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绝经后骨质疏松症中抗 RANKL 和 PTH 类似物对心血管风险无影响:系统文献回顾和荟萃分析。

No impact of anti-Rank ligand and PTH analogs on cardiovascular risk in postmenopausal osteoporosis: a systematic literature review and meta-analysis.

机构信息

Université Paul Sabatier Toulouse III, Route de Narbonne, 31330, Toulouse, France.

出版信息

Arch Osteoporos. 2020 Jan 3;15(1):10. doi: 10.1007/s11657-019-0672-4.

Abstract

UNLABELLED

The mutual effects of drugs used in osteoporosis and cardiovascular diseases are a point of interest. A literature review and meta-analysis were conducted to address the impact of PTH analogs and anti-Rank ligand on cardiovascular events and overall mortality in individuals with idiopathic osteoporosis; these treatments do not appear to have any effect.

INTRODUCTION

Two meta-analyses have been conducted to explore the cardiovascular effects of bisphosphonates. There is no review for other osteoporosis treatments. A literature review and meta-analysis were conducted to address the impact of PTH analogs and anti-Rank ligand on cardiovascular events and overall mortality in individuals with idiopathic osteoporosis.

METHODS

A systematic review was conducted in December 2017 in the PubMed, Embase, and Cochrane databases and updated on PubMed in July 2019, selecting trials with a treatment and a control group. We also conducted a search for abstracts of the French Rheumatology Society, American College of Rheumatology, and European League Against Rheumatism's annual meetings over the past 4 years. The main endpoint was the occurrence of cardiovascular events; the secondary was mortality (all causes).

RESULTS

Of the 2782 reports initially found, 16 articles were used for the meta-analysis (6 for the anti-Rank ligand and 10 for the PTH analog group). After meta-analysis, there was no significant difference between the placebo group and the anti-Rank ligand group for overall mortality (p = 0.13), the combined endpoint (overall mortality, coronary artery disease, and stroke; p 0.77), and the individual risk of coronary artery disease (p 0.53), arrhythmia (p 0.95), and stroke (p 0.62). After meta-analysis, there was no significant difference between the placebo group and the PTH analogs group for overall mortality (p 0.77), the combined endpoint (p = 0.95), and the individual risk of coronary artery disease (p = 0.74), arrhythmia (p = 0.28), and stroke (p = 0.61).

CONCLUSIONS

The anti-Rank ligand and PTH analogs have no impact on cardiovascular risk and overall mortality in idiopathic osteoporosis. To better answer the question whether these treatments can reduce the long-term cardiovascular risk, further comparative studies with longer duration are required.

摘要

目的

探讨甲状旁腺激素类似物和抗 RANK 配体对特发性骨质疏松症患者心血管事件和全因死亡率的影响。

方法

检索 2017 年 12 月至 2019 年 7 月 PubMed、Embase 和 Cochrane 数据库以及 PubMed 更新内容,筛选出有治疗组和对照组的试验。我们还检索了过去 4 年法国风湿病学会、美国风湿病学会和欧洲抗风湿病联盟年会的摘要。主要终点是心血管事件的发生;次要终点是死亡率(所有原因)。

结果

在最初发现的 2782 篇报告中,有 16 篇文章用于荟萃分析(6 篇为抗 RANK 配体组,10 篇为甲状旁腺激素类似物组)。荟萃分析后,抗 RANK 配体组与安慰剂组在全因死亡率(p=0.13)、复合终点(全因死亡率、冠心病和卒中;p=0.77)和冠心病个体风险(p=0.53)、心律失常(p=0.95)和卒中(p=0.62)方面无显著差异。荟萃分析后,甲状旁腺激素类似物组与安慰剂组在全因死亡率(p=0.77)、复合终点(p=0.95)和冠心病个体风险(p=0.74)、心律失常(p=0.28)和卒中(p=0.61)方面无显著差异。

结论

抗 RANK 配体和甲状旁腺激素类似物对特发性骨质疏松症患者的心血管风险和全因死亡率没有影响。为了更好地回答这些治疗方法是否可以降低长期心血管风险的问题,需要进行进一步的、时间更长的比较研究。

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