Relapse of varicose veins of lower extremities

G. V. Yarovenko, Яровенко Галина Викторовна, A. V. Fesun, Фесюн Алексей Витальевич
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Abstract

According to modern data, there are no signs of chronic venous disease in only 15.9% of people. Observing the clinical data of recent years, there is a tendency to increase the number of people with venous diseases and, unfortunately, the number of young patients is increasing (there are data that schoolchildren of the senior classes have signs of varicose transformation in 10-15%). Polymorphism of matrix metalloproteinase-12 is a key link in the pathogenesis of varicose veins.We conducted surveys of 50 patients. The average age is 43.7 ± 15.9 years, of them women 32, men 18 people. All patients with the class C2-C6 varicose veins (CEAP-classifier) ​​were divided into two groups by the method of serial sampling: group I (n = 20) - with relapse of varicose veins; Group II (n = 30) - patients treated with varicose disease for the first time. The only exception was patients with deferred vein thrombosis. Ultrasound diagnosis of the main veins of the lower extremities and genomic analysis of blood samples of patients was used.The obtained results confirm that in patients of the I group the MMP-12 gene occurs in 80% of cases (homo- and heterozygous variation), whereas in group II only in 33.3% of cases. The Pearson consensus criterion is 10.4 (the critical value of the criterion is 6.63). The significance level of this relationship corresponds to p <0.01. The statistical significance of the frequency of recurrence of varicose disease and the MMP-12 gene was established using the Spearman rank correlation coefficient, which is equal to 1,000 (criterion value is 0.398). Dependence of signs is statistically significant, with p <0.05
下肢静脉曲张复发
根据现代数据,只有15.9%的人没有慢性静脉疾病的迹象。观察近年来的临床资料,静脉疾病患者有增加的趋势,不幸的是,年轻患者的数量正在增加(有数据显示,10-15%的高年级学童有静脉曲张转化的迹象)。基质金属蛋白酶-12多态性是静脉曲张发病的关键环节。我们对50名患者进行了调查。平均年龄43.7±15.9岁,其中女性32人,男性18人。所有C2-C6级静脉曲张(ceap分类)患者通过连续抽样的方法分为两组:I组(n = 20) -静脉曲张复发;II组(n = 30) -首次治疗静脉曲张的患者。唯一的例外是延迟静脉血栓患者。对患者下肢主静脉进行超声诊断,并对患者血液样本进行基因组分析。所获得的结果证实,在I组患者中,MMP-12基因出现在80%的病例中(同源和杂合变异),而在II组中仅出现在33.3%的病例中。Pearson共识标准为10.4(该标准的临界值为6.63)。这种关系的显著性水平对应于p <0.01。采用Spearman秩相关系数,确定静脉曲张疾病复发频率与MMP-12基因的相关性为1000(判据值为0.398),具有统计学意义。体征相关性有统计学意义,p <0.05
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