首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Longitudinal changes in BMD and fracture risk in orthotopic liver transplant recipients not using bone-modifying treatment
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Longitudinal changes in BMD and fracture risk in orthotopic liver transplant recipients not using bone-modifying treatment

机译:未采用骨修饰治疗的原位肝移植患者骨密度的纵向变化和骨折风险

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Osteoporosis is prevalent in end-stage liver disease, but data on long-term changes in bone mineral density (BMD) and related fracture incidence after orthotopic liver transplantation (OLT) are scarce. We evaluated BMD changes up to 5 years in consecutive recipients of a successful OLT at the Leiden University Medical Centre between 2000 and 2011, in whom sequential BMD data were available. Spinal radiographs were available at time of screening and at 6 and 12 months post-OLT and were assessed for vertebral fractures by two independent observers using Genant's semiquantitative method. Patients were excluded from the study when started on bisphosphonates. A total of 201 patients (71% men), median age 53 years (range, 18-70 years) were included in the study. Most common liver pathology was viral (27%) or alcoholic liver disease (25%). All patients received prednisone for at least 6 months after transplantation and the majority received either tacrolimus or cyclosporine for immunosuppression. At time of screening for OLT, osteoporosis and osteopenia were found in 18% and 36% of patients at the lumbar spine (LS), respectively, and in 9% and 42% at the femoral neck (FN), respectively. T-scores declined significantly at both sites 6 months after OLT, but increased thereafter at the LS, reaching pretransplantation values at 2 years and remaining stable thereafter. FN T-scores remained consistently lower than pretransplantation values. The prevalence of vertebral fractures increased from 56% at screening to 71% at 1 year after OLT, with a fracture incidence of 34%. BMD changes did not predict fracture risk. Osteoporosis, osteopenia, and vertebral fractures are prevalent in patients with end-stage liver disease. An overall decline in BMD is observed within the first 6 months after OLT, with subsequent recovery to pretransplantation values at the LS, but not at the FN. Vertebral fracture risk is high after OLT regardless of changes in BMD.
机译:骨质疏松症在终末期肝病中很普遍,但是关于原位肝移植(OLT)后骨矿物质密度(BMD)和相关骨折发生率的长期变化的数据很少。我们评估了2000年至2011年期间在莱顿大学医学中心成功获得OLT的连续接受者中连续5年内BMD的变化,其中可获得连续的BMD数据。筛查时以及OLT后6个月和12个月时可获得脊柱X光片,并由两名独立的观察员使用Genant的半定量方法对椎骨骨折进行了评估。开始使用双膦酸盐治疗时,患者被排除在研究之外。该研究共纳入201名患者(男性占71%),中位年龄53岁(范围18-70岁)。最常见的肝脏病理是病毒性(27%)或酒精性肝病(25%)。移植后所有患者均接受泼尼松治疗至少6个月,大多数患者接受他克莫司或环孢素的免疫抑制。在进行OLT筛查时,分别在18%和36%的腰椎(LS)患者以及9%和42%的股骨颈(FN)患者中发现骨质疏松和骨质减少。 OLT术后6个月,两个部位的T值均显着下降,但之后LS的T值上升,在2年时达到移植前的值,此后保持稳定。 FN T分数始终低于移植前值。 OLT术后一年,椎骨骨折的发生率从筛查时的56%增加到71%​​,骨折发生率是34%。 BMD变化并未预测骨折风险。终末期肝病患者中普遍存在骨质疏松,骨质减少和椎骨骨折。在OLT后的前6个月内观察到BMD总体下降,随后在LS处恢复到移植前的值,但在FN处未恢复。不管BMD的变化如何,OLT后椎骨骨折的风险很高。

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