Bone mineral metabolism disease, which included persistent hyperparathyroidism, is common after successful kidney transplantation (KT) and is related with negative outcomes in kidney transplant recipients. ere is a lack of information about bone mineral metabolism, persistent hyperparathyroidism, and its risk factors in Latin kidney transplant recipients (KTRs). Material and Methods: A retrospective study was conducted in 74 patients aged 18-50 years with evolution of 12 months after KT and estimated glomerular filtration rate (eGFR) >60 ml/min; biochemical data of bone mineral metabolism before and at 1, 3, 6, and 12 months of KT were registered. Results. Age was 33 (IQR 27-37) years; 54% (n � 40) were men. Before KT, all patients had hyperparathyroidism, 40% (n � 30) hypocalcemia, 86% (n � 64) hyperphosphatemia, and 42% (n � 31) hyperphosphatasemia. After KT, an increase of calcium and a diminution of PTH, phosphorus, and alkaline phosphatase were corroborated (p � 0.001). All patients had hypovitaminosis D (deficiency: 91% (n � 67); insufficiency: 9% (n � 7)); 40% (n � 30) had persistent hyperparathyroidism at 12 months. Hyperphosphatasemia before KT (OR � 4.17 (95% CI: 1.21-14.44); p � 0.04), hyperparathyroidism at 6 months (OR � 1.84 (95% CI; 1.67-2.06); p � 0.02), hypovitaminosis D at 6 months (OR � 3.94 (95% CI: 1.86-17.9); p � 0.01), and hyperphosphatasemia at 6 months (OR � 1.47 (95% CI: 1.07-2.86); p � 0.03) were risk factors for persistent hyperparathyroidism at 12 months after KT. Conclusion. Persistent hyperparathyroidism at 6 months, hypovitaminosis D, and hyperphosphatasemia are risk factors for persistent hyperparathyroidism at 1 year of KT in Latin population.