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[原发性胆汁性肝硬化中的骨病]

[Bone disease in primary biliary cirrhosis].

作者信息

Shibata Hidetaka, Nakao Kazuhiko

机构信息

Department of Gastroenterology and Hepatology,Nagasaki University Graduate School of Biomedical Sciences, Japan.

出版信息

Clin Calcium. 2015 Nov;25(11):1633-8.

Abstract

Primary biliary cirrhosis(PBC)is a chronic autoimmune cholestatic liver disease. Metabolic bone disease is recognized in a complication of chronic liver disease, particularly in PBC. Bone disease in PBC includes osteoporosis and, osteomalacia which is more frequent in advanced liver disease. It is important that PBC occurs mainly in middle-aged women who are highest risk group in primary osteoporosis. In patients with PBC, the dysfunction in enterohepatic circulation of bile acids is associated with the impaired absorption of fats and fat soluble vitamins. Vitamin D and K deficiency leads to osteoporosis resulting in increased risk of bone fracture. This article describes the characteristic and molecular mechanism in bone disease of PBC.

摘要

原发性胆汁性肝硬化(PBC)是一种慢性自身免疫性胆汁淤积性肝病。代谢性骨病是慢性肝病的一种并发症,在PBC中尤为常见。PBC中的骨病包括骨质疏松症和骨软化症,后者在晚期肝病中更为常见。重要的是,PBC主要发生在中年女性中,她们是原发性骨质疏松症的最高风险人群。在PBC患者中,胆汁酸肠肝循环功能障碍与脂肪和脂溶性维生素吸收受损有关。维生素D和K缺乏会导致骨质疏松症,从而增加骨折风险。本文描述了PBC骨病的特征和分子机制。

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