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Osteoporosis and fractures in liver disease: Relevance, pathogenesis and therapeutic implications

机译:肝病中的骨质疏松症和骨折:相关性,发病机制和治疗意义

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It is being increasingly recognized that patients with liver disease develop bone loss that can be severe enough to lead to atraumatic fractures and thus markedly diminish life quality and expectancy. The estimated prevalence for liver-related osteoporosis is between 20-420/100000 of the general population, and fractures between 60-880/100000. It should be kept in mind that up to 40% of patients with chronic liver disease may experience a fracture. The pathogenic mediators include fibronectin, insulin like growth factor-I, and various cytokines, but decreased vitamin D and/or treatment with corticosteroids contribute to worsening bone health. Despite the advances in bone biology that have shed some light on the pathogenesis of this bone loss, treatment options remain nonspecific and tightly linked to treatments of other forms of osteoporosis. Thus, treatment should include calcium and vitamin D supplementation in all patients with chronic liver disease. Therapy with bisphosphonates should be considered, especially in patients receiving corticosteroids. This review focuses on the prevalence of this entity as well as the evidence available with regard to the pathogenesis of bone loss in liver disease, the diagnostic steps required in all patients, and the therapeutic options available.
机译:越来越多的人认识到,患有肝病的患者会发生骨质流失,严重程度足以导致无创伤性骨折,从而显着降低生活质量和预期寿命。肝相关性骨质疏松症的估计患病率在一般人群中20-420 / 100000之间,骨折在60-880 / 100000之间。应该记住的是,多达40%的慢性肝病患者可能会发生骨折。病原体包括纤连蛋白,胰岛素样生长因子-I和各种细胞因子,但维生素D减少和/或皮质类固醇激素治疗会加剧骨骼健康。尽管骨骼生物学的进步为这种骨质流失的发病机理提供了一些线索,但治疗选择仍然是非特异性的,并且与其他形式的骨质疏松症的治疗紧密相关。因此,对于所有患有慢性肝病的患者,治疗应包括补充钙和维生素D。应该考虑用双膦酸盐治疗,特别是在接受皮质类固醇激素的患者中。这篇综述着重于该实体的流行以及有关肝病中骨丢失的发病机制,所有患者所需的诊断步骤以及可用的治疗选择的可用证据。

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