4.7 Article

Effects of CYP3A5 Genotypes on Thrombocytopenia in Liver Transplantation Patients Treated with Tacrolimus

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BIOMEDICINES
卷 11, 期 11, 页码 -

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MDPI
DOI: 10.3390/biomedicines11113088

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deceased-donor liver transplantation (DDLT); tacrolimus; thrombocytopenia

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Platelet counts declined significantly after DDLT, especially on postoperative day 3, and continued at low levels for a week thereafter in all groups. Tacrolimus nadir levels were significantly higher in GG/GG genotype patients compared to A*/A* genotype patients, leading to a higher incidence of hemorrhage. Risk of thrombocytopenia after DDLT on postoperative day 3 was increased with a combination of specific tacrolimus blood concentration and spleen size.
Background: Thrombocytopenia is a complication after liver transplantation. This study's aims were to evaluate the role of CYP3A5 genotypes on tacrolimus-induced thrombocytopenia after orthotopic liver transplantation. Methods: In this retrospective case-control study, data from 100 patients who underwent deceased-donor liver transplantation (DDLT) were divided into CYP3A5*3 genotype (donor/recipient) tacrolimus fast- (A*/A*, n = 22), intermediate- (A*/GG, n = 20; GG/A*, n = 31) and slow-metabolizer (GG/GG, n = 27) groups. Platelet count changes and prognosis for 180 days after surgery were compared. Results: Platelet counts declined significantly after DDLT, especially on postoperative day (POD) 3, and continued at low levels for a week thereafter in all groups. In the GG/GG group, platelet counts on POD3 (50.29 +/- 5.44 x 10(9)/L) were the lowest among the groups (A*/A*, 71.00 +/- 6.22 x 10(9)/L; A*/GG, 57.95 +/- 6.21 x 10(9)/L; GG/A*, 75.90 +/- 5.56 x 10(9)/L) (p = 0.006). Compared with the A*/A* genotype, tacrolimus nadir levels were significantly higher in GG/GG genotype patients, who also exhibited a higher incidence of hemorrhage (22.2%, p = 0.011). A combination of a nadir blood concentration of tacrolimus >= 4.74 ng/mL and spleen size >= 165.5 mm was a risk factor for increased thrombocytopenia after DDLT on POD3, with an AUC of 0.735 (sensitivity, 77.2%; specificity, 41.7%). Conclusions: A high blood concentration of tacrolimus after the early stage of DDLT is a major risk factor for hemorrhage. For the CYP3A5 genotype (GG/GG), controlling the blood concentration of tacrolimus below the target concentration until POD3 can avoid thrombocytopenia-related complications.

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