评估四棱松对绝经后骨质疏松妇女的疗效的研究。

IF 0.7 Q4 PHARMACOLOGY & PHARMACY
Journal of pharmacy & bioallied sciences Pub Date : 2024-07-01 Epub Date: 2024-07-31 DOI:10.4103/jpbs.jpbs_574_24
R Sindhu Priya, R Swathi, S Tamil Selvi, D Anitha, M Kavitha, R Hemavathi, C Keerthika
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引用次数: 0

摘要

背景:骨质疏松症是指骨密度不仅正常,而且不像骨质疏松症那样低。骨质疏松会导致骨质疏松症,增加骨折风险。目前的研究主要集中在能够预防或减缓骨质流失的药物上:研究目的:评估绝经后妇女骨质疏松症的测试前和测试后水平,并评估四棱接骨木(CQ)对绝经后骨质疏松症妇女的疗效:采用真正的实验研究设计,使用有针对性的抽样技术,对 60 名骨质增生患者进行调查。通过结构化问卷收集数据。整个过程均保密。收集到的数据采用描述性和推论性统计方法进行分析:共有 60 名参与者完成了这项研究。与安慰剂相比,CQ 治疗组在 24 周后任何部位的 BMD 百分比变化均无差异。两组 CQ 治疗者的骨重塑活性均有所降低。这些结果与组内比较相关,组内比较显示,安慰剂组的两个 BTM 均持续显著增加:这是第一份显示口服 CQ 24 周对延缓骨质流失有良好效果的临床报告。然而,并未观察到 BMD 发生变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Study to Assess the Effectiveness of Cissus Quadrangularis among Postmenopausal Women with Osteopenia.

Background: Osteopenia refers to bone density that is not only normal but also not as low as that noted in osteoporosis. Osteopenia leads to osteoporosis and increases the risk of fractures. Current research is focused on agents that will prevent or slow the progression of bone loss.

The objectives of the study: To assess the pretest and posttest levels of osteopenia among postmenopausal women, and to assess the effectiveness of Cissus quadrangularis (CQ) on postmenopausal women with osteopenia.

Methodology: A true experimental study design using targeted sampling techniques was used to conduct 60 patients with osteopenia. The data were collected with the help of structured questionnaires. Confidentiality was maintained throughout the process. The data collected were analyzed using descriptive and inference statistics.

Result: A total of 60 participants completed this study. The percent BMD changes in the CQ-treated groups did not differ at any site after 24 weeks compared to the placebo. Reduced bone remodeling activity was detected in both CQ-treated groups. These results correlated with the within-group comparison, which showed a continuously significant increase in both BTMs in the placebo group.

Conclusion: This is the first clinical report that showed a promising effect on delaying bone loss of oral administration of CQ for 24 weeks, as indicated by a slower bone remodeling process via a reduction in BTMs. However, no change in BMD was observed.

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