Evidence for a genetic role in varicose veins and chronic venous insufficiency

被引:46
作者
Krysa, J. [1 ]
Jones, G. T. [1 ]
van Rij, A. M. [1 ]
机构
[1] Univ Otago, Dunedin Sch Med, Dept Surg, Dunedin 9053, New Zealand
关键词
varicose veins; venous; genome-wide scan; genetics; DIFFERENTIALLY EXPRESSED GENES; CORONARY-ARTERY-DISEASE; LEG ULCERATION; GENOMEWIDE ASSOCIATION; EPIGENETIC REGULATION; C677T MUTATION; FACTOR-XIII; TNF-ALPHA; PREVALENCE; POLYMORPHISMS;
D O I
10.1258/phleb.2011.011030
中图分类号
R61 [外科手术学];
学科分类号
摘要
There is a strong body of circumstantial evidence which implicates genetics in the aetiology and pathology of varicose veins and venous ulcer disease. The aim of this review is to consider the current knowledge of the genetic associations and the ways in which new genetic technologies may be applied to advancing our understanding of the cause and progression of these venous diseases. A number of publications have used a candidate gene approach to identify genes implicated in venous disease. Although these studies have opened up important new insights, there has been a general failure to replicate results in an independent cohort of patients. With our limited knowledge of the biological pathways involved in the pathogenesis of venous disease we are not in a strong position to formulate truly erudite a priori candidate gene hypothesis-directed studies. A genome-wide association study should therefore be considered to help further our understanding of the genetic basis of venous disease. Due to the large sample sizes required for discovery and validation, using the new generations of molecular technologies, it will be necessary to form collaborating groups in order to successfully advance the field of venous disease genetics.
引用
收藏
页码:329 / 335
页数:7
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