Kamei Hideya, Nakamura Taro, Nagai Shunji, Ishigami Masatoshi, Hamajima Nobuyuki
From the Department of Transplantation Surgery, Nagoya University, Nagoya, Japan.
Exp Clin Transplant. 2016 Jun;14(3):313-6.
Liver transplant in patients with preexisting portal vein thrombosis involves complicated surgical procedures and increased blood loss, indicating the need for further surgical innovations to overcome these difficulties. Patients who are at high risk of developing portal vein thrombosis may benefit from prophylactic anticoagulant therapy while on the transplant wait list. Homozygosity for C677T polymorphism in the methylenetetrahydrofolate reductase gene has been associated with a high plasma homocysteine concentration, which is a risk factor for venous thrombosis. This study investigated the association between C677T polymorphism in the methylenetetrahydrofolate reductase gene and preexisting portal vein thrombosis in patients with liver cirrhosis undergoing liver transplant.
C677T polymorphism in the methylenetetrahydrofolate reductase gene was investigated in 48 patients who underwent liver transplant at Nagoya University.
Of 48 patients, 7 (14.6%) had preexisting portal vein thrombosis confirmed at transplant. The frequency of methylenetetrahydrofolate reductase gene C677T genotype in recipients was significantly associated with preexisting portal vein thrombosis (P = .009, with P ≤ .013 considered significant). Logistic regression analysis showed that the TT genotype of the methylenetetrahydrofolate reductase gene was significantly associated with a higher incidence of preexisting portal vein thrombosis compared with the CC and CT genotypes (odds ratio of 14.6, 95% confidence interval, 1.86-115.21; P = .011).
The TT genotype of the methylenetetrahydrofolate reductase gene may be associated with a higher incidence of preexisting portal vein thrombosis, as confirmed at liver transplant. Identification of this genotype in patients with liver cirrhosis at the time of placement on a wait list for liver transplant may enable preventive therapy for portal vein thrombosis in these patients, reducing the complexity of surgical procedures.
已有门静脉血栓形成的患者进行肝移植,手术操作复杂,失血量大,这表明需要进一步的手术创新来克服这些困难。在等待肝移植期间,有发生门静脉血栓形成高风险的患者可能会从预防性抗凝治疗中获益。亚甲基四氢叶酸还原酶基因C677T多态性的纯合子与高血浆同型半胱氨酸浓度相关,而高血浆同型半胱氨酸浓度是静脉血栓形成的一个危险因素。本研究调查了亚甲基四氢叶酸还原酶基因C677T多态性与肝硬化患者肝移植时已有门静脉血栓形成之间的关联。
对在名古屋大学接受肝移植的48例患者进行了亚甲基四氢叶酸还原酶基因C677T多态性研究。
48例患者中,7例(14.6%)在移植时被证实已有门静脉血栓形成。受体中亚甲基四氢叶酸还原酶基因C677T基因型的频率与已有门静脉血栓形成显著相关(P = 0.009,P≤0.013被认为具有显著性)。逻辑回归分析显示,与CC和CT基因型相比,亚甲基四氢叶酸还原酶基因的TT基因型与已有门静脉血栓形成的较高发生率显著相关(比值比为14.6,95%置信区间为1.86 - 115.21;P = 0.011)。
如在肝移植时所证实的,亚甲基四氢叶酸还原酶基因的TT基因型可能与已有门静脉血栓形成的较高发生率相关。在肝硬化患者被列入肝移植等待名单时识别该基因型,可能使这些患者能够接受门静脉血栓形成的预防性治疗,降低手术操作的复杂性。