依普利酮和螺内酯治疗慢性中枢性浆液性脉络膜视网膜病变:一项系统评价和荟萃分析:依普利酮和螺内酯治疗CSCR。

IF 4.1 1区 医学 Q1 OPHTHALMOLOGY
Ryan S Huang, Andrew Mihalache, Ali Benour, Michele Zaman, Marko M Popovic, Peter J Kertes, Rajeev H Muni, David Sarraf, SriniVas R Sadda, Radha P Kohly
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引用次数: 0

摘要

主题:评价矿皮质激素受体拮抗剂(MRAs),特别是eplerenone和螺内酯,与观察、光动力治疗(PDT)和阈下微脉冲激光(SML)治疗慢性中枢性浆液性脉络膜视网膜病变(cCSCR)的疗效和安全性。临床相关性:在cCSCR的背景下,MRAs被认为通过抑制导致液体积聚的矿皮质激素受体途径来降低脉络膜血管的高渗透性和厚度。方法:从2000年1月至2024年3月,使用Ovid MEDLINE、Embase和Cochrane Library进行系统的文献检索,比较MRAs与其他cCSCR治疗组的疗效。主要结果是最后一次研究访问时的最佳矫正视力(BCVA),以及特定随访时间点(即1个月、3个月、6个月、12个月)。次要结局包括同一时间点视网膜厚度(RT)、视网膜下液(SRF)高度和SRF分辨率。采用随机效应模型进行meta分析,分别对依普利酮和螺内酯进行亚组分析。p值小于0.05被认为具有统计学意义。结果:纳入13篇文献(4篇rct报告253只眼,9篇观察性研究报告393只眼,平均随访时间=7.02±3.78个月)。MRA组与观察组最后一次研究访视时的平均BCVA相似(WMD=-0.01 logMAR, 95%CI=[-0.05, 0.02], p=0.40, n=5项研究)。然而,MRAs导致1个月时SRF平均高度显著降低(WMD=-69.56µm, 95% CI [-127.26, -11.86], p=0.02, n=2项研究),而观察组在12个月时SRF高度显著降低(WMD=48.23µm, 95% CI [45.99, 50.46], p结论:MRAs在降低SRF方面具有短期益处,但根据目前的证据,可能具有有限的长期持久性,强调需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eplerenone and Spironolactone for Chronic Central Serous Chorioretinopathy: A Systematic Review and Meta-Analysis: Eplerenone and Spironolactone for CSCR.

Topic: To evaluate the efficacy and safety of mineralocorticoid receptor antagonists (MRAs), specifically eplerenone and spironolactone, in comparison to observation, photodynamic therapy (PDT), and subthreshold micropulse laser (SML) for chronic central serous chorioretinopathy (cCSCR).

Clinical relevance: In the context of cCSCR, MRAs are thought to reduce choroidal vascular hyperpermeability and thickness by inhibiting the mineralocorticoid receptor pathways that contribute to fluid accumulation.

Methods: A systematic literature search was performed using Ovid MEDLINE, Embase, and the Cochrane Library from January 2000 to March 2024 for comparative studies evaluating the efficacy of MRAs against other treatment arms for cCSCR. The primary outcome was the best-corrected visual acuity (BCVA) at the last study visit, as well as at specific follow-up timepoints (i.e., 1 month, 3 months, 6 months, 12 months). Secondary outcomes included retinal thickness (RT), subretinal fluid (SRF) height, and SRF resolution at the same timepoints. Meta-analyses were performed using a random-effects model, with subgroup analyses performed for eplerenone and spironolactone separately. A p-value of less than 0.05 was considered statistically significant.

Results: Thirteen articles (four RCTs reporting on 253 eyes and nine observational studies reporting on 393 eyes, mean follow-up duration=7.02 ± 3.78 months) were included. The mean BCVA at the last study visit was similar between the MRA and observation groups (WMD=-0.01 logMAR, 95%CI=[-0.05, 0.02], p=0.40, n=5 studies). However, MRAs resulted in a significantly lower mean SRF height at 1 month (WMD=-69.56 µm, 95% CI [-127.26, -11.86], p=0.02, n=2 studies), while the observation group had a significantly lower SRF height at 12 months (WMD=48.23 µm, 95% CI [45.99, 50.46], p<0.00001, n=2 studies). Likewise, Similarly, MRAs demonstrated a higher rate of SRF resolution at 1 month (RR=4.24, 95%CI=[1.54, 11.72], p=0.005), whereas the observation group showed a higher resolution rate at 12 months (RR=0.45, 95%CI=[0.22, 0.95], p=0.04). On subgroup analysis, spironolactone showed a significantly reduced mean RT at the last study visit compared to observation (WMD=-46.44 µm, 95% CI [-74.76, -18.13], p=0.001, n=2 studies). When compared to PDT, MRAs were associated with a significantly higher mean SRF height at the last study visit (WMD=51.99 µm, 95% CI [2.70, 101.27], p=0.04, n=2 studies). In contrast, efficacy outcomes were largely similar between patients treated with MRAs and SML at the last study visit, with no significant differences in SRF resolution (p=0.22, n=2 studies).

Conclusion: MRAs offer short-term benefits in reducing SRF but may have limited long-term durability based on current evidence, highlighting the need for further studies.

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来源期刊
CiteScore
9.20
自引率
7.10%
发文量
406
审稿时长
36 days
期刊介绍: The American Journal of Ophthalmology is a peer-reviewed, scientific publication that welcomes the submission of original, previously unpublished manuscripts directed to ophthalmologists and visual science specialists describing clinical investigations, clinical observations, and clinically relevant laboratory investigations. Published monthly since 1884, the full text of the American Journal of Ophthalmology and supplementary material are also presented online at www.AJO.com and on ScienceDirect. The American Journal of Ophthalmology publishes Full-Length Articles, Perspectives, Editorials, Correspondences, Books Reports and Announcements. Brief Reports and Case Reports are no longer published. We recommend submitting Brief Reports and Case Reports to our companion publication, the American Journal of Ophthalmology Case Reports. Manuscripts are accepted with the understanding that they have not been and will not be published elsewhere substantially in any format, and that there are no ethical problems with the content or data collection. Authors may be requested to produce the data upon which the manuscript is based and to answer expeditiously any questions about the manuscript or its authors.
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