Jo Yeon Ji, Lee Jong Soo
Department of Ophthalmology, Pusan National University School of Medicine&Medical Research Institute of Pusan National University Hospital, Busan 49241, Republic of Korea.
Int J Ophthalmol. 2021 Nov 18;14(11):1700-1706. doi: 10.18240/ijo.2021.11.08. eCollection 2021.
To evaluate the clinical efficacy of dietary supplement of high dose DHA omega-3 in dry eye with meibomian gland dysfunction (MGD).
Prospective randomized double-masked, placebo-controlled clinical trial was conducted in mild to moderate dry eye patients with MGD. Patients have no history of taking any dietary omega-3 supplements before 3mo. Patients were divided into two groups: 24 patients in the omega-3 group and 26 patients in the placebo group. The omega-3 group received two capsules of Easyeye Dry, total containing 600 mg of EPA and 1640 mg of DHA, while the placebo group received two capsules containing 3000 mg of olive oil. All patients take two pills once a day. The examination of MGD scores, tear break-up time (TBUT), corneal staining test (NEI), strip meniscometry (SM tube), and ocular surface disease index (OSDI) scores were performed at baseline, after 4 and 8wk.
A total of 50 patients were included. There were no differences in baseline characteristics between the two groups, such as age, sex, and other ocular examination findings. The TBUT, NEI, and OSDI scores significantly improved after 4 and 8wk in both groups. While after 8wk TBUT (6.00±1.62s 5.08±1.28s, =0.034) and MGD score (7.2±1.8 8.1±2.6, =0.033) in the omega-3 group was more significantly improved than that of the placebo group.
Dry eye with the MGD patient, a high dose of DHA omega-3 dietary supplement can improve TBUT and MGD score after 8wk, effective in stabilizing the tear film.
评估高剂量ω-3二十二碳六烯酸(DHA)膳食补充剂对睑板腺功能障碍(MGD)型干眼症的临床疗效。
对轻至中度MGD型干眼症患者进行前瞻性随机双盲、安慰剂对照临床试验。患者在3个月内无服用任何ω-3膳食补充剂的病史。患者分为两组:ω-3组24例,安慰剂组26例。ω-3组服用两粒易视明软胶囊,共含600毫克二十碳五烯酸(EPA)和1640毫克DHA,而安慰剂组服用两粒含3000毫克橄榄油的胶囊。所有患者每天服用一次两粒胶囊。在基线、4周和8周后进行MGD评分、泪膜破裂时间(TBUT)、角膜染色试验(NEI)、泪河测量(SM管)和眼表疾病指数(OSDI)评分检查。
共纳入50例患者。两组患者的基线特征如年龄、性别和其他眼部检查结果无差异。两组在4周和8周后TBUT、NEI和OSDI评分均显著改善。而8周后ω-3组的TBUT(6.00±1.62秒对5.08±1.28秒,P = 0.034)和MGD评分(7.2±1.8对8.1±2.6,P = 0.033)比安慰剂组改善更显著。
对于MGD型干眼症患者,高剂量ω-3 DHA膳食补充剂在8周后可改善TBUT和MGD评分,有效稳定泪膜。