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Gestational age and risk of intellectual disability: a population-based cohort study
OBJECTIVE: To examine the association between gestational age at birth and risk of clinically diagnosed intellectual disability (ID) week by week to provide a detailed description of ID risk across the entire range of gestational ages and by severity of ID. METHODS: All individuals born alive in Swe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411878/ https://www.ncbi.nlm.nih.gov/pubmed/35470219 http://dx.doi.org/10.1136/archdischild-2021-323308 |
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author | Yin, Weiyao Döring, Nora Persson, Monica S M Persson, Martina Tedroff, Kristina Ådén, Ulrika Sandin, Sven |
author_facet | Yin, Weiyao Döring, Nora Persson, Monica S M Persson, Martina Tedroff, Kristina Ådén, Ulrika Sandin, Sven |
author_sort | Yin, Weiyao |
collection | PubMed |
description | OBJECTIVE: To examine the association between gestational age at birth and risk of clinically diagnosed intellectual disability (ID) week by week to provide a detailed description of ID risk across the entire range of gestational ages and by severity of ID. METHODS: All individuals born alive in Sweden 1974–2017 were prospectively followed up from birth until 2017 using national registers. The HRs for ID according to weekly gestational age and gestational age categories were determined using Cox models. Sibling analyses were conducted to adjust for familial confounding. RESULTS: The study included 3 572 845 live births. During the follow-up, 26 596 ID cases were registered. The adjusted weekly estimates showed a gradual increase in risk of ID from week 40 to week 24 (adjusted HR(37weeks)=1.80 (1.74 to 1.87), aHR(32weeks)=3.93 (3.73 to 4.13), aHR(28weeks)=7.53 (6.95 to 8.16), aHR(24weeks)=21.58 (18.62 to 25.00)) and from week 41 onwards (aHR(42weeks)=1.26 (1.19 to 1.32)), with statistically significantly higher risks across the range of gestational age compared with infants born at week 40. The associations were consistent in mild, moderate and severe/profound ID but most prominent for severe/profound ID. CONCLUSION: The risk of ID increased weekly as the date of delivery moved away from 40 weeks, both preterm and post-term. The results remained robust after detailed adjustment for confounding, including familial confounding. |
format | Online Article Text |
id | pubmed-9411878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-94118782022-09-12 Gestational age and risk of intellectual disability: a population-based cohort study Yin, Weiyao Döring, Nora Persson, Monica S M Persson, Martina Tedroff, Kristina Ådén, Ulrika Sandin, Sven Arch Dis Child Original Research OBJECTIVE: To examine the association between gestational age at birth and risk of clinically diagnosed intellectual disability (ID) week by week to provide a detailed description of ID risk across the entire range of gestational ages and by severity of ID. METHODS: All individuals born alive in Sweden 1974–2017 were prospectively followed up from birth until 2017 using national registers. The HRs for ID according to weekly gestational age and gestational age categories were determined using Cox models. Sibling analyses were conducted to adjust for familial confounding. RESULTS: The study included 3 572 845 live births. During the follow-up, 26 596 ID cases were registered. The adjusted weekly estimates showed a gradual increase in risk of ID from week 40 to week 24 (adjusted HR(37weeks)=1.80 (1.74 to 1.87), aHR(32weeks)=3.93 (3.73 to 4.13), aHR(28weeks)=7.53 (6.95 to 8.16), aHR(24weeks)=21.58 (18.62 to 25.00)) and from week 41 onwards (aHR(42weeks)=1.26 (1.19 to 1.32)), with statistically significantly higher risks across the range of gestational age compared with infants born at week 40. The associations were consistent in mild, moderate and severe/profound ID but most prominent for severe/profound ID. CONCLUSION: The risk of ID increased weekly as the date of delivery moved away from 40 weeks, both preterm and post-term. The results remained robust after detailed adjustment for confounding, including familial confounding. BMJ Publishing Group 2022-09 2022-04-25 /pmc/articles/PMC9411878/ /pubmed/35470219 http://dx.doi.org/10.1136/archdischild-2021-323308 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Yin, Weiyao Döring, Nora Persson, Monica S M Persson, Martina Tedroff, Kristina Ådén, Ulrika Sandin, Sven Gestational age and risk of intellectual disability: a population-based cohort study |
title | Gestational age and risk of intellectual disability: a population-based cohort study |
title_full | Gestational age and risk of intellectual disability: a population-based cohort study |
title_fullStr | Gestational age and risk of intellectual disability: a population-based cohort study |
title_full_unstemmed | Gestational age and risk of intellectual disability: a population-based cohort study |
title_short | Gestational age and risk of intellectual disability: a population-based cohort study |
title_sort | gestational age and risk of intellectual disability: a population-based cohort study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411878/ https://www.ncbi.nlm.nih.gov/pubmed/35470219 http://dx.doi.org/10.1136/archdischild-2021-323308 |
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