MbrlCatalogueTitleDetail

Do you wish to reserve the book?
Microvascular impairment as a biomarker of diabetic retinopathy progression in the long-term follow up in type 1 diabetes
Microvascular impairment as a biomarker of diabetic retinopathy progression in the long-term follow up in type 1 diabetes
Hey, we have placed the reservation for you!
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Microvascular impairment as a biomarker of diabetic retinopathy progression in the long-term follow up in type 1 diabetes
Oops! Something went wrong.
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Title added to your shelf!
Title added to your shelf!
View what I already have on My Shelf.
Oops! Something went wrong.
Oops! Something went wrong.
While trying to add the title to your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Microvascular impairment as a biomarker of diabetic retinopathy progression in the long-term follow up in type 1 diabetes
Microvascular impairment as a biomarker of diabetic retinopathy progression in the long-term follow up in type 1 diabetes

Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
How would you like to get it?
We have requested the book for you! Sorry the robot delivery is not available at the moment
We have requested the book for you!
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Microvascular impairment as a biomarker of diabetic retinopathy progression in the long-term follow up in type 1 diabetes
Microvascular impairment as a biomarker of diabetic retinopathy progression in the long-term follow up in type 1 diabetes
Journal Article

Microvascular impairment as a biomarker of diabetic retinopathy progression in the long-term follow up in type 1 diabetes

2020
Request Book From Autostore and Choose the Collection Method
Overview
This study aimed to explore differences in vascular and structural parameters using optical coherence tomography angiography in patients with type 1 diabetes (DM1) with mild signs of diabetic retinopathy (DR) over a two-year follow-up period. Parafoveal vessel density (PVD) and foveal avascular zone (FAZ) area were analyzed. The thickness of three predefined retinal slabs was measured, including the inner limiting membrane (ILM)–inner plexiform layer (IPL), IPL–inner nuclear layer (INL), and the IPL–outer nuclear layer (ONL). Twenty-two patients with DM1 and 21 controls were included. There was no significant difference in the FAZ area, perimeter and acircularity index between cohorts over time. Baseline superficial capillary plexus PVD was approximately 10% lower in patients with diabetes than in controls ( p  = 0.001), and was 12% lower at 2 years ( p  = 0.002). There was no difference in the annual linear trend between the groups (− 0.5% in diabetics vs. controls, p  = 0.736). Baseline deep capillary plexus (DCP) PVD was slightly lower in diabetics than in controls (− 4.4%, p  = 0.047) and the difference increased at 2 years (− 12.6%, p  < 0.001). The annual linear trend was − 2.7% in diabetic patients compared to controls ( p  = 0.009) . In addition, the PVD of the DCP and the intermediate capillary plexus (ICP) were evaluated separately. Regarding the DCP PVD, no statistically significant difference at any time points in diabetic patients compared to controls and no statistically significant difference in the linear trend was found ( p  > 0.1). Conversely, no difference was recorded for parafoveal ICP density at individual time points ( p  > 0.1), but a statistically significant difference in the linear trend over time in diabetic patients compared to controls was recoded (− 3.2% per year, p  = 0.001). Despite the apparent intergroup differences at baseline in structural OCT parameters, the differences including ILM–IPL ( p  = 0.273), IPL–INL ( p  = 0.708), and IPL–ONL ( p  = 0.054) were modest and not statistically significant with time. Therefore, the microvascular change of the deeper vessels might be a robust biomarker to evaluate the clinical progression of DR in DM1.