{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Woof WA"],"funding":["National Institute for Health Research (NIHR)","Wellcome Trust","NIHR Moorfields Biomedical Research Centre"],"pagination":["100652"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11782848"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["5(2)"],"pubmed_abstract":["<h4>Purpose</h4>To quantify relevant fundus autofluorescence (FAF) features cross-sectionally and longitudinally in a large cohort of patients with inherited retinal diseases (IRDs).<h4>Design</h4>Retrospective study of imaging data.<h4>Participants</h4>Patients with a clinical and molecularly confirmed diagnosis of IRD who have undergone 55° FAF imaging at Moorfields Eye Hospital (MEH) and the Royal Liverpool Hospital between 2004 and 2019.<h4>Methods</h4>Five FAF features of interest were defined: vessels, optic disc, perimacular ring of increased signal (ring), relative hypo-autofluorescence (hypo-AF), and hyper-autofluorescence (hyper-AF). Features were manually annotated by 6 graders in a subset of patients based on a defined grading protocol to produce segmentation masks to train an artificial intelligence model, AIRDetect, which was then applied to the entire imaging data set.<h4>Main outcome measures</h4>Quantitative FAF features, including area and vessel metrics, were analyzed cross-sectionally by gene and age, and longitudinally. AIRDetect feature segmentation and detection were validated with Dice score and precision/recall, respectively.<h4>Results</h4>A total of 45 749 FAF images from 3606 patients with IRD from MEH covering 170 genes were automatically segmented using AIRDetect. Model-grader Dice scores for the disc, hypo-AF, hyper-AF, ring, and vessels were, respectively, 0.86, 0.72, 0.69, 0.68, and 0.65. Across patients at presentation, the 5 genes with the largest hypo-AF areas were <i>CHM</i>, <i>ABCC6</i>, <i>RDH12</i>, <i>ABCA4</i>, and <i>RPE65</i>, with mean per-patient areas of 43.72, 29.57, 20.07, 19.65, and 16.92 mm<sup>2</sup>, respectively. The 5 genes with the largest hyper-AF areas were <i>BEST1</i>, <i>CDH23</i>, <i>NR2E3</i>, <i>MYO7A</i>, and <i>RDH12</i>, with mean areas of 0.50, 047, 0.44, 0.38, and 0.33 mm<sup>2</sup>, respectively. The 5 genes with the largest ring areas were <i>NR2E3, CDH23</i>, <i>CRX</i>, <i>EYS</i>, and <i>PDE6B</i>, with mean areas of 3.60, 2.90, 2.89, 2.56, and 2.20 mm<sup>2</sup>, respectively. Vessel density was found to be highest in <i>EFEMP1</i>, <i>BEST1</i>, <i>TIMP3</i>, <i>RS1</i>, and <i>PRPH2</i> (11.0%, 10.4%, 10.1%, 10.1%, 9.2%) and was lower in retinitis pigmentosa (RP) and Leber congenital amaurosis genes. Longitudinal analysis of decreasing ring area in 4 RP genes (<i>RPGR</i>, <i>USH2A</i>, <i>RHO</i>, and <i>EYS</i>) found <i>EYS</i> to be the fastest progressor at -0.178 mm<sup>2</sup>/year.<h4>Conclusions</h4>We have conducted the first large-scale cross-sectional and longitudinal quantitative analysis of FAF features across a diverse range of IRDs using a novel AI approach.