Isosorbide mononitrate increases bone formation and decreases bone resorption in postmenopausal women: A randomized trial

被引:62
作者
Jamal, SA
Cummings, SR
Hawker, GA
机构
[1] Univ Toronto, St Michaels Hosp, Dept Med, Div Endocrinol & Metab, Toronto, ON M5C 2T2, Canada
[2] Calif Pacific Med Ctr, San Francisco Coordinating Ctr, San Francisco, CA USA
[3] Univ Toronto, Dept Med, Div Rheumatol,Womens Coll Hlth Sci Ctr, Womens Coll Ambulatory Care Ctr, Toronto, ON, Canada
[4] Calif Pacific Med Ctr, Res Inst, San Francisco, CA USA
关键词
postmenopausal osteoporosis; markers of bone turnover; NO donors; randomized controlled trial;
D O I
10.1359/JBMR.040716
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
NO regulates bone remodeling in cellular and animal models. We examined the effect of administering ISMO, a NO donor, on bone turnover in 144 postmenopausal women. After 3 months, women randomized to ISMO had a greater decrease in bone resorption and a greater increase in bone formation compared with placebo. NO donors may prevent postmenopausal bone loss. Introduction: NO both stimulates bone formation and inhibits bone resorption in vitro. NO donors (nitrates) are inexpensive and widely available, but their value for postmenopausal osteoporosis has never been evaluated in a randomized trial. Materials and Methods: We randomly assigned 144 healthy postmenopausal women with a hip BMD T score between 0 and -2.5 to 5 or 20 mg/day of isosorbide mononitrate (ISMO) or placebo for 12 weeks. We measured urine N-telopeptide (NTx), a marker of bone resorption, and serum bone-specific alkaline phosphatase (BSALP), a marker of bone formation. Markers were measured immediately before randomization and after 12 weeks of treatment. We calculated the percent change in NTx and BSALP for each of the treatment groups (placebo, 5 mg ISMO, and 20 mg ISMO). Our primary outcome was the percent change in NTx and BSALP in the 5- and 20-mg ISMO groups compared with placebo. Results and Conclusions: Compared with women randomized to placebo, women randomized to 20 mg of ISMO had a 45.4% decrease in NTx (95% CI, 25.8-64.9) and a 23.3% increase (95% CI, 8.9-37.8) in BSALP. Women randomized to 5 mg of ISMO had a 36.3% decrease in NTx (95% CI, 14.8-57.8) and a 15.9% increase in BSALP (95% CI, 1.1-30.7). ISMO decreases bone resorption and increases bone formation. These findings suggest that nitrates may be useful for the prevention of postmenopausal osteoporosis.
引用
收藏
页码:1512 / 1517
页数:6
相关论文
共 25 条
[1]   Choosing the most appropriate treatment for stable angina - Safety considerations [J].
Asirvatham, S ;
Sebastian, C ;
Thadani, U .
DRUG SAFETY, 1998, 19 (01) :23-44
[2]   BIDIRECTIONAL REGULATION OF OSTEOCLAST FUNCTION BY NITRIC-OXIDE SYNTHASE ISOFORMS [J].
BRANDI, ML ;
HUKKANEN, M ;
UMEDA, T ;
MORADIBIDHENDI, N ;
BIANCHI, S ;
GROSS, SS ;
POLAK, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :2954-2958
[3]   Role of nitric oxide and prostaglandins in mechanically induced bone formation [J].
Chow, JWM ;
Fox, SW ;
Lean, JM ;
Chambers, TJ .
JOURNAL OF BONE AND MINERAL RESEARCH, 1998, 13 (06) :1039-1044
[4]  
Clowes JA, 2002, OSTEOPOROSIS EVIDENC, P59
[5]  
FEELISCH M, 1993, EUR HEART J, V14, P123
[6]   COMPARISON OF NEW BIOCHEMICAL MARKERS OF BONE TURNOVER IN LATE POSTMENOPAUSAL OSTEOPOROTIC WOMEN IN RESPONSE TO ALENDRONATE TREATMENT [J].
GARNERO, P ;
SHIH, WCJ ;
GINEYTS, E ;
KARPF, DB ;
DELMAS, PD .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (06) :1693-1700
[7]   Markers of bone turnover for the prediction of fracture risk [J].
Garnero P. .
Osteoporosis International, 2000, 11 (Suppl 6) :S55-S65
[8]  
GOMEZ B, 1995, CLIN CHEM, V41, P1560
[9]  
HANSON DA, 1992, J BONE MINER RES, V7, P1251
[10]   Changes in bone density and turnover explain the reductions in incidence of nonvertebral fractures that occur during treatment with antiresorptive agents [J].
Hochberg, MC ;
Greenspan, S ;
Wasnich, RD ;
Miller, P ;
Thompson, DE ;
Ross, PD .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (04) :1586-1592