扩散张量成像磁共振成像评估在糖尿病肾病自体树突状细胞转移的临床试验:分子方法。

IF 2.9 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Ernaldi Kapusin, Aditya Pratama Lokeswara, Yudo Rantung, Bhimo Aji Hernowo, Jonny Jonny, Chrismis Novalinda Ginting, Terawan Agus Putranto
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引用次数: 0

摘要

背景:2型糖尿病(T2DM)全球患病率持续上升,导致糖尿病肾病(DKD)患病率随之增加。DKD与较高水平的炎症和肾功能受损有关。许多患者没有得到适当的治疗。本研究旨在通过弥散张量成像(DTI) MRI检查其对肾脏微结构变化的影响,以及分析关键炎症生物标志物,即基质金属蛋白酶-9 (MMP-9)和细胞间粘附分子-1 (ICAM-1),来评估自体树突状细胞转移的治疗效果。方法:采用开放标签设计的临床试验,在Gatot Soebroto陆军医院接受门诊治疗的25例DKD患者进行临床试验。每个参与者都注射了一次自体树突状细胞。评估分别在治疗前和治疗后一个月进行。主要测量包括扩散张量成像(DTI) mri衍生的分数各向异性(FA)扫描和炎症生物标志物MMP-9。结果:树突状细胞注射1个月后,FA明显增加,从基线时的242.57±63.97上升到305.61±152.32。然而,MMP-9和ICAM-1水平无明显变化。此外,FA与MMP-9呈负相关(r = -0.324, p = 0.025)。结论:自体树突状细胞的转移显著增强了FA,这与炎症生物标志物MMP-9的减少有关,表明其对DKD患者的肾脏修复有潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diffusion Tensor Imaging Magnetic Resonance Imaging Assessment in a Clinical Trial of Autologous Dendritic Cell Transfer for Diabetic Kidney Disease: A Molecular Approach.

Background: Continuous rise of type 2 diabetes mellitus (T2DM) global prevalence, has led to a subsequent increase in the prevalence of diabetic kidney disease (DKD). DKD is associated with higher levels of inflammation and impaired kidney function. Many patients do not receive adequate treatment for this condition. This research aims to evaluate the therapeutic impact of autologous dendritic cell transfer by examining its effects on renal microstructural changes as assessed through Diffusion Tensor Imaging (DTI) MRI, alongside the analysis of key inflammatory biomarkers, namely Matrix Metalloproteinase-9 (MMP-9) and Intercellular Adhesion Molecule-1 (ICAM-1).

Methods: A clinical trial with an open-label design was performed with 25 DKD patients receiving outpatient care at Gatot Soebroto Army Hospital. Each participant was administered a single injection of autologous dendritic cells. Evaluations were conducted both prior to and one month following the treatment. The primary measurements included Diffusion Tensor Imaging (DTI) MRI-derived Fractional Anisotropy (FA) scans and the inflammatory biomarker MMP-9.

Results: A notable increase in FA was observed, rising from 242.57 ± 63.97 at baseline to 305.61 ± 152.32 one month after the dendritic cell injection. However, there were no significant changes in MMP-9 and ICAM-1 levels. Additionally, a negative correlation was found between FA and MMP-9 (r = -0.324, p = 0.025).

Conclusion: The transfer of autologous dendritic cells significantly enhanced FA, which correlates with a reduction in the inflammatory biomarker MMP-9, suggesting a potential impact on renal repair in DKD.

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