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肝硬化合并肝性骨病的研究进展
作者:高学松  段雪飞 
单位:首都医科大学附属北京地坛医院 综合科 北京 100015 
关键词:肝硬化 骨质疏松症 肝性骨病 
分类号:
出版年,卷(期):页码:2015,7(4):14-18
摘要:

摘要:骨质疏松症是肝硬化患者一种常见的骨骼系统并发症。症状多不明显,如果不及时治疗,易
导致骨折并影响生活质量。本文对肝硬化合并骨质疏松症的病因及发病机制、诊断、治疗等方面的
研究进展进行综述。骨质疏松症诊断采用双能X线吸收法检测骨密度,根据骨密度诊断骨质疏松症和
骨量减少。骨质疏松症的病因有病毒性肝炎肝硬化、胆汁淤积性肝病和酒精性肝硬化。发病机制考虑
为胰岛素生长因子-1、细胞因子、维生素D和钙的缺乏,核因子-κB受体活化因子(receptor activation
of nuclear factor-κB,RANK)、核因子-κB受体活化因子配体(the receptor of nuclear factor-κB ligand,
RANKL)、骨保护素系统(osteoprotegerin,OPG)、高胆红素血症、糖皮质激素、性腺功能低下,
维生素K缺乏和遗传多态性等多种因素共同作用的结果。建议所有肝性骨病患者补充维生素D和钙,
治疗骨质疏松症的药物包括双膦酸盐、降钙素和激素替代治疗,必要时行肝移植术。双膦酸盐类药物
已成为预防和治疗骨质疏松症的主要药物。建议肝硬化尤其是胆汁淤积性肝硬化患者每年采用双能X
线吸收法检测骨密度。

Abstract: Osteoporosis is a common skeletal complication in patients with liver cirrhosis. Osteoporosis is
usually asymptomatic and can result in fractures and impaired quality of life if untreated in time. We review
the diagnosis, pathophysiology and management of osteoporosis in cirrhosis. Osteoporosis is diagnosed based
on the bone mineral density (BMD) assessment using dual-energy X-ray absorptiometry scan. The etiology
of hepatic osteoporosis is multifactorial, including decreased level of insulin growth factor-1, cytokines,
deficiency of vitamin D and calcium, receptor activation of nuclear factor-κB (RANK), the receptor of
nuclear factor-κB ligand (RANKL) and osteoprotegerin (OPG), hyperbilirubinemia, the use of corticosteroid,
hypogonadism, deficiency of vitamin K and genetic polymorphisms. Vitamin D and calcium supplementation
is recommended for all patients with osteoporosis. Specific agents used for treatment of osteoporosis include
bisphosphonates, calcitonin, hormonal therapy and liver transplantation if necessary. Bisphosphonates has
become the mainstay of therapy for osteoporosis prevention and treatment. Measurement of BMD should be
considered in all patients with liver cirrhosis, especially cholestasis cirrhosis, every year.

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