Spatial distribution of early red lesions is a risk factor for development of vision-threatening diabetic retinopathy

Springer Science and Business Media LLC - Tập 60 - Trang 2361-2367 - 2017
Giovanni Ometto1, Phil Assheton2, Francesco Calivá3, Piotr Chudzik3, Bashir Al-diri3, Andrew Hunter3, Toke Bek1
1Department of Ophthalmology, Aarhus University Hospital, Aarhus C, Denmark
2Maths and Stats Help Centre, University of Lincoln, Lincoln, UK
3School of Computer Science, University of Lincoln, Lincoln, UK

Tóm tắt

Diabetic retinopathy is characterised by morphological lesions related to disturbances in retinal blood flow. It has previously been shown that the early development of retinal lesions temporal to the fovea may predict the development of treatment-requiring diabetic maculopathy. The aim of this study was to map accurately the area where lesions could predict progression to vision-threatening retinopathy. The predictive value of the location of the earliest red lesions representing haemorrhages and/or microaneurysms was studied by comparing their occurrence in a group of individuals later developing vision-threatening diabetic retinopathy with that in a group matched with respect to diabetes type, age, sex and age of onset of diabetes mellitus who did not develop vision-threatening diabetic retinopathy during a similar observation period. The probability of progression to vision-threatening diabetic retinopathy was higher in a circular area temporal to the fovea, and the occurrence of the first lesions in this area was predictive of the development of vision-threatening diabetic retinopathy. The calculated peak value showed that the risk of progression was 39.5% higher than the average. There was no significant difference in the early distribution of lesions in participants later developing diabetic maculopathy or proliferative diabetic retinopathy. The location of early red lesions in diabetic retinopathy is predictive of whether or not individuals will later develop vision-threatening diabetic retinopathy. This evidence should be incorporated into risk models used to recommend control intervals in screening programmes for diabetic retinopathy.

Tài liệu tham khảo

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