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Updated: Jul 7, 2026

Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Paternal skeletal size predicts intrauterine bone mineral accrual
N C Harvey1, M K Javaid, J R Poole
1Medical Research Council Epidemiology Resource Centre, University of Southampton, and Southampton General Hospital, Southampton, United Kingdom.
Insights
Fathers’ bone mass significantly predicts their daughters’ bone size and density, independent of maternal factors. This paternal influence on skeletal development is stronger in female infants than in males.
Area of Science:
- Human genetics
- Pediatrics
- Bone health
Background:
- Maternal factors influence neonatal bone accrual.
- Paternal determinants of neonatal bone mass remain largely unknown.
Purpose of the Study:
- To investigate the relationship between paternal bone mass and offspring bone mass.
- To explore parental determinants of neonatal bone mass.
Main Methods:
- 278 pregnancies were recruited from the Southampton Women's Survey.
- Neonates and fathers underwent whole body dual-x-ray absorptiometry (DXA).
- Correlation and regression analyses were used.
Main Results:
- Significant positive associations were found between paternal and female infant bone indices (bone area, bone mineral content, bone mineral density).
- These associations were independent of maternal height and fat stores.
- Associations were not statistically significant for male infants.
Conclusions:
- Paternal skeletal size predicts offspring skeletal size more strongly in female than male infants.
- Paternal genotype is important in understanding the developmental origins of osteoporotic fracture.
- Gender-specific influences on intrauterine bone accrual warrant further investigation.
Background:
We have previously demonstrated that maternal body build and lifestyle factors predict neonatal bone mineral accrual. However, the paternal determinants of neonatal bone mass are not known. In this study we explored the relationship between a father's bone mass and that of his offspring.
Methods:
A total of 278 pregnancies (142 male and 136 female neonates) were recruited from the Southampton Women's Survey, a unique, well-established cohort of women, aged 20-34 yr, who had been assessed before and during pregnancy. The neonates and their fathers underwent whole body dual-x-ray absorptiometry (DXA) within 2 wk of birth using a Lunar DPX (General Electric Corp., Madison, WI) and Hologic Discovery instrument (Hologic Inc., Bedford, MA), respectively; correlation and regression methods were used to explore the parental determinants of neonatal bone mass.
Results:
After adjusting the paternal DXA indices for father's age and the neonatal for baby's gestational age and age at DXA scan, there were highly significant positive associations between baby's whole body bone area, bone mineral content, and bone mineral density and the corresponding indices in the father (P = 0.003, 0.0002, 0.046, respectively) among female infants. These relationships were independent of maternal height and fat stores. The associations for male infants with paternal DXA indices did not achieve statistical significance.
Conclusions:
The father's skeletal size predicts skeletal size more strongly in female than male offspring, independently of the mother's body build. These data point toward the importance of considering paternal genotype in studies exploring the developmental origins of osteoporotic fracture and raise intriguing mechanistic questions about the gender specificity of influences on intrauterine bone mineral accrual.
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