Efficacy of Carbonic Anhydrase Inhibitors on Cystoid Fluid Collections and Visual Acuity in Patients with X-Linked Retinoschisis

被引:5
作者
Hensman, Jonathan [1 ]
Hahn, Leo C. [1 ]
van Schooneveld, Mary J. [1 ]
Diederen, Roselie M. H. [1 ]
ten Brink, Jacoline B.
Florijn, Ralph J. [2 ]
Bergen, Arthur A. [2 ]
Strubbe, Ine [3 ]
Heutinck, Pam [4 ]
van Genderen, Maria M. [3 ,5 ]
van den Born, Ingeborgh [6 ,7 ]
Thiadens, Alberta A.
Leroy, Bart P.
Hoyng, Carel B. [8 ]
Boon, Camiel J. F. [9 ]
机构
[1] Univ Amsterdam, Med Ctr, Dept Ophthalmol, Amsterdam Univ, Amsterdam, Netherlands
[2] Univ Amsterdam, Med Ctr, Dept Human Genet, Amsterdam Univ, Amsterdam, Netherlands
[3] Ghent Univ Hosp, Dept Ophthalmol, Ghent, Belgium
[4] Erasmus MC, Dept Ophthalmol, Rotterdam, Netherlands
[5] Diagnost Ctr Complex Visual Disorders, Bartimeus, Zeist, Netherlands
[6] Rotterdam Eye Hosp, Rotterdam, Netherlands
[7] Rotterdam Ophthalm Inst, Rotterdam, Netherlands
[8] Radboud Univ Nijmegen, Dept Ophthalmol, Med Ctr, Nijmegen, Netherlands
[9] Leiden Univ, Dept Ophthalmol, Med Ctr, Leiden, Netherlands
来源
OPHTHALMOLOGY RETINA | 2024年 / 8卷 / 06期
关键词
CYSTIC MACULAR LESIONS; DORZOLAMIDE HYDROCHLORIDE; GENE-THERAPY; DELIVERY;
D O I
10.1016/j.oret.2023.12.003
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To date, there is no standard treatment regimen for carbonic anhydrase inhibitors (CAIs) in X-linked retinoschisis (XLRS) patients. This retrospective study aims to evaluate the efficacy of CAIs on visual acuity and cystoid fluid collections (CFC) in XRLS patients in Dutch and Belgian tertiary referral centers. Design:Retrospective cohort study Participants: Forty-two patients with XLRS. Methods: In total, 42 patients were enrolled. To be included, patients had to have previous treatment with an oral CAI (acetazolamide), a topical CAI (brinzolamide/dorzolamide), or a combination of an oral and a topical CAI for at least 4 consecutive weeks. We evaluated the effect of the CAI on best-corrected visual acuity (BCVA) and central foveal thickness (CFT) on OCT. Main Outcome Measures: Central foveal thickness and BCVA. Results: The median age at the baseline visit of the patients in this cohort study was 14.7 (range, 43.6) years, with a median (interquartile range [IQR]) follow-up period of 4.0 (2.2e5.2) years. During the follow-up period, 25 patients were treated once with an oral CAI (60%), 24 patients were treated once with a topical CAI (57%), and 11 patients were treated once with a combination of both topical and oral CAI (26%). We observed a significant reduction of CFT for oral CAI by 14.37 gm per 100 mg per day (P < 0.001; 95% confidence interval [CI], -19.62 to -9.10 gm) and for topical CAI by 7.52 gm per drop per day (P = 0.017; 95% CI, -13.67 to -1.32 gm). The visual acuity changed significantly while on treatment with oral CAI by -0.0059 logMAR per 100 mg (P = 0.008; 95% CI, -0.010 to -0.0013 logMAR). Seven patients (17%) had side effects leading to treatment discontinuation. Conclusions: Our data indicate that treatment with (oral) CAI may be beneficial for short-term management of CFC in patients with XLRS. Despite a significant reduction in CFT, the change in visual acuity was modest and not of clinical significance. Nonetheless, the anatomic improvement of the central retina in these patients may be of value to create an optimal retinal condition for future potential treatment options such as gene therapy. Financial Disclosure(s): The authors have no proprietary or commercial interest in any materials discussed in this article. Ophthalmology Retina 2024;8:600-606 (c) 2023 by the American Academy of Ophthalmology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:600 / 606
页数:7
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