Gestational age at birth and hospitalisations for infections among individuals aged 0-50 years in Norway: a longitudinal, register-based, cohort study.

Gestational age Hospitalisation risk Infectious disease Preterm Respiratory tract infection

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 15 04 2023
revised: 30 06 2023
accepted: 03 07 2023
medline: 4 8 2023
pubmed: 4 8 2023
entrez: 4 8 2023
Statut: epublish

Résumé

Preterm birth is associated with increased risk of childhood infections. Whether this risk persists into adulthood is unknown and limited information is available on risk patterns across the full range of gestational ages. In this longitudinal, register-based, cohort study, we linked individual-level data on all individuals born in Norway (January 01, 1967-December 31, 2016) to nationwide hospital data (January 01, 2008-December 31, 2017). Gestational age was categorised as 23-27, 28-31, 32-33, 34-36, 37-38, 39-41, and 42-44 completed weeks. The analyses were stratified by age at follow-up: 0-11 months and 1-5, 6-14, 15-29, and 30-50 years. The primary outcome was hospitalisation due to any infectious disease, with major infectious disease groups as secondary outcomes. Adjusted hospitalisation rate ratios (RRs) for any infection and infectious disease groups were estimated using negative binomial regression. Models were adjusted for year of birth, maternal age at birth, parity, and sex, and included an offset parameter adjusted for person-time at risk. Among 2,695,830 individuals with 313,940 hospitalisations for infections, we found a pattern of higher hospitalisation risk in lower gestational age groups, which was the strongest in childhood but still evident in adulthood. Comparing those born very preterm (28-31) and late preterm (34-36) to full-term (39-41 weeks), RRs (95% confidence interval) for hospitalisation for any infectious disease at ages 1-5 were 3.3 (3.0-3.7) and 1.7 (1.6-1.8), respectively. At 30-50 years, the corresponding estimates were 1.4 (1.2-1.7) and 1.2 (1.1-1.3). The patterns were similar for the infectious disease groups, including bacterial and viral infections, respiratory tract infections (RTIs), and infections not attributable to RTIs. Increasing risk of hospitalisations for infections in lower gestational age groups was most prominent in children but still evident in adolescents and adults. Possible mechanisms and groups that could benefit from vaccinations and other prevention strategies should be investigated. St. Olav's University Hospital and Norwegian University of Science and Technology, Norwegian Research Council, Liaison Committee for education, research and innovation in Central Norway, European Commission, Academy of Finland, Sigrid Jusélius Foundation, Foundation for Pediatric Research, and Signe and Ane Gyllenberg Foundation.

Sections du résumé

Background UNASSIGNED
Preterm birth is associated with increased risk of childhood infections. Whether this risk persists into adulthood is unknown and limited information is available on risk patterns across the full range of gestational ages.
Methods UNASSIGNED
In this longitudinal, register-based, cohort study, we linked individual-level data on all individuals born in Norway (January 01, 1967-December 31, 2016) to nationwide hospital data (January 01, 2008-December 31, 2017). Gestational age was categorised as 23-27, 28-31, 32-33, 34-36, 37-38, 39-41, and 42-44 completed weeks. The analyses were stratified by age at follow-up: 0-11 months and 1-5, 6-14, 15-29, and 30-50 years. The primary outcome was hospitalisation due to any infectious disease, with major infectious disease groups as secondary outcomes. Adjusted hospitalisation rate ratios (RRs) for any infection and infectious disease groups were estimated using negative binomial regression. Models were adjusted for year of birth, maternal age at birth, parity, and sex, and included an offset parameter adjusted for person-time at risk.
Findings UNASSIGNED
Among 2,695,830 individuals with 313,940 hospitalisations for infections, we found a pattern of higher hospitalisation risk in lower gestational age groups, which was the strongest in childhood but still evident in adulthood. Comparing those born very preterm (28-31) and late preterm (34-36) to full-term (39-41 weeks), RRs (95% confidence interval) for hospitalisation for any infectious disease at ages 1-5 were 3.3 (3.0-3.7) and 1.7 (1.6-1.8), respectively. At 30-50 years, the corresponding estimates were 1.4 (1.2-1.7) and 1.2 (1.1-1.3). The patterns were similar for the infectious disease groups, including bacterial and viral infections, respiratory tract infections (RTIs), and infections not attributable to RTIs.
Interpretation UNASSIGNED
Increasing risk of hospitalisations for infections in lower gestational age groups was most prominent in children but still evident in adolescents and adults. Possible mechanisms and groups that could benefit from vaccinations and other prevention strategies should be investigated.
Funding UNASSIGNED
St. Olav's University Hospital and Norwegian University of Science and Technology, Norwegian Research Council, Liaison Committee for education, research and innovation in Central Norway, European Commission, Academy of Finland, Sigrid Jusélius Foundation, Foundation for Pediatric Research, and Signe and Ane Gyllenberg Foundation.

Identifiants

pubmed: 37538542
doi: 10.1016/j.eclinm.2023.102108
pii: S2589-5370(23)00285-7
pmc: PMC10393616
doi:

Types de publication

Journal Article

Langues

eng

Pagination

102108

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

All authors declare no competing interests.

