CHOROIDAL VASCULARITY INDEX IN YOUNG CHOROIDEREMIA PATIENTS.


Journal

Retina (Philadelphia, Pa.)
ISSN: 1539-2864
Titre abrégé: Retina
Pays: United States
ID NLM: 8309919

Informations de publication

Date de publication:
01 May 2021
Historique:
pubmed: 23 8 2020
medline: 15 12 2021
entrez: 23 8 2020
Statut: ppublish

Résumé

To evaluate choroidal features in young patients affected by choroideremia (CHM). Young CHM patients and control subjects were recruited at the Eye Clinic in Florence. High-resolution choroidal imaging was obtained using swept-source optical coherence tomography with long optical coherence tomography scans (12 × 9 mm optical coherence tomography scans). We considered the subfoveal choroidal area within 9 mm of the optic disk in the horizontal plane and the subfoveal choroidal area within a 3-mm diameter centered over the fovea. The subfoveal choroidal thickness, total choroidal area, luminal area, stromal area, and choroidal vascularity index were assessed using the "ImageJ" software in both groups. Eight patients (16 eyes; mean age, 19.3 ± 5.2 years) and seven control subjects (14 eyes; mean age, 19.0 ± 5.0 years) were included in this study. Best-corrected visual acuity was 20/20 in both eyes of seven CHM patients and in all control subjects and 20/25 in both eyes in one CHM patient. Mean subfoveal choroidal thickness did not differ between CHM patients and control subjects. Luminal area9mm, stromal area9mm, and total choroidal area9mm were reduced in patients compared with the control group. Luminal area3mm, stromal area3mm, and total choroidal area3mm did not differ between patients and control subjects. Choroidal vascularity index9mm and choroidal vascularity index3mm were not different between patients and control subjects. There are no differences in the choroidal vascularity index between young CHM patients and control subjects; this result suggests a simultaneous, proportional impairment of both the stromal and vascular components of the choroid in the early stages of the disease.

Identifiants

pubmed: 32826791
pii: 00006982-202105000-00016
doi: 10.1097/IAE.0000000000002960
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1018-1025

