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D-003(10 毫克/天)对绝经后妇女腰椎和股骨颈骨密度的影响:一项随机、双盲研究。

Effects of D-003 (10 mg/day) on bone mineral density of the lumbar spine and femoral neck in postmenopausal women: a randomized, double-blinded study.

机构信息

Medical Surgical Research Centre, Havana, Cuba.

出版信息

Korean J Intern Med. 2011 Jun;26(2):168-78. doi: 10.3904/kjim.2011.26.2.168. Epub 2011 Jun 1.

Abstract

BACKGROUND/AIMS: Increased osteoclast activity is a pivotal finding in osteoporosis. This increase is mediated via the mevalonate-to-cholesterol pathway, which is involved in producing the intermediates required for osteoclast activity. D-003, a mixture of high molecular weight sugarcane wax acids, has been shown to inhibit cholesterol synthesis prior to mevalonate production, resulting in a reduction of bone loss and resorption in ovariectomized rats. Moreover, previous studies have demonstrated that short-term D-003 treatment reduces urinary excretion of deoxypyridinoline/creatinine in postmenopausal women.

METHODS

We performed a double-blinded, placebo-controlled study to investigate the effects of D-003 (10 mg/day) treatment for 3 years on bone mineral density (BMD) in 83 postmenopausal women with low BMD.

RESULTS

Over 3 years, D-003 treatment increased lumbar spine BMD (5.1%, p < 0.01) and improved osteoporosis-related quality of life scores as compared with placebo-treated controls. D-003 was also well tolerated; the frequency of adverse events in the bone, joints, or muscle with D-003 treatment (p < 0.05) was lower than in the placebo group.

CONCLUSIONS

D-003 treatment (10 mg/day) for 3 years increased lumbar spine BMD and produced clinical improvements in postmenopausal women with low BMD. Further studies, however, will be required to confirm these results.

摘要

背景/目的:破骨细胞活性增加是骨质疏松症的一个关键发现。这种增加是通过甲羟戊酸到胆固醇途径介导的,该途径参与产生破骨细胞活性所需的中间产物。D-003 是一种高分子量甘蔗蜡酸的混合物,已被证明可在甲羟戊酸产生之前抑制胆固醇合成,从而减少去卵巢大鼠的骨丢失和吸收。此外,先前的研究表明,D-003 的短期治疗可减少绝经后妇女尿脱氧吡啶啉/肌酐的排泄。

方法

我们进行了一项双盲、安慰剂对照研究,以调查 D-003(10 毫克/天)治疗 3 年对 83 名低骨密度绝经后妇女骨密度(BMD)的影响。

结果

经过 3 年的治疗,D-003 治疗组的腰椎 BMD 增加了 5.1%(p<0.01),并改善了与骨质疏松症相关的生活质量评分,与安慰剂对照组相比。D-003 也具有良好的耐受性;与安慰剂组相比,D-003 治疗组的骨骼、关节或肌肉不良事件的发生频率较低(p<0.05)。

结论

D-003 治疗(10 毫克/天)3 年可增加腰椎 BMD,并改善低骨密度绝经后妇女的临床状况。然而,需要进一步的研究来证实这些结果。

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