Vitamin D replacement for cirrhosis-related bone disease

被引:47
作者
Crawford, Bronwyn A.
Labio, Eternity D.
Strasser, Simone I.
McCaughan, Geoffrey W.
机构
[1] Royal Prince Alfred Hosp, Ctr Med, Washington, DC 20422 USA
[2] Concord Gen Repatriat Hosp, Washington, DC 20422 USA
[3] Univ Sydney, Fac Med, Sydney, NSW 2006, Australia
[4] Royal Prince Alfred Hosp, AW Morrow Gastroenterol & Liver Transplant Unit, Washington, DC 20422 USA
[5] Univ Philippines, Philippine Gen Hosp, Dept Med, Manila, Philippines
来源
NATURE CLINICAL PRACTICE GASTROENTEROLOGY & HEPATOLOGY | 2006年 / 3卷 / 12期
关键词
cirrhosis; osteoporosis; parathyroid hormone; vitamin D;
D O I
10.1038/ncpgasthep0637
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The osteoporotic fracture rate in patients with chronic liver disease is approximately twice that of age-matched, control individuals. About 66% of patients with moderately severe cirrhosis and 96% of patients awaiting liver transplantation have vitamin D deficiency. Studies have strong correlation between vitamin D deficiency and bone density, particularly in the hip. Previous studies of vitamin D therapy in cirrhosis-related bone disease have had major design flaws. Most reports and guidelines on the treatment of hepatic bone disease have concluded that vitamin D deficiency does not have a significant pathogenic role in the development of osteoporosis in cirrhosis, and that there us no evidence for a therapeutic effect of vitamin D supplementation. Conversely, it is generally recommended that patients with cirrhosis and low bone density should receive calcium and vitamin D supplementation; yet there is a paucity of reliable data on the optimal doses to use, as well as a lack of clearly demonstrated benefit. We believe that clinical trials of vitamin D therapy in these patients with liver disease are warranted. As low-dose oral supplementation often will not normalize vitamin D levels or suppress parathyroid hormone activity in cirrhotic patients, high-dose, parenteral vitamin D might be preferable, but further long-term studies are required to assess the benefits and safety of this approach.
引用
收藏
页码:689 / 699
页数:11
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