IRCCS Fondazione Bietti, Rome, Italy.
Adv Ther. 2020 Apr;37(4):1646-1663. doi: 10.1007/s12325-020-01284-3. Epub 2020 Mar 16.
This study aimed to evaluate the effect of treatment with eye drops containing citicoline and vitamin B on changes in function of the inner retina, morphology of the inner and outer retina, and microvascular condition in patients with type 1 diabetes (DM1) with mild signs of non-proliferative diabetic retinopathy (NPDR) during 3 years of follow-up.
A pilot study with prospective, randomized, and double-masked design was conducted to address the aims. Twenty patients with DM1 were enrolled and randomly divided into two groups: the DC group comprising patients treated with citicoline and vitamin B eye drops (10 patients; mean age ± standard deviation, 46.86 ± 8.78 years) and the DP group comprising those treated with placebo (10 patients; mean age ± standard deviation, 47.89 ± 7.74 years). In the DC group, one eye of each patient was treated with citicoline and vitamin B eye drops (OMK2, Omikron Italia srl, Italy, 3 drops/day), while in the DP group, it was treated with placebo (eye drops containing hypromellose 0.3%, 3 drops/day) for a 3-year period. In both groups, Humphrey Matrix frequency doubling technology (FDT), spectral domain optical coherence tomography (SD-OCT) and OCT angiography (OCTA), and adaptive optics (AO) were applied at baseline and 12, 24, and 36 months of the follow-up period.
In the results of follow-up evaluation, the DC and DP groups were significantly different: Significant reduction in function in terms of 10-2 FDT mean sensitivity and in morphology reflected by an increase in inner nuclear layer thickness and decrease in other plexiform layer thickness and foveal vessel density were observed in the DP group, while no such significant changes were observed in the DC group in the long term.
This pilot study indicated that patients with DM1 with mild signs of diabetic retinopathy (DR) who underwent treatment with citicoline and vitamin B eye drops for a 3-year duration achieved stabilization or decreased rate of functional impairment, neuroretinal degeneration, and microvascular damage.
ClinicalTrials.gov identifier, NCT04009980.
本研究旨在评估含有胞磷胆碱和维生素 B 的滴眼液治疗对 1 型糖尿病(DM1)合并轻度非增殖性糖尿病视网膜病变(NPDR)患者的内视网膜功能变化、内、外视网膜形态以及微血管状态的影响,随访 3 年。
采用前瞻性、随机、双盲设计进行了一项试点研究,以解决这些目标。共纳入 20 例 DM1 患者,随机分为两组:胞磷胆碱和维生素 B 滴眼液治疗组(DC 组,10 例;平均年龄±标准差,46.86±8.78 岁)和安慰剂治疗组(DP 组,10 例;平均年龄±标准差,47.89±7.74 岁)。在 DC 组,每位患者的一只眼接受胞磷胆碱和维生素 B 滴眼液治疗(意大利 Omikron Italia srl 公司的 OMK2,3 滴/天),而 DP 组则接受安慰剂(含羟丙甲纤维素 0.3%的滴眼液,3 滴/天)治疗,为期 3 年。在两组中,均在基线及随访 12、24 和 36 个月时应用 Humphrey 矩阵频域加倍技术(FDT)、光谱域光学相干断层扫描(SD-OCT)和 OCT 血管造影(OCTA)及自适应光学(AO)。
在随访评估结果中,DC 组和 DP 组有显著差异:DP 组的 10-2 FDT 平均敏感性和形态学的功能显著降低,表现为内核层厚度增加,其他神经丛层厚度和黄斑血管密度降低,而在 DC 组中未观察到长期的显著变化。
这项试点研究表明,接受胞磷胆碱和维生素 B 滴眼液治疗 3 年的 1 型糖尿病合并轻度糖尿病视网膜病变(DR)患者,其功能损害、神经视网膜变性和微血管损伤的稳定或减缓。
ClinicalTrials.gov 标识符,NCT04009980。