Journal
ARCHIVES OF OSTEOPOROSIS
Volume 16, Issue 1, Pages -Publisher
SPRINGER LONDON LTD
DOI: 10.1007/s11657-021-01023-3
Keywords
Vitamin D; Pregnancy; Bone; Child; Fracture; 25(OH)D
Categories
Funding
- National Health and Medical and Research Council (NHMRC), Australia
- Bupa Health Foundation
- Deakin University
- Alfred Deakin Postdoctoral Research Fellowships (Deakin University)
- NHMRC Emerging Leadership Fellowship [1174060]
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Research suggests that maternal 25(OH)D levels at different stages of pregnancy may have gender-specific effects on offspring fracture risk, with higher levels in early gestation associated with lower risk in boys and higher levels in late gestation associated with increased risk in girls.
A Summary Vitamin D is important for bone health and strength. Previous studies report 25-hydroxyvitamin D (25(OH)D) exposure during pregnancy may impact offspring bone health later in life. In this study, maternal 25(OH)D at recruitment was associated with a lower fracture risk in boys and an increased fracture risk in girls at 28-32 weeks gestation. Purpose Maternal 25-hydroxyvitamin D (25(OH)D) in pregnancy has been shown to be associated with offspring bone measures in some studies, but few have examined fracture risk. We aimed to determine associations between maternal vitamin D status and offspring fracture risk. Methods In total, 475 mother-child pairs participating in the Vitamin D in Pregnancy study in southeastern Australia were recruited. Maternal serum samples were taken at recruitment (<16 weeks gestation) and/or 28-32 weeks gestation and analysed for 25(OH)D. Incident fractures in children were ascertained from date of birth (2002-2004) until December 31, 2012. Cox proportional hazard models included maternal age at recruitment, offspring sex, birth weight, gestation length and season of vitamin D sample. Results Complete follow-up data were available for 400 children (median age= 9.5 years). There were 68 (17.0%) children who sustained at least one fracture. Higher maternal 25(OH)D (per 10 nmol/L) in early gestation was weakly associated with a decreased fracture risk in boys (HR 0.82; 95% CI 0.68, 0.99; p= 0.048) but not girls (HR 1.10; 95% CI 0.98, 1.25; p= 0.11). At late gestation, higher maternal 25(OH)D was associated with increased fracture risk in girls (HR 1.11; 95% CI 1.01, 1.23; p= 0.038) but not boys (HR 0.94; 95% CI 0.80, 1.10; p= 0.42). No statistically significant relationships were detected in analyses investigating 25(OH)D as a categorical variable. Conclusion There is some evidence that higher maternal 25(OH)D at recruitment was associated with lower fracture risk in boys, while higher maternal 25(OH)D at 28-32 weeks gestation was associated with an increased fracture risk in girls.
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