Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Ocul Surf. 2016 Apr;14(2):255-63. doi: 10.1016/j.jtos.2015.12.005. Epub 2016 Jan 18.
To examine the effect of a combined dietary supplement containing fish oil, lactoferrin, zinc, vitamin C, lutein, vitamin E, γ-aminobutanoic acid, and Enterococcus faecium WB2000 on dry eye.
A preliminary study in a rat model and a prospective, randomized, double-blind, placebo-controlled study in humans were conducted. Forty Japanese volunteers aged 22 to 59 years were randomized into combined dietary supplement (2 capsules/day; 20 participants) and placebo (vehicle; 19 participants) groups and treated once daily for 8 weeks. Rats received the combined dietary supplement components (10 or 50 mg/kg orally) or vehicle (2% DMSO), and dry eye was mechanically induced for 2 days. Tear production was measured in rats after dry eye was induced. Humans were assessed at baseline and weeks 4 and 8 post-supplementation based on keratoconjunctival epithelial damage; fluorescein tear film breakup time; tear production; biochemical data; information regarding subjective dry eye symptoms by answering a questionnaire; and information regarding adverse events via medical interviews.
Supplementation dose-dependently mitigated the decrease in tear production in rats. Among subjects with confirmed dry eye, clinical symptoms improved at weeks 4 and 8 more significantly in the supplementation group than in the placebo group (P<.05). The rate of increase in the Schirmer value was greater in the supplementation group. No adverse events occurred.
Supplementation improved objective and subjective dry eye symptoms.
研究一种含有鱼油、乳铁蛋白、锌、维生素 C、叶黄素、维生素 E、γ-氨基丁酸和屎肠球菌 WB2000 的复合膳食补充剂对干眼症的影响。
在大鼠模型中进行了初步研究,并在人类中进行了前瞻性、随机、双盲、安慰剂对照研究。40 名年龄在 22 至 59 岁的日本志愿者被随机分为复合膳食补充剂(每天 2 粒;20 名参与者)和安慰剂(载体;19 名参与者)组,每天治疗一次,持续 8 周。大鼠接受复合膳食补充剂成分(10 或 50mg/kg 口服)或载体(2% DMSO),并在 2 天内机械诱导干眼症。在诱导干眼症后测量大鼠的泪液产生。在补充后 4 周和 8 周,根据角结膜上皮损伤、荧光素泪膜破裂时间、泪液产生、生化数据、通过回答问卷了解主观干眼症症状的信息以及通过医疗访谈了解不良事件的信息,对人类进行评估。
补充剂剂量依赖性地减轻了大鼠泪液产生的减少。在确诊干眼症的受试者中,与安慰剂组相比,补充组在第 4 周和第 8 周时临床症状改善更为明显(P<.05)。补充组的泪液分泌量增加率更高。未发生不良反应。
补充剂改善了客观和主观的干眼症症状。