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Modelling of longitudinal data to predict cardiovascular disease risk: a methodological review
OBJECTIVE: The identification of methodology for modelling cardiovascular disease (CVD) risk using longitudinal data and risk factor trajectories. METHODS: We screened MEDLINE-Ovid from inception until 3 June 2020. MeSH and text search terms covered three areas: data type, modelling type and disease...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684210/ https://www.ncbi.nlm.nih.gov/pubmed/34922465 http://dx.doi.org/10.1186/s12874-021-01472-x |
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author | Stevens, David Lane, Deirdre A. Harrison, Stephanie L. Lip, Gregory Y. H. Kolamunnage-Dona, Ruwanthi |
author_facet | Stevens, David Lane, Deirdre A. Harrison, Stephanie L. Lip, Gregory Y. H. Kolamunnage-Dona, Ruwanthi |
author_sort | Stevens, David |
collection | PubMed |
description | OBJECTIVE: The identification of methodology for modelling cardiovascular disease (CVD) risk using longitudinal data and risk factor trajectories. METHODS: We screened MEDLINE-Ovid from inception until 3 June 2020. MeSH and text search terms covered three areas: data type, modelling type and disease area including search terms such as “longitudinal”, “trajector*” and “cardiovasc*” respectively. Studies were filtered to meet the following inclusion criteria: longitudinal individual patient data in adult patients with ≥3 time-points and a CVD or mortality outcome. Studies were screened and analyzed by one author. Any queries were discussed with the other authors. Comparisons were made between the methods identified looking at assumptions, flexibility and software availability. RESULTS: From the initial 2601 studies returned by the searches 80 studies were included. Four statistical approaches were identified for modelling the longitudinal data: 3 (4%) studies compared time points with simple statistical tests, 40 (50%) used single-stage approaches, such as including single time points or summary measures in survival models, 29 (36%) used two-stage approaches including an estimated longitudinal parameter in survival models, and 8 (10%) used joint models which modelled the longitudinal and survival data together. The proportion of CVD risk prediction models created using longitudinal data using two-stage and joint models increased over time. CONCLUSIONS: Single stage models are still heavily utilized by many CVD risk prediction studies for modelling longitudinal data. Future studies should fully utilize available longitudinal data when analyzing CVD risk by employing two-stage and joint approaches which can often better utilize the available data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-021-01472-x. |
format | Online Article Text |
id | pubmed-8684210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86842102021-12-20 Modelling of longitudinal data to predict cardiovascular disease risk: a methodological review Stevens, David Lane, Deirdre A. Harrison, Stephanie L. Lip, Gregory Y. H. Kolamunnage-Dona, Ruwanthi BMC Med Res Methodol Research OBJECTIVE: The identification of methodology for modelling cardiovascular disease (CVD) risk using longitudinal data and risk factor trajectories. METHODS: We screened MEDLINE-Ovid from inception until 3 June 2020. MeSH and text search terms covered three areas: data type, modelling type and disease area including search terms such as “longitudinal”, “trajector*” and “cardiovasc*” respectively. Studies were filtered to meet the following inclusion criteria: longitudinal individual patient data in adult patients with ≥3 time-points and a CVD or mortality outcome. Studies were screened and analyzed by one author. Any queries were discussed with the other authors. Comparisons were made between the methods identified looking at assumptions, flexibility and software availability. RESULTS: From the initial 2601 studies returned by the searches 80 studies were included. Four statistical approaches were identified for modelling the longitudinal data: 3 (4%) studies compared time points with simple statistical tests, 40 (50%) used single-stage approaches, such as including single time points or summary measures in survival models, 29 (36%) used two-stage approaches including an estimated longitudinal parameter in survival models, and 8 (10%) used joint models which modelled the longitudinal and survival data together. The proportion of CVD risk prediction models created using longitudinal data using two-stage and joint models increased over time. CONCLUSIONS: Single stage models are still heavily utilized by many CVD risk prediction studies for modelling longitudinal data. Future studies should fully utilize available longitudinal data when analyzing CVD risk by employing two-stage and joint approaches which can often better utilize the available data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-021-01472-x. BioMed Central 2021-12-18 /pmc/articles/PMC8684210/ /pubmed/34922465 http://dx.doi.org/10.1186/s12874-021-01472-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Stevens, David Lane, Deirdre A. Harrison, Stephanie L. Lip, Gregory Y. H. Kolamunnage-Dona, Ruwanthi Modelling of longitudinal data to predict cardiovascular disease risk: a methodological review |
title | Modelling of longitudinal data to predict cardiovascular disease risk: a methodological review |
title_full | Modelling of longitudinal data to predict cardiovascular disease risk: a methodological review |
title_fullStr | Modelling of longitudinal data to predict cardiovascular disease risk: a methodological review |
title_full_unstemmed | Modelling of longitudinal data to predict cardiovascular disease risk: a methodological review |
title_short | Modelling of longitudinal data to predict cardiovascular disease risk: a methodological review |
title_sort | modelling of longitudinal data to predict cardiovascular disease risk: a methodological review |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684210/ https://www.ncbi.nlm.nih.gov/pubmed/34922465 http://dx.doi.org/10.1186/s12874-021-01472-x |
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