Références

Mitsios A, Dubis AM, Moosajee M. Choroideremia: from genetic and clinical phenotyping to gene therapy and future treatments. Ther Adv Ophthalmol 2018;10:2515841418817490.
Jacobson SG, Cideciyan AV, Sumaroka A, et al. Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutations. Invest Ophthalmol Vis Sci 2006;47:4113–4120.
Aleman TS, Han G, Serrano LW, et al. Natural history of the central structural abnormalities in choroideremia: a prospective cross-sectional study. Ophthalmology 2017;124:359–373.
Duncan JL, Aleman TS, Gardner LM, et al. Macular pigment and lutein supplementation in choroideremia. Exp Eye Res 2002;74:371–381.
Drexler W, Fujimoto JG. State-of-the-art retinal optical coherence tomography. Prog Retin Eye Res 2008;27:45–88. Review.
Xue K, Oldani M, Jolly JK, et al. Correlation of optical coherence tomography and autofluorescence in the outer retina and choroid of patients with choroideremia. Invest Ophthalmol Vis Sci 2016;57:3674–3684.
Spaide RF. Enhanced depth imaging optical coherence tomography of retinal pigment epithelial detachment in age-related macular degeneration. Am J Ophthalmol 2009;147:644–652.
Abbouda A, Dubis AM, Webster AR, Moosajee M. Identifying characteristic features of the retinal and choroidal vasculature in choroideremia using optical coherence tomography angiography. Eye (Lond) 2018;32:563–571.
Murro V, Mucciolo DP, Giorgio D, et al. Optical coherence tomography angiography (OCT-A) in young choroideremia (CHM) patients. Ophthalmic Genet 2019;40:201–206.
Agrawal R, Gupta P, Tan K, et al. Choroidal vascularity index as a measure of vascular status of the choroid: measurements in healthy eyes from a population-based study. Sci Rep 2016;6:21090.
Agrawal R, Ding J, Sen P, et al.; CVI.grid. Exploring choroidal angioarchitecture in health and disease using choroidal vascularity index. Prog Retin Eye Res 2020:100829.
Agrawal R, Salman M, Tan KA, et al. Choroidal vascularity index (CVI): a novel optical coherence tomography parameter for monitoring patients with panuveitis? PLoS One 2016;11:e0146344.
Agrawal R, Chhablani J, Tan KA, et al. Choroidal vascularity index in central serous chorioretinopathy. Retina 2016;36:1646–1651.
Iovino C, Au A, Hilely A, et al. Evaluation of the choroid in eyes with retinitis pigmentosa and cystoid macular edema. Invest Ophthalmol Vis Sci 2019;60:5000–5006.
Cetin EN, Parca O, Akkaya HS, Pekel G. Association of retinal biomarkers and choroidal vascularity index on optical coherence tomography using binarization method in retinitis pigmentosa. Graefes Arch Clin Exp Ophthalmol 2020;258:23–30.
Iovino C, Pellegrini M, Bernabei F, et al. Choroidal vascularity index: an in-depth analysis of this novel optical coherence tomography parameter. J Clin Med 2020;9:595.
Khan KN, Islam F, Moore AT, Michaelides M. Clinical and genetic features of choroideremia in childhood. Ophthalmology 2016;123:2158–2165.
Mucciolo DP, Murro V, Sodi A, et al. Peculiar clinical findings in young choroideremia patients: a retrospective case review. Ophthalmologica 2019;242:195–207.
Abbouda A, Lim WS, Sprogyte L, et al. Quantitative and qualitative features of spectral-domain optical coherence tomography provide prognostic indicators for visual acuity in patients with choroideremia. Ophthalmic Surg Lasers Imaging Retina 2017;48:711–716.
Murro V, Mucciolo DP, Giorgio D, et al. Optical coherence tomography (OCT) features of cystoid spaces in choroideremia (CHM). Graefes Arch Clin Exp Ophthalmol 2019;257:2655–2663.
Touhami S, Philippakis E, Mrejen S, et al. Topographic variations of choroidal thickness in healthy eyes on swept-source optical coherence tomography. Invest Ophthalmol Vis Sci 2020;61:38.
Rodrigues MM, Ballantine EJ, Wiggert BN, et al. Choroideremia: clinical, electron microscopic and biochemical report. Ophthalmology 1984;91 :873–883.
McCulloch C. Choroideremia: a clinical and pathologic review. Can J Ophthalmol 1969;67:142–195.
Ghosh M, McCulloch JC. Pathological findings from two cases of choroideremia. Can J Ophthalmol 1980;15:147–153.
Flannery JG, Bird AC, Farber DD, et al. A histopathologic study of a choroideremio carrier. Invest Ophthalmol Vis Sci 1990;31:229–236.
Agarwal A, Agrawal R, Khandelwal N, et al. Choroidal structural changes in tubercular multifocal serpiginoid choroiditis. Ocul Immunol Inflamm 2018;26:838–844.
Wei X, Ting DSW, Ng WY, et al. Choroidal vascularity index: a novel optical coherence tomography based parameter in patients with exudative age-related macular degeneration. Retina 2017;37:1120–1125.
Cameron JD, Fine BS, Shapiro I. Histopathologic observations in choroideremia with emphasis on vascular changes of the uveal tract. Ophthalmology 1987;94:187–196.
Noble KG, Carr RE, Siegel IM. Fluorescein angiography of the hereditary choroidal dystrophies. Br J Ophthalmol 1977;61:43–53.
Forsius H, Hyvärinen L, Nieminen H, Flower R. Fluorescein and indocyanine green fluorescence angiography in study of affected males and in female carriers with choroidermia. A preliminary report. Acta Ophthalmol (Copenh) 1977;55:459–470.
MacDonald IM, Russell L, Chan CC. Choroideremia: new findings from ocular pathology and review of recent literature. Surv Ophthalmol 2009;54:401–407.
Kim RY, Chung DH, Kim M, Park YH. Use of choroidal vascularity index for choroidal structural evaluation in central serous chorioretinopathy with choroidal neovascularization. Retina 2019;40:1395–1402.

Auteurs

Vittoria Murro (V)

Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy; and.

Dario Pasquale Mucciolo (DP)

Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy; and.

Dario Giorgio (D)

Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy; and.

Ilaria Passerini (I)

Department of Genetic Diagnosis, Careggi University Hospital, Florence, Italy.

Francesca Cipollini (F)

Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy; and.

Gianni Virgili (G)

Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy; and.

Fabrizio Giansanti (F)

Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy; and.

Andrea Sodi (A)

Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy; and.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH