Hung Kuo-Chuan, Chang Li-Chen, Chang Ying-Jen, Hsu Chih-Wei, Yew Ming, Wu Jheng-Yan, Chen I-Wen
Department of Anesthesiology, Chi Mei Medical Center, Tainan city, Taiwan.
School of Medicine, College of Medicine, National Sun Yat-sen University, Kaohsiung city, Taiwan.
Eye (Lond). 2025 Sep 6. doi: 10.1038/s41433-025-03982-0.
Diabetic retinopathy (DR) is the leading cause of preventable blindness. Although hyperglycaemia is the primary driver, other modifiable risk factors may contribute to DR development. This study investigated the association between haemoglobin levels and DR risk in adults with type 2 diabetes.
We conducted a retrospective cohort study using the TriNetX network (2010-2022). Adults aged ≥45 years with type 2 diabetes were divided into low haemoglobin (LHB, 8-12 g/dL) and control (≥12 g/dL) groups. Propensity score matching was used to address potential confounders. The primary outcome was new-onset DR occurring 6-36 months after the index date. The secondary outcomes included DR subtypes and diabetic ophthalmic complications. Subgroup analyses examined effect modifications by hypertension status, glycaemic control, and sex.
After propensity score matching (28,882 patients per group), patients in the LHB group showed significantly higher risk of overall DR (HR: 1.33, 95% CI: 1.24-1.44), proliferative DR (HR: 1.95, 95% CI: 1.62-2.35), and non-proliferative DR (HR: 1.19, 95% CI: 1.06-1.33). Even mild haemoglobin reductions (10-12 g/dL) were associated with increased DR risk. The association was stronger in patients without hypertension (HR: 1.58 vs 1.21), remained consistent regardless of HbA1c levels, and was more pronounced in males than females.
Low haemoglobin levels independently increased the risk of DR in adults with type 2 diabetes, with the strongest association for proliferative DR. Routine haemoglobin monitoring and maintenance of optimal levels may represent a modifiable risk factor for DR prevention along with glycaemic control and blood pressure management.
糖尿病视网膜病变(DR)是可预防失明的主要原因。尽管高血糖是主要驱动因素,但其他可改变的风险因素可能会促使DR的发展。本研究调查了2型糖尿病成年人血红蛋白水平与DR风险之间的关联。
我们使用TriNetX网络(2010 - 2022年)进行了一项回顾性队列研究。年龄≥45岁的2型糖尿病成年人被分为低血红蛋白(LHB,8 - 12 g/dL)组和对照组(≥12 g/dL)。倾向评分匹配用于处理潜在的混杂因素。主要结局是在索引日期后6 - 36个月发生的新发DR。次要结局包括DR亚型和糖尿病眼部并发症。亚组分析检验了高血压状态、血糖控制和性别对效应的修饰作用。
在倾向评分匹配后(每组28,882例患者),LHB组患者发生总体DR(HR:1.33,95%CI:1.24 - 1.44)、增殖性DR(HR:1.95,95%CI:1.62 - 2.35)和非增殖性DR(HR:1.19,95%CI:1.06 - 1.33)的风险显著更高。即使是轻度的血红蛋白降低(10 - 12 g/dL)也与DR风险增加相关。在无高血压的患者中这种关联更强(HR:1.58对1.21),无论糖化血红蛋白水平如何均保持一致,且在男性中比女性更明显。
低血红蛋白水平独立增加了2型糖尿病成年人发生DR的风险,与增殖性DR的关联最强。常规血红蛋白监测和维持最佳水平可能是除血糖控制和血压管理之外预防DR的一个可改变的风险因素。