Associations between late pregnancy Dietary Inflammatory Index (DII) and offspring bone mass: a meta-analysis of the Southampton Women's Survey (SWS) and the Avon Longitudinal Study of Parents and Children (ALSPAC)
Associations between late pregnancy Dietary Inflammatory Index (DII) and offspring bone mass: a meta-analysis of the Southampton Women's Survey (SWS) and the Avon Longitudinal Study of Parents and Children (ALSPAC)
Systemic inflammation is associated with reduced bone mineral density and may be influenced by pro-inflammatory diets. We undertook an observational analysis of associations between late pregnancy energy-adjusted dietary inflammatory index (E-DII) scores and offspring bone outcomes in childhood. E-DII scores (higher scores indicating pro-inflammatory diets) were derived from food frequency questionnaires in late pregnancy in two prospective mother-offspring cohorts: the Southampton Women's Survey (SWS) and the Avon Longitudinal Study of Parents and Children (ALSPAC). The mean (SD) offspring age at dual-energy X-ray absorptiometry (DXA) scanning was 9.2 (0.2) years. Linear regression was used to assess associations between E-DII and bone outcomes, adjusting for offspring sex and age at DXA and maternal age at childbirth, educational level, pre-pregnancy body mass index (BMI), parity, physical activity level, and smoking in pregnancy. Associations were synthesized using fixed-effect meta-analysis. Beta coefficients represent the association per unit E-DII increment. In fully adjusted models (total n = 5910) late pregnancy E-DII was negatively associated with offspring whole body minus head bone area (BA: β = −3.68 [95% confidence interval −6.09, −1.27] cm
2/unit), bone mineral content (BMC: β = −4.16 [95% CI −6.70, −1.62] g/unit), and areal bone mineral density (aBMD: β = −0.0012 [95% CI −0.0020, −0.0004] g.cm
−2/unit), but there was only a weak association with BMC adjusted for BA (β = −0.48 [95% CI −1.11, 0.15] g/unit) at 9 years. Adjustment for child height partly or, for weight, fully attenuated the associations. Higher late pregnancy E-DII scores (representing a more pro-inflammatory diet) are negatively associated with offspring bone measures, supporting the importance of maternal and childhood diet on longitudinal offspring bone health.
ALSPAC, BONE, CHILDHOOD, DIET, DXA, E-DII, EPIDEMIOLOGY, INFLAMMATION, OSTEOPOROSIS, SWS
1511-1519
Woolford, Stephen
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D'angelo, Stefania
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Mancano, Giulia
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Curtis, Elizabeth
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Ashai, Shanze
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Shivappa, Nitin
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Hebert, James
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Crozier, Sarah
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Phillips, Catherine
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Suderman, Matthew
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Relton, Caroline L.
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Cooper, Cyrus
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Harvey, Nicholas
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August 2022
Woolford, Stephen
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D'angelo, Stefania
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Mancano, Giulia
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Curtis, Elizabeth
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Ashai, Shanze
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Shivappa, Nitin
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Hebert, James
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Crozier, Sarah
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Phillips, Catherine
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Suderman, Matthew
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Relton, Caroline L.
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Cooper, Cyrus
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Harvey, Nicholas
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Woolford, Stephen, D'angelo, Stefania, Mancano, Giulia, Curtis, Elizabeth, Ashai, Shanze, Shivappa, Nitin, Hebert, James, Crozier, Sarah, Phillips, Catherine, Suderman, Matthew, Relton, Caroline L., Cooper, Cyrus and Harvey, Nicholas
(2022)
Associations between late pregnancy Dietary Inflammatory Index (DII) and offspring bone mass: a meta-analysis of the Southampton Women's Survey (SWS) and the Avon Longitudinal Study of Parents and Children (ALSPAC).
Journal of Bone and Mineral Research, 37 (8), .
(doi:10.1002/jbmr.4623).
