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Joint modelling of longitudinal lipids and time to coronary heart disease in the Jackson Heart Study

BACKGROUND: Multiple longitudinal responses together with time-to-event outcome are common in biomedical studies. There are several instances where the longitudinal responses are correlated with each other and at the same time each longitudinal response is associated with the survival outcome. The m...

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Autores principales: Kassahun-Yimer, Wondwosen, Valle, Karen A., Oshunbade, Adebamike A., Hall, Michael E., Min, Yuan-I., Cain-Shields, Loretta, Anugu, Pramod, Correa, Adolfo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713018/
https://www.ncbi.nlm.nih.gov/pubmed/33272219
http://dx.doi.org/10.1186/s12874-020-01177-7
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author Kassahun-Yimer, Wondwosen
Valle, Karen A.
Oshunbade, Adebamike A.
Hall, Michael E.
Min, Yuan-I.
Cain-Shields, Loretta
Anugu, Pramod
Correa, Adolfo
author_facet Kassahun-Yimer, Wondwosen
Valle, Karen A.
Oshunbade, Adebamike A.
Hall, Michael E.
Min, Yuan-I.
Cain-Shields, Loretta
Anugu, Pramod
Correa, Adolfo
author_sort Kassahun-Yimer, Wondwosen
collection PubMed
description BACKGROUND: Multiple longitudinal responses together with time-to-event outcome are common in biomedical studies. There are several instances where the longitudinal responses are correlated with each other and at the same time each longitudinal response is associated with the survival outcome. The main purpose of this study is to present and explore a joint modeling approach for multiple correlated longitudinal responses and a survival outcome. The method will be illustrated using the Jackson Heart Study (JHS), which is one of the largest cardiovascular studies among African Americans. METHODS: Four longitudinal responses, i.e., total cholesterol (TC), high density lipoprotein (HDL) cholesterol, triglyceride (TG) and inflammation measured by high-sensitivity C-reactive protein (hsCRP); and time-to-coronary heart disease (CHD) were considered from the JHS. The repeated lipid and hsCRP measurements from a given subject overtime are likely correlated with each other and could influence the subject’s risk for CHD. A joint modeling framework is considered. To deal with the high dimensionality due to the multiple longitudinal profiles, we use a pairwise bivariate model fitting approach that was developed in the context of multivariate Gaussian random effects models. The method is further explored through simulations. RESULTS: The proposed model performed well in terms of bias and relative efficiency. The JHS data analysis showed that lipid and hsCRP trajectories could exhibit interdependence in their joint evolution and have impact on CHD risk. CONCLUSIONS: We applied a unified and flexible joint modeling approach to analyze multiple correlated longitudinal responses and survival outcome. The method accounts for the correlation among the longitudinal responses as well as the association between each longitudinal response and the survival outcome at once. This helps to explore how the combination of multiple longitudinal trajectories could be related to the survival process.
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spelling pubmed-77130182020-12-03 Joint modelling of longitudinal lipids and time to coronary heart disease in the Jackson Heart Study Kassahun-Yimer, Wondwosen Valle, Karen A. Oshunbade, Adebamike A. Hall, Michael E. Min, Yuan-I. Cain-Shields, Loretta Anugu, Pramod Correa, Adolfo BMC Med Res Methodol Research Article BACKGROUND: Multiple longitudinal responses together with time-to-event outcome are common in biomedical studies. There are several instances where the longitudinal responses are correlated with each other and at the same time each longitudinal response is associated with the survival outcome. The main purpose of this study is to present and explore a joint modeling approach for multiple correlated longitudinal responses and a survival outcome. The method will be illustrated using the Jackson Heart Study (JHS), which is one of the largest cardiovascular studies among African Americans. METHODS: Four longitudinal responses, i.e., total cholesterol (TC), high density lipoprotein (HDL) cholesterol, triglyceride (TG) and inflammation measured by high-sensitivity C-reactive protein (hsCRP); and time-to-coronary heart disease (CHD) were considered from the JHS. The repeated lipid and hsCRP measurements from a given subject overtime are likely correlated with each other and could influence the subject’s risk for CHD. A joint modeling framework is considered. To deal with the high dimensionality due to the multiple longitudinal profiles, we use a pairwise bivariate model fitting approach that was developed in the context of multivariate Gaussian random effects models. The method is further explored through simulations. RESULTS: The proposed model performed well in terms of bias and relative efficiency. The JHS data analysis showed that lipid and hsCRP trajectories could exhibit interdependence in their joint evolution and have impact on CHD risk. CONCLUSIONS: We applied a unified and flexible joint modeling approach to analyze multiple correlated longitudinal responses and survival outcome. The method accounts for the correlation among the longitudinal responses as well as the association between each longitudinal response and the survival outcome at once. This helps to explore how the combination of multiple longitudinal trajectories could be related to the survival process. BioMed Central 2020-12-03 /pmc/articles/PMC7713018/ /pubmed/33272219 http://dx.doi.org/10.1186/s12874-020-01177-7 Text en © The Author(s) 2020 Open Access This 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, visithttp://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Kassahun-Yimer, Wondwosen
Valle, Karen A.
Oshunbade, Adebamike A.
Hall, Michael E.
Min, Yuan-I.
Cain-Shields, Loretta
Anugu, Pramod
Correa, Adolfo
Joint modelling of longitudinal lipids and time to coronary heart disease in the Jackson Heart Study
title Joint modelling of longitudinal lipids and time to coronary heart disease in the Jackson Heart Study
title_full Joint modelling of longitudinal lipids and time to coronary heart disease in the Jackson Heart Study
title_fullStr Joint modelling of longitudinal lipids and time to coronary heart disease in the Jackson Heart Study
title_full_unstemmed Joint modelling of longitudinal lipids and time to coronary heart disease in the Jackson Heart Study
title_short Joint modelling of longitudinal lipids and time to coronary heart disease in the Jackson Heart Study
title_sort joint modelling of longitudinal lipids and time to coronary heart disease in the jackson heart study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713018/
https://www.ncbi.nlm.nih.gov/pubmed/33272219
http://dx.doi.org/10.1186/s12874-020-01177-7
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