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The association of telomere length with substance use disorders: systematic review and meta-analysis protocol

BACKGROUND: The present protocol was designed for a systematic review and meta-analysis aimed at determining the association of telomere length with substance use disorders with the exclusion of nicotine addiction, and to identify potential moderators of the effect of telomere length. Such methodolo...

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Autores principales: Navarro-Mateu, Fernando, Rubio-Aparicio, María, Cayuela, Pedro, Álvarez, Francisco-Javier, Roca-Vega, Agustín, Chirlaque, María Dolores, Cayuela, María Luisa, Husky, Mathilde, Martínez, Salvador, Sánchez-Meca, Julio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886210/
https://www.ncbi.nlm.nih.gov/pubmed/31787100
http://dx.doi.org/10.1186/s13643-019-1199-x
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author Navarro-Mateu, Fernando
Rubio-Aparicio, María
Cayuela, Pedro
Álvarez, Francisco-Javier
Roca-Vega, Agustín
Chirlaque, María Dolores
Cayuela, María Luisa
Husky, Mathilde
Martínez, Salvador
Sánchez-Meca, Julio
author_facet Navarro-Mateu, Fernando
Rubio-Aparicio, María
Cayuela, Pedro
Álvarez, Francisco-Javier
Roca-Vega, Agustín
Chirlaque, María Dolores
Cayuela, María Luisa
Husky, Mathilde
Martínez, Salvador
Sánchez-Meca, Julio
author_sort Navarro-Mateu, Fernando
collection PubMed
description BACKGROUND: The present protocol was designed for a systematic review and meta-analysis aimed at determining the association of telomere length with substance use disorders with the exclusion of nicotine addiction, and to identify potential moderators of the effect of telomere length. Such methodological information may provide guidance to improve the quality of future research on this important topic. METHODS: Potential studies will be identified through electronic databases (PubMed/MEDLINE, EMBASE, PsycINFO, and Web of Science) up from inception onwards. The inclusion criteria will include published or unpublished observational studies (cohort, case–control, and cross-sectional studies) reporting telomere length in adult patients with substance use disorder compared with a control group. Non-human studies or other study designs such as reviews, case-only, family-based, and/or population studies with only healthy participants will be excluded, as well as those focused solely on nicotine addiction. The main outcome will be telomere length in adults with substance use disorder (primary) and, specifically, in those with alcohol use disorder (secondary). Two investigators will independently evaluate the preselected studies for possible inclusion and will extract data following a standardized protocol. Disagreements will be resolved by consensus. The risk of bias of all included studies will be assessed using the Newcastle–Ottawa Quality Assessment Scale for non-randomized studies. Data will be converted into standardized mean differences as effect size index, and random-effects models will be used for the meta-analysis. Cochran’s Q statistic, I(2) index, and visual inspection of the forest plot will be used to verify study heterogeneity. Subgroup analyses and meta-regressions will be conducted to ascertain heterogeneity. Several sensitivity analyses will be conducted to address the influence of potential confounding factors. Publication bias will be examined using the “funnel plot” method with Duval and Tweedie’s trim-and-fill method and Egger test. DISCUSSION: This systematic review will assess the association of telomere length with substance use disorders aside from nicotine addiction. SYSTEMATIC REVIEW REGISTRATION: PROSPERO registration number CRD42019119785
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spelling pubmed-68862102019-12-11 The association of telomere length with substance use disorders: systematic review and meta-analysis protocol Navarro-Mateu, Fernando Rubio-Aparicio, María Cayuela, Pedro Álvarez, Francisco-Javier Roca-Vega, Agustín Chirlaque, María Dolores Cayuela, María Luisa Husky, Mathilde Martínez, Salvador Sánchez-Meca, Julio Syst Rev Protocol BACKGROUND: The present protocol was designed for a systematic review and meta-analysis aimed at determining the association of telomere length with substance use disorders with the exclusion of nicotine addiction, and to identify potential moderators of the effect of telomere length. Such methodological information may provide guidance to improve the quality of future research on this important topic. METHODS: Potential studies will be identified through electronic databases (PubMed/MEDLINE, EMBASE, PsycINFO, and Web of Science) up from inception onwards. The inclusion criteria will include published or unpublished observational studies (cohort, case–control, and cross-sectional studies) reporting telomere length in adult patients with substance use disorder compared with a control group. Non-human studies or other study designs such as reviews, case-only, family-based, and/or population studies with only healthy participants will be excluded, as well as those focused solely on nicotine addiction. The main outcome will be telomere length in adults with substance use disorder (primary) and, specifically, in those with alcohol use disorder (secondary). Two investigators will independently evaluate the preselected studies for possible inclusion and will extract data following a standardized protocol. Disagreements will be resolved by consensus. The risk of bias of all included studies will be assessed using the Newcastle–Ottawa Quality Assessment Scale for non-randomized studies. Data will be converted into standardized mean differences as effect size index, and random-effects models will be used for the meta-analysis. Cochran’s Q statistic, I(2) index, and visual inspection of the forest plot will be used to verify study heterogeneity. Subgroup analyses and meta-regressions will be conducted to ascertain heterogeneity. Several sensitivity analyses will be conducted to address the influence of potential confounding factors. Publication bias will be examined using the “funnel plot” method with Duval and Tweedie’s trim-and-fill method and Egger test. DISCUSSION: This systematic review will assess the association of telomere length with substance use disorders aside from nicotine addiction. SYSTEMATIC REVIEW REGISTRATION: PROSPERO registration number CRD42019119785 BioMed Central 2019-12-01 /pmc/articles/PMC6886210/ /pubmed/31787100 http://dx.doi.org/10.1186/s13643-019-1199-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Protocol
Navarro-Mateu, Fernando
Rubio-Aparicio, María
Cayuela, Pedro
Álvarez, Francisco-Javier
Roca-Vega, Agustín
Chirlaque, María Dolores
Cayuela, María Luisa
Husky, Mathilde
Martínez, Salvador
Sánchez-Meca, Julio
The association of telomere length with substance use disorders: systematic review and meta-analysis protocol
title The association of telomere length with substance use disorders: systematic review and meta-analysis protocol
title_full The association of telomere length with substance use disorders: systematic review and meta-analysis protocol
title_fullStr The association of telomere length with substance use disorders: systematic review and meta-analysis protocol
title_full_unstemmed The association of telomere length with substance use disorders: systematic review and meta-analysis protocol
title_short The association of telomere length with substance use disorders: systematic review and meta-analysis protocol
title_sort association of telomere length with substance use disorders: systematic review and meta-analysis protocol
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886210/
https://www.ncbi.nlm.nih.gov/pubmed/31787100
http://dx.doi.org/10.1186/s13643-019-1199-x
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