Effect of common pregnancy and perinatal complications on offspring metabolic traits across the life course: a multi-cohort study

dc.contributor.authorElhakeem Ahmed
dc.contributor.authorRonkainen Justiina
dc.contributor.authorMansell Toby
dc.contributor.authorLange Katherine
dc.contributor.authorMikkola Tuija M
dc.contributor.authorMishra Binisha H
dc.contributor.authorWahab Rama J
dc.contributor.authorCadman Tim
dc.contributor.authorYang Tiffany
dc.contributor.authorBurgner David
dc.contributor.authorEriksson Johan G
dc.contributor.authorJärvelin Marjo-Riitta
dc.contributor.authorGaillard Romy
dc.contributor.authorJaddoe Vincent WV
dc.contributor.authorLehtimäki Terho
dc.contributor.authorRaitakari Olli T
dc.contributor.authorSaffery Richard
dc.contributor.authorWake Melissa
dc.contributor.authorWright John
dc.contributor.authorSebert Sylvain
dc.contributor.authorLawlor Deborah A
dc.contributor.organizationfi=InFLAMES Lippulaiva|en=InFLAMES Flagship|
dc.contributor.organizationfi=sydäntutkimuskeskus|en=Cardiovascular Medicine (CAPC)|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organizationfi=väestötutkimuskeskus|en=Centre for Population Health Research (POP Centre)|
dc.contributor.organization-code1.2.246.10.2458963.20.35734063924
dc.contributor.organization-code1.2.246.10.2458963.20.42471027641
dc.contributor.organization-code1.2.246.10.2458963.20.68445910604
dc.converis.publication-id178701402
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/178701402
dc.date.accessioned2025-08-28T01:49:57Z
dc.date.available2025-08-28T01:49:57Z
dc.description.abstract<p><strong>Background</strong><br></p><p>Common pregnancy and perinatal complications are associated with offspring cardiometabolic risk factors. These complications may influence multiple metabolic traits in the offspring and these associations might differ with offspring age.<br></p><p><strong>Methods</strong><br></p><p>We used data from eight population-based cohort studies to examine and compare associations of pre-eclampsia (PE), gestational hypertension (GH), gestational diabetes (GD), preterm birth (PTB), small (SGA) and large (LGA) for gestational age (vs. appropriate size for gestational age (AGA)) with up to 167 plasma/serum-based nuclear magnetic resonance-derived metabolic traits encompassing lipids, lipoproteins, fatty acids, amino acids, ketones, glycerides/phospholipids, glycolysis, fluid balance, and inflammation. Confounder-adjusted regression models were used to examine associations (adjusted for maternal education, parity age at pregnancy, ethnicity, pre/early pregnancy body mass index and smoking, and offspring sex and age at metabolic trait assessment), and results were combined using meta-analysis by five age categories representing different periods of the offspring life course: neonates (cord blood), infancy (mean ages: 1.1-1.6 years), childhood (4.2-7.5 years); adolescence (12.0-16.0 years), and adulthood (22.0-67.8 years).<br></p><p><strong>Results</strong><br></p><p>Offspring numbers for each age category/analysis varied from 8925 adults (441 PTB) to 1181 infants (135 GD); 48.4% to 60.0% were females. Pregnancy complications (PE, GH, GD) were each associated with up to three metabolic traits in neonates (<em>P</em>≤0.001) with some evidence of persistence to older ages. PTB and SGA were associated with 32 and 12 metabolic traits in neonates respectively, which included an adjusted standardised mean difference of -0.89 standard deviation (SD) units for <em>albumin</em> with PTB (95% CI: -1.10 to -0.69, <em>P</em>=1.3x10<sup>-17</sup>) and -0.41 SD for <em>total lipids in medium</em> HDL with SGA (95% CI: -0.56 to -0.25, <em>P</em>=2.6x10<sup>-7</sup>), with some evidence of persistence to older ages. LGA was inversely associated with 19 metabolic traits including lower levels of cholesterol, lipoproteins, fatty acids, and amino acids, with associations emerging in adolescence, (e.g. -0.11 SD <em>total fatty acids</em>, 95% CI: -0.18 to -0.05, <em>P</em>=0.0009), and attenuating with older age across adulthood.<br></p><p><strong>Conclusions</strong><br></p><p>These reassuring findings suggest little evidence of wide-spread and long-term impact of common pregnancy and perinatal complications on offspring metabolic traits, with most associations only observed for newborns rather than older ages, and for perinatal rather than pregnancy complications.<br></p>
dc.identifier.eissn1741-7015
dc.identifier.jour-issn1741-7015
dc.identifier.olddbid208122
dc.identifier.oldhandle10024/191149
dc.identifier.urihttps://www.utupub.fi/handle/11111/57524
dc.identifier.urlhttps://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-022-02711-8
dc.identifier.urnURN:NBN:fi-fe2023022528656
dc.language.isoen
dc.okm.affiliatedauthorRaitakari, Olli
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3123 Gynaecology and paediatricsen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.discipline3123 Naisten- ja lastentauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherBMC
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumber23
dc.relation.doi10.1186/s12916-022-02711-8
dc.relation.ispartofjournalBMC Medicine
dc.relation.volume21
dc.source.identifierhttps://www.utupub.fi/handle/10024/191149
dc.titleEffect of common pregnancy and perinatal complications on offspring metabolic traits across the life course: a multi-cohort study
dc.year.issued2023

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