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凝血因子V Leiden与高同型半胱氨酸血症或亚甲基四氢叶酸还原酶677TT基因型在静脉血栓形成中无相互作用。已发表研究的荟萃分析及一项大型单病例研究结果。

No interaction between factor V Leiden and hyperhomocysteinemia or MTHFR 677TT genotype in venous thrombosis. Results of a meta-analysis of published studies and a large case-only study.

作者信息

Keijzer Miranda B A J, Borm George F, Blom Henk J, Bos Gerard M J, Rosendaal Frits R, den Heijer Martin

机构信息

Department of Endocrinology, Radboud University Nijmegen Medical Centre, Geert Grooteplein 8, 6525 GA Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.

出版信息

Thromb Haemost. 2007 Jan;97(1):32-7.

PMID:17200768
Abstract

Homocysteine may have a thrombogenic effect through inhibition of inactivation of factor Va by activated protein C. Because factor V Leiden also leads to resistance of factor V to activated protein C, it would be possible that both factors show interaction for the risk of venous thrombosis. This has been reported in some studies, but not in others. We performed a metaanalysis to investigate a possible interaction between factor V Leiden and hyperhomocysteinemia, including 825 subjects with venous thrombosis and 2,109 controls, for the risk of venous thrombosis. In addition, we assessed a possible interaction between factor V Leiden and MTHFR 677TT genotype (the most common genetic determinant of homocysteine levels), including 2,547 subjects with venous thrombosis and 4,327 controls. We also investigated the interaction effect of factor V Leiden and hyperhomocysteinemia in a large case-only study using data of the VITRO study, including 2,077 subjects with first-time venous thrombosis. The meta-analysis yielded no evidence for additive or multiplicative interaction between factor V Leiden and hyperhomocysteinemia [relative excess risk due to interaction (RERI) -1.77 (95%CI -8.61 to 5.08) and multiplicative interaction term 0.86 (95%CI 0.35 to 2.14)]. The case-only study also showed no interaction effect [0.58 (95%CI 0.29 to 1.16)]. Also the metaanalysis on factor V Leiden and MTHFR 677TT yielded no evidence of interaction; RERI 0.13 (95%CI -3.60 to 3.86) and multiplicative interaction term 1.23 (95%CI 0.72 to 2.11). Both the meta-analyses of published studies and a large case-only study did not show evidence for interaction between factor V Leiden and hyperhomocysteinemia for risk of venous thrombosis.

摘要

同型半胱氨酸可能通过抑制活化蛋白C对因子Va的失活作用而产生致血栓形成效应。由于因子V莱顿突变也会导致因子V对活化蛋白C产生抵抗,因此这两种因素在静脉血栓形成风险方面可能存在相互作用。一些研究报道了这种情况,但其他研究并未发现。我们进行了一项荟萃分析,以研究因子V莱顿突变与高同型半胱氨酸血症之间可能存在的相互作用,纳入了825例静脉血栓形成患者和2109例对照,以评估静脉血栓形成风险。此外,我们评估了因子V莱顿突变与亚甲基四氢叶酸还原酶(MTHFR)677TT基因型(同型半胱氨酸水平最常见的遗传决定因素)之间可能存在的相互作用,纳入了2547例静脉血栓形成患者和4327例对照。我们还利用VITRO研究的数据,在一项大型单纯病例研究中调查了因子V莱顿突变与高同型半胱氨酸血症的相互作用效应,该研究纳入了2077例首次发生静脉血栓形成的患者。荟萃分析未发现因子V莱顿突变与高同型半胱氨酸血症之间存在相加或相乘相互作用的证据[交互作用所致相对超额危险度(RERI)为-1.77(95%可信区间为-8.61至5.08),相乘交互作用项为0.86(95%可信区间为0.35至2.14)]。单纯病例研究也未显示交互作用效应[0.58(95%可信区间为0.29至1.16)]。对因子V莱顿突变与MTHFR 677TT的荟萃分析也未发现相互作用的证据;RERI为0.13(95%可信区间为-3.60至3.86),相乘交互作用项为1.23(95%可信区间为0.72至2.11)。已发表研究的荟萃分析和一项大型单纯病例研究均未显示因子V莱顿突变与高同型半胱氨酸血症在静脉血栓形成风险方面存在相互作用的证据。

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