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Differential relationships between parent-child DXA and pQCT bone measures: Results from the Southampton women’s survey.

Differential relationships between parent-child DXA and pQCT bone measures: Results from the Southampton women’s survey.
Differential relationships between parent-child DXA and pQCT bone measures: Results from the Southampton women’s survey.

AIM: To investigate the associations between indices of bone health in childhood and corresponding parental measures.

METHODS: The Southampton Women's Survey characterised 12,583 non-pregnant women aged 20-34 years; 3158 subsequently had singleton live births. In a subset, dual-energy X-ray absorptiometry (DXA) measurements of bone area (BA), bone mineral content (BMC) and areal bone mineral density (aBMD) lumbar spine and total hip were obtained in the parent/offspring (aged 8-9 years) trios. Another subset of children (aged 6-7 years), and their parents, had peripheral quantitative computed tomography (pQCT; 4% and 38% tibia) measures. Using multivariable linear regression we examined relationships between mother/father and offspring, adjusting for parental age, habitual walking speed and education; offspring age and sex; and the corresponding bone measure in the other parent (β-coefficients (95%CI) unit/unit for each bone measure).

RESULTS: Data were available for 260 trios with DXA and 99 with pQCT. There were positive associations for BA, BMC and aBMD between either parent and offspring. Mother-child associations were of greater magnitude than father-child; for example, mother-child aBMD (β = 0.26 g·cm -2/g·cm -2 (0.21,0.32)) and father-child aBMD (β = 0.16 g·cm -2/g·cm -2 (0.11,0.21)), P-difference in β = 0.007. In the subset with pQCT there was a positive association for mother-offspring 4% tibial total area (β = 0.33 mm 2/mm 2 (0.17,0.48)), but little evidence of a father-offspring association (β = -0.06 mm 2/mm 2 (-0.17,0.06)). In contrast offspring 38% cortical density was more strongly associated with this measure in fathers (β = 0.48 mg·cm -3/mg·cm -3 (0.15,0.82)) than mothers (β = 0.27 mg·cm -3/mg·cm -3 (-0.03,0.56)). In general mother-father differences were attenuated by adjustment for height.

CONCLUSIONS: Whilst offspring bone measures are independently associated with those of either parent, the magnitude of the association is often greater for maternal than paternal relationships. These findings are consistent with an in utero influence on offspring growth but might also reflect genetic and/or epigenetic parent of origin effects.

SUMMARY: In an established parent-offspring cohort, associations between parent and offspring bone indices were generally greater in magnitude for mother-offspring than father-offspring relationships.

BMD, Developmental origins, Epidemiology, Mother-offspring, Osteoporosis
8756-3282
Holroyd, Christopher R.
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Carter, Sarah A
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Crozier, Sarah
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D'angelo, Stefania
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Curtis, Elizabeth
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Moon, Rebecca
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Davies, Justin
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Ward, Kate
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Dennison, Elaine
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Inskip, Hazel
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Godfrey, Keith
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Cooper, Cyrus
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Harvey, Nicholas
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Holroyd, Christopher R.
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Carter, Sarah A
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Crozier, Sarah
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D'angelo, Stefania
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Curtis, Elizabeth
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Moon, Rebecca
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Davies, Justin
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Ward, Kate
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Dennison, Elaine
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Inskip, Hazel
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Godfrey, Keith
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Cooper, Cyrus
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Harvey, Nicholas
ce487fb4-d360-4aac-9d17-9466d6cba145

Holroyd, Christopher R., Carter, Sarah A, Crozier, Sarah, D'angelo, Stefania, Curtis, Elizabeth, Moon, Rebecca, Davies, Justin, Ward, Kate, Dennison, Elaine, Inskip, Hazel, Godfrey, Keith, Cooper, Cyrus and Harvey, Nicholas (2021) Differential relationships between parent-child DXA and pQCT bone measures: Results from the Southampton women’s survey. Bone, 153, [116134]. (doi:10.1016/j.bone.2021.116134).

Record type: Article

Abstract

AIM: To investigate the associations between indices of bone health in childhood and corresponding parental measures.

METHODS: The Southampton Women's Survey characterised 12,583 non-pregnant women aged 20-34 years; 3158 subsequently had singleton live births. In a subset, dual-energy X-ray absorptiometry (DXA) measurements of bone area (BA), bone mineral content (BMC) and areal bone mineral density (aBMD) lumbar spine and total hip were obtained in the parent/offspring (aged 8-9 years) trios. Another subset of children (aged 6-7 years), and their parents, had peripheral quantitative computed tomography (pQCT; 4% and 38% tibia) measures. Using multivariable linear regression we examined relationships between mother/father and offspring, adjusting for parental age, habitual walking speed and education; offspring age and sex; and the corresponding bone measure in the other parent (β-coefficients (95%CI) unit/unit for each bone measure).

