HYPERREFLECTIVE FOCI AS A PATHOGENETIC BIOMARKER IN CHOROIDEREMIA

Standard

HYPERREFLECTIVE FOCI AS A PATHOGENETIC BIOMARKER IN CHOROIDEREMIA. / Romano, Francesco; Arrigo, Alessandro; MacLaren, Robert E; Charbel Issa, Peter; Birtel, Johannes; Bandello, Francesco; Battaglia Parodi, Maurizio.

In: RETINA-J RET VIT DIS, Vol. 40, No. 8, 08.2020, p. 1634-1640.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Romano, F, Arrigo, A, MacLaren, RE, Charbel Issa, P, Birtel, J, Bandello, F & Battaglia Parodi, M 2020, 'HYPERREFLECTIVE FOCI AS A PATHOGENETIC BIOMARKER IN CHOROIDEREMIA', RETINA-J RET VIT DIS, vol. 40, no. 8, pp. 1634-1640. https://doi.org/10.1097/IAE.0000000000002645

APA

Romano, F., Arrigo, A., MacLaren, R. E., Charbel Issa, P., Birtel, J., Bandello, F., & Battaglia Parodi, M. (2020). HYPERREFLECTIVE FOCI AS A PATHOGENETIC BIOMARKER IN CHOROIDEREMIA. RETINA-J RET VIT DIS, 40(8), 1634-1640. https://doi.org/10.1097/IAE.0000000000002645

Vancouver

Romano F, Arrigo A, MacLaren RE, Charbel Issa P, Birtel J, Bandello F et al. HYPERREFLECTIVE FOCI AS A PATHOGENETIC BIOMARKER IN CHOROIDEREMIA. RETINA-J RET VIT DIS. 2020 Aug;40(8):1634-1640. https://doi.org/10.1097/IAE.0000000000002645

Bibtex

@article{737c19253b334eeabe5c28d577017922,
title = "HYPERREFLECTIVE FOCI AS A PATHOGENETIC BIOMARKER IN CHOROIDEREMIA",
abstract = "PURPOSE: To assess hyperreflective foci (HF) number and distribution in choroideremia (CHM) using spectral domain optical coherence tomography.METHODS: Observational, cross-sectional case series. Consecutive patients and matched controls (20 eyes each) underwent best-corrected visual acuity measurement, fundoscopy, blue-light autofluorescence (BL-FAF) and spectral domain optical coherence tomography. Hyperreflective foci were assessed on a horizontal spectral domain optical coherence tomography scan, in the 500-µm area centered on the umbo, and in the 500-μm-wide areas internal (preserved border) and external (pathologic border) to the chorioretinal atrophy of CHM patients, and in the parafovea of controls. Hyperreflective foci were subclassified as retinal or choroidal. The spared central islet was measured on BL-FAF. Primary outcome was HF quantification in CHM. Secondary outcomes included their relationships with atrophy extent.RESULTS: Choroideremia eyes disclosed a significantly higher HF number across the pathologic border and in the fovea when compared with controls; in particular, these HF were primarily located in the choroid (59-87%). Moreover, choroidal HF in the pathologic border inversely correlated with the area of the preserved central islet.CONCLUSION: Hyperreflective foci might turn out to be a potential biomarker of CHM activity or severity. In this regard, we hypothesize that HF may be related to macrophages activation or progressive retinal pigment epithelium degeneration.",
keywords = "Adaptor Proteins, Signal Transducing/genetics, Adult, Biomarkers, Choroid/pathology, Choroideremia/diagnosis, Cross-Sectional Studies, Humans, Male, Middle Aged, Tomography, Optical Coherence, Visual Acuity/physiology",
author = "Francesco Romano and Alessandro Arrigo and MacLaren, {Robert E} and {Charbel Issa}, Peter and Johannes Birtel and Francesco Bandello and {Battaglia Parodi}, Maurizio",
year = "2020",
month = aug,
doi = "10.1097/IAE.0000000000002645",
language = "English",
volume = "40",
pages = "1634--1640",
journal = "RETINA-J RET VIT DIS",
issn = "0275-004X",
publisher = "Lippincott Williams and Wilkins",
number = "8",

