Correlating Changes in the Macular Microvasculature and Capillary Network to Peripheral Vascular Pathologic Features in Familial Exudative Vitreoretinopathy.


Journal

Ophthalmology. Retina
ISSN: 2468-6530
Titre abrégé: Ophthalmol Retina
Pays: United States
ID NLM: 101695048

Informations de publication

Date de publication:
07 2019
Historique:
received: 14 10 2018
revised: 26 02 2019
accepted: 26 02 2019
entrez: 7 7 2019
pubmed: 7 7 2019
medline: 27 6 2020
Statut: ppublish

Résumé

To evaluate the macular microvasculature in patients with familial exudative vitreoretinopathy (FEVR) using OCT angiography (OCTA) and to assess for peripheral vascular changes using widefield fluorescein angiography (WFA). Multicenter, retrospective, comparative, observational case series. We identified 411 patients with FEVR, examined between September 2014 and June 2018. Fifty-seven patients with FEVR and 60 healthy controls had OCTA images of sufficient quality for analysis. Custom software was used to assess for layer-specific, quantitative changes in vascular density and morphologic features on OCTA by way of vessel density (VD), skeletal density (SD), fractal dimension (FD), vessel diameter index (VDI), and foveal avascular zone (FAZ). Widefield fluorescein angiography images were reviewed for peripheral vascular changes including capillary dropout, late-phase angiographic posterior and peripheral vascular leakage (LAPPEL), vascular dragging, venous-venous shunts, and arteriovenous shunts. Macular microvascular parameters on OCTA and peripheral angiographic findings on WFA. OCT angiography analysis of 117 patients (187 eyes; 92 FEVR patients and 95 control participants) demonstrated significantly reduced VD, SD, and FD and greater VDI in patients with FEVR compared with controls in the nonsegmented retina, superficial retinal layer (SRL), and deep retinal layer (DRL). The FAZ was larger compared with that in control eyes in the DRL (P < 0.0001), but not the SRL (P = 0.52). Subanalysis by FEVR stage showed the same microvascular changes compared with controls for all parameters. Widefield fluorescein angiography analysis of 95 eyes (53 patients) with FEVR demonstrated capillary nonperfusion in all eyes: 47 eyes (49.5%) showed LAPPEL, 32 eyes (33.7%) showed vascular dragging, 30 eyes (31.6%) had venous-venous shunts, and 33 eyes (34.7%) had arteriovenous shunts. Decreasing macular VD on OCTA correlated with increasing peripheral capillary nonperfusion on WFA. Decreasing fractal dimension on OCTA correlated with increasing LAPPEL severity on WFA. Patients with FEVR demonstrated abnormalities in the macular microvasculature and capillary network, in addition to the peripheral retina. The macular microvascular parameters on OCTA may serve as biomarkers of changes in the retinal periphery on WFA.

Identifiants

pubmed: 31277801
pii: S2468-6530(18)30712-7
doi: 10.1016/j.oret.2019.02.013
pii:
doi:

Types de publication

Comparative Study Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

597-606

Subventions

Organisme : NEI NIH HHS
ID : K08 EY028999
Pays : United States

Informations de copyright

Published by Elsevier Inc.

Auteurs

Nicole Koulisis (N)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan; USC Roski Eye Institute, Department of Ophthalmology, Keck School of Medicine, University of Southern California, Los Angeles, California.

Stavros N Moysidis (SN)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan.

Yoshihiro Yonekawa (Y)

Retina Service, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts.

Yi Ling Dai (YL)

William Beaumont School of Medicine, Oakland University, Rochester, Michigan.

Bruce Burkemper (B)

USC Roski Eye Institute, Department of Ophthalmology, Keck School of Medicine, University of Southern California, Los Angeles, California.

Edward H Wood (EH)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan.

Itsara Lertjirachai (I)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan; Department of Ophthalmology, Srinakharinwirot University, Bangkok, Thailand.

Bozho Todorich (B)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan.

Tahsin Z Khundkar (TZ)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan.

Zhongdi Chu (Z)

Department of Bioengineering, University of Washington, Seattle, Washington.

Ruikang K Wang (RK)

Department of Bioengineering, University of Washington, Seattle, Washington.

George A Williams (GA)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan.

Kimberly A Drenser (KA)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan.

Antonio Capone (A)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan.

Michael T Trese (MT)

Associated Retinal Consultants, PC, William Beaumont Hospital, Royal Oak, Michigan.

Eric Nudleman (E)

Department of Ophthalmology, Shiley Eye Institute and Jacobs Retina Center, University of California, San Diego, La Jolla, California. Electronic address: eric.nudleman@gmail.com.

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