Division of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA USA.
Division of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA USA.
J Clin Densitom. 2020 Apr-Jun;23(2):212-222. doi: 10.1016/j.jocd.2019.01.004. Epub 2019 Jan 18.
Osteoporosis is the most common bone disease in chronic liver disease (CLD) resulting in frequent fractures and leading to significant morbidity in this population. In addition to patients with cirrhosis and chronic cholestasis, patients with CLD from other etiologies may be affected in the absence of cirrhosis. The mechanism of osteoporosis in CLD varies according to etiology, but in cirrhosis and cholestatic liver disease it is driven primarily by decreased bone formation, which differs from the increased bone resorption seen in postmenopausal osteoporosis. Direct toxic effects from iron and alcohol play a role in hemochromatosis and alcoholic liver disease, respectively. Chronic inflammation also has been proposed to mediate bone disease in viral hepatitis and nonalcoholic fatty liver disease. Treatment trials specific to osteoporosis in CLD are small, confined to primary biliary cholangitis and post-transplant patients, and have not consistently demonstrated a benefit in this population. As it stands, prevention of osteoporosis in CLD relies on the mitigation of risk factors such as smoking and alcohol use, treatment of underlying hypogonadism, and encouraging a healthy diet and weight-bearing exercise. The primary medical intervention for the treatment of osteoporosis in CLD remains bisphosphonates though a benefit in terms of fracture reduction has never been shown. This review outlines what is known regarding the pathogenesis of bone disease in CLD and summarizes current and emerging therapies.
骨质疏松症是慢性肝病(CLD)中最常见的骨骼疾病,导致频繁骨折,并使该人群产生重大发病率。除了肝硬化和慢性胆汁淤积症患者外,来自其他病因的 CLD 患者在没有肝硬化的情况下也可能受到影响。CLD 中的骨质疏松症的发病机制因病因而异,但在肝硬化和胆汁淤积性肝病中,主要是由骨形成减少引起的,这与绝经后骨质疏松症中所见的增加的骨吸收不同。铁和酒精的直接毒性作用分别在血色病和酒精性肝病中起作用。慢性炎症也被认为介导了病毒性肝炎和非酒精性脂肪性肝病中的骨骼疾病。专门针对 CLD 中骨质疏松症的治疗试验规模较小,仅限于原发性胆汁性胆管炎和移植后患者,并且在该人群中并未一致证明其获益。目前,CLD 中骨质疏松症的预防依赖于减轻危险因素,如吸烟和饮酒,治疗潜在的性腺功能减退症,并鼓励健康饮食和负重锻炼。治疗 CLD 中骨质疏松症的主要医学干预仍然是双膦酸盐,尽管从未显示出骨折减少的益处。这篇综述概述了已知的 CLD 中骨骼疾病的发病机制,并总结了目前和新兴的治疗方法。