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2
Coronary artery calcium in primary prevention.冠状动脉钙在一级预防中的应用。
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3
Impact of denosumab on cardiovascular calcification in patients with secondary hyperparathyroidism undergoing dialysis: a pilot study.唑来膦酸对接受透析治疗的继发性甲状旁腺功能亢进症患者心血管钙化的影响:一项初步研究。
Osteoporos Int. 2020 Aug;31(8):1507-1516. doi: 10.1007/s00198-020-05391-3. Epub 2020 Apr 3.
4
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J Bone Miner Res. 2019 Jun;34(6):1014-1024. doi: 10.1002/jbmr.3676. Epub 2019 Mar 4.
5
Impact of Statins on Cardiovascular Outcomes Following Coronary Artery Calcium Scoring.他汀类药物对冠状动脉钙评分后心血管结局的影响。
J Am Coll Cardiol. 2018 Dec 25;72(25):3233-3242. doi: 10.1016/j.jacc.2018.09.051.
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Bisphosphonates, atherosclerosis and vascular calcification: update and systematic review of clinical studies.双膦酸盐、动脉粥样硬化和血管钙化:临床研究的更新和系统评价。
Clin Interv Aging. 2017 Oct 30;12:1819-1828. doi: 10.2147/CIA.S138002. eCollection 2017.
7
Cardiac Society of Australia and New Zealand Position Statement: Coronary Artery Calcium Scoring.澳大利亚和新西兰心脏学会立场声明:冠状动脉钙化评分
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9
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双磷酸盐和 RANKL 抑制剂是否会改变冠状动脉钙化的进展?系统评价和荟萃分析方案。

Do bisphosphonates and RANKL inhibitors alter the progression of coronary artery calcification? A systematic review and meta-analysis protocol.

机构信息

Gosford Hospital, Gosford, New South Wales, Australia

Gosford Hospital, Gosford, New South Wales, Australia.

出版信息

BMJ Open. 2022 Oct 7;12(10):e066255. doi: 10.1136/bmjopen-2022-066255.

DOI:10.1136/bmjopen-2022-066255
PMID:36207048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9558804/
Abstract

INTRODUCTION

Whether bisphosphonates and RANKL inhibitors play a novel role in delaying cardiovascular calcification is unknown. Their action on regulatory enzymes in the mevalonic acid pathway, which is implicated in both bone and lipid metabolism, may be a novel therapeutic target to manage coronary artery disease (CAD). Such therapies may particularly be relevant in those for whom traditional cardiovascular therapies are no longer sufficient to control disease progression.

METHODS AND ANALYSIS

We will perform a systematic review which aims to synthesise evidence regarding whether use of bisphosphonates or use of the RANKL inhibitor denosumab delays coronary artery calcium (CAC) progression. Eligible studies will include longitudinal studies investigating CAC progression in patients aged >18 years taking either a bisphosphonate or denosumab compared with those who do not. Embase, MEDLINE and Cochrane will be searched using prespecified search terms. Studies will be screened by title and abstract independently and then in full to determine suitability for inclusion in the review. Extracted data will include that relating to study and participant characteristics. The primary outcome will be the CAC score. Secondary outcomes will include aortic and carotid artery calcification. Meta-analysis will be performed if sufficient data are available.

ETHICS AND DISSEMINATION

This study does not require ethics as it is a systematic review of the literature. The results of the review described within this protocol will be distributed via presentations at relevant conferences and publication within a peer-reviewed journal.

PROSPERO REGISTRATION NUMBER

The systematic review pertaining to this protocol is registered with PROSPERO (Registration ID: CRD42022312377).

摘要

简介

双膦酸盐和 RANKL 抑制剂在延缓心血管钙化方面是否发挥新作用尚不清楚。它们对甲羟戊酸途径中的调节酶的作用,该途径与骨和脂代谢都有关,可能是管理冠状动脉疾病(CAD)的新治疗靶点。对于那些传统心血管治疗方法已不足以控制疾病进展的患者,此类治疗方法可能特别相关。

方法和分析

我们将进行一项系统评价,旨在综合关于使用双膦酸盐或使用 RANKL 抑制剂地舒单抗是否会延缓冠状动脉钙(CAC)进展的证据。合格的研究将包括对年龄>18 岁的服用双膦酸盐或地舒单抗的患者与未服用的患者进行 CAC 进展的纵向研究。将使用预设的搜索词在 Embase、MEDLINE 和 Cochrane 中进行搜索。将通过标题和摘要独立筛选研究,然后进行全文筛选以确定是否适合纳入审查。提取的数据将包括与研究和参与者特征相关的数据。主要结局将是 CAC 评分。次要结局将包括主动脉和颈动脉钙化。如果有足够的数据,将进行荟萃分析。

伦理和传播

由于这是对文献的系统评价,因此该研究不需要伦理。本协议中描述的审查结果将通过在相关会议上的演示和在同行评审期刊上的发表来分发。

PROSPERO 注册号:与本方案相关的系统评价已在 PROSPERO(注册号:CRD42022312377)中注册。