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Quantitative Fundus Autofluorescence in HCQ Retinopathy

PURPOSE: To increase our understanding of the mechanisms underlying hydroxychloroquine (HCQ) retinopathy, analyses by quantitative fundus autofluorescence (qAF) and near-infrared fundus autofluorescence (NIR-AF) were compared to results obtained by recommended screening tests. METHODS: Thirty-one pa...

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Autores principales: Greenstein, Vivienne C., Lima de Carvalho, Jose Ronaldo, Parmann, Rait, Amaro-Quireza, Luz, Lee, Winston, Hood, Donald C., Tsang, Stephen H., Sparrow, Janet R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521180/
https://www.ncbi.nlm.nih.gov/pubmed/32976563
http://dx.doi.org/10.1167/iovs.61.11.41
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author Greenstein, Vivienne C.
Lima de Carvalho, Jose Ronaldo
Parmann, Rait
Amaro-Quireza, Luz
Lee, Winston
Hood, Donald C.
Tsang, Stephen H.
Sparrow, Janet R.
author_facet Greenstein, Vivienne C.
Lima de Carvalho, Jose Ronaldo
Parmann, Rait
Amaro-Quireza, Luz
Lee, Winston
Hood, Donald C.
Tsang, Stephen H.
Sparrow, Janet R.
author_sort Greenstein, Vivienne C.
collection PubMed
description PURPOSE: To increase our understanding of the mechanisms underlying hydroxychloroquine (HCQ) retinopathy, analyses by quantitative fundus autofluorescence (qAF) and near-infrared fundus autofluorescence (NIR-AF) were compared to results obtained by recommended screening tests. METHODS: Thirty-one patients (28 females, 3 males) were evaluated with standard automated perimetry and spectral domain optical coherence tomography (SD-OCT); 28 also had multifocal electroretinography (mfERG). Measurement of short-wavelength fundus autofluorescence (SW-AF) by qAF involved the use of an internal fluorescent reference and intensity measurements in eight concentric segments at 7° to 9° eccentricity. For semiquantitative analysis of NIR-AF, intensities were acquired along a vertical axis through the fovea. RESULTS: Four of 15 high-dose (total dose >1000 g, daily dose >5.0 mg/kg) patients and one of 16 low-dose (total dose <1000 g, daily dose 4.4 mg/kg) patients were diagnosed with HCQ-associated retinopathy based on abnormal 10-2 visual fields, SD-OCT, and SW-AF imaging. Three of the high-dose patients also had abnormal mfERG results. Of the five patients exhibiting retinopathy, two had qAF color-coded images revealing higher intensities inferior, nasal, and lateral to the fovea. The abnormal visual fields also exhibited superior-inferior differences. Mean NIR-AF gray-level intensities were increased in four high-dose patients with no evidence of retinopathy. In two patients with retinopathy, NIR-AF intensity within the parafovea was below the normal range. One high-dose patient (6.25 mg/kg) had only abnormal mfERG results. CONCLUSIONS: These findings indicate that screening for HCQ retinopathy should take into consideration superior-inferior differences in susceptibility to HCQ retinopathy.
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spelling pubmed-75211802020-10-05 Quantitative Fundus Autofluorescence in HCQ Retinopathy Greenstein, Vivienne C. Lima de Carvalho, Jose Ronaldo Parmann, Rait Amaro-Quireza, Luz Lee, Winston Hood, Donald C. Tsang, Stephen H. Sparrow, Janet R. Invest Ophthalmol Vis Sci Retina PURPOSE: To increase our understanding of the mechanisms underlying hydroxychloroquine (HCQ) retinopathy, analyses by quantitative fundus autofluorescence (qAF) and near-infrared fundus autofluorescence (NIR-AF) were compared to results obtained by recommended screening tests. METHODS: Thirty-one patients (28 females, 3 males) were evaluated with standard automated perimetry and spectral domain optical coherence tomography (SD-OCT); 28 also had multifocal electroretinography (mfERG). Measurement of short-wavelength fundus autofluorescence (SW-AF) by qAF involved the use of an internal fluorescent reference and intensity measurements in eight concentric segments at 7° to 9° eccentricity. For semiquantitative analysis of NIR-AF, intensities were acquired along a vertical axis through the fovea. RESULTS: Four of 15 high-dose (total dose >1000 g, daily dose >5.0 mg/kg) patients and one of 16 low-dose (total dose <1000 g, daily dose 4.4 mg/kg) patients were diagnosed with HCQ-associated retinopathy based on abnormal 10-2 visual fields, SD-OCT, and SW-AF imaging. Three of the high-dose patients also had abnormal mfERG results. Of the five patients exhibiting retinopathy, two had qAF color-coded images revealing higher intensities inferior, nasal, and lateral to the fovea. The abnormal visual fields also exhibited superior-inferior differences. Mean NIR-AF gray-level intensities were increased in four high-dose patients with no evidence of retinopathy. In two patients with retinopathy, NIR-AF intensity within the parafovea was below the normal range. One high-dose patient (6.25 mg/kg) had only abnormal mfERG results. CONCLUSIONS: These findings indicate that screening for HCQ retinopathy should take into consideration superior-inferior differences in susceptibility to HCQ retinopathy. The Association for Research in Vision and Ophthalmology 2020-09-25 /pmc/articles/PMC7521180/ /pubmed/32976563 http://dx.doi.org/10.1167/iovs.61.11.41 Text en Copyright 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Retina
Greenstein, Vivienne C.
Lima de Carvalho, Jose Ronaldo
Parmann, Rait
Amaro-Quireza, Luz
Lee, Winston
Hood, Donald C.
Tsang, Stephen H.
Sparrow, Janet R.
Quantitative Fundus Autofluorescence in HCQ Retinopathy
title Quantitative Fundus Autofluorescence in HCQ Retinopathy
title_full Quantitative Fundus Autofluorescence in HCQ Retinopathy
title_fullStr Quantitative Fundus Autofluorescence in HCQ Retinopathy
title_full_unstemmed Quantitative Fundus Autofluorescence in HCQ Retinopathy
title_short Quantitative Fundus Autofluorescence in HCQ Retinopathy
title_sort quantitative fundus autofluorescence in hcq retinopathy
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521180/
https://www.ncbi.nlm.nih.gov/pubmed/32976563
http://dx.doi.org/10.1167/iovs.61.11.41
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