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1型糖尿病患者视网膜病变前期检测的新标志物:全身免疫炎症指数。

New marker for the detection of pre-retinopathy in patients with type 1 diabetes mellitus: systemic immuno-inflammation index.

作者信息

Kahraman Hazan Gül, Güven Yusuf Ziya, Akay Fahrettin, Üzüm Yusuf, Aysin Murat

机构信息

Department of Ophthalmology, İzmir Democracy University Buca Seyfi Demirsoy Training and Research Hospital, İzmir, Turkey.

Department of Ophthalmology, İzmir Katip Çelebi University Atatürk Training and Research Hospital, İzmir, Turkey.

出版信息

BMC Ophthalmol. 2025 May 19;25(1):296. doi: 10.1186/s12886-025-04138-0.

Abstract

PURPOSE

This study aimed to investigate the relationships among urine parameters, systemic inflammation and retinal microvascular changes in patients with type 1 diabetes mellitus (T1DM) without clinical signs of diabetic retinopathy (DR), via optical coherence tomography angiography (OCTA) and the systemic immune-inflammation index (SII).

METHODS

A total of 64 participants, including 33 patients with T1DM and 31 healthy controls matched by age and sex, were examined. All the subjects underwent detailed eye assessments and OCTA imaging. Retinal and choroidal parameters were measured along with systemic markers such as C-reactive protein (CRP), Erythrocyte Sedimentation Rate (ESR), haemoglobin-A1C (HbA1c), spot urine tests and the SII. Relationships between systemic inflammation, renal and metabolic parameters, and ocular measurements were analyzed.

RESULTS

The T1DM group had significantly higher SII values (381.78 ± 57.30 vs. 284.86 ± 67.88, p < 0.001), HbA1c values (8.21 ± 1.80 vs. 5.15 ± 0.32, p < 0.001), spot microalbumin levels (13.50 ± 26.56 vs. 0.69 ± 0.57, p = 0.009), and albumin/creatinine ratios (0.13 ± 0.31 vs. 0.01 ± 0.01, p = 0.031). No significant differences in macular thickness, vascular density (VD), or foveal avascular zone (FAZ) area were detected between the groups. However, the mean retinal nerve fiber layer (RNFL) thickness and perifoveal ganglion cell complex (GCC) thickness were significantly lower in the diabetic group (p < 0.05). The SII was strongly positively correlated with choroidal thickness (r = 0.686, p < 0.001) and negatively correlated with parafoveal GCC thickness (r=-0.357, p = 0.041). HbA1c was negatively correlated with mean VD (r=-0.261, p = 0.037). No significant correlation was found between the SII and the FAZ or VD. Significant correlations were found between the mean vascular density and both the spot creatinine level (r = -0.527, p = 0.002) and the spot microalbumin level (r = -0.355, p = 0.043).

CONCLUSION

This study highlights the potential of the SII as a biomarker for detecting early subclinical retinal and choroidal changes in T1DM patients before the onset of retinopathy. The observed correlations among spot urine tests, the SII and OCTA parameters support the role of systemic inflammation in the early microvascular alterations associated with diabetes. These findings may contribute to early diagnosis and novel preventive strategies in DR. However, given the limited sample size, these findings should be interpreted with caution. Larger, well-stratified prospective studies are warranted to validate these preliminary observations.

摘要

目的

本研究旨在通过光学相干断层扫描血管造影(OCTA)和全身免疫炎症指数(SII),调查无糖尿病视网膜病变(DR)临床体征的1型糖尿病(T1DM)患者的尿液参数、全身炎症与视网膜微血管变化之间的关系。

方法

共检查了64名参与者,包括33名T1DM患者和31名年龄和性别匹配的健康对照者。所有受试者均接受了详细的眼部评估和OCTA成像。测量了视网膜和脉络膜参数以及全身标志物,如C反应蛋白(CRP)、红细胞沉降率(ESR)、糖化血红蛋白(HbA1c)、随机尿检测和SII。分析了全身炎症、肾脏和代谢参数与眼部测量之间的关系。

结果

T1DM组的SII值(381.78±57.30对284.86±67.88,p<0.001)、HbA1c值(8.21±1.80对5.15±0.32,p<0.001)、随机微量白蛋白水平(13.50±26.56对0.69±0.57,p=0.009)和白蛋白/肌酐比值(0.13±0.31对0.01±0.01,p=0.031)显著更高。两组之间在黄斑厚度、血管密度(VD)或中心凹无血管区(FAZ)面积方面未检测到显著差异。然而,糖尿病组的平均视网膜神经纤维层(RNFL)厚度和中心凹周围神经节细胞复合体(GCC)厚度显著更低(p<0.05)。SII与脉络膜厚度呈强正相关(r=0.686,p<0.001),与中心凹旁GCC厚度呈负相关(r=-0.357,p=0.041)。HbA1c与平均VD呈负相关(r=-0.261,p=0.037)。未发现SII与FAZ或VD之间存在显著相关性。发现平均血管密度与随机肌酐水平(r=-0.527,p=0.002)和随机微量白蛋白水平(r=-0.355,p=0.043)均存在显著相关性。

结论

本研究强调了SII作为检测T1DM患者在视网膜病变发作前早期亚临床视网膜和脉络膜变化的生物标志物的潜力。随机尿检测、SII和OCTA参数之间观察到的相关性支持全身炎症在与糖尿病相关的早期微血管改变中的作用。这些发现可能有助于DR的早期诊断和新的预防策略。然而,鉴于样本量有限,这些发现应谨慎解释。需要进行更大规模、分层良好的前瞻性研究来验证这些初步观察结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b67/12090412/96c8927d87de/12886_2025_4138_Fig1_HTML.jpg

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