Demographic and Metabolic Risk Factors Associated with Development of Diabetic Macular Edema among Persons with Diabetes Mellitus

IF 3.2 Q1 OPHTHALMOLOGY
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引用次数: 0

Abstract

Purpose

Diabetic macular edema (DME), a leading cause of visual impairment, can occur regardless of diabetic retinopathy (DR) stage. Poor metabolic control is hypothesized to contribute to DME development, although large-scale studies have yet to identify such an association. This study aims to determine whether measurable markers of dysmetabolism are associated with DME development in persons with diabetes.

Design

Retrospective cohort study.

Participants

Using data from the Sight Outcomes Research Collaborative (SOURCE) repository, patients with diabetes mellitus and no preexisting DME were identified and followed over time to see what factors associated with DME development.

Methods

Cox proportional hazard modeling was used to assess the relationship between demographic variables, diabetes type, smoking history, baseline DR status, blood pressure (BP), lipid profile, body mass index (BMI), hemoglobin A1C (HbA1C), and new onset of DME.

Main Outcome Measures

Adjusted hazard ratio (HR) of developing DME with 95% confidence intervals (CIs).

Results

Of 47 509 eligible patients from 10 SOURCE sites (mean age 63 ± 12 years, 58% female sex, 48% White race), 3633 (7.6%) developed DME in the study period. The mean ± standard deviation time to DME was 875 ± 684 days (∼2.4 years) with those with baseline nonproliferative DR (HR 3.67, 95% CI: 3.41–3.95) and proliferative DR (HR 5.19, 95% CI: 4.61–5.85) more likely to develop DME. There was no difference in DME risk between type 1 and type 2 patients; however, Black race was associated with a 40% increase in DME risk (HR 1.40, 95% CI: 1.30–1.51). Every 1 unit increase in HbA1C had a 15% increased risk of DME (HR 1.15, 95% CI: 1.13–1.17), and each 10 mmHg increase in systolic BP was associated with a 6% increased DME risk (HR 1.06, 95% CI: 1.02–1.09). No association was identified between DME development and BMI, triglyceride levels, or high-density lipoprotein levels.

Conclusions

These findings suggest that in patients with diabetes modifiable risk factors such as elevated HbA1C and BP confer a higher risk of DME development; however, other modifiable systemic markers of dysmetabolism such as obesity and dyslipidemia did not. Further work is needed to identify the underlying contributions of race in DME.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

糖尿病患者发生糖尿病性黄斑水肿的相关人口和代谢风险因素
目的糖尿病黄斑水肿(DME)是视力损伤的主要原因之一,无论糖尿病视网膜病变(DR)处于哪个阶段都可能发生。据推测,代谢控制不佳会导致 DME 的发生,但大规模的研究尚未发现这种关联。本研究旨在确定代谢紊乱的可测量标志物是否与糖尿病患者的 DME 发展相关。研究对象利用视力结果研究合作组织 (SOURCE) 存储库中的数据,确定了未患有 DME 的糖尿病患者,并对其进行了长期随访,以了解与 DME 发展相关的因素。方法采用Cox比例危险模型评估人口统计学变量、糖尿病类型、吸烟史、基线DR状态、血压(BP)、血脂状况、体重指数(BMI)、血红蛋白A1C(HbA1C)与新发DME之间的关系。结果来自 10 个 SOURCE 地区的 47 509 名符合条件的患者(平均年龄 63 ± 12 岁,女性占 58%,白人占 48%)中,有 3633 人(7.6%)在研究期间患上了 DME。发生 DME 的平均时间(± 标准差)为 875 ± 684 天(∼ 2.4 年),基线为非增殖性 DR(HR 3.67,95% CI:3.41-3.95)和增殖性 DR(HR 5.19,95% CI:4.61-5.85)的患者更容易发生 DME。1 型和 2 型患者的 DME 风险没有差异;但是,黑人种族的 DME 风险增加了 40%(HR 1.40,95% CI:1.30-1.51)。HbA1C 每增加 1 个单位,DME 风险增加 15%(HR 1.15,95% CI:1.13-1.17),收缩压每增加 10 mmHg,DME 风险增加 6%(HR 1.06,95% CI:1.02-1.09)。结论:这些研究结果表明,在糖尿病患者中,HbA1C 和血压升高等可改变的危险因素会增加发生 DME 的风险;但肥胖和血脂异常等其他可改变的代谢紊乱系统标志物则不会增加发生 DME 的风险。还需要进一步的工作来确定种族在DME中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ophthalmology science
Ophthalmology science Ophthalmology
CiteScore
3.40
自引率
0.00%
发文量
0
审稿时长
89 days
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