Assessing whether genetic scores explain extra variation in birthweight, when added to clinical and anthropometric measures
dc.contributor.author | Haulder, M | |
dc.contributor.author | Hughes, AE | |
dc.contributor.author | Beaumont, RN | |
dc.contributor.author | Knight, BA | |
dc.contributor.author | Hattersley, AT | |
dc.contributor.author | Shields, BM | |
dc.contributor.author | Freathy, RM | |
dc.date.accessioned | 2022-10-18T08:49:36Z | |
dc.date.issued | 2022-08-25 | |
dc.date.updated | 2022-10-17T21:34:44Z | |
dc.description.abstract | BACKGROUND: Human birthweight is a complex, multifactorial trait. Maternal characteristics contribute to birthweight variation by influencing the intrauterine environment. Variation explained by genetic effects is also important, but their contributions have not been assessed alongside other key determinants. We aimed to investigate variance in birthweight explained by genetic scores in addition to easily-measurable clinical and anthropometric variables. METHODS: We analysed 549 European-ancestry parent-offspring trios from a UK community-based birth cohort. We investigated variance explained in birthweight (adjusted for sex and gestational age) in multivariable linear regression models including genetic scores, routinely-measured maternal characteristics, and parental anthropometric variables. We used R-Squared (R2) to estimate variance explained, adjusted R-squared (Adj-R2) to assess improvement in model fit from added predictors, and F-tests to compare nested models. RESULTS: Maternal and fetal genetic scores together explained 6.0% variance in birthweight. A model containing maternal age, weight, smoking, parity and 28-week fasting glucose explained 21.7% variance. Maternal genetic score explained additional variance when added to maternal characteristics (Adj-R2 = 0.233 vs Adj-R2 = 0.210, p < 0.001). Fetal genetic score improved variance explained (Adj-R2 = 0.264 vs 0.248, p < 0.001) when added to maternal characteristics and parental heights. CONCLUSIONS: Genetic scores account for variance explained in birthweight in addition to easily measurable clinical variables. Parental heights partially capture fetal genotype and its contribution to birthweight, but genetic scores explain additional variance. While the genetic contribution is modest, it is comparable to that of individual clinical characteristics such as parity, which suggests that genetics could be included in tools aiming to predict risk of high or low birthweights. | en_GB |
dc.description.sponsorship | Diabetes UK | en_GB |
dc.description.sponsorship | Wellcome Trust | en_GB |
dc.description.sponsorship | National Institute for Health and Care Research (NIHR) | en_GB |
dc.format.extent | 504- | |
dc.format.medium | Electronic | |
dc.identifier.citation | Vol. 22, article 504 | en_GB |
dc.identifier.doi | https://doi.org/10.1186/s12887-022-03554-1 | |
dc.identifier.grantnumber | 18/0005929 | en_GB |
dc.identifier.grantnumber | WT220390 | en_GB |
dc.identifier.grantnumber | WT220390 | en_GB |
dc.identifier.uri | http://hdl.handle.net/10871/131300 | |
dc.identifier | ORCID: 0000-0003-1352-4447 (Hughes, Alice E) | |
dc.identifier | ScopusID: 55882698900 (Hughes, Alice E) | |
dc.identifier | ORCID: 0000-0003-0750-8248 (Beaumont, Robin N) | |
dc.identifier | ScopusID: 57156164500 (Beaumont, Robin N) | |
dc.identifier | ORCID: 0000-0003-3785-327X (Shields, Beverley M) | |
dc.identifier | ORCID: 0000-0003-4152-2238 (Freathy, Rachel M) | |
dc.language.iso | en | en_GB |
dc.publisher | BMC | en_GB |
dc.relation.url | https://www.ncbi.nlm.nih.gov/pubmed/36008798 | en_GB |
dc.relation.url | http://egg-consortium.org/ | en_GB |
dc.rights | © The Author(s) 2022. 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, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativeco mmons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. | en_GB |
dc.subject | Birthweight | en_GB |
dc.subject | Fetal | en_GB |
dc.subject | Genetic score | en_GB |
dc.subject | Intrauterine environment | en_GB |
dc.subject | Maternal | en_GB |
dc.subject | Variance | en_GB |
dc.title | Assessing whether genetic scores explain extra variation in birthweight, when added to clinical and anthropometric measures | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2022-10-18T08:49:36Z | |
dc.identifier.issn | 1471-2431 | |
exeter.article-number | 504 | |
exeter.place-of-publication | England | |
dc.description | This is the final version. Available on open access from BMC via the DOI in this record | en_GB |
dc.description | Availability of data and materials The datasets analysed during the current study (EFSOCH) can be requested for access by writing in the first instance to the EFSOCH data team via the Exeter Clinical Research Facility crf@exeter.ac.uk. The GWAS summary statistics for birthweight that were used to generate the genetic scores are publicly available can be downloaded from http://egg-consortium.org/ | en_GB |
dc.identifier.eissn | 1471-2431 | |
dc.identifier.journal | BMC Pediatrics | en_GB |
dc.relation.ispartof | BMC Pediatr, 22(1) | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_GB |
dcterms.dateAccepted | 2022-08-12 | |
dc.rights.license | CC BY | |
rioxxterms.version | VoR | en_GB |
rioxxterms.licenseref.startdate | 2022-08-25 | |
rioxxterms.type | Journal Article/Review | en_GB |
refterms.dateFCD | 2022-10-18T08:45:44Z | |
refterms.versionFCD | VoR | |
refterms.dateFOA | 2022-10-18T08:49:42Z | |
refterms.panel | A | en_GB |
refterms.dateFirstOnline | 2022-08-25 |
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