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原发性静脉曲张与静脉壁凋亡失调的关联。

Association of primary varicose veins with dysregulated vein wall apoptosis.

作者信息

Ducasse E, Giannakakis K, Speziale F, Midy D, Sbarigia E, Baste J C, Faraggiana T

机构信息

Unit of Vascular Surgery, Hospital Tripode-Pellegrin, Université de Bordeaux 2, CHU de Bordeaux, Bordeaux, France.

出版信息

Eur J Vasc Endovasc Surg. 2008 Feb;35(2):224-9. doi: 10.1016/j.ejvs.2007.08.015. Epub 2007 Oct 23.

Abstract

BACKGROUND

Disordered programmed cell death may play a role in the development of superficial venous incompetence. We have determined the number of cells in apoptosis, and the mediators regulating the intrinsic and extrinsic pathways in specimens of varicose vein.

METHODS

Venous segments were obtained from 46 patients undergoing surgical treatment for primary varicose veins. Controls samples were obtained from 20 patients undergoing distal arterial bypass grafting surgery. Segments of the distal and proximal saphenous trunk as well as tributaries were studied. Cell apoptoses and mediators of the mitochondrial and trans membrane pathway were evaluated with peroxidase in situ apoptosis detection, Bax and Fas detection, caspase-9 and 8 detection in the medial layer.

RESULTS

Disorganised histological architecture was observed in varicose veins. Primary varicose veins also contained fewer peroxidase in situ-positive cells than control veins (2.6% S.D. 0.2% versus 12% S.D. 0.93%, P=.0001, Mann-Whitney u test), fewer Bax positive cells (2.1.% S.D. 0.3% versus 13% S.D. 0.9%, P=.0001) and fewer Caspase 9 positive cells (3.2% S.D. 1% versus 12% S.D. 1.3%, P=.0001). Similar findings were observed in saphenous trunk, main tributaries and accessory veins. In patients with recurrent varicose veins in whom the saphenous trunk had been preserved showed similar findings to primary varicose veins. Residual varicose veins contained fewer peroxidase in situ-positive cells than healthy veins (3.2% S.D. 0.6% versus 11% S.D. 2%, P=.0001), fewer Bax positive cells (2.2% S.D. 0.3% versus 12% S.D. 0.7%, P=.0001) and fewer Caspase 9 positive cells (2.6% S.D. 0.6% versus 12% S.D. 1%, P=.0001). Immunohistochemical detection for Fas and caspase 8 remained equal was the same in the varicose vein and control groups.

CONCLUSION

Apoptosis is down regulated in the medial layer of varicose veins. This dysregulation is attributable to a disorder of the intrinsic pathway and involves the great saphenous vein trunk, major tributaries and accessory veins. This process may be among the causes of primary varicose veins.

摘要

背景

程序性细胞死亡紊乱可能在浅静脉功能不全的发生发展中起作用。我们已确定了静脉曲张标本中凋亡细胞的数量,以及调节内源性和外源性途径的介质。

方法

从46例接受原发性静脉曲张手术治疗的患者中获取静脉段。对照样本取自20例接受远端动脉搭桥手术的患者。对大隐静脉主干的远端和近端段以及属支进行研究。通过过氧化物酶原位凋亡检测、Bax和Fas检测、中层caspase-9和8检测来评估细胞凋亡以及线粒体和跨膜途径的介质。

结果

在静脉曲张中观察到组织结构紊乱。原发性静脉曲张中过氧化物酶原位阳性细胞也比对照静脉少(2.6%标准差0.2%对12%标准差0.93%,P = 0.0001,曼-惠特尼U检验),Bax阳性细胞少(2.1.%标准差0.3%对13%标准差0.9%,P = 0.0001),Caspase 9阳性细胞少(3.2%标准差1%对12%标准差1.3%,P = 0.0001)。在大隐静脉主干、主要属支和副静脉中观察到类似结果。在保留了大隐静脉主干的复发性静脉曲张患者中也显示出与原发性静脉曲张类似的结果。残留的静脉曲张中过氧化物酶原位阳性细胞比健康静脉少(3.2%标准差0.6%对11%标准差2%,P = 0.0001),Bax阳性细胞少(2.2%标准差0.3%对12%标准差0.7%,P = 0.0001),Caspase 9阳性细胞少(2.6%标准差0.6%对12%标准差1%,P = 0.0001)。静脉曲张组和对照组中Fas和caspase 8的免疫组化检测结果保持相同。

结论

静脉曲张中层的细胞凋亡下调。这种调节异常归因于内源性途径的紊乱,涉及大隐静脉主干、主要属支和副静脉。这一过程可能是原发性静脉曲张的病因之一。

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