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Therapeutic effect of lutein supplement on non-proliferative diabetic retinopathy: A retrospective study

机译:叶黄素补充剂对非增生性糖尿病视网膜病变的治疗作用:回顾性研究

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This study retrospectively evaluated the effect of lutein supplement (LS) on patients with non-proliferative diabetic retinopathy (NPDR). A total of 72 patients with NPDR were included in this study. All patients received Zeaxanthin during the study period. In addition, 36 patients also received LS and were assigned to the treatment group, while the other 36 patients did not receive LS and were assigned to the control group. All patients were treated for a total of 4 months. The endpoints included visual acuity (VA), contrast sensitivity (CS), and glare sensitivity (GS). In addition, any adverse events were also assessed. All endpoints were measured before and after 4-month treatment. Before treatment, there were no significant differences in VA ( P = .75), CS ( P = .71), and GS ( P = .73) between two groups. After 4-month treatment, there were still no significant differences in all endpoints of VA ( P = .66), CS ( P = .58), and GS ( P = .61) between two groups. No adverse events were recorded in either group. The results of this retrospective study showed that LS may not benefit for patients with NPDR after 4-month treatment. More high quality randomized controlled trials should still be needed to warrant the results of this study.
机译:这项研究回顾性评估了叶黄素补充剂(LS)对非增殖性糖尿病视网膜病变(NPDR)患者的作用。本研究共纳入72名NPDR患者。在研究期间,所有患者均接受玉米黄质。此外,也有36例患者接受了LS并被分配到治疗组,而其他36例未接受LS的患者被分配到对照组。所有患者共接受了4个月的治疗。终点包括视敏度(VA),对比敏感度(CS)和眩光敏感度(GS)。此外,还评估了任何不良事件。在治疗4个月之前和之后测量所有终点。治疗前,两组之间的VA(P = .75),CS(P = .71)和GS(P = .73)没有显着差异。经过4个月的治疗,两组之间VA(P = .66),CS(P = .58)和GS(P = .61)的所有终点均无显着差异。两组均未记录不良事件。这项回顾性研究的结果表明,LS对4个月治疗后的NPDR患者可能无益。仍然需要更多高质量的随机对照试验来保证这项研究的结果。

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