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肝性骨营养不良

Hepatic osteodystrophy.

作者信息

Goel Varun, Kar Premashis

机构信息

Department of Medicine, Maulana Azad Medical College, B.L.Taneja Block, New Delhi-India.

出版信息

Trop Gastroenterol. 2010 Apr-Jun;31(2):82-6.

Abstract

UNLABELLED

Hepatic Osteodystrophy (HO) is a generic definition for the metabolic bone disease that may occur in individuals with chronic liver disease. Hepatic Osteodystrophy is an important but frequently overlooked complication, seen in chronic liver disease patients. This review article illustrates its significance, various causes and methods to diagnose this complication and recent advances and recommendations to treat Hepatic Osteodystrophy. Two distinct bone metabolic processes, osteoporosis (OP) and osteomalacia (OM) are combined together in various proportions in HO syndromes. It has been described in association with most types of chronic liver disease both cholestatic and non-cholestatic. Primary biliary cirrhosis (PBC) is the condition causing osteopenia more frequently, but other cholestatic liver diseases like primary sclerosing cholangitis (PSC), haemochromatosis and alcoholic liver disease are also frequently associated with this disorder. The pathogenesis of bone disease in both adults and children with chronic cholestasis is not completely understood. There has been considerable disagreement regarding the relative importance of osteomalacia versus osteoporosis as the factors leading to osteopenia of liver disease. It can significantly affect morbidity, and quality of life of these patients. Fractures are also associated with an excess mortality. Bone mineral density measurement is the best way to assess the presence and severity of osteopenia in CLD patients, while laboratory tests give important information about the metabolic status of the bone. Since advanced HO is difficult to treat and adversely affects both the quality of life and the long-term prognosis of patients with chronic liver disease, special care is required in order to prevent the development of clinical bone disease in individuals with advanced hepatic disease.

CONCLUSION

Hepatic Osteodystrophy is under-recognized and less attended complication of CLD. Multiple factors contribute to the development of hepatic Osteodystrophy. Newer diagnostic modalities have improved the detection of HO and Vitamin D repletion, calcium supplementation and Bisphosphonates seem promising. The best course of management for these patients is to review the individual risk factors for osteoporosis, obtain a bone mass measurement, and prescribe age and disease-specific therapies.

摘要

未标注

肝性骨营养不良(HO)是对可能发生于慢性肝病患者的代谢性骨病的统称。肝性骨营养不良是慢性肝病患者中一种重要但常被忽视的并发症。这篇综述文章阐述了其重要性、各种病因、诊断该并发症的方法以及治疗肝性骨营养不良的最新进展和建议。在肝性骨营养不良综合征中,两种不同的骨代谢过程,即骨质疏松(OP)和骨软化(OM)以不同比例合并存在。它已被描述与大多数类型的慢性肝病相关,包括胆汁淤积性和非胆汁淤积性肝病。原发性胆汁性肝硬化(PBC)是更常导致骨质减少的疾病,但其他胆汁淤积性肝病,如原发性硬化性胆管炎(PSC)、血色素沉着症和酒精性肝病也常与该病症相关。慢性胆汁淤积的成人和儿童骨病的发病机制尚未完全明确。关于骨软化与骨质疏松作为导致肝病骨质减少的因素的相对重要性存在相当大的分歧。它可显著影响这些患者的发病率和生活质量。骨折还与额外的死亡率相关。骨密度测量是评估慢性肝病患者骨质减少的存在和严重程度的最佳方法,而实验室检查可提供有关骨代谢状态的重要信息。由于晚期肝性骨营养不良难以治疗且对慢性肝病患者的生活质量和长期预后产生不利影响,因此需要特别关注以预防晚期肝病患者临床骨病的发生。

结论

肝性骨营养不良是慢性肝病中未得到充分认识和较少关注的并发症。多种因素促成了肝性骨营养不良的发生。更新的诊断方法改善了对肝性骨营养不良的检测,补充维生素D、补钙和使用双膦酸盐似乎前景良好。对这些患者的最佳管理方法是审查个体骨质疏松风险因素、进行骨量测量并开具针对年龄和疾病的特定疗法。

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