Comparisons of diabetic retinopathy events associated with glucose‐lowering drugs in patients with type 2 diabetes mellitus: A network meta‐analysis

医学 内科学 优势比 荟萃分析 安慰剂 2型糖尿病 糖尿病性视网膜病变 糖尿病 置信区间 随机对照试验 相对风险 2型糖尿病 低风险 内分泌学 替代医学 病理
作者
Huilin Tang,Guangyao Li,Ying Zhao,Fei Wang,Emily W. Gower,Luwen Shi,Tiansheng Wang
出处
期刊:Diabetes, Obesity and Metabolism [Wiley]
卷期号:20 (5): 1262-1279 被引量:72
标识
DOI:10.1111/dom.13232
摘要

Aim To assess the comparative effects of glucose‐lowering drugs (GLDs) on the risk of diabetic retinopathy (DR) in patients with type 2 diabetes mellitus (T2DM). Methods We systematically searched Cochrane Central Register of Controlled Trials, PUBMED and EMBASE from inception to January 17, 2017 to identify randomized controlled trials (RCTs) that reported DR events among T2DM patients receiving any GLD. Random‐effects pairwise and network meta‐analyses were performed to calculate odds ratios (ORs) with 95% confidence intervals (CIs). Results A total of 37 independent RCTs with 1806 DR events among 100 928 patients with T2DM were included. The mean duration of diabetes was 8.7 years and mean baseline HbA1c was 8.2% (SD, 0.5%). Our network meta‐analysis found that DPP‐4i (OR, 1.20; 95% CI, 0.87‐1.65), GLP‐1RA (OR, 1.19; 95% CI, 0.94‐1.52) and SGLT2 inhibitors (OR, 0.79; 95% CI, 0.49‐1.28) were not associated with a higher risk of DR than placebo; however, a significantly increased risk of DR was associated with DPP‐4i in the pairwise meta‐analysis (OR, 1.27; 95% CI, 1.05‐1.53). Sulfonylureas, on the other hand, were associated with a significantly increased risk of DR compared to placebo (OR, 1.67; 95% CI, 1.01‐2.76). Conclusions Current evidence indicates that the association between DPP‐4i, GLP‐1RA or SGLT2 inhibitors and risk of DR remains uncertain in patients with T2DM. Some evidence suggests that sulfonylureas may be associated with increased risk of DR. However, given that DR events were not systematically assessed, these effects should be explored further in large‐scale, well‐designed studies.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Lyubb完成签到,获得积分10
1秒前
unaive完成签到,获得积分10
1秒前
文艺的枫完成签到,获得积分10
2秒前
左左完成签到,获得积分10
3秒前
3秒前
糖炒栗子完成签到 ,获得积分10
5秒前
wjzhan完成签到,获得积分10
6秒前
wxxl完成签到,获得积分10
6秒前
海茵完成签到,获得积分10
6秒前
Owen应助永毅采纳,获得10
6秒前
左西完成签到 ,获得积分10
8秒前
研友_nPxRRn完成签到,获得积分10
9秒前
poly完成签到,获得积分10
9秒前
解语花031发布了新的文献求助10
9秒前
我不到啊完成签到,获得积分10
9秒前
文刀刘完成签到 ,获得积分10
9秒前
接accept完成签到 ,获得积分10
10秒前
11完成签到,获得积分10
11秒前
学无止境完成签到 ,获得积分10
11秒前
天南地北完成签到,获得积分10
11秒前
记上没文献了完成签到 ,获得积分10
12秒前
舒心的青亦完成签到 ,获得积分10
13秒前
13秒前
白粥粥完成签到 ,获得积分10
13秒前
15秒前
火星上白羊完成签到,获得积分10
15秒前
条条大路完成签到,获得积分10
16秒前
小马甲应助MINGXING采纳,获得10
16秒前
自由逐风完成签到,获得积分10
17秒前
杨胜菲完成签到,获得积分10
18秒前
雪儿发布了新的文献求助10
19秒前
收集快乐完成签到 ,获得积分10
19秒前
不安莺完成签到,获得积分10
20秒前
Lijunjie完成签到,获得积分10
22秒前
mechefy完成签到,获得积分10
22秒前
神奇五子棋完成签到 ,获得积分10
22秒前
一个正经人完成签到,获得积分0
23秒前
LYH完成签到,获得积分10
24秒前
advance完成签到,获得积分0
24秒前
24秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 2000
Digital Twins of Advanced Materials Processing 2000
晋绥日报合订本24册(影印本1986年)【1940年9月–1949年5月】 1000
Social Cognition: Understanding People and Events 1000
Polymorphism and polytypism in crystals 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6034769
求助须知:如何正确求助?哪些是违规求助? 7746610
关于积分的说明 16206614
捐赠科研通 5181101
什么是DOI,文献DOI怎么找? 2772929
邀请新用户注册赠送积分活动 1756072
关于科研通互助平台的介绍 1640913