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Risk factors for cardiovascular events in patients with heterozygous familial hypercholesterolaemia: protocol for a systematic review

INTRODUCTION: Heterozygous familial hypercholesterolaemia (heFH) is the most common monogenic cause of premature atherosclerotic cardiovascular disease. The precise diagnosis of heFH is established by genetic testing. This systematic review will investigate the risk factors that predict cardiovascul...

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Autores principales: Mansilla-Rodríguez, María Elena, Romero-Jimenez, Manuel J, Rigabert Sánchez-Junco, Alina, Gutierrez-Cortizo, Eva Nadiedja, Sánchez-Ramos, José Luis, Mata, Pedro, Pang, Jing, Watts, Gerald F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069512/
https://www.ncbi.nlm.nih.gov/pubmed/36990476
http://dx.doi.org/10.1136/bmjopen-2022-065551
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author Mansilla-Rodríguez, María Elena
Romero-Jimenez, Manuel J
Rigabert Sánchez-Junco, Alina
Gutierrez-Cortizo, Eva Nadiedja
Sánchez-Ramos, José Luis
Mata, Pedro
Pang, Jing
Watts, Gerald F
author_facet Mansilla-Rodríguez, María Elena
Romero-Jimenez, Manuel J
Rigabert Sánchez-Junco, Alina
Gutierrez-Cortizo, Eva Nadiedja
Sánchez-Ramos, José Luis
Mata, Pedro
Pang, Jing
Watts, Gerald F
author_sort Mansilla-Rodríguez, María Elena
collection PubMed
description INTRODUCTION: Heterozygous familial hypercholesterolaemia (heFH) is the most common monogenic cause of premature atherosclerotic cardiovascular disease. The precise diagnosis of heFH is established by genetic testing. This systematic review will investigate the risk factors that predict cardiovascular events in patients with a genetic diagnosis of heFH. METHODS AND ANALYSIS: Our literature search will cover publications from database inception until June 2023. We will undertake a search of CINAHL (trial), clinicalKey, Cochrane Library, DynaMed, Embase, Espacenet, Experiments (trial), Fisterra, ÍnDICEs CSIC, LILACS, LISTA, Medline, Micromedex, NEJM Resident 360, OpenDissertations, PEDro, Trip Database, PubPsych, Scopus, TESEO, UpToDate, Web of Science and the grey literature for eligible studies. We will screen the title, abstract and full-text papers for potential inclusion and assess the risk of bias. We will employ the Cochrane tool for randomised controlled trials and non-randomised clinical studies and the Newcastle–Ottawa Scale for assessing the risk of bias in observational studies. We will include full-text peer-reviewed publications, reports of a cohort/registry, case–control and cross-sectional studies, case report/series and surveys related to adults (≥18 years of age) with a genetic diagnostic heFH. The language of the searched studies will be restricted to English or Spanish. The Grading of Recommendations, Assessment, Development and Evaluation approach will be used to assess the quality of the evidence. Based on the data available, the authors will determine whether the data can be pooled in meta-analyses. ETHICS AND DISSEMINATION: All data will be extracted from published literature. Hence, ethical approval and patient informed consent are not required. The findings of the systematic review will be submitted for publication in a peer-reviewed journal and presentation at international conferences. PROSPERO REGISTRATION NUMBER: CRD42022304273.
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spelling pubmed-100695122023-04-04 Risk factors for cardiovascular events in patients with heterozygous familial hypercholesterolaemia: protocol for a systematic review Mansilla-Rodríguez, María Elena Romero-Jimenez, Manuel J Rigabert Sánchez-Junco, Alina Gutierrez-Cortizo, Eva Nadiedja Sánchez-Ramos, José Luis Mata, Pedro Pang, Jing Watts, Gerald F BMJ Open Cardiovascular Medicine INTRODUCTION: Heterozygous familial hypercholesterolaemia (heFH) is the most common monogenic cause of premature atherosclerotic cardiovascular disease. The precise diagnosis of heFH is established by genetic testing. This systematic review will investigate the risk factors that predict cardiovascular events in patients with a genetic diagnosis of heFH. METHODS AND ANALYSIS: Our literature search will cover publications from database inception until June 2023. We will undertake a search of CINAHL (trial), clinicalKey, Cochrane Library, DynaMed, Embase, Espacenet, Experiments (trial), Fisterra, ÍnDICEs CSIC, LILACS, LISTA, Medline, Micromedex, NEJM Resident 360, OpenDissertations, PEDro, Trip Database, PubPsych, Scopus, TESEO, UpToDate, Web of Science and the grey literature for eligible studies. We will screen the title, abstract and full-text papers for potential inclusion and assess the risk of bias. We will employ the Cochrane tool for randomised controlled trials and non-randomised clinical studies and the Newcastle–Ottawa Scale for assessing the risk of bias in observational studies. We will include full-text peer-reviewed publications, reports of a cohort/registry, case–control and cross-sectional studies, case report/series and surveys related to adults (≥18 years of age) with a genetic diagnostic heFH. The language of the searched studies will be restricted to English or Spanish. The Grading of Recommendations, Assessment, Development and Evaluation approach will be used to assess the quality of the evidence. Based on the data available, the authors will determine whether the data can be pooled in meta-analyses. ETHICS AND DISSEMINATION: All data will be extracted from published literature. Hence, ethical approval and patient informed consent are not required. The findings of the systematic review will be submitted for publication in a peer-reviewed journal and presentation at international conferences. PROSPERO REGISTRATION NUMBER: CRD42022304273. BMJ Publishing Group 2023-03-28 /pmc/articles/PMC10069512/ /pubmed/36990476 http://dx.doi.org/10.1136/bmjopen-2022-065551 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Cardiovascular Medicine
Mansilla-Rodríguez, María Elena
Romero-Jimenez, Manuel J
Rigabert Sánchez-Junco, Alina
Gutierrez-Cortizo, Eva Nadiedja
Sánchez-Ramos, José Luis
Mata, Pedro
Pang, Jing
Watts, Gerald F
Risk factors for cardiovascular events in patients with heterozygous familial hypercholesterolaemia: protocol for a systematic review
title Risk factors for cardiovascular events in patients with heterozygous familial hypercholesterolaemia: protocol for a systematic review
title_full Risk factors for cardiovascular events in patients with heterozygous familial hypercholesterolaemia: protocol for a systematic review
title_fullStr Risk factors for cardiovascular events in patients with heterozygous familial hypercholesterolaemia: protocol for a systematic review
title_full_unstemmed Risk factors for cardiovascular events in patients with heterozygous familial hypercholesterolaemia: protocol for a systematic review
title_short Risk factors for cardiovascular events in patients with heterozygous familial hypercholesterolaemia: protocol for a systematic review
title_sort risk factors for cardiovascular events in patients with heterozygous familial hypercholesterolaemia: protocol for a systematic review
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069512/
https://www.ncbi.nlm.nih.gov/pubmed/36990476
http://dx.doi.org/10.1136/bmjopen-2022-065551
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