Macular Alterations in a Cohort of Caucasian Patients Affected by Retinitis Pigmentosa.

IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Diagnostics Pub Date : 2024-10-29 DOI:10.3390/diagnostics14212409
Marcella Nebbioso, Elvia Mastrogiuseppe, Eleonora Gnolfo, Marco Artico, Antonietta Moramarco, Fabiana Mallone, Samanta Taurone, Annarita Vestri, Alessandro Lambiase
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Abstract

Objectives: Our objective was to investigate the prevalence of macular complications detected by spectral-domain optical coherence tomography (SD-OCT) in a large Caucasian cohort of RP patients, highlight the major alterations in chorioretinal structure, and compare the macular structural changes in eyes affected by retinal dystrophies with those in healthy controls.

Methods: This was an observational, retrospective, and cross-sectional study. Three hundred and seven patients with RP were consecutively enrolled and underwent clinical assessment. In particular, SD-OCT images were used to ascertain the morphology of the posterior pole of patients with RP by evaluating the residual ellipsoid zone (EZ), the volume and thickness of the outer nuclear layer (ONLT), and subfoveal choroid thickness (SCT). At the same time, the pathological finding that the patients' vision was reduced under treatment was analyzed.

Results: A total of 436 eyes of 218 patients with RP were studied. Considering all of the eyes studied, 103 had cystoid macular edema (CME) (23.62%), 123 (28.21%) had vitreomacular traction (VMT), and 199 (45.75%) had epiretinal membranes (ERMs). There were also 12 (2.75%) cases of lamellar macular holes (LMHs), of which 3 (1.38% of all patients) cases were bilateral. Only 137 eyes (31.42%) did not have the above-mentioned alterations. SCT was significantly reduced compared to that of the control group (193.03 µm ± 67.90 SD vs. 295 µm ± 69.04 SD), while the foveal central macular thickness (FCMT) was greater (270.91 μm ± 74.04 SD vs. 221 µm ± 37.25 SD).

Conclusions: This research highlights the high incidence of macular complications. The results of our study indicate the importance of regular monitoring of RP patients and early intervention to avoid further complications in this group of subjects with severe visual field impairment to avoid further central vision loss.

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一组白种人视网膜色素变性患者的黄斑变化
目的我们的目的是在一大群白种人视网膜营养不良症患者中调查通过光谱域光学相干断层扫描(SD-OCT)检测到的黄斑并发症的发病率,重点研究脉络膜视网膜结构的主要改变,并将视网膜营养不良症患者的黄斑结构变化与健康对照组的黄斑结构变化进行比较:这是一项观察性、回顾性和横断面研究。方法:这是一项观察性、回顾性和横断面研究,连续纳入了 37 名 RP 患者,并对他们进行了临床评估。其中,SD-OCT 图像通过评估残留的椭圆形区(EZ)、核外层(ONLT)的体积和厚度以及脉络膜下厚度(SCT)来确定 RP 患者后极的形态。同时,还对治疗过程中患者视力下降的病理结果进行了分析:共对 218 名 RP 患者的 436 只眼睛进行了研究。在所有被研究的眼球中,103 只(23.62%)患有囊样黄斑水肿(CME),123 只(28.21%)患有玻璃体黄斑牵引(VMT),199 只(45.75%)患有视网膜外膜(ERM)。此外,还有 12 例(2.75%)黄斑片状孔(LMH),其中 3 例(占所有患者的 1.38%)为双侧。只有 137 只眼睛(31.42%)没有上述改变。与对照组相比,SCT 明显减少(193.03 μm ± 67.90 SD 对 295 μm ± 69.04 SD),而眼窝中央黄斑厚度(FCMT)则增加(270.91 μm ± 74.04 SD 对 221 μm ± 37.25 SD):这项研究强调了黄斑并发症的高发生率。我们的研究结果表明,必须对 RP 患者进行定期监测和早期干预,以避免这部分视野严重受损的受试者出现进一步的并发症,从而避免中心视力进一步丧失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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