Kapoor Ishani, Sarvepalli Swara M, Grewal Dilraj S, Hadziahmetovic Majda
Drexel University College of Medicine, Philadelphia, Pennsylvania.
Department of Ophthalmology, Indiana University School of Medicine, Indianapolis, Indiana.
Ophthalmol Sci. 2024 Sep 12;5(1):100622. doi: 10.1016/j.xops.2024.100622. eCollection 2025 Jan-Feb.
Autoimmune retinopathy (AIR) is a group of rare inflammatory diseases treated with immunosuppression; however, there is no treatment consensus. This meta-analysis and review aims to investigate treatment effectiveness in slowing AIR progression.
Autoimmune retinopathy is a group of diseases characterized by progressive vision loss that is both difficult to diagnose and treat. While there is some consensus regarding diagnostic criteria, evidence-based treatment consensus remains poorly understood. Current first-line treatment is systemic steroids and conventional steroid-sparing agents. However, patients often experience treatment failure and systemic adverse effects with these medications. Understanding the effect of medications on slowing multiple visual outcomes in AIR can help to guide future treatment protocols.
PubMed, Cochrane Library, Embase, and ClinicalTrials.gov were systematically searched from inception to November 2023. Included studies treated patients with AIR with systemic, local, and biologic therapy and reported visual acuity (VA), visual field (VF), cystoid macular edema (CME), electroretinogram, central retinal thickness (CRT), and/or ellipsoid zone (EZ) loss. Risk of bias was assessed using the Critical Appraisal Skills Programme checklist. Data for meta-analysis were pooled using a random-effects model.
Analysis of 40 case reports demonstrated that treatment type significantly affects the improvement of VA in patients with nonparaneoplastic retinopathy. Meta-analysis of 12 studies demonstrated that any treatment decreases the risk of progression of all 6 outcomes. Systemic therapy slows VA loss (risk ratio [RR] = 0.04, 95% confidence interval [0.00, 0.91], = 0.04), VF loss (RR = 0.01, 95% confidence interval [0.00, 0.14], = 0.0007), and CME (RR = 0.02, 95% confidence interval [0.00, 0.34], = 0.007). Local therapy slows VA loss (RR = 0.02, 95% confidence interval [0.00, 0.12], < 0.00001), CME (RR = 0.06, 95% confidence interval [0.01, 0.43], = 0.005), CRT loss (RR = 0.02, 95% confidence interval [0.00, 0.36], = 0.007), and EZ loss (RR = 0.31, 95% confidence interval [0.14, 0.70], = 0.004). Biologics slow VA loss (RR = 0.28, 95% confidence interval [0.12, 0.65], = 0.003), VF loss (RR = 0.25, 95% confidence interval [0.15, 0.42], < 0.00001), and CRT loss (RR = 0.19, 95% confidence interval [0.04, 0.79], = 0.02).
Systemic therapy significantly reduces the risk of progressive visual loss. Local therapy significantly decreases the risk of both progressive visual loss and retinal morphology loss, and therefore may offer precise targeting of the retina. Biologics significantly reduce both functional and morphological retinal changes. Immunosuppressive therapy may slow AIR progression; however, additional research is needed to assess long-term outcomes.
The author(s) have no proprietary or commercial interest in any materials discussed in this article.
自身免疫性视网膜病变(AIR)是一组采用免疫抑制治疗的罕见炎症性疾病;然而,目前尚无治疗共识。本荟萃分析及综述旨在研究减缓AIR进展的治疗效果。
自身免疫性视网膜病变是一组以进行性视力丧失为特征的疾病,诊断和治疗都很困难。虽然在诊断标准方面存在一些共识,但基于证据的治疗共识仍知之甚少。目前的一线治疗是全身用类固醇和传统的类固醇替代药物。然而,患者使用这些药物时经常出现治疗失败和全身不良反应。了解药物对减缓AIR多种视觉结局的作用有助于指导未来的治疗方案。
对PubMed、Cochrane图书馆、Embase和ClinicalTrials.gov进行系统检索,检索时间从建库至2023年11月。纳入的研究对AIR患者采用全身、局部和生物治疗,并报告了视力(VA)、视野(VF)、黄斑囊样水肿(CME)、视网膜电图、中心视网膜厚度(CRT)和/或椭圆体带(EZ)损失。使用关键评估技能计划清单评估偏倚风险。采用随机效应模型汇总荟萃分析的数据。
对40例病例报告的分析表明,治疗类型对非副肿瘤性视网膜病变患者的VA改善有显著影响。对12项研究的荟萃分析表明,任何治疗均可降低所有6种结局进展的风险。全身治疗减缓VA损失(风险比[RR]=0.04,95%置信区间[0.00,0.91],P=0.04)、VF损失(RR=0.01,95%置信区间[0.00,0.14],P=0.0007)和CME(RR=0.02,95%置信区间[0.00,0.34],P=0.007)。局部治疗减缓VA损失(RR=0.02,95%置信区间[0.00,0.12],P<0.00001)、CME(RR=0.06,95%置信区间[0.01,0.43],P=0.005)、CRT损失(RR=0.02,95%置信区间[0.00,0.36],P=0.007)和EZ损失(RR=0.31,95%置信区间[0.14,0.70],P=0.004)。生物制剂减缓VA损失(RR=0.28,95%置信区间[0.12,0.65],P=0.003)、VF损失(RR=0.25,95%置信区间[0.15,0.42],P<0.00001)和CRT损失(RR=0.19,95%置信区间[0.04,0.79],P=0.02)。
全身治疗显著降低进行性视力丧失的风险。局部治疗显著降低进行性视力丧失和视网膜形态学丧失的风险,因此可能对视网膜具有精确的靶向作用。生物制剂显著减少视网膜的功能和形态学改变。免疫抑制治疗可能减缓AIR的进展;然而,需要进一步研究来评估长期结局。
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