Transferrin saturation can serve as a novel biomarker for predicting the
occurrence and development of BK virus-related nephropathy after kidney
transplantation.
Abstract
Background It is unclear whether iron levels affect BKPyV
reactivation after kidney transplantation. Our goal is to analyze the
relationship between preoperative iron levels in kidney transplant
recipients and postoperative BK virus reactivation. Additionally, we aim
to develop and validate a personalized prediction model for BK virus
reactivation. Methods We retrospectively analyzed the
relationship between preoperative iron levels and BK virus reactivation
in 626 kidney transplant recipients. The cohort was randomly divided
into a training cohort and a validation cohort in a 2:1 ratio.
Independent risk factors associated with BK virus reactivation were
identified in the training cohort using COX proportional hazards
regression. Based on the analysis results, a nomogram was constructed to
develop individualized risk prediction models for BK viremia and BK
virus nephropathy. Results Among the 626 kidney transplant
recipients, 38 cases (6.1%) of BK viremia and 18 cases (2.9%) of BK
virus nephropathy were diagnosed. Univariate analysis revealed that
UIBC, TIBC, and TSAT were associated with the occurrence of BK viremia
and BKPyVAN. In the training cohort, multivariate analysis showed that
preoperative TSAT was an independent risk factor for BK viremia (1.03
[1.01-1.05], P=0.009) and BK virus nephropathy (1.05
[1.01-1.09], P=0.011). The C-index for the nomogram model predicting
BK viremia and BK virus nephropathy after kidney transplantation was
0.77 and 0.82 in the training cohort, and 0.88 and 0.92 in the
validation cohort, respectively. Conclusions Preoperative
transferrin saturation levels in kidney transplant recipients are
closely associated with the reactivation and progression of BK virus
after transplantation.