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系统评价和荟萃分析方案:他汀类药物作为免疫调节剂对慢性病成人炎症标志物的影响。

Protocol for systematic review and meta-analysis: impact of statins as immune-modulatory agents on inflammatory markers in adults with chronic diseases.

机构信息

International Centre for Genetic Engineering and Biotechnology (ICGEB) Cape Town Component, Cape Town, South Africa.

Institute of Infectious Diseases and Molecular Medicine (IDM), Department of Pathology, Division of Immunology, South African Medical Research Council (SAMRC) Immunology of Infectious Diseases, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

出版信息

BMJ Open. 2020 Aug 13;10(8):e039034. doi: 10.1136/bmjopen-2020-039034.

Abstract

INTRODUCTION

Statins, also known as 3-hydroxy-3-methylglutaryl coenzyme-A (HMG-CoA) reductase inhibitors, are lipid-lowering agents that are central in preventing or reducing the complications of atherosclerotic cardiovascular disease. Because statins have anti-inflammatory properties, there is considerable interest in their therapeutic potential in other chronic inflammatory conditions. We aim to identify the statin with the greatest ability to reduce systemic inflammation, independent of the underlying disease entity.

METHODS AND ANALYSIS

We aim to conduct a comprehensive search of published and peer-reviewed randomised controlled clinical trials, with at least one intervention arm of a Food & Drug Administration-licensed or European Medicines Agency-licensed statin and a minimum treatment duration of 12 weeks. Our objective is to investigate the effect of statins (atorvastatin, fluvastatin, pitavastatin, pravastatin, rosuvastatin, simvastatin) on lipid profile, particularly, cholesterol low-density lipoprotein and inflammation markers such as high-sensitive C reactive protein (hsCRP), CRP, tumour necrosis factor alpha (TNF-α), interleukin-1β (IL-1β), IL-6, IL-8, soluble cluster of differentiation 14 (sCD14) or sCD16 in adults, published in the last 20 years (between January 1999 and December 2019). We aim to identify the most potent statin to reduce systemic inflammation and optimal dosing. The following databases will be searched: Medline, Scopus, Web of Science and Cochrane Library of Systematic Reviews. The risk of bias of included studies will be assessed by Cochrane Risk of Bias Tool and Quality Assessment Tool for Quantitative Studies. The quality of studies will be assessed, to show uncertainty, by the Jadad Score. If sufficient evidence is identified, a meta-analysis will be conducted with risk ratios or ORs with 95% CIs in addition to mean differences.

ETHICS AND DISSEMINATION

Ethics approval is not required as no primary data will be collected. Results will be presented at conferences and published in a peer-reviewed journal.

PROSPERO REGISTRATION NUMBER

CRD42020169919.

摘要

简介

他汀类药物,也称为 3-羟基-3-甲基戊二酰辅酶 A(HMG-CoA)还原酶抑制剂,是降脂药物,在预防或减少动脉粥样硬化性心血管疾病的并发症方面发挥着核心作用。由于他汀类药物具有抗炎特性,因此人们对其在其他慢性炎症性疾病中的治疗潜力产生了浓厚的兴趣。我们旨在确定具有最大降低全身炎症能力的他汀类药物,而与潜在疾病实体无关。

方法和分析

我们旨在对已发表和同行评议的随机对照临床试验进行全面检索,至少有一个经美国食品和药物管理局(FDA)或欧洲药品管理局(EMA)批准的他汀类药物干预组,且治疗时间至少为 12 周。我们的目的是研究他汀类药物(阿托伐他汀、氟伐他汀、匹伐他汀、普伐他汀、罗苏伐他汀、辛伐他汀)对血脂谱的影响,特别是胆固醇低密度脂蛋白和炎症标志物,如高敏 C 反应蛋白(hsCRP)、CRP、肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、可溶性 CD14(sCD14)或可溶性 CD16,在过去 20 年(1999 年 1 月至 2019 年 12 月)内成年人群中的作用。我们旨在确定降低全身炎症和最佳剂量的最有效他汀类药物。将检索以下数据库:Medline、Scopus、Web of Science 和 Cochrane 系统评价图书馆。将使用 Cochrane 偏倚风险工具和定量研究质量评估工具评估纳入研究的偏倚风险。将使用 Jadad 评分评估研究质量,以显示不确定性。如果确定了足够的证据,将使用风险比或 OR 与 95%CI 以及均值差异进行荟萃分析。

伦理和传播

由于不会收集原始数据,因此不需要伦理批准。研究结果将在会议上展示,并发表在同行评议的期刊上。

PROSPERO 注册号:CRD42020169919。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56f1/7430409/3b26acfc9996/bmjopen-2020-039034f01.jpg

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