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依普黄酮治疗绝经后骨质疏松症:一项随机对照试验。

Ipriflavone in the treatment of postmenopausal osteoporosis: a randomized controlled trial.

作者信息

Alexandersen P, Toussaint A, Christiansen C, Devogelaer J P, Roux C, Fechtenbaum J, Gennari C, Reginster J Y

机构信息

Center for Clinical and Basic Research, Ballerup Byvej 222, 2750 Ballerup, Denmark.

出版信息

JAMA. 2001 Mar 21;285(11):1482-8. doi: 10.1001/jama.285.11.1482.

Abstract

CONTEXT

Data on the efficacy and safety of ipriflavone for prevention of postmenopausal bone loss are conflicting.

OBJECTIVES

To investigate the effect of oral ipriflavone on prevention of postmenopausal bone loss and to assess the safety profile of long-term treatment with ipriflavone in postmenopausal osteoporotic women.

DESIGN AND SETTING

Prospective, randomized, double-blind, placebo-controlled, 4-year study conducted in 4 centers in Belgium, Denmark, and Italy from August 1994 to July 1998.

PARTICIPANTS

Four hundred seventy-four postmenopausal white women, aged 45 to 75 years, with bone mineral densities (BMDs) of less than 0.86 g/cm(2).

INTERVENTIONS

Patients were randomly assigned to receive ipriflavone, 200 mg 3 times per day (n = 234), or placebo (n = 240); all received 500 mg/d of calcium.

MAIN OUTCOME MEASURES

Efficacy measures included spine, hip, and forearm BMD and biochemical markers of bone resorption (urinary hydroxyproline corrected for creatinine and urinary CrossLaps [Osteometer Biotech, Herlev, Denmark] corrected for creatinine), assessed every 6 months. Laboratory safety measures and adverse events were recorded every 3 months.

RESULTS

Based on intent-to-treat analysis, after 36 months of treatment, the annual percentage change from baseline in BMD of the lumbar spine for ipriflavone vs placebo (0.1% [95% confidence interval (CI), -7.9% to 8.1%] vs 0.8% [95% CI, -9.1% to 10.7%]; P =.14), or in any of the other sites measured, did not differ significantly between groups. The response in biochemical markers was also similar between groups (eg, for hydroxyproline corrected for creatinine, 20.13 mg/g [95% CI, 18.85-21.41 mg/g] vs 20.67 mg/g [95% CI, 19.41-21.92 mg/g]; P =.96); urinary CrossLaps corrected for creatinine, 268 mg/mol (95% CI, 249-288 mg/mol) vs 268 mg/mol (95% CI, 254-282 mg/mol); P =.81. The number of women with new vertebral fracture was identical or nearly so in the 2 groups at all time points. Lymphocyte concentrations decreased significantly (500/microL (0.5 x 10(9)/L]) in women treated with ipriflavone. Thirty-one women (13.2%) in the ipriflavone group developed subclinical lymphocytopenia, of whom 29 developed it during ipriflavone treatment. Of these, 15 (52%) of 29 had recovered spontaneously by 1 year and 22 (81%) of 29 by 2 years.

CONCLUSIONS

Our data indicate that ipriflavone does not prevent bone loss or affect biochemical markers of bone metabolism. Additionally, ipriflavone induces lymphocytopenia in a significant number of women.

摘要

背景

关于异黄酮预防绝经后骨质流失的疗效和安全性的数据存在矛盾。

目的

研究口服异黄酮对预防绝经后骨质流失的作用,并评估异黄酮长期治疗绝经后骨质疏松症女性的安全性。

设计与地点

1994年8月至1998年7月在比利时、丹麦和意大利的4个中心进行的前瞻性、随机、双盲、安慰剂对照的4年研究。

参与者

474名45至75岁的绝经后白人女性,骨矿物质密度(BMD)低于0.86 g/cm²。

干预措施

患者被随机分配接受异黄酮,每日3次,每次200 mg(n = 234),或安慰剂(n = 240);所有患者均接受每日500 mg的钙。

主要观察指标

疗效指标包括脊柱、髋部和前臂的骨密度以及骨吸收的生化标志物(校正肌酐后的尿羟脯氨酸和校正肌酐后的尿交联N-端肽[丹麦赫勒夫的Osteometer Biotech公司产品]),每6个月评估一次。每3个月记录实验室安全指标和不良事件。

结果

基于意向性分析,治疗36个月后,异黄酮组与安慰剂组腰椎骨密度相对于基线的年变化百分比(0.1%[95%置信区间(CI),-7.9%至8.1%]对0.8%[95% CI,-9.1%至10.7%];P = 0.14),或在其他任何测量部位,两组之间均无显著差异。两组生化标志物的反应也相似(例如,校正肌酐后的羟脯氨酸,20.13 mg/g[95% CI,18.85 - 21.41 mg/g]对20.67 mg/g[95% CI,19.41 - 21.92 mg/g];P = 0.96);校正肌酐后的尿交联N-端肽,268 mg/mol(95% CI,249 - 288 mg/mol)对268 mg/mol(95% CI,254 - 282 mg/mol);P = 0.81。在所有时间点,两组中发生新椎体骨折的女性数量相同或几乎相同。接受异黄酮治疗的女性淋巴细胞浓度显著降低(500/μL(0.5×10⁹/L))。异黄酮组有31名女性(13.2%)出现亚临床淋巴细胞减少,其中29名在异黄酮治疗期间出现。其中,29名中的15名(52%)在1年内自发恢复,29名中的22名(81%)在2年内恢复。

结论

我们的数据表明,异黄酮不能预防骨质流失或影响骨代谢的生化标志物。此外,异黄酮在相当数量的女性中会引起淋巴细胞减少。

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