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校准钠-葡萄糖共转运蛋白 2 抑制剂、胰高血糖素样肽-1 受体激动剂和二肽基肽酶-4 抑制剂治疗糖尿病试验的网络荟萃分析,以适应代表性的常规人群:系统评价方案。

Calibrating a network meta-analysis of diabetes trials of sodium glucose cotransporter 2 inhibitors, glucagon-like peptide-1 receptor analogues and dipeptidyl peptidase-4 inhibitors to a representative routine population: a systematic review protocol.

机构信息

School of Health and Wellbeing, University of Glasgow, Glasgow, UK.

Diabetes Trials Unit, University of Oxford, Oxford, UK.

出版信息

BMJ Open. 2022 Oct 27;12(10):e066491. doi: 10.1136/bmjopen-2022-066491.

Abstract

INTRODUCTION

Participants in randomised controlled trials (trials) are generally younger and healthier than many individuals encountered in clinical practice. Consequently, the applicability of trial findings is often uncertain. To address this, results from trials can be calibrated to more representative data sources. In a network meta-analysis, using a novel approach which allows the inclusion of trials whether or not individual-level participant data (IPD) is available, we will calibrate trials for three drug classes (sodium glucose cotransporter 2 (SGLT2) inhibitors, glucagon-like peptide-1 (GLP1) receptor analogues and dipeptidyl peptidase-4 (DPP4) inhibitors) to the Scottish diabetes register.

METHODS AND ANALYSIS

Medline and EMBASE databases, the US clinical trials registry (clinicaltrials.gov) and the Chinese Clinical Trial Registry (chictr.org.cn) will be searched from 1 January 2002. Two independent reviewers will apply eligibility criteria to identify trials for inclusion. Included trials will be phase 3 or 4 trials of SGLT2 inhibitors, GLP1 receptor analogues or DPP4 inhibitors, with placebo or active comparators, in participants with type 2 diabetes, with at least one of glycaemic control, change in body weight or major adverse cardiovascular event as outcomes. Unregistered trials will be excluded.We have identified a target population from the population-based Scottish diabetes register. The chosen cohort comprises people in Scotland with type 2 diabetes who either (1) require further treatment due to poor glycaemic control where any of the three drug classes may be suitable, or (2) who have adequate glycaemic control but are already on one of the three drug classes of interest or insulin.

ETHICS AND DISSEMINATION

Ethical approval for IPD use was obtained from the University of Glasgow MVLS College Ethics Committee (Project: 200160070). The Scottish diabetes register has approval from the Scottish A Research Ethics Committee (11/AL/0225) and operates with Public Benefit and Privacy Panel for Health and Social Care approval (1617-0147).

PROSPERO REGISTRATION NUMBER

CRD42020184174.

摘要

简介

随机对照试验(试验)的参与者通常比许多在临床实践中遇到的个体更年轻、更健康。因此,试验结果的适用性往往不确定。为了解决这个问题,可以根据更具代表性的数据来源对试验结果进行校准。在网络荟萃分析中,我们将采用一种新方法,无论是否有个体水平参与者数据(IPD),都可以纳入试验,以苏格兰糖尿病登记处的数据对三种药物类别(钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂、胰高血糖素样肽-1(GLP1)受体类似物和二肽基肽酶-4(DPP4)抑制剂)的试验进行校准。

方法和分析

从 2002 年 1 月 1 日起,将对 Medline 和 EMBASE 数据库、美国临床试验注册处(clinicaltrials.gov)和中国临床试验注册中心(chictr.org.cn)进行搜索。两名独立的审查员将应用纳入标准,以确定纳入试验。纳入的试验将是 SGLT2 抑制剂、GLP1 受体类似物或 DPP4 抑制剂的 3 期或 4 期试验,使用安慰剂或活性对照剂,在 2 型糖尿病患者中,以血糖控制、体重变化或主要不良心血管事件作为结局。未注册的试验将被排除在外。我们已经从基于人群的苏格兰糖尿病登记处确定了目标人群。所选队列由苏格兰 2 型糖尿病患者组成,这些患者(1)由于血糖控制不佳需要进一步治疗,其中任何三种药物类别都可能适用,或(2)血糖控制良好,但已经使用了三种感兴趣的药物类别之一或胰岛素。

伦理和传播

苏格兰格拉斯哥大学 MVLS 学院伦理委员会已获得 IPD 使用的伦理批准(项目:200160070)。苏格兰糖尿病登记处已获得苏格兰 A 研究伦理委员会的批准(11/AL/0225),并获得健康和社会护理公共利益和隐私小组的批准(1617-0147)。

前瞻性登记号

CRD42020184174。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc4/9621152/175982d8d15c/bmjopen-2022-066491f01.jpg

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