首页> 外文期刊>Digestive and liver disease: official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver >A 4-year treatment with clodronate plus calcium and vitamin D supplements does not improve bone mass in primary biliary cirrhosis.
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A 4-year treatment with clodronate plus calcium and vitamin D supplements does not improve bone mass in primary biliary cirrhosis.

机译:氯膦酸盐加上钙和维生素D补充剂的4年治疗不能改善原发性胆汁性肝硬化的骨量。

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INTRODUCTION: International guidelines for managing osteoporosis in cirrhosis or severe cholestasis indicate a <-2.5 t-score as a cut-off for medical treatment, while no treatment is recommended in the case of osteopenia (t-scores ranging from -1.0 to -2.5). AIM: We conducted a prospective study in primary biliary cirrhosis with a view to optimizing the rationale for the medical treatment of bone loss. METHODS: All naive post-menopausal women with primary biliary cirrhosis were enrolled in the study. Bone metabolism was evaluated by measuring 25-hydroxy-vitamin D, parathyroid hormone, osteocalcin. Bone mineral density was assessed at the lumbar spine by dual-photon X-ray absorptiometry at the baseline and every 2 years for up to 4 years. Patients with either osteopenia or osteoporosis received the following treatment: oral calcium carbonate (1000mg/day)+vitamin D3 (880IU/day)+i.m. disodium clodronate 100mg every 10 days for 4 years. RESULTS: Ninety-six patients completed the study: 30 had a normal bonemineral density (group 1), 37 had osteopenia (group 2), 29 had osteoporosis (group 3). No significant differences in biochemical parameters of bone metabolism were observed between the three groups. A total of 288 bone mineral density measurements were taken. Linear regression analysis failed to reveal significant changes in t-score over the follow-up in all groups. CONCLUSIONS: A 4-year treatment with clodronate+calcium/vitamin D3 supplements does not significantly improve osteoporosis or osteopenia in primary biliary cirrhosis women in menopause, but prevents the natural bone loss in these patients. Extensive international trials are warranted to optimize the prevention and treatment of bone loss in primary biliary cirrhosis.
机译:简介:在肝硬化或严重胆汁淤积症中管理骨质疏松症的国际准则表明,<-2.5 t分值作为医疗的临界值,而骨质减少的情况则不建议治疗(t分值介于-1.0至-2.5之间)。目的:我们对原发性胆汁性肝硬化进行了一项前瞻性研究,以优化骨丢失的医学治疗原理。方法:所有未婚绝经后原发性胆汁性肝硬化妇女均纳入研究。通过测量25-羟基维生素D,甲状旁腺激素,骨钙素评估骨代谢。通过双光子X线骨密度仪在基线和每2年(最多4年)评估腰椎的骨矿物质密度。患有骨质减少或骨质疏松症的患者接受以下治疗:口服碳酸钙(1000mg /天)+维生素D3(880IU /天)+ i.m。氯膦酸二钠100mg每10天一次,持续4年。结果:96名患者完成了研究:30名骨密度正常(第1组),37名骨质减少(第2组),29名骨质疏松(第3组)。三组之间在骨代谢的生化参数上没有观察到显着差异。总共进行了288次骨矿物质密度测量。线性回归分析未能揭示所有组随访中t得分的显着变化。结论:使用氯膦酸盐+钙/维生素D3补充剂治疗4年,并不能显着改善绝经期原发性胆汁性肝硬化妇女的骨质疏松或骨质减少,但可以防止这些患者的自然骨质流失。有必要进行广泛的国际试验,以优化对原发性胆汁性肝硬化的骨丢失的预防和治疗。

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