RESULTS: Data were available for 260 trios with DXA and 99 with pQCT. There were positive associations for BA, BMC and aBMD between either parent and offspring. Mother-child associations were of greater magnitude than father-child; for example, mother-child aBMD (β = 0.26 g·cm -2/g·cm -2 (0.21,0.32)) and father-child aBMD (β = 0.16 g·cm -2/g·cm -2 (0.11,0.21)), P-difference in β = 0.007. In the subset with pQCT there was a positive association for mother-offspring 4% tibial total area (β = 0.33 mm 2/mm 2 (0.17,0.48)), but little evidence of a father-offspring association (β = -0.06 mm 2/mm 2 (-0.17,0.06)). In contrast offspring 38% cortical density was more strongly associated with this measure in fathers (β = 0.48 mg·cm -3/mg·cm -3 (0.15,0.82)) than mothers (β = 0.27 mg·cm -3/mg·cm -3 (-0.03,0.56)). In general mother-father differences were attenuated by adjustment for height.

CONCLUSIONS: Whilst offspring bone measures are independently associated with those of either parent, the magnitude of the association is often greater for maternal than paternal relationships. These findings are consistent with an in utero influence on offspring growth but might also reflect genetic and/or epigenetic parent of origin effects.

SUMMARY: In an established parent-offspring cohort, associations between parent and offspring bone indices were generally greater in magnitude for mother-offspring than father-offspring relationships.

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CH Parent child bone 2021_07_12 R1 clean - Accepted Manuscript
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Accepted/In Press date: 24 July 2021
e-pub ahead of print date: 29 July 2021
Published date: December 2021
Additional Information: Acknowledgements We thank the administrative staff, research nurses and participants of the SWS for their contributions. CRH and SC are joint first author. CC and NCH are joint senior author. This work was supported by grants from Medical Research Council (MRC) [4050502589 (MRC LEU)], 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. EMC has been supported by the Wellcome Trust (201268/Z/ 16/Z) and an NIHR Clinical Lectureship. KMG is supported by the Na-tional Institute for Health Research (NIHR) Senior Investigator (NF-SI- 0515-10042), the European Union (Erasmus+Programme ImpENSA 598488-EPP-1-2018-1-DE-EPPKA2-CBHE-JP) the British Heart Foun-dation (RG/15/17/3174) and the US National Institute On Aging of the National Institutes of Health (Award No. U24AG047867). 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), 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.
Keywords: BMD, Developmental origins, Epidemiology, Mother-offspring, Osteoporosis

Identifiers

Local EPrints ID: 450700
URI: http://eprints.soton.ac.uk/id/eprint/450700
ISSN: 8756-3282
PURE UUID: 2e6b77a2-466f-4573-93f2-7e86de2d602e
ORCID for Sarah Crozier: ORCID iD orcid.org/0000-0002-9524-1127
ORCID for Stefania D'angelo: ORCID iD orcid.org/0000-0002-7267-1837
ORCID for Elizabeth Curtis: ORCID iD orcid.org/0000-0002-5147-0550
ORCID for Kate Ward: ORCID iD orcid.org/0000-0001-7034-6750
ORCID for Elaine Dennison: ORCID iD orcid.org/0000-0002-3048-4961
ORCID for Hazel Inskip: ORCID iD orcid.org/0000-0001-8897-1749
ORCID for Keith Godfrey: ORCID iD orcid.org/0000-0002-4643-0618
ORCID for Cyrus Cooper: ORCID iD orcid.org/0000-0003-3510-0709
ORCID for Nicholas Harvey: ORCID iD orcid.org/0000-0002-8194-2512

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Date deposited: 06 Aug 2021 16:32
Last modified: 18 Mar 2024 05:11

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Contributors

Author: Christopher R. Holroyd
Author: Sarah A Carter
Author: Sarah Crozier ORCID iD
Author: Stefania D'angelo ORCID iD
Author: Rebecca Moon
Author: Justin Davies
Author: Kate Ward ORCID iD
Author: Elaine Dennison ORCID iD
Author: Hazel Inskip ORCID iD
Author: Keith Godfrey ORCID iD
Author: Cyrus Cooper ORCID iD
Author: Nicholas Harvey ORCID iD

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