Hertzberg Mark S
Department of Haematology, Westmead Hospital, Westmead, New South Wales, Australia.
Semin Thromb Hemost. 2005 Feb;31(1):33-8. doi: 10.1055/s-2005-863803.
Venous thrombosis is a multicausal disease due to the interaction of genetic and environmental risk factors. Some of the recently discovered genetic risk factors, such as factor V Leiden and prothrombin G20210A mutations, are quite common in the population. Accordingly, laboratory investigation of thrombophilic disorders has expanded to incorporate molecular assays, which unlike functional assays, are unequivocal with no borderline values. When testing for these mutations, specific issues of patient management need to be addressed, such as the duration of anticoagulant therapy, risk stratification for primary or secondary prophylaxis, and family studies. Criteria used to select specific DNA methodologies will center on the issues of cost, automation, speed, reliability, and simplicity. A variety of molecular methods fulfill many but not all of these criteria, whereas the new, semiautomated methodologies of real-time polymerase chain reaction and DNA microarrays offer the potential for widespread application and utility in the future.
静脉血栓形成是一种由遗传和环境风险因素相互作用导致的多病因疾病。一些最近发现的遗传风险因素,如因子V莱顿突变和凝血酶原G20210A突变,在人群中相当常见。因此,血栓形成倾向疾病的实验室检查已扩展到纳入分子检测,与功能检测不同,分子检测明确无误,没有临界值。在检测这些突变时,需要解决患者管理的特定问题,如抗凝治疗的持续时间、一级或二级预防的风险分层以及家族研究。用于选择特定DNA方法的标准将围绕成本、自动化、速度、可靠性和简单性等问题。多种分子方法满足了其中许多但并非全部标准,而实时聚合酶链反应和DNA微阵列等新的半自动方法在未来具有广泛应用和实用的潜力。