Association between salivary microbiota and tacrolimus pharmacokinetic variability in kidney transplant

被引:2
作者
Xiang, Xuyu [1 ,2 ]
Zhu, Yi [1 ,2 ]
Wang, Tianyin [1 ,2 ]
Ding, Peng [1 ,2 ]
Cheng, Ke [1 ,2 ]
Ming, Yingzi [1 ,2 ]
机构
[1] Cent South Univ, Xiangya Hosp 3, Transplantat Ctr, Changsha 410013, Peoples R China
[2] Natl Hlth Commiss, Engn & Technol Res Ctr Transplantat Med, Changsha, Peoples R China
关键词
Biomarker; Salivary microbiota; Tacrolimus; Pharmacokinetic variability; Immunosuppressive efficacy; Kidney transplantation; HIGH INTRAPATIENT VARIABILITY; CAPNOCYTOPHAGA; FK-506; IMMUNOSUPPRESSANT; CYCLOSPORINE;
D O I
10.1016/j.ygeno.2024.110952
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Kidney transplantation (KT) serves as a highly effective treatment for end-stage renal disease (ESRD). Nonetheless, the administration of tacrolimus, a commonly used immunosuppressant in KT, faces challenges due to the lack of dependable biomarkers for its efficacy and the considerable variability in tacrolimus pharmacokinetics (TacIPV). In this study, 183 saliva samples from 48 KT recipients under tacrolimus therapy, alongside 9 healthy control samples, were subjected to 16S rRNA sequencing. The analysis revealed significant differences in the composition of salivary microbiota among KT recipients, patients with ESRD, and healthy controls. Moreover, trough blood concentrations (C0) of tacrolimus were associated with alterations in microbiota composition. Notably, Capnocytophage consistently exhibited a negative correlation in both group-level and individual trends. Furthermore, distinct taxa were identified that effectively distinguished recipients with varying TacIPV, as demonstrated by a cross-validation random forest model (mean AUC = 0.7560), with Anaerolinea emerging as a prominent contributor to the classifier. These findings suggest that salivary microbiota is closely linked to tacrolimus C0 levels and could aid clinicians in differentiating KT recipients based on TacIPV.
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页数:11
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