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未接受骨改良治疗的原位肝移植受者骨密度和骨折风险的纵向变化。

Longitudinal changes in BMD and fracture risk in orthotopic liver transplant recipients not using bone-modifying treatment.

作者信息

Krol Charlotte G, Dekkers Olaf M, Kroon Herman M, Rabelink Ton J, van Hoek Bart, Hamdy Neveen At

机构信息

Department of Endocrinology and Metabolic Diseases, Leiden University Medical Centre, Leiden, The Netherlands.

出版信息

J Bone Miner Res. 2014 Aug;29(8):1763-9. doi: 10.1002/jbmr.2214.

Abstract

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.

摘要

骨质疏松症在终末期肝病中很常见,但关于原位肝移植(OLT)后骨矿物质密度(BMD)的长期变化及相关骨折发生率的数据却很稀少。我们评估了2000年至2011年间在莱顿大学医学中心连续接受成功OLT的患者长达5年的BMD变化情况,这些患者有连续的BMD数据。在筛查时以及OLT后6个月和12个月可获得脊柱X线片,由两名独立观察者使用Genant半定量方法评估椎体骨折情况。开始使用双膦酸盐类药物的患者被排除在研究之外。共有201例患者(71%为男性)纳入研究,中位年龄53岁(范围18 - 70岁)。最常见的肝脏病理类型是病毒性(27%)或酒精性肝病(25%)。所有患者移植后至少接受泼尼松治疗6个月,大多数患者接受他克莫司或环孢素进行免疫抑制。在OLT筛查时,腰椎(LS)骨质疏松症和骨质减少症的患者分别为18%和36%,股骨颈(FN)分别为9%和42%。OLT后6个月时,两个部位的T值均显著下降,但此后LS部位T值升高,在2年时达到移植前水平并在此后保持稳定。FN的T值一直低于移植前水平。椎体骨折的患病率从筛查时的56%增加到OLT后1年时 的7%,骨折发生率为34%。BMD变化不能预测骨折风险。骨质疏松症、骨质减少症和椎体骨折在终末期肝病患者中很常见。OLT后最初6个月内观察到BMD总体下降,随后LS部位恢复到移植前水平,但FN部位未恢复。无论BMD如何变化,OLT后椎体骨折风险都很高。

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