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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

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 represe...

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Autores principales: Butterly, Elaine, Wei, Lili, Adler, Amanda I, Almazam, Saleh A M, Alsallumi, Khalid, Blackbourn, Luke A K, Dias, Sofia, Hanlon, Peter, Hughes, Katherine, Lewsey, Jim, Lindsay, Robert, McGurnaghan, Stuart, Petrie, John, Phillippo, David, Sattar, Naveed, Tomlinson, Laurie A, Welton, Nicky, Wild, Sarah, McAllister, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621152/
https://www.ncbi.nlm.nih.gov/pubmed/36302574
http://dx.doi.org/10.1136/bmjopen-2022-066491
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author Butterly, Elaine
Wei, Lili
Adler, Amanda I
Almazam, Saleh A M
Alsallumi, Khalid
Blackbourn, Luke A K
Dias, Sofia
Hanlon, Peter
Hughes, Katherine
Lewsey, Jim
Lindsay, Robert
McGurnaghan, Stuart
Petrie, John
Phillippo, David
Sattar, Naveed
Tomlinson, Laurie A
Welton, Nicky
Wild, Sarah
McAllister, David
author_facet Butterly, Elaine
Wei, Lili
Adler, Amanda I
Almazam, Saleh A M
Alsallumi, Khalid
Blackbourn, Luke A K
Dias, Sofia
Hanlon, Peter
Hughes, Katherine
Lewsey, Jim
Lindsay, Robert
McGurnaghan, Stuart
Petrie, John
Phillippo, David
Sattar, Naveed
Tomlinson, Laurie A
Welton, Nicky
Wild, Sarah
McAllister, David
author_sort Butterly, Elaine
collection PubMed
description 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.
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spelling pubmed-96211522022-11-01 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 Butterly, Elaine Wei, Lili Adler, Amanda I Almazam, Saleh A M Alsallumi, Khalid Blackbourn, Luke A K Dias, Sofia Hanlon, Peter Hughes, Katherine Lewsey, Jim Lindsay, Robert McGurnaghan, Stuart Petrie, John Phillippo, David Sattar, Naveed Tomlinson, Laurie A Welton, Nicky Wild, Sarah McAllister, David BMJ Open Epidemiology 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. BMJ Publishing Group 2022-10-27 /pmc/articles/PMC9621152/ /pubmed/36302574 http://dx.doi.org/10.1136/bmjopen-2022-066491 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Epidemiology
Butterly, Elaine
Wei, Lili
Adler, Amanda I
Almazam, Saleh A M
Alsallumi, Khalid
Blackbourn, Luke A K
Dias, Sofia
Hanlon, Peter
Hughes, Katherine
Lewsey, Jim
Lindsay, Robert
McGurnaghan, Stuart
Petrie, John
Phillippo, David
Sattar, Naveed
Tomlinson, Laurie A
Welton, Nicky
Wild, Sarah
McAllister, David
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
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621152/
https://www.ncbi.nlm.nih.gov/pubmed/36302574
http://dx.doi.org/10.1136/bmjopen-2022-066491
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