Sessa A, Esposito A, Iavicoli G D, Lettieri E, Dente G, Costa C, Bergallo M, Rossano R, Capuano M
Day Hospital, Post Trapianto Rene UOC, Nefrologia e Dialisi PO Dei Pellegrini, Napoli, Italy.
Transplant Proc. 2010 May;42(4):1148-55. doi: 10.1016/j.transproceed.2010.03.069.
Renal transplantation is the definitive treatment for many metabolic abnormalities of uremic patients, although it is only partially effective for renal osteodystrophy, which may interact with posttransplant renal osteopathy. Osteopenic-osteoporotic syndrome represents, together with fractures secondary to osteoporosis and osteonecrosis, the bone complication most related to renal transplantation. Several factors contribute to the pathogenesis of posttransplantation osteoporosis, particularly immunosuppressive treatment. In this study, we evaluated the prevalence of factors related to posttransplant renal osteopathy and the clinical impact of immunosuppressive protocols. We studied 24 renal transplant recipients with hypercalcemia. Glomerular filtration rate was >50 mL/min. Mean age, time on dialysis, and time from transplantation were 49.6, 5.4, and 6.9 years, respectively. We evaluated serum and urine calcium and phosphorus, calcitonin, parathormone, bone-specific alkaline phosphatase, osteocalcin, urine deoxypyridinoline, telopeptide of type 1 procollagen, 1,25-(OH)(2) and 25-OH vitamin D, parathyroid ultrasound, and computerized bone mineralometry. The combination of sirolimus and steroids resulted in the most disadvantageous outcomes regarding alkaline phosphatase and mineralometry. Calcineurin inhibitors did not significantly influence bone metabolism markers; mycophenolate mofetil evidenced no effect on bone. According to the literature, steroids account for the abnormalities found in our patients and in severe osteopenia. Several factors may contribute to the development of osteoporosis and fractures in transplantation patients, although they are overcome by the prominent effect of steroids. In patients at high risk of osteoporosis, steroid-free therapy should be considered. Everolimus is indicated for diseases with bone loss. Combined therapy with everolimus and mycophenolic acid without cyclosporine and steroids, seemed to be particularly indicated. Prophylactic treatments should be commenced early. No single marker was useful to diagnose posttransplant renal osteopathy. The definitive diagnosis should be made by bone biopsy during transplantation, and noninvasive procedures, such as densitometry and evaluation of biologic markers, may be useful during follow-up.
肾移植是治疗尿毒症患者多种代谢异常的决定性方法,尽管它对肾性骨营养不良仅部分有效,而肾性骨营养不良可能与移植后肾性骨病相互作用。骨质减少 - 骨质疏松综合征与骨质疏松和骨坏死继发的骨折一起,是与肾移植最相关的骨并发症。移植后骨质疏松的发病机制有多种因素,特别是免疫抑制治疗。在本研究中,我们评估了与移植后肾性骨病相关因素的患病率以及免疫抑制方案的临床影响。我们研究了24例高钙血症的肾移植受者。肾小球滤过率>50 mL/分钟。平均年龄、透析时间和移植后时间分别为49.6岁、5.4年和6.9年。我们评估了血清和尿钙、磷、降钙素、甲状旁腺激素、骨特异性碱性磷酸酶、骨钙素、尿脱氧吡啶啉、I型前胶原端肽、1,25 - (OH)(2)和25 - OH维生素D、甲状旁腺超声以及计算机化骨密度测定。西罗莫司和类固醇的联合使用在碱性磷酸酶和骨密度测定方面导致了最不利的结果。钙调神经磷酸酶抑制剂对骨代谢标志物没有显著影响;霉酚酸酯对骨没有影响。根据文献,类固醇是导致我们患者出现异常以及严重骨质减少的原因。移植患者骨质疏松和骨折的发生可能有多种因素,尽管它们被类固醇的显著作用所掩盖。对于骨质疏松高危患者,应考虑无类固醇治疗。依维莫司适用于有骨质流失的疾病。依维莫司与霉酚酸联合治疗,不使用环孢素和类固醇,似乎特别适用。预防性治疗应尽早开始。没有单一标志物可用于诊断移植后肾性骨病。最终诊断应在移植期间通过骨活检进行,而在随访期间,诸如骨密度测定和生物标志物评估等非侵入性程序可能有用。