Abstract
Systemic inflammation is associated with reduced bone mineral density and may be influenced by pro-inflammatory diets. We undertook an observational analysis of associations between late pregnancy energy-adjusted dietary inflammatory index (E-DII) scores and offspring bone outcomes in childhood. E-DII scores (higher scores indicating pro-inflammatory diets) were derived from food frequency questionnaires in late pregnancy in two prospective mother-offspring cohorts: the Southampton Women's Survey (SWS) and the Avon Longitudinal Study of Parents and Children (ALSPAC). The mean (SD) offspring age at dual-energy X-ray absorptiometry (DXA) scanning was 9.2 (0.2) years. Linear regression was used to assess associations between E-DII and bone outcomes, adjusting for offspring sex and age at DXA and maternal age at childbirth, educational level, pre-pregnancy body mass index (BMI), parity, physical activity level, and smoking in pregnancy. Associations were synthesized using fixed-effect meta-analysis. Beta coefficients represent the association per unit E-DII increment. In fully adjusted models (total n = 5910) late pregnancy E-DII was negatively associated with offspring whole body minus head bone area (BA: β = −3.68 [95% confidence interval −6.09, −1.27] cm
2/unit), bone mineral content (BMC: β = −4.16 [95% CI −6.70, −1.62] g/unit), and areal bone mineral density (aBMD: β = −0.0012 [95% CI −0.0020, −0.0004] g.cm
−2/unit), but there was only a weak association with BMC adjusted for BA (β = −0.48 [95% CI −1.11, 0.15] g/unit) at 9 years. Adjustment for child height partly or, for weight, fully attenuated the associations. Higher late pregnancy E-DII scores (representing a more pro-inflammatory diet) are negatively associated with offspring bone measures, supporting the importance of maternal and childhood diet on longitudinal offspring bone health.
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sw DII DXA JBMR R1 2022_04_20 R2 clean v3
- Accepted Manuscript
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J of Bone Mineral Res - 2022 - Woolford - Associations Between Late Pregnancy Dietary Inflammatory Index DII and
- Version of Record
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sw DII DXA JBMR supplement online R1 2022_03_13
More information
Accepted/In Press date: 1 June 2022
e-pub ahead of print date: 10 June 2022
Published date: August 2022
Additional Information:
Funding Information:
The UK Medical Research Council and the Wellcome Trust (grant no. 217065/Z/19/Z) and the University of Bristol provide core support for ALSPAC. Welcome Trust grants 079960 and 084632 funded the pQCT scans. The SWS work was supported by grants from Medical Research Council (MRC), Bupa Foundation, British Heart Foundation, National Institute for Health Research (NIHR) Southampton Biomedical Research Centre, University of Southampton, and University Hospital Southampton NHS Foundation Trust, NIHR Oxford Biomedical Research Centre, University of Oxford, and the UK Royal Osteoporosis Society Osteoporosis and Bone Research Academy. NCH is supported by the UK Medical Research Council (MC_PC_21003; MC_PC_21001). EMC has been supported by the Welcome Trust (201268/Z/16/Z). The work leading to these results was supported by the European Union's Seventh Framework Programme (FP7/2007–2013), projects EarlyNutrition, ODIN, and LifeCycle under grant agreements numbers 289346, 613977, and 733206, and by the BBSRC (HDHL‐Biomarkers, BB/P028179/1 and BB/P028187/1), as part of the ALPHABET project, supported by an award made through the ERA‐Net on Biomarkers for Nutrition and Health (ERA HDHL), Horizon 2020 grant agreement number 696295. CMP was supported by an award from Science Foundation Ireland, Ireland (grant no. SFI/16/ERA‐HDHL/3360).
Publisher Copyright:
© 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
Keywords:
ALSPAC, BONE, CHILDHOOD, DIET, DXA, E-DII, EPIDEMIOLOGY, INFLAMMATION, OSTEOPOROSIS, SWS
Identifiers
Local EPrints ID: 467377
URI: http://eprints.soton.ac.uk/id/eprint/467377
ISSN: 0884-0431
PURE UUID: 0c287db5-51e7-47d3-9b57-b06a60d70148
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Date deposited: 07 Jul 2022 17:10
Last modified: 18 Mar 2024 03:38
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Contributors
Author:
Stephen Woolford
Author:
Stefania D'angelo
Author:
Giulia Mancano
Author:
Shanze Ashai
Author:
Nitin Shivappa
Author:
James Hebert
Author:
Catherine Phillips
Author:
Matthew Suderman
Author:
Caroline L. Relton
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