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Alcohol exposure prior to pregnancy—does hazardous consumption affect placenta‐ and inflammatory‐mediated pregnancy outcomes? A Swedish population‐based cohort study

INTRODUCTION: Alcohol consumption during pregnancy is related to severe birth complications such as low birthweight, preterm birth and birth defects. During the last decade, the Alcohol Use Disorders Identification Test (AUDIT) has been used as a screening tool in Swedish maternal healthcare units t...

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Autores principales: Asp, Joline, Bergman, Lina, Lager, Susanne, Axelsson, Ove, Wikström, Anna‐Karin, Hesselman, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812091/
https://www.ncbi.nlm.nih.gov/pubmed/36073360
http://dx.doi.org/10.1111/aogs.14451
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author Asp, Joline
Bergman, Lina
Lager, Susanne
Axelsson, Ove
Wikström, Anna‐Karin
Hesselman, Susanne
author_facet Asp, Joline
Bergman, Lina
Lager, Susanne
Axelsson, Ove
Wikström, Anna‐Karin
Hesselman, Susanne
author_sort Asp, Joline
collection PubMed
description INTRODUCTION: Alcohol consumption during pregnancy is related to severe birth complications such as low birthweight, preterm birth and birth defects. During the last decade, the Alcohol Use Disorders Identification Test (AUDIT) has been used as a screening tool in Swedish maternal healthcare units to identify hazardous, pre‐pregnancy alcohol use. However, evaluation of the screening with AUDIT, as well as adverse maternal or neonatal outcomes, has not been assessed at a national level. MATERIAL AND METHODS: This was a population‐based cohort study of 530 458 births from 2013 to 2018 using demographic, reproductive and maternal health data from the Swedish Pregnancy Register. Self‐reported alcohol consumption in the year before pregnancy, measured as AUDIT scores, was categorized into moderate (6–13 points) and high‐risk (14–40 points) consumption, with low‐risk (0–5 points) consumption as the reference group. Associations with pregnancy‐ and birth outcomes were explored with logistic regressions using generalized estimating equation models, adjusting for maternal and socioeconomic characteristics. Estimates are presented as adjusted odds ratios (aORs) with 95% confidence intervals (CIs). RESULTS: High‐risk and moderate pre‐pregnancy alcohol consumption was associated with preeclampsia, preterm birth and birth of an infant small for gestational age (SGA), but these associations were nonsignificant after adjustments. Prior moderate‐risk (aOR 1.29, 95% CI 1.17–1.42) and high‐risk consumption (aOR 1.62, 95% CI 1.17–2.25) increased the likelihood of intrapartum and neonatal infections. CONCLUSIONS: Apart from identifying hazardous alcohol consumption prior to pregnancy and the offer of counseling, screening with the AUDIT in early pregnancy indicates a high risk of inflammatory‐/placenta‐mediated pregnancy and birth outcomes. For most outcomes, AUDIT was not an independent contributor when adjusting for confounding factors. Hazardous alcohol use prior to pregnancy was independently linked to intrapartum and neonatal infections; conditions associated with morbidity and long‐term sequalae. These associations may be explained by alcohol‐induced changes in the maternal or fetal immune system in early pregnancy or persistent alcohol intake during pregnancy, or may depend on unidentified confounding factors.
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spelling pubmed-98120912023-01-05 Alcohol exposure prior to pregnancy—does hazardous consumption affect placenta‐ and inflammatory‐mediated pregnancy outcomes? A Swedish population‐based cohort study Asp, Joline Bergman, Lina Lager, Susanne Axelsson, Ove Wikström, Anna‐Karin Hesselman, Susanne Acta Obstet Gynecol Scand Pregnancy INTRODUCTION: Alcohol consumption during pregnancy is related to severe birth complications such as low birthweight, preterm birth and birth defects. During the last decade, the Alcohol Use Disorders Identification Test (AUDIT) has been used as a screening tool in Swedish maternal healthcare units to identify hazardous, pre‐pregnancy alcohol use. However, evaluation of the screening with AUDIT, as well as adverse maternal or neonatal outcomes, has not been assessed at a national level. MATERIAL AND METHODS: This was a population‐based cohort study of 530 458 births from 2013 to 2018 using demographic, reproductive and maternal health data from the Swedish Pregnancy Register. Self‐reported alcohol consumption in the year before pregnancy, measured as AUDIT scores, was categorized into moderate (6–13 points) and high‐risk (14–40 points) consumption, with low‐risk (0–5 points) consumption as the reference group. Associations with pregnancy‐ and birth outcomes were explored with logistic regressions using generalized estimating equation models, adjusting for maternal and socioeconomic characteristics. Estimates are presented as adjusted odds ratios (aORs) with 95% confidence intervals (CIs). RESULTS: High‐risk and moderate pre‐pregnancy alcohol consumption was associated with preeclampsia, preterm birth and birth of an infant small for gestational age (SGA), but these associations were nonsignificant after adjustments. Prior moderate‐risk (aOR 1.29, 95% CI 1.17–1.42) and high‐risk consumption (aOR 1.62, 95% CI 1.17–2.25) increased the likelihood of intrapartum and neonatal infections. CONCLUSIONS: Apart from identifying hazardous alcohol consumption prior to pregnancy and the offer of counseling, screening with the AUDIT in early pregnancy indicates a high risk of inflammatory‐/placenta‐mediated pregnancy and birth outcomes. For most outcomes, AUDIT was not an independent contributor when adjusting for confounding factors. Hazardous alcohol use prior to pregnancy was independently linked to intrapartum and neonatal infections; conditions associated with morbidity and long‐term sequalae. These associations may be explained by alcohol‐induced changes in the maternal or fetal immune system in early pregnancy or persistent alcohol intake during pregnancy, or may depend on unidentified confounding factors. John Wiley and Sons Inc. 2022-09-08 /pmc/articles/PMC9812091/ /pubmed/36073360 http://dx.doi.org/10.1111/aogs.14451 Text en © 2022 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Pregnancy
Asp, Joline
Bergman, Lina
Lager, Susanne
Axelsson, Ove
Wikström, Anna‐Karin
Hesselman, Susanne
Alcohol exposure prior to pregnancy—does hazardous consumption affect placenta‐ and inflammatory‐mediated pregnancy outcomes? A Swedish population‐based cohort study
title Alcohol exposure prior to pregnancy—does hazardous consumption affect placenta‐ and inflammatory‐mediated pregnancy outcomes? A Swedish population‐based cohort study
title_full Alcohol exposure prior to pregnancy—does hazardous consumption affect placenta‐ and inflammatory‐mediated pregnancy outcomes? A Swedish population‐based cohort study
title_fullStr Alcohol exposure prior to pregnancy—does hazardous consumption affect placenta‐ and inflammatory‐mediated pregnancy outcomes? A Swedish population‐based cohort study
title_full_unstemmed Alcohol exposure prior to pregnancy—does hazardous consumption affect placenta‐ and inflammatory‐mediated pregnancy outcomes? A Swedish population‐based cohort study
title_short Alcohol exposure prior to pregnancy—does hazardous consumption affect placenta‐ and inflammatory‐mediated pregnancy outcomes? A Swedish population‐based cohort study
title_sort alcohol exposure prior to pregnancy—does hazardous consumption affect placenta‐ and inflammatory‐mediated pregnancy outcomes? a swedish population‐based cohort study
topic Pregnancy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812091/
https://www.ncbi.nlm.nih.gov/pubmed/36073360
http://dx.doi.org/10.1111/aogs.14451
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