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Postal recruitment for genetic studies of preterm birth: A feasibility study

Background: Preterm birth (PTB) represents the leading cause of neonatal death. Large-scale genetic studies are necessary to determine genetic influences on PTB risk, but prospective cohort studies are expensive and time-consuming. We investigated the feasibility of retrospective recruitment of post...

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Autores principales: Keag, Oonagh E., Murphy, Lee, Bradley, Aoibheann, Deakin, Naomi, Whyte, Sonia, Norman, Jane E., Stock, Sarah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160603/
https://www.ncbi.nlm.nih.gov/pubmed/32322692
http://dx.doi.org/10.12688/wellcomeopenres.15207.2
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author Keag, Oonagh E.
Murphy, Lee
Bradley, Aoibheann
Deakin, Naomi
Whyte, Sonia
Norman, Jane E.
Stock, Sarah J.
author_facet Keag, Oonagh E.
Murphy, Lee
Bradley, Aoibheann
Deakin, Naomi
Whyte, Sonia
Norman, Jane E.
Stock, Sarah J.
author_sort Keag, Oonagh E.
collection PubMed
description Background: Preterm birth (PTB) represents the leading cause of neonatal death. Large-scale genetic studies are necessary to determine genetic influences on PTB risk, but prospective cohort studies are expensive and time-consuming. We investigated the feasibility of retrospective recruitment of post-partum women for efficient collection of genetic samples, with self-collected saliva for DNA extraction from themselves and their babies, alongside self-recollection of pregnancy and birth details to phenotype PTB. Methods: 708 women who had participated in the OPPTIMUM trial (a randomised trial of progesterone pessaries to prevent PTB [ISRCTN14568373]) and consented to further contact were invited to provide self-collected saliva from themselves and their babies. DNA was extracted from Oragene OG-500 (adults) and OG-575 (babies) saliva kits and the yield measured by Qubit. Samples were analysed using a panel of Taqman single nucleotide polymorphism (SNP) assays. A questionnaire designed to meet the minimum data set required for phenotyping PTB was included. Questionnaire responses were transcribed and analysed for concordance with prospective trial data using Cohen’s kappa ( k). Results: Recruitment rate was 162/708 (23%) for self-collected saliva samples and 157/708 (22%) for questionnaire responses. 161 samples from the mother provided DNA with median yield 59.0µg (0.4-148.9µg). 156 samples were successfully genotyped (96.9%). 136 baby samples had a median yield 11.5µg (0.1-102.7µg); two samples failed DNA extraction. 131 baby samples (96.3%) were successfully genotyped. Concordance between self-recalled birth details and prospective birth details was excellent ( k>0.75) in 4 out of 10 key fields for phenotyping PTB (mode of delivery, labour onset, ethnicity and maternal age at birth). Conclusion: This feasibility study demonstrates that self-collected DNA samples from mothers and babies were sufficient for genetic analysis but yields were variable. Self-recollection of pregnancy and birth details was inadequate for accurately phenotyping PTB, highlighting the need for alternative strategies for investigating genetic links with PTB.
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spelling pubmed-71606032020-04-21 Postal recruitment for genetic studies of preterm birth: A feasibility study Keag, Oonagh E. Murphy, Lee Bradley, Aoibheann Deakin, Naomi Whyte, Sonia Norman, Jane E. Stock, Sarah J. Wellcome Open Res Research Article Background: Preterm birth (PTB) represents the leading cause of neonatal death. Large-scale genetic studies are necessary to determine genetic influences on PTB risk, but prospective cohort studies are expensive and time-consuming. We investigated the feasibility of retrospective recruitment of post-partum women for efficient collection of genetic samples, with self-collected saliva for DNA extraction from themselves and their babies, alongside self-recollection of pregnancy and birth details to phenotype PTB. Methods: 708 women who had participated in the OPPTIMUM trial (a randomised trial of progesterone pessaries to prevent PTB [ISRCTN14568373]) and consented to further contact were invited to provide self-collected saliva from themselves and their babies. DNA was extracted from Oragene OG-500 (adults) and OG-575 (babies) saliva kits and the yield measured by Qubit. Samples were analysed using a panel of Taqman single nucleotide polymorphism (SNP) assays. A questionnaire designed to meet the minimum data set required for phenotyping PTB was included. Questionnaire responses were transcribed and analysed for concordance with prospective trial data using Cohen’s kappa ( k). Results: Recruitment rate was 162/708 (23%) for self-collected saliva samples and 157/708 (22%) for questionnaire responses. 161 samples from the mother provided DNA with median yield 59.0µg (0.4-148.9µg). 156 samples were successfully genotyped (96.9%). 136 baby samples had a median yield 11.5µg (0.1-102.7µg); two samples failed DNA extraction. 131 baby samples (96.3%) were successfully genotyped. Concordance between self-recalled birth details and prospective birth details was excellent ( k>0.75) in 4 out of 10 key fields for phenotyping PTB (mode of delivery, labour onset, ethnicity and maternal age at birth). Conclusion: This feasibility study demonstrates that self-collected DNA samples from mothers and babies were sufficient for genetic analysis but yields were variable. Self-recollection of pregnancy and birth details was inadequate for accurately phenotyping PTB, highlighting the need for alternative strategies for investigating genetic links with PTB. F1000 Research Limited 2020-06-30 /pmc/articles/PMC7160603/ /pubmed/32322692 http://dx.doi.org/10.12688/wellcomeopenres.15207.2 Text en Copyright: © 2020 Keag OE et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Keag, Oonagh E.
Murphy, Lee
Bradley, Aoibheann
Deakin, Naomi
Whyte, Sonia
Norman, Jane E.
Stock, Sarah J.
Postal recruitment for genetic studies of preterm birth: A feasibility study
title Postal recruitment for genetic studies of preterm birth: A feasibility study
title_full Postal recruitment for genetic studies of preterm birth: A feasibility study
title_fullStr Postal recruitment for genetic studies of preterm birth: A feasibility study
title_full_unstemmed Postal recruitment for genetic studies of preterm birth: A feasibility study
title_short Postal recruitment for genetic studies of preterm birth: A feasibility study
title_sort postal recruitment for genetic studies of preterm birth: a feasibility study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160603/
https://www.ncbi.nlm.nih.gov/pubmed/32322692
http://dx.doi.org/10.12688/wellcomeopenres.15207.2
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