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Effects of CYP3A5 Genotypes on Thrombocytopenia in Liver Transplantation Patients Treated with Tacrolimus
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 und...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669143/ https://www.ncbi.nlm.nih.gov/pubmed/38002088 http://dx.doi.org/10.3390/biomedicines11113088 |
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author | Guo, Zhe Chen, Qi Liu, Juan Li, Shan Wang, He Tang, Rui Zhang, Zhenyu |
author_facet | Guo, Zhe Chen, Qi Liu, Juan Li, Shan Wang, He Tang, Rui Zhang, Zhenyu |
author_sort | Guo, Zhe |
collection | PubMed |
description | 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 × 10(9)/L) were the lowest among the groups (A*/A*, 71.00 ± 6.22 × 10(9)/L; A*/GG, 57.95 ± 6.21 × 10(9)/L; GG/A*, 75.90 ± 5.56 × 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. |
format | Online Article Text |
id | pubmed-10669143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106691432023-11-17 Effects of CYP3A5 Genotypes on Thrombocytopenia in Liver Transplantation Patients Treated with Tacrolimus Guo, Zhe Chen, Qi Liu, Juan Li, Shan Wang, He Tang, Rui Zhang, Zhenyu Biomedicines Article 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 × 10(9)/L) were the lowest among the groups (A*/A*, 71.00 ± 6.22 × 10(9)/L; A*/GG, 57.95 ± 6.21 × 10(9)/L; GG/A*, 75.90 ± 5.56 × 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. MDPI 2023-11-17 /pmc/articles/PMC10669143/ /pubmed/38002088 http://dx.doi.org/10.3390/biomedicines11113088 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Guo, Zhe Chen, Qi Liu, Juan Li, Shan Wang, He Tang, Rui Zhang, Zhenyu Effects of CYP3A5 Genotypes on Thrombocytopenia in Liver Transplantation Patients Treated with Tacrolimus |
title | Effects of CYP3A5 Genotypes on Thrombocytopenia in Liver Transplantation Patients Treated with Tacrolimus |
title_full | Effects of CYP3A5 Genotypes on Thrombocytopenia in Liver Transplantation Patients Treated with Tacrolimus |
title_fullStr | Effects of CYP3A5 Genotypes on Thrombocytopenia in Liver Transplantation Patients Treated with Tacrolimus |
title_full_unstemmed | Effects of CYP3A5 Genotypes on Thrombocytopenia in Liver Transplantation Patients Treated with Tacrolimus |
title_short | Effects of CYP3A5 Genotypes on Thrombocytopenia in Liver Transplantation Patients Treated with Tacrolimus |
title_sort | effects of cyp3a5 genotypes on thrombocytopenia in liver transplantation patients treated with tacrolimus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669143/ https://www.ncbi.nlm.nih.gov/pubmed/38002088 http://dx.doi.org/10.3390/biomedicines11113088 |
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