<h4>Financial disclosures</h4>Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article."],"journal":["Ophthalmology science"],"pubmed_title":["Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom."],"pmcid":["PMC11782848"],"funding_grant_id":["206619/Z/17/Z"],"pubmed_authors":["Shah M","Furman J","Moosajee M","Sallum J","Lin S","Downes SM","Webster AR","Liefers BJ","Fu DJ","Woof WA","Mendes B","de Guimaraes TAC","Bagga P","Patel P","Liu Y","Burke P","Georgiou M","Sousa da Silva A","Mahroo OA","Madhusudhan S","Parry D","Holz FG","Ghoshal B","Al-Khuzaei S","Fujinami-Yokokawa Y","Pontikos N","Moghul I","Daich Varela M","Nguyen Q","Fujinami K","Michaelides M","Sen S","Balaskas K","De Silva SR","Sumodhee D","Lorenz B","Naik G"],"additional_accession":[]},"is_claimable":false,"name":"Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom.","description":"<h4>Purpose</h4>To quantify relevant fundus autofluorescence (FAF) features cross-sectionally and longitudinally in a large cohort of patients with inherited retinal diseases (IRDs).<h4>Design</h4>Retrospective study of imaging data.<h4>Participants</h4>Patients with a clinical and molecularly confirmed diagnosis of IRD who have undergone 55° FAF imaging at Moorfields Eye Hospital (MEH) and the Royal Liverpool Hospital between 2004 and 2019.<h4>Methods</h4>Five FAF features of interest were defined: vessels, optic disc, perimacular ring of increased signal (ring), relative hypo-autofluorescence (hypo-AF), and hyper-autofluorescence (hyper-AF). Features were manually annotated by 6 graders in a subset of patients based on a defined grading protocol to produce segmentation masks to train an artificial intelligence model, AIRDetect, which was then applied to the entire imaging data set.<h4>Main outcome measures</h4>Quantitative FAF features, including area and vessel metrics, were analyzed cross-sectionally by gene and age, and longitudinally. AIRDetect feature segmentation and detection were validated with Dice score and precision/recall, respectively.<h4>Results</h4>A total of 45 749 FAF images from 3606 patients with IRD from MEH covering 170 genes were automatically segmented using AIRDetect. Model-grader Dice scores for the disc, hypo-AF, hyper-AF, ring, and vessels were, respectively, 0.86, 0.72, 0.69, 0.68, and 0.65. Across patients at presentation, the 5 genes with the largest hypo-AF areas were <i>CHM</i>, <i>ABCC6</i>, <i>RDH12</i>, <i>ABCA4</i>, and <i>RPE65</i>, with mean per-patient areas of 43.72, 29.57, 20.07, 19.65, and 16.92 mm<sup>2</sup>, respectively. The 5 genes with the largest hyper-AF areas were <i>BEST1</i>, <i>CDH23</i>, <i>NR2E3</i>, <i>MYO7A</i>, and <i>RDH12</i>, with mean areas of 0.50, 047, 0.44, 0.38, and 0.33 mm<sup>2</sup>, respectively. The 5 genes with the largest ring areas were <i>NR2E3, CDH23</i>, <i>CRX</i>, <i>EYS</i>, and <i>PDE6B</i>, with mean areas of 3.60, 2.90, 2.89, 2.56, and 2.20 mm<sup>2</sup>, respectively. Vessel density was found to be highest in <i>EFEMP1</i>, <i>BEST1</i>, <i>TIMP3</i>, <i>RS1</i>, and <i>PRPH2</i> (11.0%, 10.4%, 10.1%, 10.1%, 9.2%) and was lower in retinitis pigmentosa (RP) and Leber congenital amaurosis genes. Longitudinal analysis of decreasing ring area in 4 RP genes (<i>RPGR</i>, <i>USH2A</i>, <i>RHO</i>, and <i>EYS</i>) found <i>EYS</i> to be the fastest progressor at -0.178 mm<sup>2</sup>/year.<h4>Conclusions</h4>We have conducted the first large-scale cross-sectional and longitudinal quantitative analysis of FAF features across a diverse range of IRDs using a novel AI approach.<h4>Financial disclosures</h4>Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Mar-Apr","modification":"2026-05-26T20:12:04.985Z","creation":"2025-04-05T23:33:58.866Z"},"accession":"S-EPMC11782848","cross_references":{"pubmed":["39896422"],"doi":["10.1016/j.xops.2024.100652"]}}