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原发性胆汁性胆管炎患者的疾病持续时间和分期影响骨微结构。

Disease Duration and Stage Influence Bone Microstructure in Patients With Primary Biliary Cholangitis.

机构信息

Department of Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Department of Orthopaedic Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

J Bone Miner Res. 2018 Jun;33(6):1011-1019. doi: 10.1002/jbmr.3410. Epub 2018 Mar 25.

Abstract

Primary biliary cholangitis (PBC) is known to be a major risk factor for osteoporosis reflected by a reduction of bone mineral density (BMD). However, both the extent of the macro- and microstructural alterations of bone as well as the causative factors are unknown. We have retrospectively analyzed a total of 96 patients with PBC and 53 healthy controls matched for age, sex, and body mass index. In addition to dual-energy X-ray absorptiometry (DXA) measurements at the lumbar spine and hip, high-resolution peripheral quantitative computed tomography (HR-pQCT) was used to assess the geometric, volumetric, and microstructural changes of bone at the distal radius and tibia. Furthermore, serum analyses and measures of disease duration and stage including transient elastography were performed. Total, cortical, and trabecular volumetric BMD as well as geometric parameters were significantly reduced in PBC patients. Microstructural analysis revealed a significantly lower cortical thickness (p < 0.001) and bone volume per tissue volume (p < 0.001) in the radius and tibia but unchanged trabecular number in patients with PBC (radius: p = 0.42; tibia: p = 0.12). Multivariate regression models pointed out that disease duration and stage are the primary factors that are independently associated with bone loss in PBC. A subgroup analysis of patients with additional autoimmune hepatitis (AIH) revealed no significant changes in bone structure compared with PBC only. Taken together, PBC patients demonstrate severe alterations in bone microstructure that are positively associated with disease duration and stage. By applying HR-pQCT in the distal radius and tibia, a combined bone loss syndrome expressed by a predominant decrease in BMD and cortical thickness could be detected. © 2018 American Society for Bone and Mineral Research.

摘要

原发性胆汁性胆管炎(PBC)已知是骨质疏松症的一个主要危险因素,表现为骨密度(BMD)降低。然而,骨的宏观和微观结构改变的程度以及致病因素尚不清楚。我们回顾性分析了总共 96 例 PBC 患者和 53 例年龄、性别和体重指数匹配的健康对照者。除了腰椎和髋部的双能 X 线吸收法(DXA)测量外,高分辨率外周定量计算机断层扫描(HR-pQCT)还用于评估桡骨和胫骨远端的骨几何形状、体积和微观结构变化。此外,还进行了血清分析以及疾病持续时间和阶段的测量,包括瞬时弹性成像。PBC 患者的总、皮质和小梁体积 BMD 以及几何参数均显著降低。微观结构分析显示,PBC 患者桡骨和胫骨的皮质厚度(p < 0.001)和骨体积/组织体积(p < 0.001)显著降低,但小梁数量不变(桡骨:p = 0.42;胫骨:p = 0.12)。多变量回归模型指出,疾病持续时间和阶段是与 PBC 骨丢失相关的主要因素。对伴有自身免疫性肝炎(AIH)的患者进行亚组分析,与仅 PBC 患者相比,骨结构无明显变化。总之,PBC 患者表现出严重的骨微观结构改变,与疾病持续时间和阶段呈正相关。通过在桡骨和胫骨远端应用 HR-pQCT,可以检测到一种联合的骨丢失综合征,表现为 BMD 和皮质厚度的主要减少。© 2018 美国骨矿研究协会。

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