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补体基因治疗再血管化与大隐静脉在糖尿病足综合征。

Complementary Gene Therapy after Revascularization with the Saphenous Vein in Diabetic Foot Syndrome.

机构信息

Clinical Department of Vascular, General and Transplantation Surgery, Wroclaw Medical University, Borowska Street 213, 50-556 Wroclaw, Poland.

Clinical Department of Diabetology and Internal Disease, Wroclaw Medical University, Borowska Street 213, 50-556 Wroclaw, Poland.

出版信息

Genes (Basel). 2023 Oct 20;14(10):1968. doi: 10.3390/genes14101968.

DOI:10.3390/genes14101968
PMID:37895317
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10606318/
Abstract

Diabetic foot syndrome (DFS) is one of the most serious macroangiopathic complications of diabetes. The primary treatment option is revascularization, but complementary therapies are still being sought. The study group consisted of 18 patients diagnosed with ischemic ulcerative and necrotic lesions in DFS. Patients underwent revascularization procedures and, due to unsatisfactory healing of the lesions, were randomly allocated to two groups: a group in which bicistronic VEGF165/HGF plasmid was administered and a control group in which saline placebo was administered. Before gene therapy administration and after 7, 30, 90, and 180 days, color duplex ultrasonography (CDU) was performed, the ankle-brachial index (ABI) and transcutaneous oxygen pressure (TcPO2) were measured, and DFS changes were described and documented photographically. In the gene therapy group, four out of eight patients (50%) healed their DFS lesions before 12 weeks. During this time, the ABI increased by an average of 0.25 and TcPO2 by 30.4 mmHg. In the control group, healing of the lesions by week 12 occurred in six out of nine patients (66.67%), and the ABI increased by an average of 0.14 and TcPO2 by 27.1 mmHg. One major amputation occurred in each group. Gene therapy may be an attractive option for complementary treatment in DFS.

摘要

糖尿病足综合征(DFS)是糖尿病最严重的大血管并发症之一。主要的治疗选择是血管重建,但仍在寻找补充疗法。研究组包括 18 名被诊断为 DFS 缺血性溃疡性和坏死性病变的患者。这些患者接受了血管重建手术,但由于病变愈合不理想,他们被随机分配到两组:一组接受双顺反子 VEGF165/HGF 质粒治疗,另一组接受生理盐水安慰剂治疗。在基因治疗给药之前和给药后 7、30、90 和 180 天,进行彩色双功能超声(CDU)检查,测量踝肱指数(ABI)和经皮氧压(TcPO2),并描述和记录 DFS 变化。在基因治疗组中,8 名患者中有 4 名(50%)在 12 周前治愈了他们的 DFS 病变。在此期间,ABI 平均增加了 0.25,TcPO2 增加了 30.4mmHg。在对照组中,9 名患者中有 6 名(66.67%)在 12 周前治愈了病变,ABI 平均增加了 0.14,TcPO2 增加了 27.1mmHg。每组都有一例主要截肢。基因治疗可能是 DFS 补充治疗的一个有吸引力的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/10606318/2aba7dc8173a/genes-14-01968-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/10606318/2aba7dc8173a/genes-14-01968-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8567/10606318/2aba7dc8173a/genes-14-01968-g001.jpg

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