Increase of bone mineral density with sodium fluoride in patients with Crohn's disease

被引:40
作者
von Tirpitz, C [1 ]
Klaus, J [1 ]
Brückel, J [1 ]
Rieber, A [1 ]
Scholer, A [1 ]
Adler, G [1 ]
Böhm, BO [1 ]
Reinshagen, M [1 ]
机构
[1] Univ Ulm, Dept Med 1, D-89081 Ulm, Germany
关键词
bone mass density; Crohn's disease; osteoporosis; sodium fluoride;
D O I
10.1097/00042737-200012010-00005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and aims Low bone density with an increased risk of vertebral fractures is a frequent complication in inflammatory bowel disease. Since the aetiology of osteopathia in these patients is different compared to postmenopausal or steroid-induced osteoporosis, no treatment strategy is established. Supplementation of calcium and vitamin D has been shown to prevent further bone loss, but no data are available showing the anabolic effect of sodium fluoride in Crohn's disease. Methods We carried out a one-year prospective clinical trial in 33 patients with chronic active Crohn's disease who were randomly assigned to receive either calcium (500 mg b.i.d.) and 1000 IU vitamin Dg only, or retarded-release sodium fluoride (25 mg t.i.d,) additionally. The diagnosis of Crohn's disease had been made at least two years ago, and all patients had received systemic high-dose steroid therapy during the previous year. Eleven of 15 patients who received calcium/vitamin D and 15 of 18 patients who additionally received sodium fluoride completed the study. The primary endpoint of the study was the increase of bone mineral density, measured by dual energy X-ray absorptiometry (DXA) after one year of treatment. Bone-specific alkaline phosphatase and osteocalcin were used as markers for bone turnover. Results In the calcium/vitamin D only group, bone density was not significantly changed after one year of treatment, whereas in the calcium/vitamin D/fluoride group, bone density of the lumbar spine increased from -1.39 +/- 0.3 (Z-score, mean +/- SEM) to -0.65 +/- 0.3 (P < 0.05) after one year of treatment Increase of bone density was positively correlated to the osteoblastic markers bone-specific alkaline phosphatase (r = 0.53) and osteocalcin (r = 0.43). Conclusions Sodium fluoride in combination with vitamin D and calcium is an effective, well-tolerated and inexpensive treatment to increase lumbar bone density in patients with chronic active Crohn's disease and osteoporosis. (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:19 / 24
页数:6
相关论文
共 48 条
[1]   Intermittent etidronate therapy to prevent corticosteroid-induced osteoporosis [J].
Adachi, JD ;
Bensen, WG ;
Brown, J ;
Hanley, D ;
Hodsman, A ;
Josse, R ;
Kendler, DL ;
Lentle, B ;
Olszynski, W ;
SteMarie, LG ;
Tenenhouse, A ;
Chines, AA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (06) :382-387
[2]  
ALEXEEVA L, 1994, WHO TECH REP SER, V843, P1
[3]   Inflammatory bowel disease and osteoporosis [J].
Andreassen, H ;
Rungby, J ;
Dahlerup, JF ;
Mosekilde, L .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1997, 32 (12) :1247-1255
[4]  
BERNSTEIN CN, 1995, J BONE MINER RES, V10, P250
[5]   A randomized, placebo-controlled trial of calcium supplementation for decreased bone density in corticosteroid-using patients with inflammatory bowel disease: A pilot study [J].
Bernstein, CN ;
Seeger, LL ;
Anton, PA ;
Artinian, L ;
Geffrey, S ;
Goodman, W ;
Belin, TR ;
Shanahan, F .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 1996, 10 (05) :777-786
[6]   Reduced bone density in patients with inflammatory bowel disease [J].
Bjarnason, I ;
Macpherson, A ;
Mackintosh, C ;
BuxtonThomas, M ;
Forgacs, I ;
Moniz, C .
GUT, 1997, 40 (02) :228-233
[7]   CALCITONIN FOR PREVENTION AND TREATMENT OF POSTMENOPAUSAL OSTEOPOROSIS [J].
BODY, JJ .
CLINICAL RHEUMATOLOGY, 1995, 14 :18-21
[8]   LONG-TERM FLUORIDE THERAPY OF POSTMENOPAUSAL OSTEOPOROSIS [J].
DAMBACHER, MA ;
ITTNER, J ;
RUEGSEGGER, P .
BONE, 1986, 7 (03) :199-205
[9]   Effect of calcium and vitamin D supplementation on bone, density in men and women 65 years of age or older [J].
DawsonHughes, B ;
Harris, SS ;
Krall, EA ;
Dallal, GE .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (10) :670-676
[10]  
DRISCOLL RH, 1982, GASTROENTEROLOGY, V83, P1252