Klinge U, Si Z Y, Zheng H, Schumpelick V, Bhardwaj R S, Klosterhalfen B
Department of Surgery, Technical University of Aachen, Germany.
J Invest Surg. 2001 Jan-Feb;14(1):47-54. doi: 10.1080/089419301750072202.
The late appearance ofincisional hernias several years after laparotomy and the high recurrence rates after operation strongly imply the presence of a disorder of the connective tissue, although a specific defect in patients with incisional hernias has not yet been identified. In the present study we used both immunohistochemistry and Western blot analysis to evaluate the ratio of collagen I and III and the expression of the metalloproteinases (MMP) 1 and 13 in the fascia of patients with incisional or recurrent incisional hernias. Samples of healthy skin or stable skin scar in patients without hernias served as controls. Altogether, our data indicated a significantly decreased ratio of collagen I/III in the fascia of patients with incisional hernias and recurrent incisional hernias. Furthermore, in these patients the expression of MMP-1 was decreased compared to the controls, whereas MMP-13 could not be detected in any fascia sample, with or without hernias present. For the first time, our results give evidence of the existence of a possible collagen disorder in these patients. The decreased ratio ofcollagen I/III is explainable due to a relative increase of collagen type III, which is known to be characterized by thin fibril diameters and lowered mechanical strength. The altered collagen ratio might be the result of the decreased activity of MMP-1, whereas the absent MMP-13 expression did not seem to modify the scar formation. Thus, our data indicate the presence of collagen metabolic disorders in patients with incisional hernias and recurrent incisional hernias. Furthermore, these results might explain the poor results of a mesh-free hernia repair, which again builds up scar tissue of inadequate collagen composition and strength.
剖腹手术后数年切口疝才出现,且手术后复发率高,这强烈提示存在结缔组织疾病,尽管切口疝患者的具体缺陷尚未明确。在本研究中,我们使用免疫组织化学和蛋白质印迹分析来评估切口疝或复发性切口疝患者筋膜中I型和III型胶原蛋白的比例以及金属蛋白酶(MMP)1和13的表达。无疝患者的健康皮肤或稳定皮肤瘢痕样本作为对照。总体而言,我们的数据表明,切口疝和复发性切口疝患者筋膜中I型/III型胶原蛋白的比例显著降低。此外,与对照组相比,这些患者中MMP-1的表达降低,而在任何有无疝的筋膜样本中均未检测到MMP-13。我们的结果首次证明这些患者可能存在胶原蛋白紊乱。I型/III型胶原蛋白比例降低可归因于III型胶原蛋白相对增加,已知III型胶原蛋白的特征是纤维直径细且机械强度低。胶原蛋白比例的改变可能是MMP-1活性降低的结果,而MMP-13表达缺失似乎并未改变瘢痕形成。因此,我们的数据表明切口疝和复发性切口疝患者存在胶原蛋白代谢紊乱。此外,这些结果可能解释了无网片疝修补术效果不佳的原因,该手术再次形成了胶原蛋白组成和强度不足的瘢痕组织。