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Clusters and associations of adverse neonatal events with adult risk of multimorbidity: a secondary analysis of birth cohort data

Clusters and associations of adverse neonatal events with adult risk of multimorbidity: a secondary analysis of birth cohort data
Clusters and associations of adverse neonatal events with adult risk of multimorbidity: a secondary analysis of birth cohort data
Objective: to investigate associations between clustered adverse neonatal events and later-life multimorbidity.

Design: secondary analysis of birth cohort data.

Setting: prospective birth cohort study of individuals born in Britain in one week of 1970.

Population: respondents provided data at birth (n = 17,196), age 34 (n = 11,261), age 38 (n = 9,665), age 42 (n = 9,840), and age 46 (n = 8,580).

Methods: mixed components analysis determined included factors, ‘Birthweight’; ‘Neonatal cyanosis’; ‘Neonatal cerebral signs’; ‘Neonatal illnesses’; ‘Neonatal breathing difficulties’; and ‘Prolonged duration to establishment of respiratory rate at birth’, within the composite adverse neonatal event score. Log-binomial regression quantified the unadjusted and covariate-adjusted (paternal employment status and social class; maternal smoking status; maternal age; parity; cohort member smoking status and Body Mass Index) associations between the adverse neonatal event score and risk of multimorbidity in adulthood.

Outcome measures: multimorbidity at each adult data sweep, defined as the presence of two or more Long-Term Conditions (LTCs).

Result: 13.7% of respondents experienced one or more adverse neonatal event(s) at birth. The percentage reporting multimorbidity increased steadily from 14.6% at age 34 to 25.5% at age 46. A significant association was only observed at the 38 years sweep; those who had experienced two or more adverse neonatal events had a 41.0% (95% CI: 1.05 – 1.88) increased risk of multimorbidity, compared to those who had not suffered any adverse neonatal events at birth. This association was maintained following adjustment for parental confounders and adult smoking status.

Conclusions: adverse neonatal events at birth may be independently associated with the development of midlife multimorbidity. Programmes and policies aimed at tackling the growing public health burden of multimorbidity may also need to consider interventions to reduce adverse neonatal events at birth.
1932-6203
John, Jeeva
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Stannard, Seb
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Fraser, Simon D.S.
135884b6-8737-4e8a-a98c-5d803ac7a2dc
Berrington, Ann
bd0fc093-310d-4236-8126-ca0c7eb9ddde
Alwan, Nisreen A.
0d37b320-f325-4ed3-ba51-0fe2866d5382
John, Jeeva
43cfeb69-bbd6-4d6f-90e4-0587891e5fd1
Stannard, Seb
0fbf5a1c-abab-4135-a8f9-c3c9f570aaea
Fraser, Simon D.S.
135884b6-8737-4e8a-a98c-5d803ac7a2dc
Berrington, Ann
bd0fc093-310d-4236-8126-ca0c7eb9ddde
Alwan, Nisreen A.
0d37b320-f325-4ed3-ba51-0fe2866d5382

John, Jeeva, Stannard, Seb, Fraser, Simon D.S., Berrington, Ann and Alwan, Nisreen A. (2025) Clusters and associations of adverse neonatal events with adult risk of multimorbidity: a secondary analysis of birth cohort data. PLoS ONE, 20 (3), [e0319200]. (doi:10.1371/journal.pone.0319200).

Record type: Article

Abstract

Objective: to investigate associations between clustered adverse neonatal events and later-life multimorbidity.

Design: secondary analysis of birth cohort data.

Setting: prospective birth cohort study of individuals born in Britain in one week of 1970.

Population: respondents provided data at birth (n = 17,196), age 34 (n = 11,261), age 38 (n = 9,665), age 42 (n = 9,840), and age 46 (n = 8,580).

Methods: mixed components analysis determined included factors, ‘Birthweight’; ‘Neonatal cyanosis’; ‘Neonatal cerebral signs’; ‘Neonatal illnesses’; ‘Neonatal breathing difficulties’; and ‘Prolonged duration to establishment of respiratory rate at birth’, within the composite adverse neonatal event score. Log-binomial regression quantified the unadjusted and covariate-adjusted (paternal employment status and social class; maternal smoking status; maternal age; parity; cohort member smoking status and Body Mass Index) associations between the adverse neonatal event score and risk of multimorbidity in adulthood.

Outcome measures: multimorbidity at each adult data sweep, defined as the presence of two or more Long-Term Conditions (LTCs).

Result: 13.7% of respondents experienced one or more adverse neonatal event(s) at birth. The percentage reporting multimorbidity increased steadily from 14.6% at age 34 to 25.5% at age 46. A significant association was only observed at the 38 years sweep; those who had experienced two or more adverse neonatal events had a 41.0% (95% CI: 1.05 – 1.88) increased risk of multimorbidity, compared to those who had not suffered any adverse neonatal events at birth. This association was maintained following adjustment for parental confounders and adult smoking status.

Conclusions: adverse neonatal events at birth may be independently associated with the development of midlife multimorbidity. Programmes and policies aimed at tackling the growing public health burden of multimorbidity may also need to consider interventions to reduce adverse neonatal events at birth.

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Accepted/In Press date: 29 January 2025
Published date: 18 March 2025

Identifiers

Local EPrints ID: 498526
URI: http://eprints.soton.ac.uk/id/eprint/498526
ISSN: 1932-6203
PURE UUID: de490713-ce9f-42e9-ab57-bba6ea74e9a1
ORCID for Seb Stannard: ORCID iD orcid.org/0000-0002-6139-1020
ORCID for Simon D.S. Fraser: ORCID iD orcid.org/0000-0002-4172-4406
ORCID for Ann Berrington: ORCID iD orcid.org/0000-0002-1683-6668
ORCID for Nisreen A. Alwan: ORCID iD orcid.org/0000-0002-4134-8463

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Date deposited: 20 Feb 2025 17:55
Last modified: 30 Aug 2025 02:06

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Contributors

Author: Jeeva John
Author: Seb Stannard ORCID iD
Author: Ann Berrington ORCID iD

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