Références

Lancet. 2012 Jun 9;379(9832):2151-61
pubmed: 22579125
Eur Respir J. 2022 May 19;59(5):
pubmed: 34625479
J Pediatr. 2018 Oct;201:106-114.e4
pubmed: 30054165
Lancet. 2017 Apr 22;389(10079):1649-1659
pubmed: 28443559
Lancet Infect Dis. 2016 Aug;16(8):952-61
pubmed: 27052469
Pediatr Pulmonol. 2018 Feb;53(2):209-217
pubmed: 29193814
N Engl J Med. 2007 May 17;356(20):2053-63
pubmed: 17507704
JAMA. 2012 Jan 4;307(1):32; author reply 32-3
pubmed: 22215157
PLoS One. 2020 Sep 3;15(9):e0238382
pubmed: 32881953
Circulation. 2020 Nov 3;142(18):1791-1793
pubmed: 32966752
JAMA. 2015 Sep 8;314(10):1039-51
pubmed: 26348753
Scand J Public Health. 2020 Feb;48(1):49-55
pubmed: 31288711
J Leukoc Biol. 2017 Sep;102(3):645-656
pubmed: 28630102
J Allergy Clin Immunol. 2011 Apr;127(4):935-42
pubmed: 21333345
Semin Fetal Neonatal Med. 2019 Feb;24(1):66-83
pubmed: 30420114
Clin Infect Dis. 2005 Aug 1;41(3):345-51
pubmed: 16007532
Lancet Glob Health. 2019 Jun;7(6):e710-e720
pubmed: 31097275
Elife. 2021 May 25;10:
pubmed: 34032570
Clin Infect Dis. 2010 Jan 15;50(2):202-9
pubmed: 20014950
Lancet Glob Health. 2019 Jan;7(1):e37-e46
pubmed: 30389451
JAMA Pediatr. 2019 Aug 01;173(8):736-743
pubmed: 31157896
Eur Respir J. 2023 Jun 22;61(6):
pubmed: 36990472
Pediatr Res. 2015 Nov;78(5):492-7
pubmed: 26186294
N Engl J Med. 2020 Jul 30;383(5):415-425
pubmed: 32726528
JAMA Netw Open. 2021 Jan 4;4(1):e2032779
pubmed: 33416885
Nat Rev Genet. 2021 Mar;22(3):137-153
pubmed: 33277640
Am J Obstet Gynecol. 2002 Mar;186(3):433-7
pubmed: 11904603
Pediatrics. 2017 Mar;139(3):
pubmed: 28228499
Tidsskr Nor Laegeforen. 2015 May 05;135(8):768-70
pubmed: 25947599
Lancet Respir Med. 2019 Aug;7(8):677-686
pubmed: 31078498
Health Econ. 2017 Mar;26(3):352-370
pubmed: 26842217
Allergy. 2023 Apr;78(4):928-939
pubmed: 36719074
Thorax. 2022 Aug;77(8):790-798
pubmed: 35410959
Immunol Res. 2023 Apr;71(2):185-196
pubmed: 36417145
BMJ. 2020 Nov 25;371:m4075
pubmed: 33239272
Acta Paediatr. 1996 Jul;85(7):843-8
pubmed: 8819552
Clin Epidemiol. 2021 Jul 19;13:533-554
pubmed: 34321928
Acta Obstet Gynecol Scand. 2016 May;95(5):519-27
pubmed: 26867143
Early Hum Dev. 2020 Nov;150:105187
pubmed: 32948365
N Engl J Med. 2008 Jul 17;359(3):262-73
pubmed: 18635431

Auteurs

Sara Marie Nilsen (SM)

Center for Health Care Improvement, St. Olav's University Hospital, Norway.
Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

Jonas Valand (J)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

Tormod Rogne (T)

Department of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, USA.
Center for Perinatal, Pediatric and Environmental Epidemiology, Yale School of Public Health, New Haven, CT, USA.
Department of Circulation and Medical Imaging, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.

Andreas Asheim (A)

Center for Health Care Improvement, St. Olav's University Hospital, Norway.
Department of Mathematical Sciences, Norwegian University of Science and Technology, Trondheim, Norway.

Weiyao Yin (W)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

Johanna Metsälä (J)

Department of Public Health and Welfare, Population Health Unit, Finnish Institute for Health and Welfare, Helsinki, Finland.

Signe Opdahl (S)

Department of Public Health and Nursing, Norwegian University of Science and Technology, Trondheim, Norway.

Henrik Døllner (H)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Children's Clinic, St. Olav's University Hospital, Trondheim, Norway.

Jan K Damås (JK)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Clinic of Medicine, Department of Infectious Diseases, St Olav's University Hospital, Trondheim, Norway.

Eero Kajantie (E)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Department of Public Health and Welfare, Population Health Unit, Finnish Institute for Health and Welfare, Helsinki, Finland.
Clinical Medicine Research Unit, Oulu University Hospital and University of Oulu, Oulu, Finland.

Erik Solligård (E)

Department of Circulation and Medical Imaging, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Department of Research and Development, Møre and Romsdal Hospital Trust, Ålesund, Norway.

Sven Sandin (S)

Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, USA.
Seaver Center for Autism Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Kari Risnes (K)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Children's Clinic, St. Olav's University Hospital, Trondheim, Norway.

Classifications MeSH