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Jointly modelling longitudinally measured urinary human chorionic gonadotrophin and early pregnancy outcomes

Human chorionic gonadotrophin (hCG) is largely used to confirm pregnancy. Yet evidence shows that longitudinal hCG profiles are distinguishable between healthy and failing pregnancies. We retrospectively fitted a joint longitudinal-survival model to data from 127 (85 healthy and 42 failing pregnanci...

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Autores principales: Ashra, N. B., Marriott, L., Johnson, S., Abrams, K. R., Crowther, M. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067806/
https://www.ncbi.nlm.nih.gov/pubmed/32165717
http://dx.doi.org/10.1038/s41598-020-61461-w
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author Ashra, N. B.
Marriott, L.
Johnson, S.
Abrams, K. R.
Crowther, M. J.
author_facet Ashra, N. B.
Marriott, L.
Johnson, S.
Abrams, K. R.
Crowther, M. J.
author_sort Ashra, N. B.
collection PubMed
description Human chorionic gonadotrophin (hCG) is largely used to confirm pregnancy. Yet evidence shows that longitudinal hCG profiles are distinguishable between healthy and failing pregnancies. We retrospectively fitted a joint longitudinal-survival model to data from 127 (85 healthy and 42 failing pregnancies) US women, aged 18–45, who were attempting to conceive, to quantify the association between longitudinally measured urinary hCG and early miscarriage. Using subject-specific predictions, obtained uniquely from the joint model, we investigated the plausibility of adaptively monitoring early pregnancy outcomes based on updating hCG measurements. Volunteers collected daily early morning urine samples for their menstrual cycle and up to 28 days post day of missed period. The longitudinal submodel for log hCG included a random intercept and slope and fixed linear and quadratic time terms. The survival submodel included maternal age and cycle length covariates. Unit increases in log hCG corresponded to a 63.9% (HR 0.36, 95% CI 0.16, 0.47) decrease in the risk of miscarriage, confirming a strong association between hCG and miscarriage. Outputted conditional survival probabilities gave individualised risk estimates for the early pregnancy outcomes in the short term. However, longer term monitoring would require a larger sample size and prospectively followed up data, focusing on emerging extensions to the joint model, which allow assessment of the specificity and sensitivity.
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spelling pubmed-70678062020-03-19 Jointly modelling longitudinally measured urinary human chorionic gonadotrophin and early pregnancy outcomes Ashra, N. B. Marriott, L. Johnson, S. Abrams, K. R. Crowther, M. J. Sci Rep Article Human chorionic gonadotrophin (hCG) is largely used to confirm pregnancy. Yet evidence shows that longitudinal hCG profiles are distinguishable between healthy and failing pregnancies. We retrospectively fitted a joint longitudinal-survival model to data from 127 (85 healthy and 42 failing pregnancies) US women, aged 18–45, who were attempting to conceive, to quantify the association between longitudinally measured urinary hCG and early miscarriage. Using subject-specific predictions, obtained uniquely from the joint model, we investigated the plausibility of adaptively monitoring early pregnancy outcomes based on updating hCG measurements. Volunteers collected daily early morning urine samples for their menstrual cycle and up to 28 days post day of missed period. The longitudinal submodel for log hCG included a random intercept and slope and fixed linear and quadratic time terms. The survival submodel included maternal age and cycle length covariates. Unit increases in log hCG corresponded to a 63.9% (HR 0.36, 95% CI 0.16, 0.47) decrease in the risk of miscarriage, confirming a strong association between hCG and miscarriage. Outputted conditional survival probabilities gave individualised risk estimates for the early pregnancy outcomes in the short term. However, longer term monitoring would require a larger sample size and prospectively followed up data, focusing on emerging extensions to the joint model, which allow assessment of the specificity and sensitivity. Nature Publishing Group UK 2020-03-12 /pmc/articles/PMC7067806/ /pubmed/32165717 http://dx.doi.org/10.1038/s41598-020-61461-w 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ashra, N. B.
Marriott, L.
Johnson, S.
Abrams, K. R.
Crowther, M. J.
Jointly modelling longitudinally measured urinary human chorionic gonadotrophin and early pregnancy outcomes
title Jointly modelling longitudinally measured urinary human chorionic gonadotrophin and early pregnancy outcomes
title_full Jointly modelling longitudinally measured urinary human chorionic gonadotrophin and early pregnancy outcomes
title_fullStr Jointly modelling longitudinally measured urinary human chorionic gonadotrophin and early pregnancy outcomes
title_full_unstemmed Jointly modelling longitudinally measured urinary human chorionic gonadotrophin and early pregnancy outcomes
title_short Jointly modelling longitudinally measured urinary human chorionic gonadotrophin and early pregnancy outcomes
title_sort jointly modelling longitudinally measured urinary human chorionic gonadotrophin and early pregnancy outcomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067806/
https://www.ncbi.nlm.nih.gov/pubmed/32165717
http://dx.doi.org/10.1038/s41598-020-61461-w
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