Retinal Microvascular Changes in Association with Endothelial Glycocalyx Damage and Arterial Stiffness in Patients with Diabetes Mellitus Type 2: A Cross-Sectional Study in a Greek Population.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Journal of Personalized Medicine Pub Date : 2024-09-19 DOI:10.3390/jpm14090995
Chrysa Agapitou, Theodoros N Sergentanis, John Thymis, George Pavlidis, Stamatios Lampsas, Emmanouil Korakas, Aikaterini Kountouri, Loukia Pliouta, Efthymios Karmiris, Areti Lagiou, Panagiotis Theodossiadis, Vaia Lambadiari, Ignatios Ikonomidis, Irini Chatziralli
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Abstract

Purpose: To evaluate the potential association between endothelial glycocalyx damage, as well as arterial stiffness, and the retinal changes on optical coherence tomography (OCT) and OCT-angiography (OCT-A) in patients with type 2 diabetes mellitus (DM).

Methods: Participants in this cross-sectional study were 65 patients with DM type 2 and 42 age- and gender-matched controls without DM. The demographic and clinical characteristics of the participants were recorded. All patients underwent a thorough ophthalmological examination and multimodal imaging, including fundus photography, OCT, and OCT-A. In addition, evaluation of the endothelial glycocalyx thickness by measuring the perfused boundary region (PBR5-25) of the sublingual microvessel, as well as of the arterial stiffness, by measuring the carotid-femoral pulse wave velocity (PWV), the central aortic pressures and the augmentation index (Aix) was performed. Univariate and multivariate logistic regression analysis was performed for the examination of the potential association between the eye imaging variables and the cardiovascular-related variables. The odds ratios (OR) with the respective 95% confidence intervals (CI) were calculated. A p-value < 0.05 was considered statistically significant.

Results: Patients with DM presented significantly higher PBR5-25 compared to controls without DM (p = 0.023). At the univariate analysis, increased PBR5-25 (≥2.19 μm vs. <2.19 μm) was associated with decreased peripapillary VD at the superior quadrant (univariate OR (95% CI) = 0.34 (0.12-0.93), p = 0.037). Multivariate logistic regression analysis showed that increased PWV (≥13.7 m/s vs. <13.7 m/s) was associated with an increased foveal avascular zone (FAZ) area on OCT-A (p = 0.044) and increased FAZ perimeter (p = 0.048). Moreover, increased Aix (≥14.745% vs. <14.745%) was associated with diabetic macular edema (DME) presence (p = 0.050) and increased perifoveal and parafoveal superior and temporal thickness on OCT (p < 0.05 for all associations).

Conclusions: Markers of endothelial damage and arterial stiffness were associated with structural and microvascular retinal alterations in patients with DM, pointing out that OCT-A could be a useful biomarker for detecting potential cardiovascular risk in such patients.

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2 型糖尿病患者视网膜微血管变化与内皮糖萼损伤和动脉僵化的关系:希腊人群横断面研究。
目的:评估 2 型糖尿病(DM)患者内皮糖萼损伤和动脉僵化与光学相干断层扫描(OCT)和 OCT 血管造影(OCT-A)视网膜变化之间的潜在关联:这项横断面研究的参与者包括 65 名 2 型糖尿病患者和 42 名年龄和性别匹配的非 2 型糖尿病对照者。研究记录了参与者的人口统计学特征和临床特征。所有患者都接受了全面的眼科检查和多模态成像,包括眼底摄影、OCT 和 OCT-A。此外,还通过测量舌下微血管灌注边界区(PBR5-25)评估了内皮糖萼厚度,并通过测量颈动脉-股动脉脉搏波速度(PWV)、主动脉中心压和增强指数(Aix)评估了动脉僵化程度。为研究眼部成像变量与心血管相关变量之间的潜在联系,进行了单变量和多变量逻辑回归分析。计算出几率比(OR)及相应的 95% 置信区间(CI)。P值小于0.05为具有统计学意义:结果:与非 DM 对照组相比,DM 患者的 PBR5-25 明显更高(p = 0.023)。单变量分析显示,PBR5-25 增加(≥2.19 μm vs. p = 0.037)。多变量逻辑回归分析显示,脉搏波速度增加(≥13.7 m/s vs. p = 0.044)和FAZ周长增加(p = 0.048)。此外,OCT显示Aix增加(≥14.745% vs. p = 0.050),眼底周围和眼底旁的上部和颞部厚度增加(所有关联的p < 0.05):结论:内皮损伤和动脉僵化的标志物与糖尿病患者视网膜结构和微血管的改变有关,这表明OCT-A可能是检测此类患者潜在心血管风险的有用生物标志物。
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
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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