AI Article Synopsis

  • Tacrolimus, when used with mycophenolate mofetil and glucocorticoids, is a key part of immunosuppressive therapy for kidney transplant patients, and both intrapatient variability (IPV) and C/D ratio impact kidney function.
  • In a study involving 170 patients, researchers assessed the C/D ratio and IPV over a period of up to 70 months post-transplant, finding a negative correlation between the C/D ratio and creatinine levels, indicating better kidney function with higher C/D ratios.
  • Ultimately, the study concludes that while the C/D ratio is effective for evaluating tacrolimus metabolism's impact on kidney function, it does not influence IPV, and the C/D ratio tends to increase over

Article Abstract

Tacrolimus, in combination with mycophenolate mofetil and glucocorticoids, is the basis of immunosuppressive therapy after renal transplantation. Tacrolimus intrapatient variability (IPV) and the blood concentration normalized by the dose (concentration/dose ratio, C/D ratio) both have an effect on the function of the transplanted kidney. In this study, we examined whether the metabolism rate affected IPV, whether the C/D ratio value was stable in the long-term follow-up, and whether it could be used for IPV measurements. In addition, our study population was examined for the effect of the C/D ratio and IPV on long-term renal function. The C/D ratio and IPV were examined in 170 patients at appointments held at 3, 6, 12 and 24 months after RTx. The average time post renal transplantation was 70 months. Renal function defined as creatinine concentration at the last appointment was examined. Results: the mean C/D ratio in the study group was 1.63. A negative correlation between the C/D ratio and creatinine concentration at the end of the follow-up was observed. Between the C/D ratio < and ≥1.63 groups, significant differences in creatinine concentration at the last appointment were found. No relationship was identified between the mean C/D ratio and IPV. The C/D ratio values increased significantly over a longer post-transplant period (12, 24, 60 and 120 m). We did not find a correlation between the mean IPV and the creatinine concentration from the last appointment. Our study group was divided into terciles according to IPV, while no renal graft function differences were found at the same appointment. Conclusion: the C/D ratio is useful for assessing the effects of the metabolism rate of tacrolimus on the long-term renal graft function. The C/D ratio does not affect the IPV value. IPV calculated from variability of the C/D ratio does not influence transplanted kidney function. The C/D changes over time.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687762PMC
http://dx.doi.org/10.3390/biomedicines10112860DOI Listing

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