1型糖尿病患者血清趋化素水平与糖尿病视网膜病变的关系

Q2 Medicine
Ahmed Gomaa Elmahdy, Mohamed Mohamed-Aly Ibrahim, Omar Hassan Salama, Hossam Eldin Abdelmonem Ziada, Mahmoud Mohammed Ali, Ghada F Elmohaseb, Eman Mi Youssef, Eman Saad Bayoumy, Marwa Ahmed Bayomy, Sanaa Ahmed Mohamed
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引用次数: 0

摘要

背景:在2型糖尿病患者中,糖尿病视网膜病变(DR)的发展与血清趋化素水平升高呈正相关。本研究旨在探讨1型糖尿病(T1DM)患者血清趋化素水平与DR发生之间的可能关系。方法:在本横断面研究中,我们纳入埃及人并将其分为四组:1组,包括健康个体;2组,包括无DR的T1DM患者;3组,包括T1DM合并非增殖性DR (NPDR)患者;第4组,包括合并增生性DR (PDR)的T1DM患者。评估包括最佳矫正距离视力评估、裂隙灯生物显微检查、眼底镜检查、眼底荧光素血管造影和黄斑眼相干断层扫描。所有参与者的空腹血样用于测定血清趋化素、糖化血红蛋白(HbA1c)、总胆固醇、甘油三酯和肌酐水平。比较各组血清趋化素水平,并分析其与年龄、糖尿病病程、HbA1c、总胆固醇、甘油三酯和肌酐水平的相关性。结果:我们招募了209名参与者,其中第1组46名健康个体,第2组52名患者(T1DM和无DR),第3组61名患者(T1DM和NPDR),第4组50名患者(T1DM和PDR),各组之间的平均年龄和性别比例相当。糖尿病病程、体重指数、HbA1c、总胆固醇、甘油三酯和血清趋化素水平组间差异显著(均P < 0.001),而肌酐水平组间差异无统计学意义(P > 0.05)。血清趋化素水平4组显著高于3、2组,3组显著高于2组,3、4组显著高于1组(均P < 0.001)。但1组和2组间具有可比性(P > 0.05)。它与T1DM和HbA1c持续时间、总胆固醇、甘油三酯和肌酐水平相关,但与年龄无关。结论:合并DR的T1DM患者血清趋化素水平高于未合并DR的T1DM患者和健康人群。PDR患者血清趋化素水平高于NPDR患者。因此,血清趋化素水平是T1DM患者DR发展和严重程度的潜在生物标志物。然而,未来的诊断准确性研究需要确认这些潜在的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of the serum chemerin level with the development of diabetic retinopathy in patients with type 1 diabetes mellitus.

Association of the serum chemerin level with the development of diabetic retinopathy in patients with type 1 diabetes mellitus.

Background: In patients with type 2 diabetes mellitus, the development of diabetic retinopathy (DR) correlates positively with elevated serum chemerin levels. This study was aimed at investigating the probable association between the serum chemerin level and the development of DR in patients with type 1 diabetes mellitus (T1DM).

Methods: In this cross-sectional study, we included Egyptians and classified them into four groups: group 1, including healthy individuals; group 2, including patients with T1DM without DR; group 3, including patients with T1DM with non-proliferative DR (NPDR); and group 4, including patients with T1DM with proliferative DR (PDR). The assessment included best-corrected distance visual acuity assessment, slit-lamp biomicroscopy, funduscopy, fundus fluorescein angiography, and macular ocular coherence tomography. Fasting blood samples were obtained from all participants to measure serum chemerin, glycated hemoglobin (HbA1c), total cholesterol, triglyceride, and creatinine levels. Serum chemerin levels were compared among the groups, and their correlations with age, duration of diabetes, HbA1c, total cholesterol, triglyceride, and creatinine levels were analyzed.

Results: We recruited 209 participants, including 46 healthy individuals in group 1, 52 patients (T1DM and no DR) in group 2, 61 patients (T1DM and NPDR) in group 3, and 50 patients (T1DM and PDR) in group 4, with comparable mean ages and sex ratios among groups. The diabetes duration, body mass index, HbA1c, total cholesterol, triglyceride, and serum chemerin levels differed significantly among the groups (all P < 0.001), whereas the creatinine level did not (P > 0.05). The serum chemerin level was significantly higher in group 4 than in groups 3 and 2, in group 3 than in group 2, and in groups 3 and 4 than in group 1 (all P < 0.001). However, it was comparable between groups 1 and 2 (P > 0.05). It correlated with the duration of T1DM and HbA1c, total cholesterol, triglyceride, and creatinine levels but not with age.

Conclusions: Patients with T1DM with DR showed higher serum chemerin levels than those with T1DM without DR or healthy individuals. Serum chemerin levels were higher in those with PDR than in those with NPDR. Thus, serum chemerin levels are a potential biomarker of the development and severity of DR in patients with T1DM. Nevertheless, future diagnostic accuracy studies are required to confirm these potential applications.

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