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糖尿病下肢动脉阻塞性疾病伴临界性下肢缺血患者的血管腔结构功能障碍。

Dysfunctional vasa vasorum in diabetic peripheral artery obstructive disease with critical lower limb ischaemia.

机构信息

Department of Specialistic Surgical and Anaestesiological Sciences, S. Orsola-Malpighi Hospital - University of Bologna, Via Massarenti, 9 Bld 5, 40126 Bologna, Italy.

出版信息

Eur J Vasc Endovasc Surg. 2010 Sep;40(3):365-74. doi: 10.1016/j.ejvs.2010.04.011. Epub 2010 Jun 1.

Abstract

OBJECTIVES AND DESIGN

To establish whether in diabetic patients with peripheral artery obstructive disease (PAOD) vasa vasorum (vv) neoangiogenesis is altered with increased arterial damage.

MATERIALS

Thirty-three patients with PAOD and critical lower limb ischaemia, 22 with type II diabetes.

METHODS

Immunohistochemistry for endothelial cell markers (CD34 and von Willebrand Factor); real-time reverse transcription polymerase chain reaction (RT-PCR) to quantify arterial wall expression of vascular endothelial growth factor (VEGF); enzyme-linked immunosorbent assay (ELISA) to assess blood VEGF; flow cytometry to detect circulating endothelial cells (CECs).

RESULTS

Patients with PAOD and diabetes have a higher frequency (60% vs. 45%) of advanced atherosclerotic lesions and a significant reduction (p = 0.0003) in CD34(+) capillaries in the arterial media. Adventitial neoangiogenesis was increased equally (CD34(+) and vWF(+)) in all patients. Likewise, all patients have increased CEC and VEGF concentration in the blood as well as in-situ VEGF transcript expression.

CONCLUSIONS

Patients with PAOD have remarkable arterial damage despite increased in-situ and circulating expression of the pro-angiogenic VEGF; a dysfunctional vv angiogenesis was seen in diabetics which also showed a higher frequency of parietal damage; it is suggested that in diabetic arterial wall, injury is worsened by vv inability to finalise an effective VEGF-driven arterial wall neoangiogenesis.

摘要

目的与设计

研究在患有外周动脉阻塞性疾病(PAOD)的糖尿病患者中,血管新生是否因动脉损伤增加而发生改变。

材料

33 名患有 PAOD 和严重下肢缺血的患者,22 名患有 2 型糖尿病。

方法

免疫组织化学检测内皮细胞标志物(CD34 和血管性血友病因子);实时逆转录聚合酶链反应(RT-PCR)定量评估血管内皮生长因子(VEGF)在动脉壁中的表达;酶联免疫吸附试验(ELISA)评估血液 VEGF 浓度;流式细胞术检测循环内皮细胞(CECs)。

结果

PAOD 合并糖尿病患者的动脉粥样硬化晚期病变发生率更高(60% vs. 45%),动脉中层 CD34(+)毛细血管数量显著减少(p = 0.0003)。所有患者的外膜新生血管生成(CD34(+)和 vWF(+))均同等增加。同样,所有患者的血液 CEC 和 VEGF 浓度以及原位 VEGF 转录表达均增加。

结论

尽管存在促血管生成 VEGF 的原位和循环表达增加,但 PAOD 患者仍存在明显的动脉损伤;糖尿病患者的 vv 血管生成功能失调,且更容易发生壁损伤;提示在糖尿病患者的动脉壁中,vv 无法完成有效的 VEGF 驱动的动脉壁新生血管生成,从而加重了损伤。

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