2型糖尿病患者角膜地形图与高阶畸变的关系

Amir Asharlous, A. Riazi, A. Jamali, S. Rajabi, Masoud Rahimi, Alireza Akbarzadeh, M. Khabazkhoob, Samira Janani, Taghi Naghdi
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引用次数: 0

摘要

背景:血糖水平的变化引起眼球前段和视网膜的改变。本研究旨在评估未接受治疗的2型糖尿病(T2DM)患者的角膜地形图、像差测量和角膜非球形度。方法:未接受治疗的T2DM患者被纳入这项横断面研究。纳入标准为糖化血红蛋白A1c (Hb A1c)大于或等于7.5%,无其他眼部或全身性疾病。拒绝参与或有局部或全身类固醇使用史、高脂血症、高血压、贫血、既往眼部疾病或手术、糖尿病视网膜病变、青光眼、白内障、活动性眼部炎症或感染性疾病或使用隐形眼镜的患者被排除在外。所有参与者都进行了全面的眼科检查。Pentacam高分辨率成像系统(Pentacam High Resolution;Oculus, Wetzlar, Germany)用于测量前段参数。结果:纳入30例患者60只眼,男女比例为1:1;平均(标准差[SD])年龄为51.63(6.73)岁,糖化血红蛋白为8.82%(1.31%)。角膜中央厚度、总像差的均方根、低阶像差的均方根、高阶像差的均方根、球差、0°彗发、90°彗发、平角度数(K)、前角陡K、平均前角K、前面地形散光、平角后K、后角陡K、平均后角K、后角地形散光、前角非球度、后角非球度的均方根(SD)值分别为540.22(24.47)µm、1.72(0.73)µm,1.63µm(0.73), 0.51(0.17)µm + 0.31(0.09)µm - 0.06(0.15)度(D), 0.003 (0.21), 43.87 (1.49), 44.69 (1.50), (1.44) 44.28 D, D + 0.82 (0.83), - 6.25 (0.27) D, D - 6.55 (0.31), - 6.40 (0.28) D, D - 0.30(0.15), - 0.32(0.12)核反应能量,和- 0.47(0.17)核反应能量。结论:我们给出了戊他康对初治T2DM患者的像差测量、角膜测量和角膜非圆度的平均值。这些值可以作为前瞻性监测该队列的眼健康状况的基线,并与未来控制良好的T2DM患者队列进行比较。T2DM患者强化血糖控制后眼部变化的存在和适用性有待进一步研究,并进一步了解相关病理生理。
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Corneal topography and higher-order aberrations in patients with type 2 diabetes mellitus
Background: Changes in blood sugar levels cause alterations in the anterior segment and retina of the eye. This study was aimed at evaluating corneal topography, aberrometry, and corneal asphericity in patients with treatment-naive type 2 diabetes mellitus (T2DM). Methods: Participants with treatment-naive T2DM were enrolled in this cross-sectional study. The inclusion criteria were glycated hemoglobin A1c (Hb A1c) greater than or equal to 7.5% and absence of other ocular or systemic diseases. Patients who refused to participate or had a history of topical or systemic steroid use, hyperlipidemia, hypertension, anemia, prior ocular disorder or surgery, diabetic retinopathy, glaucoma, cataract, active ocular inflammatory or infectious disease, or contact lens use were excluded. All participants underwent a comprehensive ophthalmic examination. The Pentacam HR Scheimpflug tomography system (Pentacam High Resolution; Oculus, Wetzlar, Germany) was used to measure the anterior-segment parameters. Results: Sixty eyes of 30 patients with a male-to-female ratio of 1:1 were included; the mean (standard deviation [SD]) age and Hb A1c were 51.63 (6.73) years and 8.82% (1.31%), respectively. The mean (SD) values of central corneal thickness, root mean square (RMS) of total aberration, RMS of lower-order aberrations, RMS of higher-order aberrations, spherical aberration, 0° coma, 90° coma, flat anterior keratometry (K), steep anterior K, mean anterior K, anterior topographic astigmatism, flat posterior K, steep posterior K, mean posterior K, posterior topographic astigmatism, anterior corneal asphericity, and posterior corneal asphericity were 540.22 (24.47) µm, 1.72 (0.73) µm, 1.63 (0.73) µm, 0.51 (0.17) µm, + 0.31 (0.09) µm, - 0.06 (0.15) diopters (D), 0.003 (0.21) D, 43.87 (1.49) D, 44.69 (1.50) D, 44.28 (1.44) D, + 0.82 (0.83) D, - 6.25 (0.27) D, - 6.55 (0.31) D, - 6.40 (0.28) D, - 0.30 (0.15) D, - 0.32 (0.12) Q-value, and - 0.47 (0.17) Q-value, respectively. Conclusions: We presented the mean values of Pentacam parameters for aberrometry, keratometry, and corneal asphericity in patients with treatment-naive T2DM. These values could serve as a baseline for prospective monitoring of the ocular health status of this cohort and for comparison with future cohorts of patients with well-controlled T2DM. Further studies are required to assess the presence and applicability of ocular changes following intensive blood glucose control in T2DM and further understand the related pathophysiology.
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