Validation of choroidal hyperreflective foci in diabetic macular edema through a retrospective pilot study.
Choroidal hyperreflective foci
diabetic macular edema
retinal hyperreflective foci
spectral-domain optical coherence tomography
Journal
Indian journal of ophthalmology
ISSN: 1998-3689
Titre abrégé: Indian J Ophthalmol
Pays: India
ID NLM: 0405376
Informations de publication
Date de publication:
Nov 2021
Nov 2021
Historique:
entrez:
28
10
2021
pubmed:
29
10
2021
medline:
5
11
2021
Statut:
ppublish
Résumé
Choroidal hyperreflective foci (HCF) are novel spectral-domain optical coherence tomography (SDOCT) biomarkers in diabetic macular edema (DME). The present study intended to validate HCF and assess their role in the treatment outcome. It was a retrospective, longitudinal, records-based pilot study recruiting consecutive patients of nonproliferative diabetic retinopathy with treatment naïve DME. Patients were treated with three intravitreal anti-vascular endothelial growth factor injections and followed by a pro re nata regimen. A total of 43 eyes of 28 patients were included in the study. Eyes were divided into two groups. Group A (n = 19) comprised eyes with retinal hyperreflective foci (HRF) and group B (n = 24) had eyes with both HRF and HCF. The mean age of patients in group A and B was 58.5 ± 2.1 years and 55.2 ± 8.8 years, respectively. Mean best-corrected visual acuity at presentation was 0.38 ± 0.25 in group A and 0.59 ± 0.29 in group B (P = 0.01). Final BCVA was 0.35 ± 0.39 in group A and 0.47 ± 0.34 in group B (P = 0.3). External limiting membrane was intact in 19 out of 19 eyes in group A and two (8.3%) eyes in group B (P = 0). Presence of HCF meant significantly worse initial BCVA compared to the eye that had HRF alone. The final BCVA was also worse in eyes with HCF compared to those with HRF and without HCF; however, the difference did not reach a significance level, probably pointing toward the fact that HCF and HRF are pathophysiologically identical. Further studies with a larger sample size and prospective design are needed to take these findings forward.
Identifiants
pubmed: 34708773
pii: IndianJOphthalmol_2021_69_11_3203_329260
doi: 10.4103/ijo.IJO_1585_21
pmc: PMC8725089
doi:
Substances chimiques
Angiogenesis Inhibitors
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
3203-3206Commentaires et corrections
Type : CommentIn
Déclaration de conflit d'intérêts
None
Références
Asia Pac J Ophthalmol (Phila). 2019 Jul-Aug;8(4):314-318
pubmed: 31397675
J Diabetes Res. 2013;2013:491835
pubmed: 24386645
Acta Diabetol. 2020 Jul;57(7):861-866
pubmed: 32114640
Invest Ophthalmol Vis Sci. 2012 Aug 24;53(9):5814-8
pubmed: 22836760
Ophthalmology. 2009 May;116(5):914-20
pubmed: 19410950
Diabetologia. 2016 Aug;59(8):1594-608
pubmed: 27179659
Indian J Ophthalmol. 2019 Nov;67(11):1850-1854
pubmed: 31638047
JAMA Ophthalmol. 2015 Apr;133(4):398-405
pubmed: 25590640
Am J Ophthalmol Case Rep. 2016 Apr 12;3:25-30
pubmed: 29503902
Am J Ophthalmol. 2012 Apr;153(4):710-7, 717.e1
pubmed: 22137207
Ther Adv Ophthalmol. 2020 Sep 4;12:2515841420950513
pubmed: 32954207
Ophthalmologica. 2013;229(1):32-7
pubmed: 23006969