利用 68Ga-FAPI46 PET 评估成纤维细胞活化蛋白在高血压引起的组织变化中的表达情况

Jung Woo Byun, Jin Chul Paeng, Young Ju Kim, Seung-Pyo Lee, Yun-Sang Lee, Hongyoon Choi, Keon Wook Kang, Gi Jeong Cheon
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摘要

慢性高血压会导致主要器官损伤和纤维化。成纤维细胞活化蛋白(FAP)是组织纤维化的关键分子之一,68Ga标记的FAP抑制剂-46(FAPI46)PET是最近开发的一种评估FAP的方法。本研究旨在评估高血压模型中 FAP 的表达和纤维化情况,并测试 68Ga-FAPI46 PET 在高血压中的可行性。方法:通过输注血管紧张素 II 诱导小鼠患高血压 4 周。在高血压模型建立后的 1、2 和 4 周进行 68Ga-FAPI46 生物分布研究和 PET 扫描,并测量主要器官的摄取量。分析了心脏和肾脏组织的 FAP 表达和纤维化形成,并与 68Ga-FAPI46 摄取量进行了比较。为了进行比较,高血压模型的子组接受了血管紧张素受体阻滞剂治疗和大剂量 FAPI46 阻滞治疗。作为一项初步人体研究,对肺癌患者的 68Ga-FAPI46 PET 图像进行了分析,并在高血压组和对照组之间进行了比较。研究结果高血压组心脏和肾脏对 68Ga-FAPI46 的摄取早在第一周就明显高于假组,第二周后有所下降。在高剂量阻断研究中,这种摄取被特别阻断。免疫组化也显示 FAP 在心脏和肾脏组织中均有表达。然而,在心脏中观察到明显的纤维化,而在肾脏中则没有。血管紧张素受体阻滞剂治疗组的心脏和肾脏摄取量低于高血压组。在试验性人体研究中,高血压组和对照组对 68Ga-FAPI46 的肾脏摄取量存在显著差异。结论在高血压患者中,心脏和肾脏中的 FAP 表达从早期阶段就开始增加,并随着时间的推移而减少。FAP 的表达似乎代表了纤维化组织形成之前或之后的纤维化活动。68Ga-FAPI46 PET有望成为评估高血压进行性纤维化中FAP表达的有效成像方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Fibroblast Activation Protein Expression Using 68Ga-FAPI46 PET in Hypertension-Induced Tissue Changes

Chronic hypertension leads to injury and fibrosis in major organs. Fibroblast activation protein (FAP) is one of key molecules in tissue fibrosis, and 68Ga-labeled FAP inhibitor-46 (FAPI46) PET is a recently developed method for evaluating FAP. The aim of this study was to evaluate FAP expression and fibrosis in a hypertension model and to test the feasibility of 68Ga-FAPI46 PET in hypertension. Methods: Hypertension was induced in mice by angiotensin II infusion for 4 wk. 68Ga-FAPI46 biodistribution studies and PET scanning were conducted at 1, 2, and 4 wk after hypertension modeling, and uptake in the major organs was measured. The FAP expression and fibrosis formation of the heart and kidney tissues were analyzed and compared with 68Ga-FAPI46 uptake. Subgroups of the hypertension model underwent angiotensin receptor blocker administration and high-dose FAPI46 blocking, for comparison. As a preliminary human study, 68Ga-FAPI46 PET images of lung cancer patients were analyzed and compared between hypertension and control groups. Results: Uptake of 68Ga-FAPI46 in the heart and kidneys was significantly higher in the hypertension group than in the sham group as early as week 1 and decreased after week 2. The uptake was specifically blocked in the high-dose blocking study. Immunohistochemistry also revealed FAP expression in both heart and kidney tissues. However, overt fibrosis was observed in the heart, whereas it was absent from the kidneys. The angiotensin receptor blocker–treated group showed lower uptake in the heart and kidneys than did the hypertension group. In the pilot human study, renal uptake of 68Ga-FAPI46 significantly differed between the hypertension and control groups. Conclusion: In hypertension, FAP expression is increased in the heart and kidneys from the early phases and decreases over time. FAP expression appears to represent fibrosis activity preceding or underlying fibrotic tissue formation. 68Ga-FAPI46 PET has potential as an effective imaging method for evaluating FAP expression in progressive fibrosis by hypertension.

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