Jolene McCarney, Katie Curran, Tunde Peto, Giuliana Silvestri, Laura N Cushley
{"title":"The Retinal Complications of C3 Dense Deposit Disease: A Scoping Review.","authors":"Jolene McCarney, Katie Curran, Tunde Peto, Giuliana Silvestri, Laura N Cushley","doi":"10.3390/vision9030064","DOIUrl":null,"url":null,"abstract":"<p><p>People with C3 Dense Deposit Disease (C3DDD), a rare autoimmune disease, often also have ocular complications. Due to the rarity of this disease, there is little known about ocular complications in populations across the world. This paper aimed to assess literature on retinal complications in people with C3 Dense Deposit Disease. A scoping review was conducted and three databases (Embase, Medline All, and Web of Science) were searched using agreed search terms and Boolean operators. All references were imported into Covidence for screening by two reviewers. Any conflicts were resolved by a third reviewer. Data were extracted into an Excel spreadsheet and analysis was conducted using SPSS Version 29. After full text screening, 38 studies were included in the review. These studies were from 1990-2023 and most (67%) being case reports. All studies were conducted in the United States (55%) or Europe (45%). Most studies reported drusen-like deposits in the retina (75%) and retinal pigment epithelial detachment (18%) and macular atrophy (11%). Choroidal Neovascularisation (CNV) was found in 16% of cases. People with C3 Dense Deposit Disease are at risk of ocular complications, primarily drusen-like deposits. Further population-based research and progression is needed.</p>","PeriodicalId":36586,"journal":{"name":"Vision (Switzerland)","volume":"9 3","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371912/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vision (Switzerland)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/vision9030064","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
People with C3 Dense Deposit Disease (C3DDD), a rare autoimmune disease, often also have ocular complications. Due to the rarity of this disease, there is little known about ocular complications in populations across the world. This paper aimed to assess literature on retinal complications in people with C3 Dense Deposit Disease. A scoping review was conducted and three databases (Embase, Medline All, and Web of Science) were searched using agreed search terms and Boolean operators. All references were imported into Covidence for screening by two reviewers. Any conflicts were resolved by a third reviewer. Data were extracted into an Excel spreadsheet and analysis was conducted using SPSS Version 29. After full text screening, 38 studies were included in the review. These studies were from 1990-2023 and most (67%) being case reports. All studies were conducted in the United States (55%) or Europe (45%). Most studies reported drusen-like deposits in the retina (75%) and retinal pigment epithelial detachment (18%) and macular atrophy (11%). Choroidal Neovascularisation (CNV) was found in 16% of cases. People with C3 Dense Deposit Disease are at risk of ocular complications, primarily drusen-like deposits. Further population-based research and progression is needed.
C3致密沉积病(C3DDD)是一种罕见的自身免疫性疾病,常伴有眼部并发症。由于这种疾病的罕见性,对世界各地人群的眼部并发症知之甚少。本文旨在对C3致密沉积病患者视网膜并发症的文献进行评估。进行了范围审查,并使用商定的搜索条件和布尔运算符搜索了三个数据库(Embase、Medline All和Web of Science)。所有参考文献都导入到covid中,由两名审稿人进行筛选。任何冲突都由第三位审稿人解决。将数据提取到Excel电子表格中,并使用SPSS Version 29进行分析。经过全文筛选,38项研究被纳入综述。这些研究从1990年至2023年进行,大多数(67%)是病例报告。所有研究均在美国(55%)或欧洲(45%)进行。大多数研究报告了视网膜中的毒品样沉积物(75%),视网膜色素上皮脱离(18%)和黄斑萎缩(11%)。16%的病例发现脉络膜新生血管(CNV)。C3致密沉积病患者有眼部并发症的风险,主要是毒品样沉积。需要进一步以人群为基础的研究和进展。