首页> 外文期刊>Dermatologic surgery >Serum iron and matrix metalloproteinase-9 variations in limbs affected by chronic venous disease and venous leg ulcers.
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Serum iron and matrix metalloproteinase-9 variations in limbs affected by chronic venous disease and venous leg ulcers.

机译:受慢性静脉疾病和下肢静脉溃疡影响的四肢中血清铁和基质金属蛋白酶9的变化。

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BACKGROUND: Severe chronic venous disease (CVD) is characterized by both dermal hemosiderin accumulation and matrix metalloproteinase (MMP) hyperactivation. The iron-driven pathway is one of the recognized mechanisms of MMP hyperactivation. OBJECTIVE: To investigate the potential consequences of leg hemosiderin deposits on both iron metabolism and activation of MMPs. METHODS: We contemporaneously assessed the following in the serum of the arm and ankle veins of 30 patients (C4-6) with CVD and 14 normal subjects: ferritin, transferrin, iron, percentage of transferrin iron binding capacity (%TIBC), and MMP-9. Optical microscopy examinations with Perls' staining of chronic wounds were also performed. RESULTS: Histology consistently revealed iron deposits. Serum ferritin, iron, and %TIBC were significantly increased in the legs affected by severe CVD compared with the arm of the same subjects or the controls. In addition, iron and %TIBC were significantly elevated in the legs of ulcer patients. The rate ofactivation of MMP-9 was significantly elevated in CVD. CONCLUSIONS: The increased iron deposition in legs affected by CVD seems to be more instable in ulcer patients, leading to iron release in the serum of the affected leg. Our data suggest the iron-driven pathway as a further mechanism for MMP hyperexpression leading to tissue lesion.
机译:背景:严重的慢性静脉疾病(CVD)的特征是真皮含铁血黄素的积累和基质金属蛋白酶(MMP)的过度活化。铁驱动途径是MMP过度激活的公认机制之一。目的:研究腿部铁血铁蛋白的沉积物对铁代谢和MMPs活化的潜在影响。方法:我们同时评估了30例患有CVD的患者(C4-6)和14例正常受试者的手臂和踝静脉血清中的以下物质:铁蛋白,转铁蛋白,铁,转铁蛋白铁结合能力百分比(%TIBC)和MMP -9。还进行了带有Perls慢性伤口染色的光学显微镜检查。结果:组织学一直显示铁沉积。与相同受试者或对照组的手臂相比,受严重CVD影响的腿中血清铁蛋白,铁和%TIBC显着增加。此外,溃疡患者腿部铁和%TIBC明显升高。在CVD中,MMP-9的活化速率显着提高。结论:在溃疡患者中,受CVD影响的腿中铁沉积物的增加似乎更加不稳定,从而导致受累腿部血清中的铁释放。我们的数据表明铁驱动途径是导致组织损伤的MMP高表达的进一步机制。

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