}

RIS

TY - JOUR

T1 - HYPERREFLECTIVE FOCI AS A PATHOGENETIC BIOMARKER IN CHOROIDEREMIA

AU - Romano, Francesco

AU - Arrigo, Alessandro

AU - MacLaren, Robert E

AU - Charbel Issa, Peter

AU - Birtel, Johannes

AU - Bandello, Francesco

AU - Battaglia Parodi, Maurizio

PY - 2020/8

Y1 - 2020/8

N2 - PURPOSE: To assess hyperreflective foci (HF) number and distribution in choroideremia (CHM) using spectral domain optical coherence tomography.METHODS: Observational, cross-sectional case series. Consecutive patients and matched controls (20 eyes each) underwent best-corrected visual acuity measurement, fundoscopy, blue-light autofluorescence (BL-FAF) and spectral domain optical coherence tomography. Hyperreflective foci were assessed on a horizontal spectral domain optical coherence tomography scan, in the 500-µm area centered on the umbo, and in the 500-μm-wide areas internal (preserved border) and external (pathologic border) to the chorioretinal atrophy of CHM patients, and in the parafovea of controls. Hyperreflective foci were subclassified as retinal or choroidal. The spared central islet was measured on BL-FAF. Primary outcome was HF quantification in CHM. Secondary outcomes included their relationships with atrophy extent.RESULTS: Choroideremia eyes disclosed a significantly higher HF number across the pathologic border and in the fovea when compared with controls; in particular, these HF were primarily located in the choroid (59-87%). Moreover, choroidal HF in the pathologic border inversely correlated with the area of the preserved central islet.CONCLUSION: Hyperreflective foci might turn out to be a potential biomarker of CHM activity or severity. In this regard, we hypothesize that HF may be related to macrophages activation or progressive retinal pigment epithelium degeneration.

AB - PURPOSE: To assess hyperreflective foci (HF) number and distribution in choroideremia (CHM) using spectral domain optical coherence tomography.METHODS: Observational, cross-sectional case series. Consecutive patients and matched controls (20 eyes each) underwent best-corrected visual acuity measurement, fundoscopy, blue-light autofluorescence (BL-FAF) and spectral domain optical coherence tomography. Hyperreflective foci were assessed on a horizontal spectral domain optical coherence tomography scan, in the 500-µm area centered on the umbo, and in the 500-μm-wide areas internal (preserved border) and external (pathologic border) to the chorioretinal atrophy of CHM patients, and in the parafovea of controls. Hyperreflective foci were subclassified as retinal or choroidal. The spared central islet was measured on BL-FAF. Primary outcome was HF quantification in CHM. Secondary outcomes included their relationships with atrophy extent.RESULTS: Choroideremia eyes disclosed a significantly higher HF number across the pathologic border and in the fovea when compared with controls; in particular, these HF were primarily located in the choroid (59-87%). Moreover, choroidal HF in the pathologic border inversely correlated with the area of the preserved central islet.CONCLUSION: Hyperreflective foci might turn out to be a potential biomarker of CHM activity or severity. In this regard, we hypothesize that HF may be related to macrophages activation or progressive retinal pigment epithelium degeneration.

KW - Adaptor Proteins, Signal Transducing/genetics

KW - Adult

KW - Biomarkers

KW - Choroid/pathology

KW - Choroideremia/diagnosis

KW - Cross-Sectional Studies

KW - Humans

KW - Male

KW - Middle Aged

KW - Tomography, Optical Coherence

KW - Visual Acuity/physiology

U2 - 10.1097/IAE.0000000000002645

DO - 10.1097/IAE.0000000000002645

M3 - SCORING: Journal article

C2 - 31800458

VL - 40

SP - 1634

EP - 1640

JO - RETINA-J RET VIT DIS

JF - RETINA-J RET VIT DIS

SN - 0275-004X

IS - 8

ER -