Literature DB >> 29555483

Analysis of Retinal Thinning Using Spectral-domain Optical Coherence Tomography Imaging of Sickle Cell Retinopathy Eyes Compared to Age- and Race-Matched Control Eyes.

Jennifer I Lim1, Dingcai Cao2.   

Abstract

PURPOSE: To determine whether the retina is thinner in sickle cell patients than in race- and age-matched controls, and, if it is thinner, whether there is any association with systemic diseases.
METHODS: Sickle cell and control (age- and race-matched) patients were prospectively enrolled from a university retina clinic into this observational study. Participants underwent visual acuity testing, slit-lamp biomicroscopy, dilated ophthalmoscopy, and spectral-domain optical coherence tomography imaging. Sickle cell retinal lesions, degree of vascular tortuosity, caliber of arteriovenous anastomosis, and stage of retinopathy were noted. Early Treatment Diabetic Retinopathy Study (ETDRS) subfield measurements were compared between sickle cell and control subjects and also among sickle cell hemoglobin subtypes. Associations between ETDRS subfield measurements and hemoglobin subtype, retinopathy stage, and systemic diseases were assessed.
RESULTS: A total of 513 sickle cell eyes (260 patients) and 75 control eyes (39 patients) had median visual acuities of 20/20. ETDRS central (P = .002), inner (nasal P = .009, superior P = .021, temporal P < .001, inferior P = .017), and temporal outer (P = .012) subfield measurements were thinner in sickle cell eyes compared to control eyes. Hemoglobin SS eyes had significantly thinner inner ETDRS subfield measurements compared to SC and SThal eyes. Retinal thinning in all subfields was associated with age (P = .017) for sickle cell and control eyes. No association was found between retinal thinning and hydroxyurea use or arteriovenous anastomosis caliber.
CONCLUSIONS: The macula is thinner in sickle cell eyes compared to control eyes; retinal thickness decreases with increasing age and sickle cell retinopathy stage and is most severe in hemoglobin SS subtypes. NOTE: Publication of this article is sponsored by the American Ophthalmological Society.
Copyright © 2018 Elsevier Inc. All rights reserved.

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Year:  2018        PMID: 29555483      PMCID: PMC6064656          DOI: 10.1016/j.ajo.2018.03.013

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  24 in total

1.  Optical coherence tomography demonstration of macular infarction in sickle cell retinopathy.

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Journal:  Arch Ophthalmol       Date:  2006-05

2.  Relationship between peripheral vascular closure and proliferative retinopathy in sickle cell disease.

Authors:  J C van Meurs
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1991       Impact factor: 3.117

3.  Temporal macular thinning on spectral-domain optical coherence tomography in proliferative sickle cell retinopathy.

Authors:  Ravi K Murthy; Sandeep Grover; Kakarla V Chalam
Journal:  Arch Ophthalmol       Date:  2011-02

4.  Macular and perimacular vascular remodelling sickling haemoglobinopathies.

Authors:  G K Asdourian; K C Nagpal; B Busse; M Goldbaum; D Patriankos; M F Rabb; M F Goldberg
Journal:  Br J Ophthalmol       Date:  1976-06       Impact factor: 4.638

5.  Risk factors for proliferative sickle retinopathy.

Authors:  P D Fox; D T Dunn; J S Morris; G R Serjeant
Journal:  Br J Ophthalmol       Date:  1990-03       Impact factor: 4.638

6.  Classification and pathogenesis of proliferative sickle retinopathy.

Authors:  M F Goldberg
Journal:  Am J Ophthalmol       Date:  1971-03       Impact factor: 5.258

7.  CORRELATION OF MULTIMODAL IMAGING IN SICKLE CELL RETINOPATHY.

Authors:  Khalil Ghasemi Falavarjani; Adrienne W Scott; Kang Wang; Ian C Han; Xuejing Chen; Michael Klufas; Jean-Pierre Hubschman; Steven D Schwartz; Srinivas R Sadda; David Sarraf; Irena Tsui
Journal:  Retina       Date:  2016-12       Impact factor: 4.256

8.  Key endothelial cell angiogenic mechanisms are stimulated by the circulating milieu in sickle cell disease and attenuated by hydroxyurea.

Authors:  Flavia C M Lopes; Fabiola Traina; Camila B Almeida; Flavia C Leonardo; Carla F Franco-Penteado; Vanessa T Garrido; Marina P Colella; Raquel Soares; Sara T Olalla-Saad; Fernando F Costa; Nicola Conran
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9.  Temporal Macular Atrophy as a Predictor of Neovascularization in Sickle Cell Retinopathy.

Authors:  Michael P Hood; Rocio I Diaz; Eric J Sigler; Jorge I Calzada
Journal:  Ophthalmic Surg Lasers Imaging Retina       Date:  2016-01       Impact factor: 1.300

10.  Peripapillary retinal nerve fiber layer thickness in sickle-cell hemoglobinopathies using spectral-domain optical coherence tomography.

Authors:  Clement C Chow; Rohan J Shah; Jennifer I Lim; Felix Y Chau; Joelle A Hallak; Thasarat S Vajaranant
Journal:  Am J Ophthalmol       Date:  2012-12-04       Impact factor: 5.258

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