Literature DB >> 6608483

Metabolic bone disease in alcoholic cirrhosis: a comparison of the effect of vitamin D2, 25-hydroxyvitamin D, or supportive treatment.

S A Mobarhan, R M Russell, R R Recker, D B Posner, F L Iber, P Miller.   

Abstract

In a study of 56 alcoholics with liver cirrhosis, 18 (32%) had decreased bone density and low levels of serum 25-hydroxyvitamin D (25-OH-D) (less than 20 ng per ml). To compare the efficacy of vitamin D2 and 25-OH-D treatment in correcting the metabolic bone disease in alcoholic cirrhosis, the 18 patients were randomized in the following manner, in groups of six patients each: Group 1, control (received no supplemental vitamin D treatment); Group 2, given vitamin D2 (50,000 IU p.o.) two to three times weekly, and Group 3, treated with 25-OH-D (20 to 50 mg p.o.) daily as required to attain normal serum 25-OH-D levels. The study period lasted 6 to 12 months (mean, 10.7 months). Initial histomorphometric study of transiliac bone biopsy with double tetracycline labeling in nine patients in whom biopsy was feasible showed only osteoporosis without evidence of osteomalacia. By the end of the study, serum 25-OH-D levels in the control group (Group 1) raised slightly while showing marked improvement in Groups 2 and 3. Bone density results remained unchanged in control patients but demonstrated a significant increase in both treatment groups. Vitamin D2 and 25-OH-D were equally effective in increasing bone density measurements. Posttreatment biopsies were performed in three patients of Group 2 and two patients of Group 3. While the histomorphometric results in Group 3 were not conclusive, in Group 2 improvement in static measures of bone remodeling was noted. Osteoporosis is the usual form of bone disease in alcoholic cirrhosis and a response to either vitamin D2 or 25-OH-D treatment is suggested.

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Year:  1984        PMID: 6608483     DOI: 10.1002/hep.1840040216

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  14 in total

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

Authors:  Jane D Collier; M Ninkovic; J E Compston
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Review 2.  Bone changes in alcoholic liver cirrhosis. A histomorphometrical analysis of 52 cases.

Authors:  J A Jorge-Hernandez; C E Gonzalez-Reimers; A Torres-Ramirez; F Santolaria-Fernandez; C Gonzalez-Garcia; J N Batista-Lopez; M Pestana-Pestana; L Hernandez-Nieto
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3.  Bone histomorphometry and structure in corticosteroid treated chronic active hepatitis.

Authors:  A J Stellon; A Webb; J E Compston
Journal:  Gut       Date:  1988-03       Impact factor: 23.059

4.  Osteoporosis and skeletal fractures in chronic liver disease.

Authors:  T Diamond; D Stiel; M Lunzer; M Wilkinson; J Roche; S Posen
Journal:  Gut       Date:  1990-01       Impact factor: 23.059

5.  Nutritional intake and status in persons with alcohol dependency: data from an outpatient treatment programme.

Authors:  Anne Wilkens Knudsen; Jens-Erik Beck Jensen; Inge Nordgaard-Lassen; Thomas Almdal; Jens Kondrup; Ulrik Becker
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6.  Free 25-hydroxyvitamin D levels are normal in subjects with liver disease and reduced total 25-hydroxyvitamin D levels.

Authors:  D D Bikle; B P Halloran; E Gee; E Ryzen; J G Haddad
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Review 7.  Hepatic osteodystrophy: vitamin D metabolism in patients with liver disease.

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

Review 8.  Fragility fracture risk in cirrhosis: a comparison of the fracture risk assessment tool, British Society of Gastroenterology and National Institute for Health and Clinical Excellence guidelines.

Authors:  Lachlan Richard Owen Ayres; Shane Clarke; Jonathan Digby-Bell; Ashwin Deep Dhanda; Suranga Dharmasiri; Katharine Caddick; Peter Lesley Collins
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9.  Absence of hyperparathyroidism in severe liver disease.

Authors:  G L Klein; D B Endres; J D Colonna; W E Berquist; L I Goldstein; R W Busuttil; L J Deftos
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10.  Alcohol and bone.

Authors:  Peter Mikosch
Journal:  Wien Med Wochenschr       Date:  2014-01-30
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