Literature DB >> 6287835

Vitamin D, hydroxyapatite, and calcium gluconate in treatment of cortical bone thinning in postmenopausal women with primary biliary cirrhosis.

O Epstein, Y Kato, R Dick, S Sherlock.   

Abstract

Women with primary biliary cirrhosis malabsorb calcium, phosphate and vitamin D, and develop accelerated cortical bone thinning. We have assessed the value of parenteral vitamin D, oral hydroxyapatite (HA), and calcium gluconate (CG) in the treatment of cortical bone thinning in primary biliary cirrhosis. Sixty-four postmenopausal women with primary biliary cirrhosis were assigned randomly into three groups: one group receiving no mineral supplements (control), one group receiving HA, and one group receiving CG. All patients received parenteral vitamin D2 (100,000 IU monthly). Eleven patients withdrew from the study and 10 withdrew due to poor compliance (six HA, four CG). Over a 14-month follow-up period, none of the groups showed a significant change in serum calcium or inorganic phosphate levels. Pre- and posttreatment hand radiographs were used to assess changes in metacarpal cortical thickness using the technique of caliper radiogrammetry. Cortical bone loss occurred in the control group (p less than 0.01). The HA group showed a significant gain in cortical bone thickness (p less than 0.01), while no significant change occurred in the CG group. This study indicated that vitamin D2 does not halt metacarpal cortical bone thinning in primary biliary cirrhosis. The addition of CG prevents bone thinning, and HA promotes positive cortical bone balance.

Entities:  

Mesh:

Substances:

Year:  1982        PMID: 6287835     DOI: 10.1093/ajcn/36.3.426

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


  16 in total

1.  Guidelines on the management of osteoporosis associated with chronic liver disease.

Authors:  Jane D Collier; M Ninkovic; J E Compston
Journal:  Gut       Date:  2002-02       Impact factor: 23.059

Review 2.  Bone disease after liver transplantation.

Authors:  M S Losowsky; S H Hussaini
Journal:  Gut       Date:  1996-10       Impact factor: 23.059

3.  Phosphate and carbonate salts of calcium support robust bone building in osteoporosis.

Authors:  Robert P Heaney; Robert R Recker; Patrice Watson; Joan M Lappe
Journal:  Am J Clin Nutr       Date:  2010-05-19       Impact factor: 7.045

4.  Hepatic osteodystrophy: An important matter for consideration in chronic liver disease.

Authors:  Germán López-Larramona; Alfredo J Lucendo; Sonia González-Castillo; José M Tenias
Journal:  World J Hepatol       Date:  2011-12-27

Review 5.  Hepatic osteodystrophy: vitamin D metabolism in patients with liver disease.

Authors:  J E Compston
Journal:  Gut       Date:  1986-09       Impact factor: 23.059

6.  Non-hormonal treatment of osteoporosis.

Authors: 
Journal:  Br Med J (Clin Res Ed)       Date:  1983-05-21

7.  Non-hormonal treatment of osteoporosis.

Authors:  A S Dixon
Journal:  Br Med J (Clin Res Ed)       Date:  1983-03-26

8.  Comparison of the treatment effects of ossein-hydroxyapatite compound and calcium carbonate in osteoporotic females.

Authors:  P Rüegsegger; A Keller; M A Dambacher
Journal:  Osteoporos Int       Date:  1995-01       Impact factor: 4.507

Review 9.  Metabolic bone disease in patients with liver disease.

Authors:  Elizabeth Carey; Vijayan Balan
Journal:  Curr Gastroenterol Rep       Date:  2003-02

10.  Microcrystalline hydroxyapatite compound in prevention of bone loss in corticosteroid-treated patients with chronic active hepatitis.

Authors:  A Stellon; A Davies; A Webb; R Williams
Journal:  Postgrad Med J       Date:  1985-09       Impact factor: 2.401

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.