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单次给予OC-01(伐尼克兰溶液)鼻喷雾剂可导致干眼症患者结膜杯状细胞的短期改变。

A Single Administration of OC-01 (Varenicline Solution) Nasal Spray Induces Short-Term Alterations in Conjunctival Goblet Cells in Patients with Dry Eye Disease.

作者信息

Dieckmann Gabriela M, Cox Stephanie M, Lopez Maria J, Ozmen M Cuneyt, Yavuz Saricay Leyla, Bayrakutar Betul N, Binotti William W, Henry Eugenia, Nau Jeffrey, Hamrah Pedram

机构信息

Center for Translational Ocular Immunology, Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.

Cornea Service, Department of Ophthalmology, New England Eye Center, Tufts Medical Center, Tufts University School of Medicine, 800 Washington St, Boston, MA, 02111, USA.

出版信息

Ophthalmol Ther. 2022 Aug;11(4):1551-1561. doi: 10.1007/s40123-022-00530-x. Epub 2022 Jun 2.

Abstract

INTRODUCTION

Dry eye disease is characterized by a persistently unstable or deficient tear film causing discomfort or visual impairment. Varenicline is a small-molecule nicotinic acetylcholine receptor agonist recently approved for use as a preservative-free nasal spray (OC-01 [varenicline solution] nasal spray [OC-01 VNS]) to treat signs and symptoms of dry eye disease, but its effect on conjunctival goblet cells has not been studied.

METHODS

In this phase 2, single-center, vehicle-controlled study, patients aged 18 years or more with a diagnosis of dry eye disease and Ocular Surface Disease Index score of at least 23 were randomized 2:1 to receive a 50-µL single dose of OC-01 0.06 mg VNS or vehicle nasal spray in each nostril. Image assessments for area and perimeter were performed pre and 10 min post treatment for goblet cells by in vivo confocal microscopy and for meibomian glands by infrared meibography. Non-parametric Wilcoxon signed-rank test compared pre- and post-treatment measurements for each treatment group. Treatment-emergent adverse events (TEAEs) were assessed.

RESULTS

The study randomized 18 patients (mean age 61 years); 6 received vehicle (3/6 [50%] female) and 12 patients received OC-01 VNS (11/12 [92%] female). OC-01 VNS treatment decreased mean goblet cell area (pre-treatment, 106.4 µm; post-treatment, 67.6 µm; p = 0.02) and perimeter (pre-treatment, 38.9 µm; post-treatment, 31.2 µm; p = 0.03) but not vehicle did not (p = 0.25). There were no significant changes in mean meibomian gland area with either treatment (p ≥ 0.05). All TEAEs were non-ocular, non-serious, and mild.

CONCLUSIONS

This study demonstrated that a single administration of OC-01 0.06 mg VNS in patients with dry eye disease reduced conjunctival goblet cell area and perimeter, suggesting goblet cell degranulation and associated release of lubricating mucin. By activating the natural tear film, OC-01 VNS may provide benefits over topical medications.

TRIAL REGISTRATION

ClinicalTrials.gov, NCT03688802.

摘要

引言

干眼症的特征是泪膜持续不稳定或不足,导致不适或视力损害。伐尼克兰是一种小分子烟碱型乙酰胆碱受体激动剂,最近被批准用作无防腐剂的鼻喷雾剂(OC-01[伐尼克兰溶液]鼻喷雾剂[OC-01 VNS])来治疗干眼症的体征和症状,但其对结膜杯状细胞的影响尚未得到研究。

方法

在这项2期、单中心、安慰剂对照研究中,年龄在18岁及以上、诊断为干眼症且眼表疾病指数评分至少为23的患者按2:1随机分组,每组每侧鼻孔接受单剂量50μL的OC-01 0.06mg VNS或安慰剂鼻喷雾剂。在治疗前和治疗后10分钟,通过体内共聚焦显微镜对杯状细胞的面积和周长进行图像评估,通过红外睑板腺造影对睑板腺进行图像评估。采用非参数Wilcoxon符号秩检验比较各治疗组治疗前后的测量值。评估治疗中出现的不良事件(TEAE)。

结果

该研究将18例患者随机分组(平均年龄61岁);6例接受安慰剂(3/6[50%]为女性),12例患者接受OC-01 VNS(11/12[92%]为女性)。OC-01 VNS治疗使杯状细胞平均面积减小(治疗前为106.4μm,治疗后为67.6μm;p=0.02),周长减小(治疗前为38.9μm,治疗后为31.2μm;p=0.03),而安慰剂组未出现这种情况(p=0.25)。两种治疗方法对睑板腺平均面积均无显著影响(p≥0.05)。所有TEAE均为非眼部、非严重且轻度的。

结论

本研究表明,对干眼症患者单次给予0.06mg OC-01 VNS可减小结膜杯状细胞的面积和周长,提示杯状细胞脱颗粒并释放相关的润滑黏液。通过激活天然泪膜,OC-01 VNS可能比局部用药更具优势。

试验注册

ClinicalTrials.gov,NCT03688802。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0569/9253229/ef04c828d9aa/40123_2022_530_Fig1_HTML.jpg

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