Abstract: FR-PO249
Mineral Bone Disorders after Preemptive Kidney Transplantation
Session Information
- Mineral Bone Disease: Transplant and Kidney Stones
October 25, 2024 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Bone and Mineral Metabolism
- 502 Bone and Mineral Metabolism: Clinical
Authors
- Tinajero Sánchez, Denisse Nayely, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ciudad de Mexico, Ciudad de México, Mexico
- Castro Almanza, Carlos Antonio, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ciudad de Mexico, Ciudad de México, Mexico
- Berman, Nathan, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ciudad de Mexico, Ciudad de México, Mexico
- Canaviri, Vianca Anabel, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ciudad de Mexico, Ciudad de México, Mexico
- Cojuc, Gabriel, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ciudad de Mexico, Ciudad de México, Mexico
- Marino-Vazquez, Lluvia A., Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ciudad de Mexico, Ciudad de México, Mexico
- Morales-Buenrostro, Luis E., Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ciudad de Mexico, Ciudad de México, Mexico
- Ramirez-Sandoval, Juan Carlos, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ciudad de Mexico, Ciudad de México, Mexico
Background
Mineral bone disorders are common after kidney transplantation. Preemptive kidney transplantation (PKT) may reduce these risks. We aimed to assess the long-term effects of PKT on mineral metabolism outcomes
Methods
Retrospective cohort study with a median follow-up time of 4 years (range 1-9). We compared kidney transplant recipients (KTRs) who underwent PKT (n=26) with KTRs who received hemodialysis before transplantation (n=359). The outcomes included iPTH, free calcium, phosphate, and eGFR trajectories, as well as the presence of post-transplant persistent hyperparathyroidism (iPTH > upper reference level), persistent hypercalcemia (free Ca >5.2 mg/dL) and graft dysfunction (<30 mL/min/1.73m2). Asymptomatic mild hypercalcemia was monitored unless complications developed
Results
Pre-transplant iPTH levels were similar between the PKT and non-PKT groups (median 479 [238-828] Vs 392 [145-603]; p=0.064). There were no differences in the trajectory of biochemical parameters between groups after transplantation. Similarly, when comparing PKT and non-PKT KTRs, we observed no differences in persistent hyperparathyroidism (39% Vs. 45%, P=0.54), persistent hypercalcemia (73% Vs. 62%, p=0.17), and graft dysfunction (4% Vs. 6%, p=0.58). In both groups, PTH levels below 300 were a protective factor against the development of post-transplant hyperparathyroidism or hypercalcemia
Conclusion
PKT in KTRs without controlled hyperparathyroidism did not decrease the risk of hyperparathyroidism or persistent hypercalcemia after transplantation. Medical treatment of mineral bone disorders, with a target iPTH below 300, likely decreases the risk of adverse outcomes in KTRs, including individuals undergoing PKT