: 16 start-page: 11438 year: 2008 end-page: 11452 ident: CR27 article-title: In vivo volumetric imaging of vascular perfusion within human retina and choroids with optical micro-angiography publication-title: Opt Express doi: 10.1364/OE.16.011438 – volume: 16 start-page: 545 year: 2010 end-page: 554 ident: CR26 article-title: Optical microangiography: a label free 3d imaging technology to visualize and quantify blood circulations within tissue beds in vivo publication-title: IEEE J Sel Top Quantum Electron doi: 10.1109/JSTQE.2009.2033609 – volume: 53 start-page: 957 year: 2016 end-page: 964 ident: CR14 article-title: Effects of the neuroprotective drugs somatostatin and brimonidine on retinal cell models of diabetic retinopathy publication-title: Acta Diabetol doi: 10.1007/s00592-016-0895-4 – volume: 254 start-page: 1051 year: 2016 end-page: 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To analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion... To analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion cell... Aims To analyze retinal vascular plexuses and choriocapillaris by optical coherence tomography angiography (OCT-A) and retinal nerve fiber layer and ganglion... |
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SubjectTerms | Adolescent Adult Angiography Angiography - methods Diabetes Diabetes mellitus Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - diagnosis Diabetes Mellitus, Type 1 - pathology Diabetic retinopathy Diabetic Retinopathy - diagnosis Eye diseases Female Fluorescein Angiography Fundus Oculi Humans Internal Medicine Male Medical imaging Medicine Medicine & Public Health Metabolic Diseases Microvasculature Original Article Predictive Value of Tests Retina Retina - diagnostic imaging Retinal Ganglion Cells - pathology Retinal Ganglion Cells - ultrastructure Retinal Neurons - pathology Retinal Neurons - ultrastructure Retinal Vessels - diagnostic imaging Retinopathy Single-cell protein Tomography Tomography, Optical Coherence Young Adult |
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Title | Optical coherence tomography angiography analysis of retinal vascular plexuses and choriocapillaris in patients with type 1 diabetes without diabetic retinopathy |
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