Effects of Diquafosol Sodium Ophthalmic Solution on Tear Film Matrix Metallopeptidase-9 and Corneal Nerve Density in Patients with Type 2 Diabetic Dry Eye.

IF 1.9 4区 医学 Q2 OPHTHALMOLOGY
Guanghao Qin, Jiayan Chen, Liangzhe Li, Yifan Qi, Yimeng Chen, Qing Zhang, Yi Wu, Yue You, Lanting Yang, Naici Guo, Salissou Moutari, Shaochong Bu, Jonathan E Moore, Ling Xu, Wei He, Sile Yu, Xingru He, Emmanuel Eric Pazo
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引用次数: 0

Abstract

Purpose: Diabetes mellitus has been associated with increased dry eye disease (DED) and exacerbates DED's pathology. This preliminary short-term study aimed to evaluate the effects of 3% Diquafosol Sodium ophthalmic solution (DQS) on ocular surface inflammation and corneal nerve density in diabetic dry eye (DDE) patients. Methods: In this perspective, participants used 1 drop of 3% DQS (Diquas; Santen Pharmaceutical Co., Ltd., Osaka, Japan) 6 times daily for 8 weeks. Non-invasive tear breakup time (NITBUT), tear film lipid layer (TFLL), conjunctival hyperemia [redness score (RS)], corneoconjunctival staining (CFS), corneal sensitivity (CS), Meibomian gland quality (MGQ) and Meibomian gland expressibility (MGEx), corneal nerve fiber density (CNFD), and Standard Patient Evaluation Eye Dryness (SPEED) questionnaire were assessed at baseline, at weeks 4, and up to 8 weeks. Matrix metalloproteinase-9 (MMP-9) of tear samples was measured at baseline and weeks 8. Results: The mean age was 61.27 ± 11.68 years. At baseline NITBUT = 5.89 ± 2.81 s, tear meniscus height = 0.17 ± 0.05 mm, TFLL = 2.74 ± 0.51, CFS = 4.35 ± 0.68, CS = 53.83 ± 9.63 mm, MMP-9 = 49.10 ± 10.42 ng/mL, RS = 1.65 ± 0.44, MGEx = 1.85 ± 0.72, MGQ = 2.65 ± 0.50, CNFD = 20.36 ± 8.20 no./mm2, and SPEED = 12.62 ± 3.91. At week 4, significant improvements were found in all parameters except RS (1.59 ± 0.46, P = 0.172) and CNFD (21.46 ± 8.41, P = 0.163). Finally, at week 8, all parameters had significant improvements. Conclusion: Preliminary short-term findings suggest that treatment of DDE patients with DQS was found to be safe and efficacious in improving dry eye parameters. In addition, inflammatory marker and corneal nerve density were significantly improved. This study was registered with ClinicalTrials.gov (NCT05193331).

地屈孕酮钠眼药水对 2 型糖尿病干眼症患者泪膜基质金属肽酶-9 和角膜神经密度的影响
目的:糖尿病与干眼症(DED)的增加有关,并且会加重 DED 的病理变化。这项初步的短期研究旨在评估 3% Diquafosol sodium 眼科溶液(DQS)对糖尿病干眼症(DDE)患者眼表炎症和角膜神经密度的影响。方法:在本研究中,参与者使用 3% DQS(Diquas;日本大阪山田制药株式会社),每天 6 次,每次 1 滴,连续使用 8 周。无创泪液破裂时间(NITBUT)、泪膜脂质层(TFLL)、结膜充血[发红评分(RS)]、角膜结膜染色(CFS)、角膜敏感度(CS)、在基线期、第 4 周和最多 8 周时对睑板腺质量(MGQ)和睑板腺表现力(MGEx)、角膜神经纤维密度(CNFD)和标准患者眼干燥评估(SPEED)问卷进行评估。在基线和第 8 周时测量泪液样本中的基质金属蛋白酶-9 (MMP-9)。结果平均年龄为 61.27 ± 11.68 岁。基线时,NITBUT = 5.89 ± 2.81 s,泪液半月板高度 = 0.17 ± 0.05 mm,TFLL = 2.74 ± 0.51,CFS = 4.35 ± 0.68,CS = 53.83 ± 9.63 mm,MMP-9 = 49.10 ± 10.42 ng/mL,RS = 1.65 ± 0.44,MGEx = 1.85 ± 0.72,MGQ = 2.65 ± 0.50,CNFD = 20.36 ± 8.20 no./mm2,SPEED = 12.62 ± 3.91。第 4 周时,除 RS(1.59 ± 0.46,P = 0.172)和 CNFD(21.46 ± 8.41,P = 0.163)外,所有参数均有明显改善。最后,在第 8 周,所有参数均有明显改善。结论初步的短期研究结果表明,用 DQS 治疗 DDE 患者对改善干眼症参数安全有效。此外,炎症标志物和角膜神经密度也有明显改善。本研究已在 ClinicalTrials.gov (NCT05193331) 注册。
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来源期刊
CiteScore
4.60
自引率
4.30%
发文量
72
审稿时长
1 months
期刊介绍: Journal of Ocular Pharmacology and Therapeutics is the only peer-reviewed journal that combines the fields of ophthalmology and pharmacology to enable optimal treatment and prevention of ocular diseases and disorders. The Journal delivers the latest discoveries in the pharmacokinetics and pharmacodynamics of therapeutics for the treatment of ophthalmic disorders. Journal of Ocular Pharmacology and Therapeutics coverage includes: Glaucoma Cataracts Retinal degeneration Ocular infection, trauma, and toxicology Ocular drug delivery and biotransformation Ocular pharmacotherapy/clinical trials Ocular inflammatory and immune disorders Gene and cell-based therapies Ocular metabolic disorders Ocular ischemia and blood flow Proliferative disorders of the eye Eyes on Drug Discovery - written by Gary D. Novack, PhD, featuring the latest updates on drug and device pipeline developments as well as policy/regulatory changes by the FDA.
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