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Mapping domains of early life determinants of future multimorbidity across three UK longitudinal cohort studies

Mapping domains of early life determinants of future multimorbidity across three UK longitudinal cohort studies
Mapping domains of early life determinants of future multimorbidity across three UK longitudinal cohort studies
Many studies use a reductionist approach to isolate the influence of one factor in childhood on multimorbidity rather than consider the combined effect of wider determinants. We explored how potential multiple early life determinants of multimorbidity can be characterised across three UK cohort studies. We used the National Child Development Study (NCDS), the 1970 British Cohort Study (BCS70), and the Aberdeen Children of the 1950s Study (ACONF) to identified early life variables that fit into 12 conceptualised domains of early life determinants of multimorbidity. Variables were assigned into 12 domains; principal component analysis reduced the dimensionality of the data and structured variables into subgroups. The data audit identified 7 domains in ACONF, 10 domains in NCDS and 12 domains in BCS70. Dominant components included maternal fertility histories within the prenatal, antenatal and birth domain, long-term illnesses within the child health domain, educational ability within the child education and health literacy domain, ethnicity within the demography domain, parental health behaviours within the transgenerational domain, housing within the socioeconomic domain and parental-child interactions within the parental-family domain. We demonstrated that if multiple large scale longitudinal studies are used, there is enough data available for researchers to consider conceptualising early life risk factors of multimorbidity across groups or domains. Such conceptualisation can help challenge the existing understanding of disease aetiology and develop new ideas for prevention of multimorbidity.
2045-2322
Stannard, S.
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Berrington, A.
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Fraser, S.D.S.
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Paranjothy, S.
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Hoyle, R.B.
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Owen, R.K.
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Akbari, A.
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Shiranirad, M.
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Chiovoloni, R.
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Alwan, N.A.
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Stannard, S.
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Berrington, A.
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Fraser, S.D.S.
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Paranjothy, S.
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Hoyle, R.B.
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Owen, R.K.
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Akbari, A.
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Shiranirad, M.
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Chiovoloni, R.
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Alwan, N.A.
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Stannard, S., Berrington, A., Fraser, S.D.S., Paranjothy, S., Hoyle, R.B., Owen, R.K., Akbari, A., Shiranirad, M., Chiovoloni, R. and Alwan, N.A. (2024) Mapping domains of early life determinants of future multimorbidity across three UK longitudinal cohort studies. Scientific Reports, 14 (1), [21454]. (doi:10.1038/s41598-024-72275-5).

Record type: Article

Abstract

Many studies use a reductionist approach to isolate the influence of one factor in childhood on multimorbidity rather than consider the combined effect of wider determinants. We explored how potential multiple early life determinants of multimorbidity can be characterised across three UK cohort studies. We used the National Child Development Study (NCDS), the 1970 British Cohort Study (BCS70), and the Aberdeen Children of the 1950s Study (ACONF) to identified early life variables that fit into 12 conceptualised domains of early life determinants of multimorbidity. Variables were assigned into 12 domains; principal component analysis reduced the dimensionality of the data and structured variables into subgroups. The data audit identified 7 domains in ACONF, 10 domains in NCDS and 12 domains in BCS70. Dominant components included maternal fertility histories within the prenatal, antenatal and birth domain, long-term illnesses within the child health domain, educational ability within the child education and health literacy domain, ethnicity within the demography domain, parental health behaviours within the transgenerational domain, housing within the socioeconomic domain and parental-child interactions within the parental-family domain. We demonstrated that if multiple large scale longitudinal studies are used, there is enough data available for researchers to consider conceptualising early life risk factors of multimorbidity across groups or domains. Such conceptualisation can help challenge the existing understanding of disease aetiology and develop new ideas for prevention of multimorbidity.

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Accepted/In Press date: 4 September 2024
Published date: 13 September 2024
Additional Information: © 2024. The Author(s).

Identifiers

Local EPrints ID: 494468
URI: http://eprints.soton.ac.uk/id/eprint/494468
ISSN: 2045-2322
PURE UUID: c0852169-26a0-4fab-9bba-12c6cc5cd6db
ORCID for S. Stannard: ORCID iD orcid.org/0000-0002-6139-1020
ORCID for A. Berrington: ORCID iD orcid.org/0000-0002-1683-6668
ORCID for S.D.S. Fraser: ORCID iD orcid.org/0000-0002-4172-4406
ORCID for R.B. Hoyle: ORCID iD orcid.org/0000-0002-1645-1071
ORCID for M. Shiranirad: ORCID iD orcid.org/0000-0003-4346-3059
ORCID for N.A. Alwan: ORCID iD orcid.org/0000-0002-4134-8463

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Date deposited: 09 Oct 2024 16:34
Last modified: 15 Nov 2024 03:07

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Contributors

Author: S. Stannard ORCID iD
Author: A. Berrington ORCID iD
Author: S.D.S. Fraser ORCID iD
Author: S. Paranjothy
Author: R.B. Hoyle ORCID iD
Author: R.K. Owen
Author: A. Akbari
Author: M. Shiranirad ORCID iD
Author: R. Chiovoloni
Author: N.A. Alwan ORCID iD

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